<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">JTR</journal-id><journal-title-group><journal-title>Journal of Tuberculosis Research</journal-title></journal-title-group><issn pub-type="epub">2329-843X</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/jtr.2015.34024</article-id><article-id pub-id-type="publisher-id">JTR-62095</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject><subject> Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Natural Remedies against Multi-Drug Resistant &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt;
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>amesh</surname><given-names>Pandit</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pawan</surname><given-names>Kumar Singh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Vipin</surname><given-names>Kumar</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Value Addition Research and Development Department-Human Health, National Innovation Foundation (NIF)-India, Ahmedabad, India</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>pawan@nifindia.org(PKS)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>30</day><month>10</month><year>2015</year></pub-date><volume>03</volume><issue>04</issue><fpage>171</fpage><lpage>183</lpage><history><date date-type="received"><day>3</day>	<month>November</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>18</month>	<year>December</year>	</date><date date-type="accepted"><day>22</day>	<month>December</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Tuberculosis (TB), caused by 
  Mycobacterium tuberculosis is an infectious deadly disease and the treatment of which is one of the most severe challenges at the global level. Currently more than 20 chemical medications are described for the treatment of TB. Regardless of availability of several drugs to treat TB, the causative agent, 
  M. tuberculosis is nowadays getting resistant toward the conventional drugs and leading to conditions known as Multidrug-resistant tuberculosis (MDR-TB) and extensively drug resistant tuberculosis (XDR-TB). This situation has terrified the global health community and raised a demand for new anti-tuberculosis drugs. Medicinal plants have been used to cure different common as well as lethal diseases by ancient civilizations due to its virtue of variety of chemical compounds which may have some important remedial properties. The aim of the present review is to focus the anti-tubercular medicinal plants native to India as well as the plants effective against MDR or XDR-TB across the globe. In the present review, we have addressed 25 medicinal plants for TB and 16 plants effective against MDR-TB testified from India and 23 herbal plants described for MDR-TB across the world during 2011-2015. These herbal plants can serve as promising candidates for developing novel medications to combat multidrug resistant 
  M. tuberculosis.
 
</p></abstract><kwd-group><kwd>Drug Resistant</kwd><kwd> &lt;i&gt;Mycobacterium tuberculosis&lt;/i&gt;</kwd><kwd> Medicinal Plants</kwd><kwd> MDR or XDR-TB</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Tuberculosis (TB), an infectious deadly disease caused by the various species of Mycobacterium, especially Mycobacterium tuberculosis, was emerged from East Africa more than three million years ago [<xref ref-type="bibr" rid="scirp.62095-ref1">1</xref>] .</p><p>According to World Health Organization (WHO), TB is the second most fatal disease after HIV, accountable for human death across the globe and about one third of human population is estimated to be infected with M. tuberculosis. However, it is not necessary that all infected person may get the tuberculosis. The carrier stage is called latent tuberculosis, in which M. tuberculosis infected person does not show any symptoms of disease. Still, about 5% to 10% of the infected people have a chance to develop TB, depending upon the immunity of the individual. Around 6.1 million TB patients have been reported in year 2013, of these, about 5.7 million (93%) cases were new. About 9 million people were reported ill due to TB in 2013, of which approximately 1.5 million died due to the disease (<xref ref-type="fig" rid="fig1">Figure 1</xref>) [<xref ref-type="bibr" rid="scirp.62095-ref2">2</xref>] . The disease is highly progressive in Asia and Africa and more than 80% of all TB cases were reported from these two continents [<xref ref-type="bibr" rid="scirp.62095-ref3">3</xref>] . When we talk about Indian scenario, one report said that TB was reported about 3300 years ago [<xref ref-type="bibr" rid="scirp.62095-ref4">4</xref>] while according to ancient literature [<xref ref-type="bibr" rid="scirp.62095-ref5">5</xref>] TB have been reported since 1500BC. Treatment of TB is one of the most severe challenges at the global level. Presently, there are more than 20 drugs which are described for the treatment of TB [<xref ref-type="bibr" rid="scirp.62095-ref6">6</xref>] among them. Isoniazid, rifampin, ethambutol, pyrazinamide and streptomycin are most commonly used.</p><p>However, recent few years have revealed that the causative agent of Tuberculosis, M. tuberculosis is getting resistant towards conventional drugs used for treatment. The development of drug-resistant in M. tuberculosis has frightened the global health community [<xref ref-type="bibr" rid="scirp.62095-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref9">9</xref>] . Multidrug-resistant tuberculosis (MDR-TB) is a condition where the M. tuberculosis strain is resistant to two most frequently used drugs i.e. first-line oral (<xref ref-type="table" rid="table1">Table 1</xref>) specifically isoniazid, rifampicin and it was first developed in USA during 1990s [<xref ref-type="bibr" rid="scirp.62095-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref11">11</xref>] . The improper use of antimicrobial drugs, early treatment cessation, genetic mutation in M. tuberculosis, an inadequate administered treatment, etc. may cause drug resistance [<xref ref-type="bibr" rid="scirp.62095-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref13">13</xref>] which can then be transmitted to other people in the community. Among all, genetic mutation is the most important cause for the MDR-TB and 7 hotspots loci have been identified across the chromosome which includes RNA polymerase beta subunit gene, rpoB (rifampicin), nicotinamidase, pncA (pyrazinamide), catalase-peroxidase gene, katG (isoniazid); inhibin alpha, mabA(fabG1)-inhA (isoniazid), DNA gyrase subunit A&amp;B (quinolone), and 16S rRNA gene, rrs (streptomycin) [<xref ref-type="bibr" rid="scirp.62095-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref15">15</xref>] . According to WHO, around 480,000 cases of MDR-TB were reported in 2013-14 and between 20% to 30% of the new cases were from Soviet Union countries. MDR-TB treatment requires the use of second-line drugs (SLDs), which are less effective [<xref ref-type="bibr" rid="scirp.62095-ref6">6</xref>] and highly expensive compared to first-line drugs [<xref ref-type="bibr" rid="scirp.62095-ref16">16</xref>] . Other drugs which are recommended for TB treatment includes sulfamethoxazole and mefloquine, however, both the drugs require further validation [<xref ref-type="bibr" rid="scirp.62095-ref17">17</xref>] . Recently two new anti-TB drugs, bedaquiline which affects the proton pump for ATP synthase and delamanid which blocks the synthesis of mycolic acids have been approved by the US Food and Drug Administration and European Medicines Agency [<xref ref-type="bibr" rid="scirp.62095-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref19">19</xref>] . Together with MDR-TB, XDR-TB (extensively drug resistant tuberculosis) has also been described where M. tuberculosis is resistant to at least four of the core anti-</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Percentage of new TB cases with MDT-TB in 2013-2014 [<xref ref-type="bibr" rid="scirp.62095-ref7">7</xref>] </title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/8-1130121x7.png"/></fig><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> First and second line recommended by WHO [<xref ref-type="bibr" rid="scirp.62095-ref7">7</xref>] </title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Group</th><th align="center" valign="middle" >Drug</th></tr></thead><tr><td align="center" valign="middle" >First-line oral</td><td align="center" valign="middle" >Isoniazid, Rifampicin, Ethambutol, Pyrazinamide, Rifabutin and Rifapentine</td></tr><tr><td align="center" valign="middle" >Injectables</td><td align="center" valign="middle" >Streptomycin, Kanamycin, Amikacin and Capreomycin</td></tr><tr><td align="center" valign="middle" >Fluoroquinolones</td><td align="center" valign="middle" >Levofloxacin, Moxifloxacin, Gatifloxacin and Ofloxacin</td></tr><tr><td align="center" valign="middle" >Oral bacteriostatic second-line anti-TB drugs</td><td align="center" valign="middle" >Ethionamide, Prothionamide, Cycloserine, Terizidone, p-Aminosalicylic acid and p-Aminosalicylate sodium</td></tr><tr><td align="center" valign="middle" >Anti-TB drugs with limited data on efficacy and/or long-term safety in the treatment of drug-resistant TB</td><td align="center" valign="middle" >Linezolid, Clofazimine, Amoxicillin/clavulanate, Imipenem/cilastatin, Meropenem, High-dose isoniazid, Thioacetazone, Clarithromycin, Bedaquiline and Delamanid</td></tr><tr><td align="center" valign="middle" >Other drugs (need clinical trials)</td><td align="center" valign="middle" >Sulfamethoxazole, Mefloquine, Pretomanid, Sutezolid, SQ109 and Benzothiazinones</td></tr></tbody></table></table-wrap><p>TB drugs including, isoniazid, rifampicin and any of the fluoroquinolones and to one of the three injectable second line drugs (<xref ref-type="table" rid="table1">Table 1</xref>). Nowadays completely drug?resistant Mycobacterium tuberculosis strains have also been evolved which are resistant to all the first and second line drugs used for TB treatment [<xref ref-type="bibr" rid="scirp.62095-ref20">20</xref>] - [<xref ref-type="bibr" rid="scirp.62095-ref22">22</xref>] . Types of report have directed attention of researchers worldwide to find a novel potent drug molecule for the treatment of TB. Recently, [<xref ref-type="bibr" rid="scirp.62095-ref23">23</xref>] researchers have reviewed new drugs for tuberculosis including PA-824 (Nitroimidazole), Linezolid (Oxazolidinones), Sutezolid (Oxazolidinones), AZD5847 (Oxazolidinones) and SQ109 (1,2-diamine). Most of these drugs are under the clinical trial phase II. Therefore, there is an urgent demand to find out some potential anti-tuberculosis medicines which are effective against the resistant deadly strains. As usual, the “hope for the best” is the natural system and generally mankind is always looking into actinomycetes [<xref ref-type="bibr" rid="scirp.62095-ref24">24</xref>] - [<xref ref-type="bibr" rid="scirp.62095-ref26">26</xref>] , fungi [<xref ref-type="bibr" rid="scirp.62095-ref27">27</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref28">28</xref>] , cyanobactria [<xref ref-type="bibr" rid="scirp.62095-ref29">29</xref>] and plants [<xref ref-type="bibr" rid="scirp.62095-ref30">30</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref31">31</xref>] for the new drug molecules. Various drugs have already been identified and still being identified from the natural resources by the mankind.</p><p>Further, the interest in herbal medications is due to adverse effect of chemical based anti-TB drugs on the patients, who generally have to administer the drug for longer durations. The adverse effects of first-line oral and second line drugs are summarized in the <xref ref-type="table" rid="table2">Table 2</xref>. According to one survey in India, the adverse drug reactions during MDR-TB treatment ranges from 57.14% to 94.3% and the most common adversarial effect was found to be gastrointestinal problems (71.7%) [<xref ref-type="bibr" rid="scirp.62095-ref32">32</xref>] . In contrast to this, herbal medicines are naturally occurring chemical compounds which can be administrated in the form of whole plant or it particular part. The advantages of herbal medications are fewer side effects, affectivity in multiple diseases as they are crude mixture of many plant compounds and are low cost.</p></sec><sec id="s2"><title>2. Medicinal Plants for Tuberculosis</title><p>The significance of plants has been recognized and documented since ancient time due to virtue of its variety of chemical compounds, which may have some important medicinal properties that can be used to cure diverse diseases. Medicinal plants have been widely used as preventives and curative solutions against different common as well as lethal diseases by ancient cultures. There are some prehistoric data available, in which recipes for medicine preparation from the plants have been discussed [<xref ref-type="bibr" rid="scirp.62095-ref35">35</xref>] - [<xref ref-type="bibr" rid="scirp.62095-ref38">38</xref>] . The World Health Organization (WHO) estimated that about 80 percent of world’s population still relied on traditional medicinal plants for their primary health care. The uses of herbs and herbal products have been broadly being accepted in our modern way of life. Moreover [<xref ref-type="bibr" rid="scirp.62095-ref39">39</xref>] , the majority of new drugs introduced in the United States are derived primarily from the plants. As discussed, most of the chemical drugs cause adverse effects and are costlier, therefore, nowadays there is an increasing inclinations towards the use of an alternative source of medicine, especially based on medicinal plants [<xref ref-type="bibr" rid="scirp.62095-ref40">40</xref>] . A number of medicinal plants have been reported for anti-mycobacterial activity across the globe [<xref ref-type="bibr" rid="scirp.62095-ref41">41</xref>] - [<xref ref-type="bibr" rid="scirp.62095-ref46">46</xref>] .</p><p>Ayurveda, means the science of life (Ayur = Life, Veda = Science), is an ancient medical knowledge which was developed in India thousands of years ago and describes numerous plants to treat several diseases. When we particularly talk about TB, more than 250 medicinal plants from India have been reported [<xref ref-type="bibr" rid="scirp.62095-ref47">47</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref48">48</xref>] . The comprehensive safety, toxicity and clinical studies are needed for these plants before using them effectively as curative and/or preventive medications against TB. <xref ref-type="table" rid="table3">Table 3</xref> summarizes the Indian plants reported for anti-mycoba- cterial activity during last 5 (2011-2015) years.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Adversarial effects of commonly used anti-mycobacterial drugs [<xref ref-type="bibr" rid="scirp.62095-ref33">33</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref34">34</xref>] </title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Group</th><th align="center" valign="middle" >Drug</th><th align="center" valign="middle" >Adverse effects</th></tr></thead><tr><td align="center" valign="middle"  rowspan="4"  >First-line oral</td><td align="center" valign="middle" >Isoniazid</td><td align="center" valign="middle" >Nausea, vomiting, epigastric pain, hepatotoxic, psychosis, convulsive seizures, mental confusion, and coma etc.</td></tr><tr><td align="center" valign="middle" >Rifampin</td><td align="center" valign="middle" >Exanthema, hepatotoxicity, immunological reactions, nausea, anorexia, abdominal pain, fatigue, dizziness, headache, dyspnea, and ataxia etc.</td></tr><tr><td align="center" valign="middle" >Pyrazinamide</td><td align="center" valign="middle" >Nausea, vomiting, anorexia, severe exanthema, pruritus, rhabdomyolysis with myoglobinuria, kidney failure, acute arthritis in gouty individuals and hepatotoxicity.</td></tr><tr><td align="center" valign="middle" >Ethambutol</td><td align="center" valign="middle" >Retrobulbar neuritis, nausea, vomiting, abdominal pain, hepatotoxicity, hematological symptoms, hematological symptoms and hypersensitivity etc.</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >Second-line drugs</td><td align="center" valign="middle" >Aminoglycosides</td><td align="center" valign="middle" >Ototoxic, neurotoxic, nephrotoxic, neuromuscular blockage and hypersensitivity.</td></tr><tr><td align="center" valign="middle" >Fluoroquinolones</td><td align="center" valign="middle" >Affects that gastrointestinal, central nervous system, musculoskeleta, cardiovascular system, urinary tract, endocrine system and also cause skin reactions and allergies.</td></tr><tr><td align="center" valign="middle" >Oral bacteriostatic second-line anti-TB drugs</td><td align="center" valign="middle" >Neurological adverse effects (headache, vertigo, dysarthriasomnolence, convulsion, mental confusion, and memory deficit) and psychiatric adverse effects (psychotic states with catatonic, paranoid, and depressive reactions, with a risk of suicide.</td></tr></tbody></table></table-wrap><table-wrap-group id="3"><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Indian medicinal plants possessing anti-mycobacterial activity (Reported during 2011-2015)</title></caption><table-wrap id="3_1"><table><tbody><thead><tr><th align="center" valign="middle" >Plant name (Botanical)</th><th align="center" valign="middle" >Family</th><th align="center" valign="middle" >Part Used</th><th align="center" valign="middle" >Solvent used for extraction</th><th align="center" valign="middle" >Chemical constituents</th><th align="center" valign="middle" >Anti-TB activity/MIC values</th><th align="center" valign="middle" >Reference</th></tr></thead><tr><td align="center" valign="middle" >Mallotus philippensis (Linn.) Muell Arg.</td><td align="center" valign="middle" >Euphorbiaceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle" >First in 95% ethanol, than fractionation using t hexane, chloroform, ethyl acetate and metahnol</td><td align="center" valign="middle" >Ursolic acid and β-sitosterol</td><td align="center" valign="middle" >MIC for M. tuberculosis H<sub>37</sub>Rv and M. tuberculosis H<sub>37</sub>Ra is 0.25 and 0.125 mg/mL respectively in ethyl acetate fraction</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref49">49</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref50">50</xref>]</td></tr><tr><td align="center" valign="middle" >Vetiveria zizanioides L. Nash</td><td align="center" valign="middle" >Poaceae</td><td align="center" valign="middle" >Roots</td><td align="center" valign="middle" >Hexane, ethyl acetate and methanol fractions from ethanolic extract</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >MIC of the ethanolic extract of intact as well as spent root is 500 μg/mL whereas for the hexane fraction it is 50 μg/mL against M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref51">51</xref>]</td></tr><tr><td align="center" valign="middle" >Withania somnifera (Linn.)</td><td align="center" valign="middle" >Solanaceae</td><td align="center" valign="middle" >Fresh leaves and roots</td><td align="center" valign="middle" >Water</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >1.0 mg/mL - 64.47% and 0.01 mg/mL - 17.88% inhibition of M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref52">52</xref>]</td></tr><tr><td align="center" valign="middle" >Piper nigrum L.</td><td align="center" valign="middle" >Piperaceae</td><td align="center" valign="middle" >Seeds</td><td align="center" valign="middle" >Acetone, ethanol and distilled water</td><td align="center" valign="middle" >Piperine</td><td align="center" valign="middle" >MIC of acetone extract is 100 &#181;g/mL and combination of acetone and ethanol extracts is 50 &#181;g/mL against M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref53">53</xref>]</td></tr><tr><td align="center" valign="middle" >Alstonia scholaris</td><td align="center" valign="middle" >Apocynaceae</td><td align="center" valign="middle" >Bark, flower, fruit and leaf</td><td align="center" valign="middle" >Ethyl acetate, butanol and water</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >MIC of butanol extracts of flower and bark is of 500 and 100 &#181;g/mL respectively against M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref54">54</xref>]</td></tr><tr><td align="center" valign="middle" >Acacia catechu (L.) Willd</td><td align="center" valign="middle" >Mimosaceae</td><td align="center" valign="middle" >Roots</td><td align="center" valign="middle"  rowspan="5"  >Sequentially extracted in water, ethanol, chloroform and hexane</td><td align="center" valign="middle"  rowspan="5"  >Need to be identify</td><td align="center" valign="middle"  rowspan="5"  >Most potent anti-mycobacterium activity shown by ethanol extracts of A. paniculata and A. catechu with MIC value 2.5 &#177; 1.45 mg/mL (5.0 mg/mL by [<xref ref-type="bibr" rid="scirp.62095-ref55">55</xref>] followed by chloroform extract of A. paniculata and ethanol extract of D. metel (05 &#177; 1.24 mg/mL) against M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.62095-ref55">55</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref56">56</xref>]</td></tr><tr><td align="center" valign="middle" >Ailanthus excels Roxb.</td><td align="center" valign="middle" >Simaroubaceae</td><td align="center" valign="middle" >Roots</td></tr><tr><td align="center" valign="middle" >Aegle marmelos Corr.</td><td align="center" valign="middle" >Rutaceae</td><td align="center" valign="middle" >Leaf</td></tr><tr><td align="center" valign="middle" >Andrographis paniculata Nees.</td><td align="center" valign="middle" >Acanthaceae</td><td align="center" valign="middle" >Leaf</td></tr><tr><td align="center" valign="middle" >Datura metel L.</td><td align="center" valign="middle" >Solanaceae</td><td align="center" valign="middle" >Leaf</td></tr><tr><td align="center" valign="middle" >Vitex trifolia L. (syn. Vitex rotundifolia</td><td align="center" valign="middle" >Verbenaceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle" >Cold methanol followed by fractionation in hexane, chloroform and n-butanol</td><td align="center" valign="middle" >Compound-1: 13-hydroxy-5(10), 14-halimadien-6-one Compound-2: 6α,7α-diacetoxy-13-hydroxy-8(9),14-labdadiene Compound-3: 9-hydroxy-13(14)-labden-15, 16-olide) and Compound-4: Isoambreinolide</td><td align="center" valign="middle" >MIC for compound 3 and 4 is 100 and 25 μg/mL respectively against M. tuberculosis HRv (ATCC27294)</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref57">57</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="3_2"><table><tbody><thead><tr><th align="center" valign="middle" >Allium sativum</th><th align="center" valign="middle" >Amaryllidaceae</th><th align="center" valign="middle" >Bulb</th><th align="center" valign="middle"  rowspan="3"  >Petroleum ether, ethyl acetate and chloroform</th><th align="center" valign="middle"  rowspan="3"  >Either fats and fixed oils or phenol and aryl amine derivative</th><th align="center" valign="middle"  rowspan="3"  >MIC of Acalyphaindica, Adhatodavasica andAllium sativum is 5, 10 and 1.25 mg/mL respectively (80 mg/mL of garlic oil against M. tuberculosis HRv<sub>37</sub> [<xref ref-type="bibr" rid="scirp.62095-ref58">58</xref>]</th><th align="center" valign="middle"  rowspan="3"  >[<xref ref-type="bibr" rid="scirp.62095-ref58">58</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref59">59</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Acalypha indica</td><td align="center" valign="middle" >Euphorbiaceae</td><td align="center" valign="middle" >Leaves</td></tr><tr><td align="center" valign="middle" >Adhatoda vasica</td><td align="center" valign="middle" >Acanthaceae</td><td align="center" valign="middle" >Leaves</td></tr><tr><td align="center" valign="middle" >Actiniopteris radiata Linn.</td><td align="center" valign="middle" >Actiniopteridaceae</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle" >n-Hexane, chloroform and ethanol</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >MIC of n-Hexane, chloroform and ethanolic extracts was 12.5, 3.125, 25 &#181;g/mL respectively against M. tuberculosis H<sub>37</sub>RV</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref60">60</xref>]</td></tr><tr><td align="center" valign="middle" >Syzygium aromaticum</td><td align="center" valign="middle" >Fabaceae</td><td align="center" valign="middle" >Buds</td><td align="center" valign="middle"  rowspan="5"  >Hexane, acetone and methanol</td><td align="center" valign="middle" >Terpenoids, alkaloids, flavonoids and saponins</td><td align="center" valign="middle"  rowspan="5"  >Lowest MIC was of metahnol extract of Syzygium aromaticum, 0.8 &#181;g/mL against M. tuberculosis H<sub>37</sub>RV</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.62095-ref61">61</xref>]</td></tr><tr><td align="center" valign="middle" >Piper nigrum</td><td align="center" valign="middle" >Piperaceae</td><td align="center" valign="middle" >Seeds</td><td align="center" valign="middle" >Alkaloids and carbohydrates</td></tr><tr><td align="center" valign="middle" >Glycyrrhiza glabra</td><td align="center" valign="middle" >Fabaceae</td><td align="center" valign="middle" >Rhizome</td><td align="center" valign="middle" >Terpenoids, alkaloids, flavonoids, Saponins and carbohydrates</td></tr><tr><td align="center" valign="middle" >Aegele marmelos</td><td align="center" valign="middle" >Rutaceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle" >Terpenoids, alkaloids and flavonoids</td></tr><tr><td align="center" valign="middle" >Lawsonia inermis</td><td align="center" valign="middle" >Lythraceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle" >Terpenoids, alkaloids, flavonoids and saponins</td></tr><tr><td align="center" valign="middle" >Strophanthus wallichii</td><td align="center" valign="middle" >Apocynaceae</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle" >Methanol</td><td align="center" valign="middle" >2-hydroxy-4-methoxy-benzaldehyde</td><td align="center" valign="middle" >Showed anti-tubercle activity against M. tuberculosis</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref62">62</xref>]</td></tr><tr><td align="center" valign="middle" >Quercus infectoria</td><td align="center" valign="middle" >Fagaceae</td><td align="center" valign="middle" >Seed</td><td align="center" valign="middle" >Methanol crude extract</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >The MIC of pet-ether, chloroform and methanol extracts were 12.5 μg/mL, 50 μg/mL and 100 μg/mL Potential anti-tuberculosis activity against M. tuberculosis H<sub>37</sub>RV</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref63">63</xref>]</td></tr><tr><td align="center" valign="middle" >Leucas marrubioides</td><td align="center" valign="middle" >Lamiaceae</td><td align="center" valign="middle" >Roots</td><td align="center" valign="middle" >Petroleum ether, chloroform and methanol</td><td align="center" valign="middle" >Need to be identify</td><td align="center" valign="middle" >The MIC of pet-ether, chloroform and methanol extracts were 12.5 &#181;g/mL, 50 &#181;g/mL and 100 &#181;g/mL against M. tuberculosis</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref64">64</xref>]</td></tr><tr><td align="center" valign="middle" >Cassia fistula Linn</td><td align="center" valign="middle" >Fabaceae</td><td align="center" valign="middle" >Roots</td><td align="center" valign="middle" >Petroleum ether, chloroform and ethanol (95%)</td><td align="center" valign="middle" >Alkaloids and tannins could be responsible</td><td align="center" valign="middle" >A alcoholic extract showed good activity at 12.5 &#181;g/mL against M. tuberculosis H<sub>37</sub>Rv</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref65">65</xref>]</td></tr><tr><td align="center" valign="middle" >Glycyrrhiza glabra L.</td><td align="center" valign="middle" >Fabaceae</td><td align="center" valign="middle" >Rhizomes</td><td align="center" valign="middle" >Acetone and then fractionated with n-hexane and ethyl acetate</td><td align="center" valign="middle" >Isoliquiritigenin and liquiritigenin</td><td align="center" valign="middle" >MIC 12.5 - 100 &#181;g/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref66">66</xref>]</td></tr></tbody></table></table-wrap></table-wrap-group><p>The above data shows that some plants and/or their fractions have very low MIC value (&gt;25 &#181;g/mL) (<xref ref-type="table" rid="table2">Table 2</xref>) and are effective. These plants are promising candidates to find novel medication for the treatment of TB. However, the emergence of MDR and XDR-TB has further inspired the scientific community to find novel and more potent anti-mycobacterial drug molecules. Various plants across the globe possess anti-mycobacterial activity against MDR-TB [<xref ref-type="bibr" rid="scirp.62095-ref67">67</xref>] - [<xref ref-type="bibr" rid="scirp.62095-ref70">70</xref>] . <xref ref-type="table" rid="table4">Table 4</xref> summarizes the medicinal plants having anti-mycobacterial activity against MDR-TB reported during 2011-2015 in countries other than India.</p><p>India is also one of the leading countries in herbal medicines and researchers are continuously engaged in searching novel drug molecules to combat MDR/XDR-TB. Since last few years several plants have been reported for their anti-mycobacterial activity from India (<xref ref-type="table" rid="table5">Table 5</xref>).</p><p>The review suggests that many plants either confined to India or elsewhere have the unique capability to counter the deadly tuberculosis pathogen. Some plants showed very low MIC values against the clinical isolates of MDR-M. tuberculosis and few of them were also found effective against XDR-TB. These plants surely must be chosen for further researches and attempts should be made to translate this knowledge into some potential anti-TB therapies, either curative or preventive. In some cases the active molecule(s) need to be identified and where the molecule has been identified one should go for generation of safety, efficacy, pharmacokinetics, stability, etc. data through approved clinical experiments, which are essential for drug development, regulatory approval and commercialization. In few studies, it was also observed that most of the data required by the regulatory authorities are available and if some more efforts are made to find out evidences of safety, stability, etc. then these herbal leads may be converted into an alternative and novel solutions to combat MDR and XDR-TB in future.</p></sec><sec id="s3"><title>Acknowledgements</title><p>Authors are grateful to Prof. Anil Gupta, Executive Vice Chair, National Innovation Foundation India for his</p><table-wrap-group id="4"><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Medicinal plants having anti-mycobacterial activity against MDR-TB reported during 2011-2015 in countries other than India</title></caption><table-wrap id="4_1"><table><tbody><thead><tr><th align="center" valign="middle" >Plant name (Botanical)</th><th align="center" valign="middle" >Part Used</th><th align="center" valign="middle" >Solvent used for extraction</th><th align="center" valign="middle" >Chemical constituents</th><th align="center" valign="middle" >Strain and method used</th><th align="center" valign="middle" >MIC value/Anti-TB activity</th><th align="center" valign="middle" >Reference</th></tr></thead><tr><td align="center" valign="middle" >Prunella vulgaris L.</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle" >20% ethanol</td><td align="center" valign="middle" >Identification needed</td><td align="center" valign="middle" >MDR M. tuberculosis, ELISA and RT-PCR</td><td align="center" valign="middle" >The extract of Prunella vulgaris L. can enhance the cellar immunological Function in rats.</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref71">71</xref>]</td></tr><tr><td align="center" valign="middle" >Celastrus vulcanicola</td><td align="center" valign="middle" >Dried leaves</td><td align="center" valign="middle" >Ethanol</td><td align="center" valign="middle" >Dihydro-β-agarofuransesquiter penes</td><td align="center" valign="middle" >H<sub>37</sub>Rv ATCC 27,294 and clinical isolate, strain 02TBDM039EP097. MTT assay.</td><td align="center" valign="middle" >α-Acetoxy-6β,9β-dibenzoyloxy-dihydro-β-agarofuran exhibited anti-tuberculosis activity against the MDR TB strain with a MIC value of 6.2 μg/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref72">72</xref>]</td></tr><tr><td align="center" valign="middle" >Flourensia cernua</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle" >n-hexane, ethanol, ethyl acetate, n-butanol, and methanol</td><td align="center" valign="middle" >Identification needed</td><td align="center" valign="middle" >M. tuberculosis H<sub>37</sub>Rv (ATCC 27,294 and M. tuberculosis CIBIN/UMF 15:99 MDR strain, Microplate Alamar Blue Assay (MABA)</td><td align="center" valign="middle" >Decoction of F. cernua leaves combined with n-Hex fractionation is more efficient</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref73">73</xref>]</td></tr><tr><td align="center" valign="middle" >Allium sativum</td><td align="center" valign="middle" >Cloves</td><td align="center" valign="middle" >70% ethanol</td><td align="center" valign="middle" >Identification needed</td><td align="center" valign="middle" >15 MDR and 5 non-MDR MTB isolates of M. tuberculosis</td><td align="center" valign="middle" >MIC of garlic extract was ranged from 1 to 3 mg/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref74">74</xref>] [<xref ref-type="bibr" rid="scirp.62095-ref75">75</xref>]</td></tr><tr><td align="center" valign="middle" >Aristolochia brevipes</td><td align="center" valign="middle" >Root</td><td align="center" valign="middle" >Dichloromethane</td><td align="center" valign="middle" >(1) 6α-7-dehydro-N-formylnornantenine; (2) E/Z-N-formylnornantenine; (3) 7,9-dimethoxytariacuripyrone; (4) 9-methoxytariacuripyrone; (5) aristololactam I; (6) β-sitosterol; (7) stigmasterol; and (8) 3-hydroxy-α-terpineol</td><td align="center" valign="middle" >M. tuberculosis H<sub>37</sub>Rv (27,294); isoniazid-resistant H<sub>37</sub>Rv (35,822); streptomycin-resistant H<sub>37</sub>Rv (35,820); rifampicin-resistant H<sub>37</sub>Rv (35,838), and etambutol-resistant H<sub>37</sub>Rv (35,837), Microplate Alamar Blue Assay (MABA)</td><td align="center" valign="middle" >The most active compound against all mycobacterial strains tested was the compound aristolactam I (5), with MIC values ranging between 12.5 and 25 &#181;g/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref76">76</xref>]</td></tr><tr><td align="center" valign="middle" >Tiliacora triandra</td><td align="center" valign="middle" >Roots</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref77">77</xref>]</td><td align="center" valign="middle" >Bisbenzylisoquinoline alkaloids, tiliacorinine 1), 2’-nortiliacorinine 2), and tiliacorine 3)</td><td align="center" valign="middle" >59 isolates of MDR M. tuberculosis</td><td align="center" valign="middle" >All the alkaloids showed MIC 3.1 μg/mL against most MDR-MTB isolates</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref67">67</xref>]</td></tr><tr><td align="center" valign="middle" >Humulus lupulus</td><td align="center" valign="middle" >Whole plant (stems, leaves and roots)</td><td align="center" valign="middle" >Alcohol</td><td align="center" valign="middle" >Identification needed</td><td align="center" valign="middle" >Sensitivity and resistant strains of M. tuberculosis</td><td align="center" valign="middle" >MIC is 4 and 8 mg/mL for sensitive and resistant strains respectively</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref78">78</xref>]</td></tr><tr><td align="center" valign="middle" >Citrus essential oils</td><td align="center" valign="middle" >---</td><td align="center" valign="middle" >---</td><td align="center" valign="middle" >Cold pressed terpeneless Valencia oil (CPT)</td><td align="center" valign="middle" >MTB (ATCC H<sub>37</sub>Rv), M. bovis BCG (BCG, ATCC Pasteur 35,734), M. avium (ATCC 700,898) and various clarithromycin resistant clinical isolates, M. aviumsubspecies paratuberculosis (ATCC 19,698) and various drug resistant clinical isolates of M. abscessus and M. chelonae</td><td align="center" valign="middle" >CPT demonstrated potent activity against drug-resistant strains of the M. avium complex and M. abscessus</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref79">79</xref>]</td></tr><tr><td align="center" valign="middle" >Struthanthus marginatus</td><td align="center" valign="middle" >Aerial parts</td><td align="center" valign="middle"  rowspan="2"  >Water hexane, dichloromethane, ethyl acetate and n-butanol</td><td align="center" valign="middle"  rowspan="2"  >Obtusifoliol, 3-O-n-acil-lup-20(29)-en-3β,7β,15α-triol</td><td align="center" valign="middle"  rowspan="2"  >M. tuberculosis strains H<sub>37</sub>Rv (sensitive) and ATCC 35,338 (resistant to rifampicin) by the microdilution method using resazurin as an indicator of cell viability</td><td align="center" valign="middle"  rowspan="2"  >Obtusifoliol: MIC H<sub>37</sub>Rv 50 μg/mL, MIC ATCC 35338 12.5 μg/mL; 3-O-n-acil-lup-20(29)-en-3β,7β,15α-triol: MIC H<sub>37</sub>Rv 200 μg/mL, MIC ATCC 35338 100 μg/mL</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.62095-ref68">68</xref>]</td></tr><tr><td align="center" valign="middle" >Struthanthu sconcinnus</td><td align="center" valign="middle" >Leaves</td></tr></tbody></table></table-wrap><table-wrap id="4_2"><table><tbody><thead><tr><th align="center" valign="middle" >Aristolochia taliscana</th><th align="center" valign="middle" >Roots</th><th align="center" valign="middle"  colspan="2"  >Hexane</th><th align="center" valign="middle"  colspan="3"  >(−) Licarin A</th><th align="center" valign="middle" >M. tuberculosis H<sub>37</sub>Rv or MDR. TB murine model</th><th align="center" valign="middle" >Low toxicity together with the discrete bacteriostatic activity</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref80">80</xref>]</th></tr></thead><tr><td align="center" valign="middle" >Hypericum species</td><td align="center" valign="middle" >Aerial parts</td><td align="center" valign="middle"  colspan="2"  >Ethanol</td><td align="center" valign="middle"  colspan="3"  >Identification needed</td><td align="center" valign="middle" >M. tuberculosis H<sub>37</sub>Rv (ATCC 27,294), H<sub>37</sub>Rv isoniazid-resistant (ATCC 35,822), H<sub>37</sub>Rv rifampin-resistant (ATCC 35,838), H<sub>37</sub>Rv ethambutol-resistant (ATCC 35,837), M. fortuitum, M. smegmatis (ATCC 35,798), M. avium (ATCC 35,717), M. chelonaeand four drug-resistant strains. Microplate Alamar Blue Assay (MABA)</td><td align="center" valign="middle" >Potent activity was observed from H. foliosum, H. hircinum subsp. majus, H. grandifolium, H. humifusum and H. elodeswith MICs ranging from 25 to 50 μg/mL. H. elodes and H. hircinum subsp. majus were also active against drug resistant clinical isolates with MICs ranging from 12.5 to 50 μg/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref81">81</xref>]</td></tr><tr><td align="center" valign="middle" >Chamaedorea tepejilote</td><td align="center" valign="middle"  rowspan="2"  >Aerial parts</td><td align="center" valign="middle"  colspan="2"   rowspan="2"  >Hexane</td><td align="center" valign="middle"  colspan="3"   rowspan="2"  >Ursolic and oleanolic acids</td><td align="center" valign="middle"  rowspan="2"  >M. tuberculosis H<sub>37</sub>Rv (ATCC 27294), four mono-resistant strains of M. tuberculosis H<sub>37</sub>Rv. Modified Microplate Alamar Blue Assay (MABA)</td><td align="center" valign="middle"  rowspan="2"  >Both the compounds showed MIC range from 12.5 μg/mL to<sub> </sub> 50 μg/mL<sub> </sub></td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.62095-ref82">82</xref>]</td></tr><tr><td align="center" valign="middle" >Robinia hispida</td></tr><tr><td align="center" valign="middle" >Diospyros anisandra</td><td align="center" valign="middle" >Stem bark</td><td align="center" valign="middle"  colspan="2"  >n-hexane</td><td align="center" valign="middle"  colspan="3"  >Maritinone and 3,3’-biplumbagin</td><td align="center" valign="middle" >Two strains of MTB (H<sub>37</sub>Rv) susceptible and one MDR clinical isolates. Modified Microplate Alamar Blue Assay (MABA)</td><td align="center" valign="middle" >Plumbagin and its dimers maritinone and 3,3’-biplumbagin showed the strongest activity against both MTB strains (MIC = 1.56 - 3.33 μg/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref83">83</xref>]</td></tr><tr><td align="center" valign="middle" >Ranunculi Ternati Radix</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle"  colspan="2"  >Water, 70% ethanol and water eluted part of ethanol extract</td><td align="center" valign="middle"  colspan="3"  >Identification needed</td><td align="center" valign="middle" >H<sub>37</sub>Rv (ATCC 95054), MDR-TB (2314-2) and XDR-TB strains, Vivo experiments were performed on C57BL/6 mice</td><td align="center" valign="middle" >70% ethanol eluted part of EE from D101 macroporous resin showed stronger inhibitory effect on MDR2314-2 and XDR1220. MIC 1.0 mg/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref84">84</xref>]</td></tr><tr><td align="center" valign="middle" >Chiness Herble Remidies (CHM)</td><td align="center" valign="middle"  colspan="8"  >CHM as an adjuvant to anti-TB chemotherapy may have beneficial effect for MDR-TB</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref70">70</xref>]</td></tr><tr><td align="center" valign="middle" >Andrographis paniculata</td><td align="center" valign="middle"  colspan="2"  >Herbs</td><td align="center" valign="middle"  colspan="2"   rowspan="5"  >Water, methylene chlolride, ethanol, nhexane and ethyl acetate</td><td align="center" valign="middle"  rowspan="5"  >Identification needed</td><td align="center" valign="middle"  colspan="2"   rowspan="5"  >M. tuberculosis standard strain and MDR strain. Proportion methods using Lowenstein Jensen (L-J) medium</td><td align="center" valign="middle"  rowspan="5"  >The proportion of inhibition of aqueous extract (2.5 mg/ml) of Rhoeo spathacea was 100% against M. tuberculosis H<sub>37</sub>Rv and MDR strain.</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.62095-ref85">85</xref>]</td></tr><tr><td align="center" valign="middle" >Annona muricata</td><td align="center" valign="middle"  colspan="2"  >Dried leaves</td></tr><tr><td align="center" valign="middle" >Centella asiatica</td><td align="center" valign="middle"  colspan="2"  >Whole plant</td></tr><tr><td align="center" valign="middle" >Pluchea indica</td><td align="center" valign="middle"  colspan="2"  >Dried leaves</td></tr><tr><td align="center" valign="middle" >Rhoeospathacea</td><td align="center" valign="middle"  colspan="2"  >Dried leaves</td></tr><tr><td align="center" valign="middle" >Croton tonkinensis</td><td align="center" valign="middle"  colspan="2"  >Whole plants or leaves</td><td align="center" valign="middle"  colspan="2"  >---</td><td align="center" valign="middle" >Diterpenoids including ent-kaurane, kaurane and grayanane</td><td align="center" valign="middle"  colspan="2"  >M. tuberculosis H<sub>37</sub>Ra (ATCC 27,294, H<sub>37</sub>rv (ATCC 35,835), MDR TB (KMRC 00116-00250), XDR TB (KMRC 00203-00197), (KMRC 00130-00064), (KMRC 00120-00137), (KMRC 00121-00341) and (KMRC 00122-00123, Resazurin Microtitre Assay (REMA)</td><td align="center" valign="middle" >All the di-terpenoids showed activity against susceptible and resistant strains. ent-1b,7a,14b-triacetoxykaur-16-en-15-one showed highest activity, MIC-3.125 - 6.25 &#181;g/ml for MDR and XDR strains.</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref86">86</xref>]</td></tr><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></table-wrap-group><table-wrap-group id="5"><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Indian medicinal plants effective against MDR-TB</title></caption><table-wrap id="5_1"><table><tbody><thead><tr><th align="center" valign="middle" >Plant name (Botanical)</th><th align="center" valign="middle" >Family</th><th align="center" valign="middle" >Part Used</th><th align="center" valign="middle" >Solvent used for extraction</th><th align="center" valign="middle" >Chemical constituents</th><th align="center" valign="middle" >Strain and method used</th><th align="center" valign="middle" >MIC value/Anti-TB activity</th><th align="center" valign="middle" >Reference</th></tr></thead><tr><td align="center" valign="middle" >Acalypha indica L.</td><td align="center" valign="middle" >Euphorbiaceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle"  rowspan="5"  >Water extract and pure gel of Aloe vera</td><td align="center" valign="middle"  rowspan="5"  >Identification needed</td><td align="center" valign="middle"  rowspan="5"  >Drug susceptible strain M. tuberculosis H<sub>37</sub>Rv as control, multi-drug resistant isolates DKU-156, JAL-1236 and fast growing mycobacterial pathogen M. fortuitum (TMC-1529). Lowenstein Jensen (L-J) medium and colorimetric BacT/ALERT 3D system</td><td align="center" valign="middle"  rowspan="5"  >All these plants exhibited activity against MDR isolates of M. tuberculosis.</td><td align="center" valign="middle"  rowspan="5"  >[<xref ref-type="bibr" rid="scirp.62095-ref87">87</xref>]</td></tr><tr><td align="center" valign="middle" >Adhatoda vasicaNees</td><td align="center" valign="middle" >Acanthaceae</td><td align="center" valign="middle" >Leaves</td></tr><tr><td align="center" valign="middle" >Allium cepa</td><td align="center" valign="middle" >Alliaceae</td><td align="center" valign="middle" >Bulbs</td></tr><tr><td align="center" valign="middle" >Allium sativum L.</td><td align="center" valign="middle" >Alliaceae</td><td align="center" valign="middle" >Cloves</td></tr><tr><td align="center" valign="middle" >Aloe vera L.</td><td align="center" valign="middle" >Aloaceae</td><td align="center" valign="middle" >Pure gel</td></tr><tr><td align="center" valign="middle" >Kaempferia galanga</td><td align="center" valign="middle" >Zingiberaceae</td><td align="center" valign="middle" >Rhizome</td><td align="center" valign="middle" >Ethanol</td><td align="center" valign="middle" >Ethyl p-methoxycinnamate</td><td align="center" valign="middle" >M. tuberculosis H<sub>37</sub>Ra, H<sub>37</sub>Rv, drug susceptible and multidrug resistant (MDR) clinical isolates. Resazurin Microtitre Assay (REMA)</td><td align="center" valign="middle" >MIC 0.242 - 0.485 mM</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref88">88</xref>]</td></tr><tr><td align="center" valign="middle" >Piper nigrum L.</td><td align="center" valign="middle" >Piperaceae</td><td align="center" valign="middle" >Seeds</td><td align="center" valign="middle" >Acetone, ethanol and distilled water</td><td align="center" valign="middle" >Piperine</td><td align="center" valign="middle" >Reference strain H<sub>37</sub>Rv; three susceptible (S1, S2 and S3) and three MDR (MDR1, MDR2 and MDR3. Microplate Alamar Blue Assay (MABA).</td><td align="center" valign="middle" >MIC of Acetone extract is 100 &#181;g/mL</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref53">53</xref>]</td></tr><tr><td align="center" valign="middle" >Vetiveria zizanioides</td><td align="center" valign="middle" >Poaceae</td><td align="center" valign="middle" >Fresh roots</td><td align="center" valign="middle" >Chloroform and methanol</td><td align="center" valign="middle" >5,10-pentadecadiyn-1-ol, a-curcumene, hydroxyjunipene, (?) cycloisosativene, valencine and selino 3,7 (11)-diene</td><td align="center" valign="middle" >MDR M. smegmatis. Dilution and disc diffusion method</td><td align="center" valign="middle" >All these compounds showed good MIC.</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref89">89</xref>]</td></tr><tr><td align="center" valign="middle" >Urtica dioica</td><td align="center" valign="middle" >Urticaceae</td><td align="center" valign="middle" >Leaves</td><td align="center" valign="middle"  rowspan="2"  >Hexane, methanol, ethyl acetate and chloroform</td><td align="center" valign="middle"  rowspan="2"  >Anti-tubercle activity of C. sophera may be due to presence of alkaloids or flavonoids and that of HEUD due to terpenoids.</td><td align="center" valign="middle"  rowspan="2"  >M. tuberculosis standard strain H<sub>37</sub>Rv (ATCC- 35838), MDR strains, and clinical isolates CL-1 (+3) and CL-2 (+2). A disk diffusion and broth dilution method.</td><td align="center" valign="middle"  rowspan="2"  >MIC for hexane extract of U. dioica and methanol extract of C. sophera, is 250 and 125 μg/mL respectively. Semipurified fraction F2 from MECS produced 86% inhibition against clinical isolate and 60% inhibition against MDR strain of M. tuberculosis. F18 from HEUD produced 81% inhibition against clinical isolate and 60% inhibition against MDR strain of M. tuberculosis.</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.62095-ref90">90</xref>]</td></tr><tr><td align="center" valign="middle" >Cassia sophera</td><td align="center" valign="middle" >Urticaceae</td><td align="center" valign="middle" >Dried seeds</td></tr><tr><td align="center" valign="middle" >Plumeria bicolor</td><td align="center" valign="middle" >Apocynaceae</td><td align="center" valign="middle" >Bark</td><td align="center" valign="middle" >Methanol than chloroform</td><td align="center" valign="middle" >Plumericin and iso-Plumericin</td><td align="center" valign="middle" >M. tuberculosis (H<sub>37</sub>Rv) and four multi-drug resistant (MDR) clinical isolates, Tetrazolium Microplate Assay (TEMA)</td><td align="center" valign="middle" >Plumericin showed better activity against all the four sensitive as well as MDR strains of M. tuberculosis with MIC values of 2.1 &#177; 0.12, 1.3 &#177; 0.15, 2.0 &#177; 0.07, 1.5 &#177; 0.13 &amp; 2.0 &#177; 0.14 μg/mL and MBC values of 3.6 &#177; 0.22, 2.5 &#177; 0.18, 3.8 &#177; 0.27, 2.9 &#177; 0.20 &amp; 3.7 &#177; 0.32 μg/mL than isoplumericin, respectively</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref91">91</xref>]</td></tr><tr><td align="center" valign="middle" >Ventilago madraspatana</td><td align="center" valign="middle" >Rhamnaceae</td><td align="center" valign="middle" >Stem bark</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref92">92</xref>]</td><td align="center" valign="middle" >Emodin</td><td align="center" valign="middle"  rowspan="3"  >Drug resistant clinical isolates, Tetrazolium Microplate Assay (TEMA)</td><td align="center" valign="middle"  rowspan="3"  >Among all the compounds, Plumbagin was found to be the most potent MIC 0.25 - 16 μg/mL</td><td align="center" valign="middle"  rowspan="3"  >[<xref ref-type="bibr" rid="scirp.62095-ref93">93</xref>]</td></tr><tr><td align="center" valign="middle" >Plumbago indicalinn</td><td align="center" valign="middle" >Plumbaginaceae</td><td align="center" valign="middle" >Root</td><td align="center" valign="middle"  rowspan="2"  >[<xref ref-type="bibr" rid="scirp.62095-ref94">94</xref>]</td><td align="center" valign="middle" >Plumbagin</td></tr><tr><td align="center" valign="middle" >Diospyros montanaroxb</td><td align="center" valign="middle" >Ebenaceae</td><td align="center" valign="middle" >Stem bark</td><td align="center" valign="middle" >Diosyprin</td></tr><tr><td align="center" valign="middle" >Andrographis paniculata</td><td align="center" valign="middle" >Acanthaceae</td><td align="center" valign="middle" >Whole plant</td><td align="center" valign="middle" >hexane and methanol (1:5)</td><td align="center" valign="middle" >Andrographolide</td><td align="center" valign="middle" >Drug resistant susceptible clinical isolate and M. tuberculosis H<sub>37</sub>Rv, Resazurin assay</td><td align="center" valign="middle" >The methanolic extract of A. paniculata showed maximum anti-mycobacterial activity at 250 μg/mL against all the tested strains of M. tuberculosis (H37Rv, MDR, and drug sensitive</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref95">95</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="5_2"><table><tbody><thead><tr><th align="center" valign="middle" >Punica granatum</th><th align="center" valign="middle" >Lythraceae</th><th align="center" valign="middle" >Fruit</th><th align="center" valign="middle" >Water, boiling water and Methanol</th><th align="center" valign="middle" >Identification needed</th><th align="center" valign="middle" >MDR and XDR-TB strains, Tetrazolium Microplate Assay (TEMA)</th><th align="center" valign="middle" >Methanol (M) and water (W) extracts of pomegranate fruit pericarp exhibited greater antitubercular activity (MIC 64 - 512, and 64 - 1024 mg/mL, respectively) than J, the lyophilised juice (MIC 256 - &gt;1024 mg/mL)</th><th align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.62095-ref96">96</xref>]</th></tr></thead></tbody></table></table-wrap></table-wrap-group><p>honorary guidance and encouragement for carrying out research activities.</p></sec><sec id="s4"><title>Cite this paper</title><p>RameshPandit,Pawan KumarSingh,VipinKumar, (2015) Natural Remedies against Multi-Drug Resistant Mycobacterium tuberculosis. Journal of Tuberculosis Research,03,171-183. doi: 10.4236/jtr.2015.34024</p></sec><sec id="s5"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.62095-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Gutierrez, M.C., Brisse, S., Brosch, R., Fabre, M., Omais, B., et al. (2005) Ancient Origin and Gene Mosaicism of the Progenitor of Mycobacterium tuberculosis. PLoS Pathogens, 1, e5. &lt;br /&gt;http://dx.doi.org/10.1371/journal.ppat.0010005</mixed-citation></ref><ref id="scirp.62095-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">(2014) Organization WH Global Tuberculosis Report 2014. World Health Organization, Geneva.</mixed-citation></ref><ref id="scirp.62095-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Zager, E.M. and McNerney, R. (2008) Multidrug-Resistant Tuberculosis. BMC Infectious Diseases, 8, 10. 
&lt;br /&gt;http://dx.doi.org/10.1186/1471-2334-8-10</mixed-citation></ref><ref id="scirp.62095-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Brothwell, D. and Sandison, A.T. (1967) Diseases in Antiquity. A Survey of the Diseases, Injuries and Surgery of Early Populations. Diseases in Antiquity a Survey of the Diseases, Injuries and Surgery of Early Populations.</mixed-citation></ref><ref id="scirp.62095-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Herzog, B. (1998) History of Tuberculosis. Respiration, 65, 5-15. &lt;br /&gt;http://dx.doi.org/10.1159/000029220</mixed-citation></ref><ref id="scirp.62095-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">D’Ambrosio, L., Centis, R., Sotgiu, G., Pontali, E., Spanevello, A., et al. (2015) New Anti-Tuberculosis Drugs and Regimens: 2015 Update. ERJ Open Research, 1, 00010-02015. &lt;br /&gt;http://dx.doi.org/10.1183/23120541.00010-2015</mixed-citation></ref><ref id="scirp.62095-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">WHO (2014) Global Tuberculosis Report 2014. World Health Organization, Geneva.</mixed-citation></ref><ref id="scirp.62095-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Zignol, M., Hosseini, M.S., Wright, A., Lambregts-van Weezenbeek, C., Nunn, P., et al. (2006) Global Incidence of Multidrug-Resistant Tuberculosis. Journal of Infectious Diseases, 194, 479-485. &lt;br /&gt;http://dx.doi.org/10.1086/505877</mixed-citation></ref><ref id="scirp.62095-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Control, CfD. and Prevention (2006) Emergence of Mycobacterium tuberculosis with Extensive Resistance to Second- Line Drugs—Worldwide, 2000-2004. MMWR Morbidity and Mortality Weekly Report, 55, 301.</mixed-citation></ref><ref id="scirp.62095-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Dooley, S.W., Jarvis, W.R., Marione, W.J. and Snider, D.E. (1992) Multidrug-Resistant Tuberculosis. Annals of Internal Medicine, 117, 257-259. &lt;br /&gt;http://dx.doi.org/10.7326/0003-4819-117-3-257</mixed-citation></ref><ref id="scirp.62095-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Edlin, B.R., Tokars, J.I., Grieco, M.H., Crawford, J.T., Williams, J., et al. (1992) An Outbreak of Multidrug-Resistant Tuberculosis among Hospitalized Patients with the Acquired Immunodeficiency Syndrome. New England Journal of Medicine, 326, 1514-1521. &lt;br /&gt;http://dx.doi.org/10.1056/NEJM199206043262302</mixed-citation></ref><ref id="scirp.62095-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Sharma, S. and Mohan, A. (2004) Multidrug-Resistant Tuberculosis. Indian Journal of Medical Research, 120, 354- 376.</mixed-citation></ref><ref id="scirp.62095-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">India Tuberculosis (2012) Revised National Tuberculosis Control Programme. Annual Status Report. 
&lt;br /&gt;http://www.tbcindia.nic.in/showfile.php?lid=3141</mixed-citation></ref><ref id="scirp.62095-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Ohno, H., Koga, H. and Kohno, S. (1998) Multidrug-Resistant Tuberculosis. 2. Mechanisms of Drug-Resistance in Mycobacterium tuberculosis—Genetic Mechanisms of Drug-Resistance. Kekkaku: &lt;br /&gt;[Tuberculosis], 73, 657-663.</mixed-citation></ref><ref id="scirp.62095-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Flandrois, J.P., Lina, G. and Dumitrescu, O. (2014) MUBII-TB-DB: A Database of Mutations Associated with Antibiotic Resistance in Mycobacterium tuberculosis. BMC Bioinformatics, 15, 107. 
&lt;br /&gt;http://dx.doi.org/10.1186/1471-2105-15-107</mixed-citation></ref><ref id="scirp.62095-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Diel, R., Rutz, S., Castell, S. and Schaberg, T. (2012) Tuberculosis: Cost of Illness in Germany. European Respiratory Journal, 40, 143-151. &lt;br /&gt;http://dx.doi.org/10.1183/09031936.00204611</mixed-citation></ref><ref id="scirp.62095-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Alsaad, N., van Altena, R., Pranger, A.D., van Soolingen, D., de Lange, W.C., et al. (2013) Evaluation of Co-Trimoxazole in the Treatment of Multidrug-Resistant Tuberculosis. European Respiratory Journal, 42, 504-512. 
http://dx.doi.org/10.1183/09031936.00114812</mixed-citation></ref><ref id="scirp.62095-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Skripconoka, V., Danilovits, M., Pehme, L., Tomson, T., Skenders, G., et al. (2013) Delamanid Improves Outcomes and Reduces Mortality in Multidrug-Resistant Tuberculosis. European Respiratory Journal, 41, 1393-1400. 
http://dx.doi.org/10.1183/09031936.00125812</mixed-citation></ref><ref id="scirp.62095-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Diacon, A.H., Pym, A., Grobusch, M.P., de los Rios, J.M., Gotuzzo, E., et al. (2014) Multidrug-Resistant Tuberculosis and Culture Conversion with Bedaquiline. New England Journal of Medicine, 371, 723-732. 
&lt;br /&gt;http://dx.doi.org/10.1056/NEJMoa1313865</mixed-citation></ref><ref id="scirp.62095-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Migliori, G., De Iaco, G., Besozzi, G., Centis, R. and Cirillo, D. (2007) First Tuberculosis Cases in Italy Resistant to All Tested Drugs. Euro Surveillance, 12, Article ID: E070517.</mixed-citation></ref><ref id="scirp.62095-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Udwadia, Z.F., Amale, R.A., Ajbani, K.K. and Rodrigues, C. (2012) Totally Drug-Resistant Tuberculosis in India. Clinical Infectious Diseases, 54, 579-581. http://dx.doi.org/10.1093/cid/cir889</mixed-citation></ref><ref id="scirp.62095-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Klopper, M., Warren, R.M., Hayes, C., van Pittius, N.C.G., Streicher, E.M., et al. (2013) Emergence and Spread of Extensively and Totally Drug-Resistant Tuberculosis, South Africa. Emerging Infectious Diseases, 19, 449-455. 
http://dx.doi.org/10.3201/eid1903.120246</mixed-citation></ref><ref id="scirp.62095-ref23"><label>23</label><mixed-citation publication-type="other" xlink:type="simple">Parida, S., Axelsson-Robertson, R., Rao, M., Singh, N., Master, I., et al. (2015) Totally Drug-Resistant Tuberculosis and Adjunct Therapies. Journal of Internal Medicine, 277, 388-405. &lt;br /&gt;http://dx.doi.org/10.1111/joim.12264</mixed-citation></ref><ref id="scirp.62095-ref24"><label>24</label><mixed-citation publication-type="other" xlink:type="simple">Mahajan, G.B. and Balachandran, L. (2011) Antibacterial Agents from Actinomycetes—A Review. Frontiers in Bioscience (Elite Edition), 4, 240-253.</mixed-citation></ref><ref id="scirp.62095-ref25"><label>25</label><mixed-citation publication-type="book" xlink:type="simple">Adegboye, M. and Babalola, O. (2013) Actinomycetes: A Yet Inexhaustive Source of Bioactive Secondary Metabolites. In: Mendez-Vilas, A., Ed., Microbial Pathogens and Strategies for Combating Them: Science, Technology and Education, Formatex, Badajoz, 786-795.</mixed-citation></ref><ref id="scirp.62095-ref26"><label>26</label><mixed-citation publication-type="other" xlink:type="simple">Patel, J.D., Parmar, M., Patel, P., Rohit, P., Taviyad, R., et al. (2014) Dynamism of Antimicrobial Activity of Actinomycetes—A Case Study from Undisturbed Microbial Niche. Advances in Microbiology, 4, 324-334. 
&lt;br /&gt;http://dx.doi.org/10.4236/aim.2014.46039</mixed-citation></ref><ref id="scirp.62095-ref27"><label>27</label><mixed-citation publication-type="other" xlink:type="simple">Smith, D. and Ryan, M. (2009) Fungal Sources for New Drug Discovery. Access Science, &amp;copy; McGraw-Hill Companies. 
&lt;br /&gt;http://www.accessscience.com</mixed-citation></ref><ref id="scirp.62095-ref28"><label>28</label><mixed-citation publication-type="other" xlink:type="simple">Aly, A.H., Debbab, A. and Proksch, P. (2011) Fifty Years of Drug Discovery from Fungi. Fungal Diversity, 50, 3-19. 
http://dx.doi.org/10.1007/s13225-011-0116-y</mixed-citation></ref><ref id="scirp.62095-ref29"><label>29</label><mixed-citation publication-type="other" xlink:type="simple">Singh, R.K., Tiwari, S.P., Rai, A.K. and Mohapatra, T.M. (2011) Cyanobacteria: An Emerging Source for Drug Discovery. The Journal of Antibiotics, 64, 401-412. &lt;br /&gt;http://dx.doi.org/10.1038/ja.2011.21</mixed-citation></ref><ref id="scirp.62095-ref30"><label>30</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Abdallah</surname><given-names> E.M. </given-names></name>,<etal>et al</etal>. (<year>2011</year>)<article-title>Plants: An Alternative Source for Antimicrobials</article-title><source> Journal of Applied Pharmaceutilcal Science</source><volume> 1</volume>,<fpage> 16</fpage>-<lpage>20</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.62095-ref31"><label>31</label><mixed-citation publication-type="other" xlink:type="simple">Katiyar, C., Gupta, A., Kanjilal, S. and Katiyar, S. (2012) Drug Discovery from Plant Sources: An Integrated Approach. Ayu, 33, 10-19.</mixed-citation></ref><ref id="scirp.62095-ref32"><label>32</label><mixed-citation publication-type="other" xlink:type="simple">Akshata, J., Chakrabarthy, A., Swapna, R., Buggi, S. and Somashekar, M. (2015) Adverse Drug Reactions in Management of Multi Drug Resistant Tuberculosis, in Tertiary Chest Institute. Journal of Tuberculosis Research, 3, 27-33. 
http://dx.doi.org/10.4236/jtr.2015.32004</mixed-citation></ref><ref id="scirp.62095-ref33"><label>33</label><mixed-citation publication-type="other" xlink:type="simple">Arbex, M.A., Varella Mde, C., Siqueira, H.R. and Mello, F.A. (2010) Antituberculosis Drugs: Drug Interactions, Adverse Effects, and Use in Special Situations-Part 1: First-Line Drugs. Jornal Brasileiro de Pneumologia, 36, 626-640. 
http://dx.doi.org/10.1590/S1806-37132010000500016</mixed-citation></ref><ref id="scirp.62095-ref34"><label>34</label><mixed-citation publication-type="other" xlink:type="simple">Arbex, M.A., Varella Mde, C., Siqueira, H.R. and Mello, F.A. (2010) Antituberculosis Drugs: Drug Interactions, Adverse Effects, and Use in Special Situations-Part 2: Second Line Drugs. Jornal Brasileiro de Pneumologia, 36, 641- 656. http://dx.doi.org/10.1590/S1806-37132010000500017</mixed-citation></ref><ref id="scirp.62095-ref35"><label>35</label><mixed-citation publication-type="other" xlink:type="simple">Glesinger, L. (1954) Medicine through Centuries. Zora, Zagreb, 21-38.</mixed-citation></ref><ref id="scirp.62095-ref36"><label>36</label><mixed-citation publication-type="other" xlink:type="simple">Bottcher, H. (1965) Miracle Drugs. Zora, Zagreb, 23-139.</mixed-citation></ref><ref id="scirp.62095-ref37"><label>37</label><mixed-citation publication-type="other" xlink:type="simple">Castiglioni, A., Krumbhaar, E.B. and Alfred, A. (1947) A History of Medicine. Knopf, New York.</mixed-citation></ref><ref id="scirp.62095-ref38"><label>38</label><mixed-citation publication-type="other" xlink:type="simple">Petrovska, B.B. (2012) Historical Review of Medicinal Plants’ Usage. Pharmacognosy Reviews, 6, 1-5. 
&lt;br /&gt;http://dx.doi.org/10.4103/0973-7847.95849</mixed-citation></ref><ref id="scirp.62095-ref39"><label>39</label><mixed-citation publication-type="other" xlink:type="simple">Cragg, G.M. and Newman, D.J. (2013) Natural Products: A Continuing Source of Novel Drug Leads. Biochimica et Biophysica Acta (BBA)—General Subjects, 1830, 3670-3695. &lt;br /&gt;http://dx.doi.org/10.1016/j.bbagen.2013.02.008</mixed-citation></ref><ref id="scirp.62095-ref40"><label>40</label><mixed-citation publication-type="other" xlink:type="simple">Santhosh, R.S. and Suriyanarayanan, B. (2014) Plants: A Source for New Antimycobacterial Drugs. Planta Medica, 80, 9-21.</mixed-citation></ref><ref id="scirp.62095-ref41"><label>41</label><mixed-citation publication-type="other" xlink:type="simple">Newton, S.M., Lau, C. and Wright, C.W. (2000) A Review of Antimycobacterial Natural Products. Phytotherapy Research, 14, 303-322. &lt;br /&gt;http://dx.doi.org/10.1002/1099-1573(200008)14:5&lt;303::AID-PTR712&gt;3.0.CO;2-N</mixed-citation></ref><ref id="scirp.62095-ref42"><label>42</label><mixed-citation publication-type="other" xlink:type="simple">Mohamad, S., Zin, N.M., Wahab, H.A., Ibrahim, P., Sulaiman, S.F., et al. (2011) Antituberculosis Potential of Some Ethnobotanically Selected Malaysian Plants. Journal of Ethnopharmacology, 133, 1021-1026. 
&lt;br /&gt;http://dx.doi.org/10.1016/j.jep.2010.11.037</mixed-citation></ref><ref id="scirp.62095-ref43"><label>43</label><mixed-citation publication-type="other" xlink:type="simple">Babalola, I.T., Adelakun, E.A., Wang, Y. and Shode, F.O. (2012) Anti-TB Activity of Sterculia setigera Del., Leaves (Sterculiaceae). Journal of Pharmacognosy and Phytochemistry, 1, 19-26.</mixed-citation></ref><ref id="scirp.62095-ref44"><label>44</label><mixed-citation publication-type="other" xlink:type="simple">Robles-Zepeda, R.E., Coronado-Aceves, E.W., Velázquez-Contreras, C.A., Ruiz-Bustos, E., Navarro-Navarro, M., et al. (2013) In Vitro Anti-Mycobacterial Activity of Nine Medicinal Plants Used by Ethnic Groups in Sonora, Mexico. BMC Complementary and Alternative Medicine, 13, 329. &lt;br /&gt;http://dx.doi.org/10.1186/1472-6882-13-329</mixed-citation></ref><ref id="scirp.62095-ref45"><label>45</label><mixed-citation publication-type="other" xlink:type="simple">Balcha, E., Mengiste, B., Gebrelibanos, M., Worku, A. and Ameni, G. (2014) Evaluation of In-Vitro Anti-Mycobacterial Activity of Selected Medicinal Plants in Mekelle, Ethiopia. World Applied Sciences Journal, 31, 1217-1220.</mixed-citation></ref><ref id="scirp.62095-ref46"><label>46</label><mixed-citation publication-type="other" xlink:type="simple">Njeru, S.N., Obonyo, M.A., Ngari, S.M., Nyambati, S., Onsarigo, J.M.N., et al. (2015) Antituberculous, Antimicrobial, Cytotoxicity and Phytochemical Activity Study of Piliostigma thonningii Extract Fractions. Journal of Medicinal Plants Research, 9, 655-663.</mixed-citation></ref><ref id="scirp.62095-ref47"><label>47</label><mixed-citation publication-type="other" xlink:type="simple">Gautam, R., Saklani, A. and Jachak, S.M. (2007) Indian Medicinal Plants as a Source of Antimycobacterial Agents. Journal of Ethnopharmacology, 110, 200-234. &lt;br /&gt;http://dx.doi.org/10.1016/j.jep.2006.12.031</mixed-citation></ref><ref id="scirp.62095-ref48"><label>48</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Arya</surname><given-names> V. </given-names></name>,<etal>et al</etal>. (<year>2011</year>)<article-title>A Review on Anti-Tubercular Plants</article-title><source> International Journal of PharmaTech Research</source><volume> 3</volume>,<fpage> 872</fpage>-<lpage>880</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.62095-ref49"><label>49</label><mixed-citation publication-type="other" xlink:type="simple">Chattopadhyay, D., Arunachalam, G., Mandal, A.B., Sur, T.K., Mandal, S.C., et al. (2002) Antimicrobial and Anti- Inflammatory Activity of Folklore: Mallotus peltatus Leaf Extract. Journal of Ethnopharmacology, 82, 229-237. 
http://dx.doi.org/10.1016/S0378-8741(02)00165-4</mixed-citation></ref><ref id="scirp.62095-ref50"><label>50</label><mixed-citation publication-type="other" xlink:type="simple">Gupta, V., Shukla, C., Bisht, G., Saikia, D., Kumar, S., et al. (2011) Detection of Anti-Tuberculosis Activity in Some Folklore Plants by Radiometric BACTEC Assay. Letters in Applied Microbiology, 52, 33-40. 
&lt;br /&gt;http://dx.doi.org/10.1111/j.1472-765X.2010.02963.x</mixed-citation></ref><ref id="scirp.62095-ref51"><label>51</label><mixed-citation publication-type="other" xlink:type="simple">Saikia, D., Parveen, S., Gupta, V.K. and Luqman, S. (2012) Anti-Tuberculosis Activity of Indian Grass KHUS (Vetiveria zizanioides L. Nash). Complementary Therapies in Medicine, 20, 434-436. 
&lt;br /&gt;http://dx.doi.org/10.1016/j.ctim.2012.07.010</mixed-citation></ref><ref id="scirp.62095-ref52"><label>52</label><mixed-citation publication-type="other" xlink:type="simple">Adaikkappan, P., Kannapiran, M. and Anthonisamy, A. (2012) Anti-Mycobacterial Activity of Withania somnifera and Pueraria tuberosa against Mycobacterium tuberculosis H37Rv. Journal of Academia and Industrial Research, 1, 153- 156.</mixed-citation></ref><ref id="scirp.62095-ref53"><label>53</label><mixed-citation publication-type="other" xlink:type="simple">Birdi, T., D’souza, D., Tolani, M., Daswani, P., Nair, V., et al. (2012) Assessment of the Activity of Selected Indian Medicinal Plants against Mycobacterium tuberculosis: A Preliminary Screening Using the Microplate Alamar Blue Assay. European Journal of Medicinal Plants, 2, 308-323. &lt;br /&gt;http://dx.doi.org/10.9734/EJMP/2012/1638</mixed-citation></ref><ref id="scirp.62095-ref54"><label>54</label><mixed-citation publication-type="other" xlink:type="simple">Antony, M., James, J., Misra, C.S., Sagadevan, L., Veettil, A.T., et al. (2012) Anti Mycobacterial Activity of the Plant Extracts of Alstonia scholaris. International Journal of Current Pharmaceutical Research, 4, 40-42.</mixed-citation></ref><ref id="scirp.62095-ref55"><label>55</label><mixed-citation publication-type="other" xlink:type="simple">Mishra, P.K., Singh, R.K., Gupta, A., Chaturvedi, A., Pandey, R., et al. (2013) Antibacterial Activity of Andrographis paniculata (Burm. f.) Wall. ex Nees Leaves against Clinical Pathogens. Journal of Pharmacy Research, 7, 459-462. 
http://dx.doi.org/10.1016/j.jopr.2013.05.009</mixed-citation></ref><ref id="scirp.62095-ref56"><label>56</label><mixed-citation publication-type="other" xlink:type="simple">Tawde, K., Gacche, R. and Pund, M. (2012) Evaluation of Selected Indian Traditional Folk Medicinal Plants against Mycobacterium tuberculosis with Antioxidant and Cytotoxicity Study. Asian Pacific Journal of Tropical Disease, 2, S685-S691. &lt;br /&gt;http://dx.doi.org/10.1016/s2222-1808(12)60244-8</mixed-citation></ref><ref id="scirp.62095-ref57"><label>57</label><mixed-citation publication-type="other" xlink:type="simple">Tiwari, N., Thakur, J., Saikia, D. and Gupta, M.M. (2013) Antitubercular Diterpenoids from Vitex trifolia. Phytomedicine, 20, 605-610. &lt;br /&gt;http://dx.doi.org/10.1016/j.phymed.2013.01.003</mixed-citation></ref><ref id="scirp.62095-ref58"><label>58</label><mixed-citation publication-type="other" xlink:type="simple">Viswanathan, V., Phadatare, A. and Mukne, A. (2014) Antimycobacterial and Antibacterial Activity of Allium sativum Bulbs. Indian Journal of Pharmaceutical Sciences, 76, 256-261.</mixed-citation></ref><ref id="scirp.62095-ref59"><label>59</label><mixed-citation publication-type="other" xlink:type="simple">Rajiniraja, M. and Jayaraman, G. (2014) Bioautography Guided Screening of Selected Indian Medicinal Plants Reveals Potent Antimycobacterial Activity of Allium sativum Extracts-Implication of Non-Sulfur Compounds in Inhibition. International Journal of Pharmacy and Pharmaceutical Sciences, 6, 671-676.</mixed-citation></ref><ref id="scirp.62095-ref60"><label>60</label><mixed-citation publication-type="other" xlink:type="simple">Munna, S., Basha, S.C., Reddy, P.R., Pramod, N., Kumar, Y.P., et al. (2014) Antitubercular Activity of Actiniopteris radiata Linn. Journal of Global Trends in Pharmaceutical Sciences, 5, 1443-1445.</mixed-citation></ref><ref id="scirp.62095-ref61"><label>61</label><mixed-citation publication-type="other" xlink:type="simple">Kaur, R. and Kaur, H. (2015) Antitubercular Activity and Phytochemical Screening of Selected Medicinal Plants. Oriental Journal of Chemistry, 31, 597-600.</mixed-citation></ref><ref id="scirp.62095-ref62"><label>62</label><mixed-citation publication-type="other" xlink:type="simple">Suhitha, S., Devi, S.K., Gunasekaran, K., Carehome Pakyntein, H., Bhattacharjee, A., et al. (2015) Phytochemical Analyses and Activity of Herbal Medicinal Plants of North-East India for Anti-Diabetic, Anti-Cancer and Anti- Tuberculosis and Their Docking Studies. Current Topics in Medicinal Chemistry, 15, 21-36. 
&lt;br /&gt;http://dx.doi.org/10.2174/1568026615666150112104344</mixed-citation></ref><ref id="scirp.62095-ref63"><label>63</label><mixed-citation publication-type="other" xlink:type="simple">Sheeba, D.G., Gomathi, K.S. and Citarasu, D. (2015) Anti-Mycobacterial and Phytochemical Investigation of Methanol Extracts of Few Medicinal Plants. Journal of Chemical and Pharmaceutical Sciences, 8, 480-486.</mixed-citation></ref><ref id="scirp.62095-ref64"><label>64</label><mixed-citation publication-type="other" xlink:type="simple">Gowrish, A., Vagdevi, H. and Rajashekar, H. (2015) In Vitro Antioxidant and Antitubercular Activity of Leucas marrubioides Desf. Root Extracts. Journal of Applied Pharmaceutical Science, 5, 137-142. 
&lt;br /&gt;http://dx.doi.org/10.7324/JAPS.2015.50220</mixed-citation></ref><ref id="scirp.62095-ref65"><label>65</label><mixed-citation publication-type="other" xlink:type="simple">Channabasappa, H.S., Shrinivas, J.D. and Venkatrao, K.H. (2015) Evaluation of Antibacterial and Antitubercular Activity of Cassia fistula Linn Root. International Journal of Research in Pharmaceutical Sciences, 6, 82-84.</mixed-citation></ref><ref id="scirp.62095-ref66"><label>66</label><mixed-citation publication-type="other" xlink:type="simple">Gaur, R., Thakur, J.P., Yadav, D.K., Kapkoti, D.S., Verma, R.K., et al. (2015) Synthesis, Antitubercular Activity, and Molecular Modeling Studies of Analogues of Isoliquiritigenin and Liquiritigenin, Bioactive Components from Glycyrrhiza glabra. Medicinal Chemistry Research, 24, 3494-3503. &lt;br /&gt;http://dx.doi.org/10.1007/s00044-015-1401-1</mixed-citation></ref><ref id="scirp.62095-ref67"><label>67</label><mixed-citation publication-type="other" xlink:type="simple">Sureram, S., Senadeera, S.P., Hongmanee, P., Mahidol, C., Ruchirawat, S., et al. (2012) Antimycobacterial Activity of Bisbenzylisoquinoline Alkaloids from Tiliacora triandra against Multidrug-Resistant Isolates of Mycobacterium tuberculosis. Bioorganic &amp; Medicinal Chemistry Letters, 22, 2902-2905. &lt;br /&gt;http://dx.doi.org/10.1016/j.bmcl.2012.02.053</mixed-citation></ref><ref id="scirp.62095-ref68"><label>68</label><mixed-citation publication-type="other" xlink:type="simple">Leit&amp;atilde;o, F., Leit&amp;atilde;o, S.G., de Almeida, M.Z., Cantos, J., Coelho, T., et al. (2013) Medicinal Plants from Open-Air Markets in the State of Rio de Janeiro, Brazil as a Potential Source of New Antimycobacterial Agents. Journal of Ethnopharmacology, 149, 513-521. &lt;br /&gt;http://dx.doi.org/10.1016/j.jep.2013.07.009</mixed-citation></ref><ref id="scirp.62095-ref69"><label>69</label><mixed-citation publication-type="other" xlink:type="simple">Nguta, J.M., Appiah-Opong, R., Nyarko, A.K., Yeboah-Manu, D. and Addo, P.G. (2015) Medicinal Plants Used to Treat TB in Ghana. International Journal of Mycobacteriology, 4, 116-123. 
&lt;br /&gt;http://dx.doi.org/10.1016/j.ijmyco.2015.02.003</mixed-citation></ref><ref id="scirp.62095-ref70"><label>70</label><mixed-citation publication-type="other" xlink:type="simple">Wang, M., Guan, X., Chi, Y., Robinson, N. and Liu, J.P. (2015) Chinese Herbal Medicine as Adjuvant Treatment to Chemotherapy for Multidrug-Resistant Tuberculosis (MDR-TB): A Systematic Review of Randomized Clinical Trials. Tuberculosis, 95, 364-372. &lt;br /&gt;http://dx.doi.org/10.1016/j.tube.2015.03.003</mixed-citation></ref><ref id="scirp.62095-ref71"><label>71</label><mixed-citation publication-type="other" xlink:type="simple">Lu, J., Qin, R., Ye, S. and Yang, M. (2011) Prunella vulgaris L. Extract Improves Cellular Immunity in MDR-TB Challenged Rats. Journal of Medical Colleges of PLA, 26, 230-237. &lt;br /&gt;http://dx.doi.org/10.1016/S1000-1948(11)60040-3</mixed-citation></ref><ref id="scirp.62095-ref72"><label>72</label><mixed-citation publication-type="other" xlink:type="simple">Torres-Romero, D., Jimenez, I.A., Rojas, R., Gilman, R.H., Lopez, M., et al. (2011) Dihydro-Beta-Agarofuran Sesquiterpenes Isolated from Celastrus vulcanicola as Potential Anti-Mycobacterium tuberculosis Multidrug-Resistant Agents. Bioorganic &amp; Medicinal Chemistry, 19, 2182-2189. &lt;br /&gt;http://dx.doi.org/10.1016/j.bmc.2011.02.034</mixed-citation></ref><ref id="scirp.62095-ref73"><label>73</label><mixed-citation publication-type="other" xlink:type="simple">Molina-Salinas, G.M., Pena-Rodriguez, L.M., Mata-Cardenas, B.D., Escalante-Erosa, F., Gonzalez-Hernandez, S., et al. (2011) Flourensia cernua: Hexane Extracts a Very Active Mycobactericidal Fraction from an Inactive Leaf Decoction against Pansensitive and Panresistant Mycobacterium tuberculosis. Evidence-Based Complementary and Alternative Medicine: eCAM, 2011, Article ID: 782503.</mixed-citation></ref><ref id="scirp.62095-ref74"><label>74</label><mixed-citation publication-type="other" xlink:type="simple">Hannan, A., Ikram Ullah, M., Usman, M., Hussain, S., Absar, M., et al. (2011) Anti-Mycobacterial Activity of Garlic (Allium sativum) against Multi-Drug Resistant and Non-Multi-Drug Resistant Mycobacterium tuberculosis. Pakistan Journal of Pharmaceutical Sciences, 24, 81-85.</mixed-citation></ref><ref id="scirp.62095-ref75"><label>75</label><mixed-citation publication-type="other" xlink:type="simple">Dini, C., Fabbri, A. and Geraci, A. (2011) The Potential Role of Garlic (Allium sativum) against the Multi-Drug Resistant Tuberculosis Pandemic: A Review. Annali dell’Istituto Superiore di Sanita, 47, 465-473.</mixed-citation></ref><ref id="scirp.62095-ref76"><label>76</label><mixed-citation publication-type="other" xlink:type="simple">Navarro-Garcia, V.M., Luna-Herrera, J., Rojas-Bribiesca, M.G., Alvarez-Fitz, P. and Rios, M.Y. (2011) Antibacterial Activity of Aristolochia brevipes against Multidrug-Resistant Mycobacterium tuberculosis. Molecules, 16, 7357-7364. 
http://dx.doi.org/10.3390/molecules16097357</mixed-citation></ref><ref id="scirp.62095-ref77"><label>77</label><mixed-citation publication-type="other" xlink:type="simple">Patra, A., Ghosh, S. and Mukherjee, B. (2010) Structure Elucidation of Two New Bisbenzylisoquinoline Alkaloids and NMR Assignments of the Alkaloids from the Fruits of Tiliacora racemosa. Magnetic Resonance in Chemistry, 48, 823-828. http://dx.doi.org/10.1002/mrc.2670</mixed-citation></ref><ref id="scirp.62095-ref78"><label>78</label><mixed-citation publication-type="other" xlink:type="simple">Serkani, J.E., Isfahani, B.N., Safaei, H.G., Kermanshahi, R.K. and Asghari, G. (2012) Evaluation of the Effect of Humulus lupulus Alcoholic Extract on Rifampin-Sensitive and Resistant Isolates of Mycobacterium tuberculosis. Research in Pharmaceutical Sciences, 7, 235-242.</mixed-citation></ref><ref id="scirp.62095-ref79"><label>79</label><mixed-citation publication-type="other" xlink:type="simple">Crandall, P.G., Ricke, S.C., O’Bryan, C.A. and Parrish, N.M. (2012) In Vitro Effects of Citrus Oils against Mycobacterium tuberculosis and Non-Tuberculous Mycobacteria of Clinical Importance. Journal of Environmental Science and Health Part B, Pesticides, Food Contaminants, and Agricultural Wastes, 47, 736-741. 
http://dx.doi.org/10.1080/03601234.2012.669331</mixed-citation></ref><ref id="scirp.62095-ref80"><label>80</label><mixed-citation publication-type="other" xlink:type="simple">Leon-Diaz, R., Meckes-Fischer, M., Valdovinos-Martinez, L., Campos, M.G., Hernandez-Pando, R., et al. (2013) Antitubercular Activity and the Subacute Toxicity of (-)-Licarin A in BALB/c Mice: A Neolignan Isolated from Aristolochia taliscana. Archives of Medical Research, 44, 99-104. &lt;br /&gt;http://dx.doi.org/10.1016/j.arcmed.2012.12.006</mixed-citation></ref><ref id="scirp.62095-ref81"><label>81</label><mixed-citation publication-type="other" xlink:type="simple">Nogueira, T., Medeiros, M.A., Marcelo-Curto, M.J., García-Pérez, B., Luna-Herrera, J., et al. (2013) Profile of Antimicrobial Potential of Fifteen Hypericum Species from Portugal. Industrial Crops and Products, 47, 126-131. 
http://dx.doi.org/10.1016/j.indcrop.2013.03.005</mixed-citation></ref><ref id="scirp.62095-ref82"><label>82</label><mixed-citation publication-type="other" xlink:type="simple">Jimenez-Arellanes, A., Luna-Herrera, J., Cornejo-Garrido, J., Lopez-Garcia, S., Castro-Mussot, M.E., et al. (2013) Ursolic and Oleanolic Acids as Antimicrobial and Immunomodulatory Compounds for Tuberculosis Treatment. BMC Complementory and Alternative Medicines, 13, 258. &lt;br /&gt;http://dx.doi.org/10.1186/1472-6882-13-258</mixed-citation></ref><ref id="scirp.62095-ref83"><label>83</label><mixed-citation publication-type="other" xlink:type="simple">Uc-Cachon, A.H., Borges-Argaez, R., Said-Fernandez, S., Vargas-Villarreal, J., Gonzalez-Salazar, F., et al. (2014) Naphthoquinones Isolated from Diospyros anisandra Exhibit Potent Activity against Pan-Resistant First-Line Drugs Mycobacterium tuberculosis Strains. Pulmonary Pharmacology and Therapeutics, 27, 114-120. 
http://dx.doi.org/10.1016/j.pupt.2013.08.001</mixed-citation></ref><ref id="scirp.62095-ref84"><label>84</label><mixed-citation publication-type="other" xlink:type="simple">Zhang, L., Li, R., Li, M., Qi, Z. and Tian, J. (2015) In Vitro and in Vivo Study of Anti-Tuberculosis Effect of Extracts Isolated from Ranunculi Ternati Radix. Sarcoidosis Vasculitis and Diffuse Lung Diseases. Official Journal of WASOG/ World Association of Sarcoidosis and Other Granulomatous Disorders, 31, 336-342.</mixed-citation></ref><ref id="scirp.62095-ref85"><label>85</label><mixed-citation publication-type="other" xlink:type="simple">Radji, M., Kurniati, M. and Kiranasari, A. (2015) Comparative Antimycobacterial Activity of Some Indonesian Medicinal Plants against Multi-Drug Resistant Mycobacterium tuberculosis. Journal of Applied Pharmaceutical Science, 5, 19-22.</mixed-citation></ref><ref id="scirp.62095-ref86"><label>86</label><mixed-citation publication-type="other" xlink:type="simple">Jang, W.S., Jyoti, M.A., Kim, S., Nam, K.W., Ha, T.K., et al. (2015) In Vitro Antituberculosis Activity of Diterpenoids from the Vietnamese Medicinal Plant Croton tonkinensis. Journal of Natural Medicines, 70, 127-132.</mixed-citation></ref><ref id="scirp.62095-ref87"><label>87</label><mixed-citation publication-type="other" xlink:type="simple">Gupta, R., Thakur, B., Singh, P., Singh, H., Sharma, V., et al. (2010) Anti-Tuberculosis Activity of Selected Medicinal Plants against Multi-Drug Resistant Mycobacterium tuberculosis Isolates. Indian Journal of Medical Research, 131, 809-813.</mixed-citation></ref><ref id="scirp.62095-ref88"><label>88</label><mixed-citation publication-type="other" xlink:type="simple">Lakshmanan, D., Werngren, J., Jose, L., Suja, K., Nair, M.S., et al. (2011) Ethyl p-Methoxycinnamate Isolated from a Traditional Anti-Tuberculosis Medicinal Herb Inhibits Drug Resistant Strains of Mycobacterium tuberculosis in Vitro. Fitoterapia, 82, 757-761. &lt;br /&gt;http://dx.doi.org/10.1016/j.fitote.2011.03.006</mixed-citation></ref><ref id="scirp.62095-ref89"><label>89</label><mixed-citation publication-type="other" xlink:type="simple">Gupta, S., Dwivedi, G.R., Darokar, M.P. and Srivastava, S.K. (2012) Antimycobacterial Activity of Fractions and Isolated Compounds from Vetiveria zizanioides. Medicinal Chemistry Research, 21, 1283-1289. 
&lt;br /&gt;http://dx.doi.org/10.1007/s00044-011-9639-8</mixed-citation></ref><ref id="scirp.62095-ref90"><label>90</label><mixed-citation publication-type="other" xlink:type="simple">Singh, R., Hussain, S., Verma, R. and Sharma, P. (2013) Anti-Mycobacterial Screening of Five Indian Medicinal Plants and Partial Purification of Active Extracts of Cassia sophera and Urtica dioica. Asian Pacific Journal of Tropical Medicine, 6, 366-371. &lt;br /&gt;http://dx.doi.org/10.1016/S1995-7645(13)60040-1</mixed-citation></ref><ref id="scirp.62095-ref91"><label>91</label><mixed-citation publication-type="other" xlink:type="simple">Kumar, P., Singh, A., Sharma, U., Singh, D., Dobhal, M., et al. (2013) Anti-Mycobacterial Activity of Plumericin and Isoplumericin against MDR Mycobacterium tuberculosis. Pulmonary Pharmacology &amp; Therapeutics, 26, 332-335. 
http://dx.doi.org/10.1016/j.pupt.2013.01.003</mixed-citation></ref><ref id="scirp.62095-ref92"><label>92</label><mixed-citation publication-type="other" xlink:type="simple">Basu, S., Ghosh, A. and Hazra, B. (2005) Evaluation of the Antibacterial Activity of Ventilago madraspatana Gaertn., Rubia cordifolia Linn. and Lantana camara Linn.: Isolation of Emodin and Physcion as Active Antibacterial Agents. Phytotherapy Research, 19, 888-894. &lt;br /&gt;http://dx.doi.org/10.1002/ptr.1752</mixed-citation></ref><ref id="scirp.62095-ref93"><label>93</label><mixed-citation publication-type="other" xlink:type="simple">Dey, D., Ray, R. and Hazra, B. (2014) Antitubercular and Antibacterial Activity of Quinonoid Natural Products against Multi-Drug Resistant Clinical Isolates. Phytotherapy Research, 28, 1014-1021. &lt;br /&gt;http://dx.doi.org/10.1002/ptr.5090</mixed-citation></ref><ref id="scirp.62095-ref94"><label>94</label><mixed-citation publication-type="other" xlink:type="simple">Hazra, B., Sarkar, R., Bhattacharyya, S., Ghosh, P.K., Chel, G., et al. (2002) Synthesis of Plumbagin Derivatives and Their Inhibitory Activities against Ehrlich ascites Carcinoma in Vivo and Leishmania donovani Promastigotes in Vitro. Phytotherapy Research, 16, 133-137. &lt;br /&gt;http://dx.doi.org/10.1002/ptr.867</mixed-citation></ref><ref id="scirp.62095-ref95"><label>95</label><mixed-citation publication-type="other" xlink:type="simple">Prabu, A., Hassan, S., Prabuseenivasan Shainaba, A.S., Hanna, L.E., et al. (2015) Andrographolide: A Potent Antituberculosis Compound That Targets Aminoglycoside 2’-N-Acetyltransferase in Mycobacterium tuberculosis. Journal of Molecular Graphics &amp; Modelling, 61, 133-140. &lt;br /&gt;http://dx.doi.org/10.1016/j.jmgm.2015.07.001</mixed-citation></ref><ref id="scirp.62095-ref96"><label>96</label><mixed-citation publication-type="other" xlink:type="simple">Dey, D., Ray, R. and Hazra, B. (2015) Antimicrobial Activity of Pomegranate Fruit Constituents against Drug-Resistant Mycobacterium tuberculosis and β-Lactamase Producing Klebsiella pneumoniae. Pharmaceutical Biology, 53, 1474- 1418. &lt;br /&gt;http://dx.doi.org/10.3109/13880209.2014.986687</mixed-citation></ref></ref-list></back></article>