<?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">PP</journal-id><journal-title-group><journal-title>Pharmacology &amp; Pharmacy</journal-title></journal-title-group><issn pub-type="epub">2157-9423</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/pp.2020.119020</article-id><article-id pub-id-type="publisher-id">PP-103205</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject><subject> Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Assessment of Anti-Salmonella Activity of Aqueous and Ethanolic Extract of Senna siamae, Used in Traditional Management of Salmonellosis in Benin
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Brice</surname><given-names>Boris Legba</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>Victorien</surname><given-names>Dougnon</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>Jerrold</surname><given-names>Agbankpe</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>Kafayath</surname><given-names>Fabiyi</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>Christelle</surname><given-names>Lougbegnon</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>Arnaud</surname><given-names>Soha</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>Césaire</surname><given-names>Ayena</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>Esther</surname><given-names>Deguenon</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hornel</surname><given-names>Koudokpon</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>Lamine</surname><given-names>Baba-Moussa</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Laboratory of Biology and Molecular Typing in Microbiology, Faculty of Sciences and Techniques, University of Abomey-Calavi, Abomey-Calavi, Benin</addr-line></aff><aff id="aff1"><addr-line>Research Unit in Applied Microbiology and Pharmacology of Natural Substances, Research Laboratory in Applied Biology, Polytechnic School of Abomey-Calavi, University of Abomey-Calavi, Abomey-Calavi, Benin</addr-line></aff><pub-date pub-type="epub"><day>15</day><month>09</month><year>2020</year></pub-date><volume>11</volume><issue>09</issue><fpage>226</fpage><lpage>234</lpage><history><date date-type="received"><day>17,</day>	<month>August</month>	<year>2020</year></date><date date-type="rev-recd"><day>26,</day>	<month>September</month>	<year>2020</year>	</date><date date-type="accepted"><day>29,</day>	<month>September</month>	<year>2020</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>
 
 
  Recent ethnopharmacological data cited 
  Senna siamea
   as one of the most widely used medicinal plants in the management of salmonellosis in Benin. However,
   
  data related to its activity on non-typhoidal Salmonella spp are limited. This study aimed to assess the antibacterial activity of Senna siamea on multidrug-resistant Salmonella. Ethanolic and aqueous extracts of S. siamea were tested for their antibacterial activity on four multidrug-resistant Salmonella: Salmonella Typhimurium ATCC 14028 and three Salmonella spp
  . 
  isolated from animals intended for human consumption in Benin. Well diffusion technique combined with the determination by microdilution of Minimum Bactericidal Concentration (MBC) and Minimum Inhibitory Concentration (MIC) were used for antibacterial testing. From antibacterial testing, inhibition diameters of the extracts ranged from 7 to 11 mm, for the susceptible strains. Colistin (reference antibiotic) was active on all Salmonella spp. with inhibition diameters between 18 and 19 mm. The MICs ranged from 3.125 to 25 mg/ml while MBCs of the extracts are greater than 100 mg/ml, so none of the extracts have antibacterial power (p.a). From these results, it appears that 
  the 
  use of Senna siamea in the traditional treatment of salmonellosis is justified. These results must be valued in the development of anti-salmonella phytomedicines.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Salmonella&lt;/i&gt; spp.</kwd><kwd> &lt;i&gt;Senna siamea&lt;/i&gt;</kwd><kwd> Salmonellosis</kwd><kwd> MIC</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Non-typhoid Salmonella enterica associated with various foods, particularly poultry products, are major causes of bacterial gastroenteritis worldwide [<xref ref-type="bibr" rid="scirp.103205-ref1">1</xref>]. Non-typhoid salmonellosis is endemic in sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.103205-ref2">2</xref>]. Approximately 1.4 million people are affected each year in the United States, with nearly 15,000 hospitalizations and more than 400 deaths [<xref ref-type="bibr" rid="scirp.103205-ref3">3</xref>].</p><p>Salmonellosis is a public health problem in Benin (West Africa). A recent study led in southern Benin revealed Salmonella spp. in the faeces of animals intended for human consumption. These strains were resistant to aminoglycosides, cephalosporins of generations 1 and 2 and penicillins, with the presence of virulence genes such as invA, fimA and stn [<xref ref-type="bibr" rid="scirp.103205-ref4">4</xref>]. These data show how emergent it is to implement an effective strategy to control multidrug resistance and virulence of Salmonella circulating in Benin.</p><p>Fluoroquinolones are involved in the treatment of serious Salmonella infections [<xref ref-type="bibr" rid="scirp.103205-ref5">5</xref>]. Unfortunately, there is an increase in the resistance of Salmonella to quinolone [<xref ref-type="bibr" rid="scirp.103205-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.103205-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.103205-ref7">7</xref>]. Lack of sanitation, limited access to safe drinking water and inappropriate use of antimicrobials also complicate the management and treatment of salmonellosis. In recent years, several alternatives to conventional antibiotics have been proposed in the fight against antimicrobial resistance. The use of medicinal plants is one of the most explored alternatives in West Africa.</p><p>In Benin, an ethnopharmacological survey performed in Benin identified 57 medicinal plants used by herbalists in the traditional management of Senna siamea (Lam) was one of the most quoted plants [<xref ref-type="bibr" rid="scirp.103205-ref8">8</xref>]. A study performed by Legba et al. [<xref ref-type="bibr" rid="scirp.103205-ref9">9</xref>] provided interesting data on the antibacterial activity of Senna siamea on enteric pathogens, and its chemical and toxicological characteristics. In addition, several authors demonstrated in vitro anti-Salmonella activity of S. siamea. In 2013, Dahiru et al. [<xref ref-type="bibr" rid="scirp.103205-ref10">10</xref>] demonstrated inhibition of Salmonella Typhi by S. siamea leaf extracts. Furthermore, in Doughari and Okafor [<xref ref-type="bibr" rid="scirp.103205-ref11">11</xref>] study, the aqueous extract of S. siamea leaves inhibited Salmonella Typhi with a MIC of 1 mg/ml and a MBC of 1.3 mg/ml. These data are of interest and show the potential of S. siamea in the control of salmonellosis, but there are two major shortcomings: There is a wealth of data on the antibacterial activity of S. siamea on Salmonella Typhi, but little information on its activity on non-typhoid Salmonella. In addition, no data on the antibacterial activities of the plant on multidrug-resistant Salmonella isolated in Benin have been identified.</p><p>This work aims to assess the antibacterial activity of S. siamea on multidrug resistant strains of Salmonella isolated in Benin.</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Material</title><sec id="s2_1_1"><title>2.1.1. Plant Material</title><p>Leaves of Senna siamea (Leguminosae, Caesalpinioideae) were collected in Porto-Novo (Benin) in March 2018. Samples were identified by Professor Hounnankpon Yedomonhan from National Herbarium of Benin, University of Abomey-Calavi (Benin). Reference number is AA6691/HNB.</p></sec><sec id="s2_1_2"><title>2.1.2. Bacterial Strains</title><p>The reference strain Salmonella Typhimurium ATCC 14028 was obtained from Research Unit in Applied Microbiology and Pharmacology of natural substances, University of Abomey-Calavi, Benin. The three multiresistant Salmonella spp were isolated from animals intended for human consumption by Deguenon et al. [<xref ref-type="bibr" rid="scirp.103205-ref4">4</xref>]. The three strains were multidrug-resistant to first generation cephalosporins, some aminoglycosides and penicillins, and some <xref ref-type="table" rid="table1">Table 1</xref> below presents bacterial strains’s characteristics.</p></sec></sec><sec id="s2_2"><title>2.2. Methodology</title><sec id="s2_2_1"><title>2.2.1. Obtaining Extracts</title><p>The leaves were sorted (decomposed leaves exlusion), washed with distilled water (to avoid contamination), dried in the laboratory’s temperature (16˚C) for 10 days. Thus, leaves were powdered using a Retsch SM 2000/1430/Upm/Smf type mill. The extracts were prepared from powders using the Maceration technique [<xref ref-type="bibr" rid="scirp.103205-ref9">9</xref>]. After extraction, the crude extracts obtained were kept at 4˚C.</p></sec><sec id="s2_2_2"><title>2.2.2. Antibacterial Tests</title><p>&#183; Preparation of Extracts</p><p>For the antibacterial tests, aqueous and ethanol extracts were dissolved in sterile distilled water at a concentration of 100 mg/ml.</p><p>&#183; Preparation of bacterial suspension</p><p>From young colonies of 18 to 24 hours, a bacterial suspension was prepared at 0.5 Mc Farland, with sterile distilled water [<xref ref-type="bibr" rid="scirp.103205-ref12">12</xref>].</p><p>&#183; Antibiogram by well diffusion technique</p><p>Each inoculum was swabbed onto Petri dishes containing Mueller Hinton agar [<xref ref-type="bibr" rid="scirp.103205-ref12">12</xref>]. Wells of 6 mm diameter were dug, using a sterile Pasteur pipette tip. 50 μl of each extract were deposited in the wells. One well containing sterile distilled water was used as a negative control while colistin (reference antibiotic) was used as a positive control. Petri dishes were left for 1 hour at room temperature for pre-diffusion of the extracts and then incubated at 37˚C for 18 hours. The inhibition diameters were measured at the end of the incubation period. To</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Characteristics of bacterial strains (Deguenon et al., 2019)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Strains</th><th align="center" valign="middle"  colspan="5"  >Virulence genes</th></tr></thead><tr><td align="center" valign="middle" ></td><td align="center" valign="middle" >invA</td><td align="center" valign="middle" >spvR</td><td align="center" valign="middle" >spvC</td><td align="center" valign="middle" >fimA</td><td align="center" valign="middle" >Stn</td></tr><tr><td align="center" valign="middle" >P14</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><tr><td align="center" valign="middle" >P16</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><tr><td align="center" valign="middle" >P19</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><tr><td align="center" valign="middle" >Salmonella Typhimurium ATCC 14028</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><p>P14; P16; P19 are identified Salmonella Spp.; + = Presence; − = Absence.</p><p>avoid bias and to determine the means and standard deviations, the test was carried out three times.</p><p>The standard used for interpreting the results of the antibiogram tests is presented in <xref ref-type="table" rid="table2">Table 2</xref>.</p><p>&#183; Determination of MIC and MBC.</p><p>Microdilution method with 96-well plate was used for determination of MIC [<xref ref-type="bibr" rid="scirp.103205-ref13">13</xref>]. 100 μl of the stock solution of each extract prepared at 200 mg/ml were added to 100 μl of Mueller-Hinton Broth (MHB). Then, a series of two-fold dilution from well to well was made then 100 μl of different bacterial suspensions were added. Positive and negative controls were prepared respectively by adding 100 μl of MHB to 100 μl of bacterial suspension and 100 μl of MHB to 100 μl of the extracts. The microplates were coated with parafilm paper and incubated at 37˚C for 24 hours. Resazurin is used as an indicator of cell viability. After incubation, each well was cultured on MH Agar and incubated at 37˚C for 24 hours for the determination of MBC. MBC is the lowest concentration of extract to which no colony of bacteria can be observed. The antibiotic power (p.a) of each extract was then calculated with the formula MBC/MIC.</p></sec><sec id="s2_2_3"><title>2.2.3. Data Analysis</title><p>The experiments were done with three replicates (n = 3) and the results were subjected to Two-way ANOVA according to Turkey’s multiple comparison test, p &lt; 0.05.</p></sec></sec></sec><sec id="s3"><title>3. Results and Discussion</title><sec id="s3_1"><title>3.1. Results</title><p>The anti-Salmonella activity of the aqueous and ethanolic extracts was evaluated in vitro by performing antibiogram and MIC and MBC determinations. Four strains were used: Salmonella Typhimurium ATCC 14028 (reference strain) and three strains of Salmonella spp isolated in Benin</p></sec><sec id="s3_2"><title>3.2. Antibiogram results</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> presents Antibacterial activity of leaves extracts of Senna siamea and Colistin (reference antibiotic) on Salmonella Typhimurium ATCC 14028. The reference strain was sensitive to aqueous extract of Senna siamae (7 mm) and Colistin (19 mm), but resistant to Senna siamae ethanolic extract.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Interpretation of the susceptibility tests of the plant extracts [<xref ref-type="bibr" rid="scirp.103205-ref14">14</xref>]</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Diameter of the inhibition zone (Δ)</th><th align="center" valign="middle" >sensitivity of the germ</th><th align="center" valign="middle" >Symbol</th></tr></thead><tr><td align="center" valign="middle" >Δ &lt; 7 mm</td><td align="center" valign="middle" >Resistant</td><td align="center" valign="middle" >−</td></tr><tr><td align="center" valign="middle" >7 mm ≤ Δ &lt; 8 mm</td><td align="center" valign="middle" >Sensitive</td><td align="center" valign="middle" >+</td></tr><tr><td align="center" valign="middle" >8 mm ≤ Δ &lt; 9 mm</td><td align="center" valign="middle" >Moderately sensitive</td><td align="center" valign="middle" >++</td></tr><tr><td align="center" valign="middle" >Δ ≥ 9 mm</td><td align="center" valign="middle" >Very sensitive</td><td align="center" valign="middle" >+++</td></tr></tbody></table></table-wrap><p>Aqueous and ethanolic extracts of Senna siamea and Colistin had variable activities on Salmonella spp strains isolated from animals intended for human consumption. Colistin was active on all three strains with inhibition diameters between 18 and 19 mm. On Salmonella spp (P19), aqueous and ethanolic extracts of Senna siamea had inhibition diameters of 8 &#177; 1 mm (moderately sensitive) and 11 &#177; 1 m (very sensitive) respectively. On Salmonella spp (P14), only aqueous extract of Senna siamea was active with an inhibition diameter of 7 &#177; 0.57 mm. Finally, Salmonella spp (P16) was resistant to all Senna siamea extracts with inhibition diameters less than 7 mm (<xref ref-type="fig" rid="fig2">Figure 2</xref>). Two-way Anova showed significative difference between inhibition diameter of extracts and Colistin (P = 0.0003) and between sensitivity of strains (P &lt; 0.0001).</p></sec><sec id="s3_3"><title>3.3. MIC and MBC</title><p>The well diffusion test was coupled with the determination of the MIC and MBC of the extracts in order to determine the antibacterial power of the extracts. <xref ref-type="table" rid="table3">Table 3</xref> below shows MICMIC and MBC results obtained during this study.</p><p>The MICs of the extracts ranged from 3.125 to 25 mg/ml. The MBCs of the extracts are greater than 100 mg/ml, so none of the extracts have antibacterial properties.</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>This study was aimed to assess the antibacterial activity of Senna siamea on multidrug resistant Salmonella. For Well diffusion test, the choice of 100 mg/ml concentration is explained by the fact that in previous work, aqueous and ethanolic extracts of Senna siamea have not been active on enteropathogens strains at concentrations lower than 100 mg/ml [<xref ref-type="bibr" rid="scirp.103205-ref9">9</xref>].</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> MIC (mg/ml), MBC (mg/ml) and a. p. of the aqueous and Ethanolic extracts of Senna siamea on Salmonella spp</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Extracts</th><th align="center" valign="middle" >Parameters</th><th align="center" valign="middle" >P19</th><th align="center" valign="middle" >P14</th></tr></thead><tr><td align="center" valign="middle"  rowspan="3"  >S. siamea aqueous extract</td><td align="center" valign="middle" >MIC</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >3125</td></tr><tr><td align="center" valign="middle" >MBC</td><td align="center" valign="middle" >&gt;100</td><td align="center" valign="middle" >&gt;100</td></tr><tr><td align="center" valign="middle" >a.p.</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >S. siamea ethanolic extract</td><td align="center" valign="middle" >MIC</td><td align="center" valign="middle" >25</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >MBC</td><td align="center" valign="middle" >&gt;100</td><td align="center" valign="middle" >-</td></tr><tr><td align="center" valign="middle" >a.p.</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td></tr></tbody></table></table-wrap><p>Legends: MIC: Maximum inhibitory concentration, MBC: Minimum Bactericidal Concentration, PA: Antibacterial Power.</p><sec id="s4_1"><title>4.1. An Interesting Anti-Salmonella Activity</title><p>The aqueous extract of Senna siamea was active on the reference strain (Salmonella Typhimurium ATCC 14028) and on two of the three Salmonella isolates, while the ethanolic extract was only active on one strain of Salmonella. However, the largest inhibition diameter was obtained with the ethanolic extract of Senna siamea which had an inhibition diameter of 11 mm on Salmonella spp. (P19). The MICs of the extracts ranged from 3.125 to 25 mg/ml. The interesting data reported reinforces some previous studies. For example, in 2013, Dahiru et al. [<xref ref-type="bibr" rid="scirp.103205-ref10">10</xref>] showed that S. siamea leaf extracts have antibacterial activity on Salmonella Typhi. In Doughari and Okafor [<xref ref-type="bibr" rid="scirp.103205-ref11">11</xref>] study, leaves aqueous extract of S. siamea has in vitro inhibitory activity on Salmonella Typhi with a MIC of 1 mg/ml and a MBC of 1.3 mg/ml. In another study, at 100 mg/ml, the aqueous extract of Senna siamea leaves had an inhibition diameter of 15.45 &#177; 0.26 mm on Salmonella Typhi while the ethanolic extract had an inhibition diameter of 17.20 &#177; 0.20 mm on the same strain [<xref ref-type="bibr" rid="scirp.103205-ref15">15</xref>]. However, these studies differed from ours in that they focused on strains of Salmonella Typhi, the cause of typhoid fever, whereas we worked on Non Typhoid Salmonella isolated from animals intended for human consumption.</p><p>The interesting antibacterial activity of Senna siamea on these Salmonella strains encourages its traditional use in the management of salmonellosis, according to reports by Dougnon et al. [<xref ref-type="bibr" rid="scirp.103205-ref8">8</xref>]. However, the great inhibition diameters of Colistin could be due to the fact that the reference molecule is a pure molecule while the extract used is not yet one. In our study, extracts are raw, unpurified. The difference in activity between the aqueous extract and the ethanolic extract could be due to the likely variability in chemical composition between the two extracts. The differences in polarity between the two solvents (Water and ethanol) certainly led to the extraction of different chemical compounds not having the same pharmacological activities. Moreover, this result reinforces the traditional use of the plant. The decoction with water from the leaves is the essential method of preparation reported [<xref ref-type="bibr" rid="scirp.103205-ref8">8</xref>].</p></sec><sec id="s4_2"><title>4.2. Chemical Composition as a Source of Antibacterial Activity?</title><p>Work on medicinal plants is unanimous on the fact that the activity of the plant extracts is mainly linked to the presence of molecules usually known under the term ‘‘Secondary metabolites’’. The works of Legba et al. [<xref ref-type="bibr" rid="scirp.103205-ref9">9</xref>] revealed an interesting composition of aqueous and ethanolic extracts in polyphenols and flavonoids, molecules known for their antibacterial properties. Abdulrasheed et al. [<xref ref-type="bibr" rid="scirp.103205-ref16">16</xref>] also identified alkaloids, flavonoids, tannin and steroids in Senna siamea leaves while Nas et al. [<xref ref-type="bibr" rid="scirp.103205-ref15">15</xref>] identified glycosides, tannin, anthraquinone, flavonoid saponin, phenol, terpenoid and steroid. We hypothesize that the presence of these molecules explains the activity of the extracts.</p></sec><sec id="s4_3"><title>4.3. Can Senna siamea Be Potential Source of Phytomedicines against Salmonellosis?</title><p>In vitro antibacterial activity is not enough. In vivo anti-Salmonella activity tests are needed to support the plant activity data. The model developed by Legba et al. [<xref ref-type="bibr" rid="scirp.103205-ref13">13</xref>] seems interesting for this type of test. The evidence of non-toxicity of Senna siamea exists and attests to the harmlessness of this plant. Using the model Artemia salina, Legba et al. [<xref ref-type="bibr" rid="scirp.103205-ref9">9</xref>] showed that the extracts were non-cytotoxic. In addition, in vitro, leaves aqueous and ethanol extracts were devoid of toxicity against vero cells [<xref ref-type="bibr" rid="scirp.103205-ref17">17</xref>]. A few cases of toxicity were reported in vivo, but these were at very high doses up to 8000 and 9600 mg/kg body weight [<xref ref-type="bibr" rid="scirp.103205-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.103205-ref19">19</xref>]. Senna siamea could be valued in the development of anti-salmonellosis phytomedicine.</p></sec></sec><sec id="s5"><title>5. Conclusion</title><p>The results of this study showed that aqueous and ethanolic extract of Senna siamea have an antibacterial activity on multiresistant Salmonella spp., with inhibition diameters ranged from 7 to 11 mm and MICs ranged from 3.125 to 25 mg/ml. The traditional use of Senna siamea leaves in the treatment of salmonellosis is justified. Senna siamea could be a good candidate for the development of anti-Salmonellosis phytomedicine, and in vivo efficacy testing, quality control of the powder, plus testing of formulations will be required.</p></sec><sec id="s6"><title>Funding</title><p>The authors are very grateful to the World Academy of Sciences for the Advancement of Science in Developing Countries (TWAS) and the United Nations Educational, Scientific and Cultural Organization (UNESCO). These two institutions have made this research possible through research funding allocated to the research team under the number 487 RG/BIO/AF/AC G-FR3240293303.</p></sec><sec id="s7"><title>Limitations</title><p>Our study did not exhibit the way the extract gives the beneficial effect on Salmonella spp. Further investigations will assess it.</p></sec><sec id="s8"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s9"><title>Cite this paper</title><p>Legba, B.B., Dougnon, V., Agbankpe, J., Fabiyi, K., Lougbegnon, C., Soha, A., Ayena, C., Deguenon, E., Koudokpon, H. and Baba-Moussa, L. (2020) Assessment of Anti-Salmonella Activity of Aqueous and Ethanolic Extract of Senna siamae, Used in Traditional Management of Salmonellosis in Benin. Pharmacology &amp; Pharmacy, 11, 226-234. https://doi.org/10.4236/pp.2020.119020</p></sec></body><back><ref-list><title>References</title><ref id="scirp.103205-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Gay, K., Robicsek, A., Strahilevitz, J., Park, C.H., Jacoby, G., Barrett, T.J., et al. (2006) Plasmid-Mediated Quinolone Resistance in Non-Typhi Serotypes of Salmonella enterica. Clinical Infectious Diseases, 43, 297-304. https://doi.org/10.1086/505397</mixed-citation></ref><ref id="scirp.103205-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Agbaje, M., Lettini, A.A., Olufemi, O.E., Longo, A., Marafin, E., Antonello, K., et al. (2019) Antimicrobial Resistance Profiles of Salmonella serovars Isolated from Dressed Chicken Meat at Slaughter in Kaduna, Nigeria. Revue d’élevage et de Médecine Vétérinaire des Pays Tropicaux, 72. https://doi.org/10.19182/remvt.31484</mixed-citation></ref><ref id="scirp.103205-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Voetsch, A.C., Van Gilder, T.J., Angulo, F.J., Farley, M.M., Shallow, S., Marcus, R., et al. (2004) FoodNet Estimate of the Burden of Illness Caused by Nontyphoidal Salmonella Infections in the United States. Clinical Infectious Diseases, 38, S127-S134. https://doi.org/10.1086/381578</mixed-citation></ref><ref id="scirp.103205-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Deguenon, E., Dougnon, V., Lozes, E., Maman, N., Agbankpe, J., Abdel-Massih, R.M., et al. (2019) Resistance and Virulence Determinants of Faecal Salmonella spp. Isolated from Slaughter Animals in Benin. BMC Research Notes, 12, Article No. 317.https://doi.org/10.1186/s13104-019-4341-x</mixed-citation></ref><ref id="scirp.103205-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Ruiz, M., Rodríguez, J.C., Escribano, I. and Royo, G. (2004) Available Options in the Management of Non-Typhi Salmonella. Expert Opinion on Pharmacotherapy, 5, 1737-1743. https://doi.org/10.1517/14656566.5.8.1737</mixed-citation></ref><ref id="scirp.103205-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Elkenany, R.M., Eladl, A.H. and El-Shafei, R.A. (2018) Genetic Characterisation of Class 1 Integrons among Multidrug-Resistant Salmonella Serotypes in Broiler Chicken Farms. Journal of Global Antimicrobial Resistance, 14, 202-208.https://doi.org/10.1016/j.jgar.2018.04.009</mixed-citation></ref><ref id="scirp.103205-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Voss-Rech, D., Potter, L., Vaz, C.S.L., Pereira, D.I.B., Sangioni, L.A., Vargas, á.C., et al. (2017) Antimicrobial Resistance in Nontyphoidal Salmonella Isolated from Human and Poultry-Related Samples in Brazil: 20-Year Meta-Analysis. Foodborne Pathogens and Disease, 14, 116-124.</mixed-citation></ref><ref id="scirp.103205-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Dougnon, T.V., Yadouleton, A., Legba, B., Agbankpe, J., Koudokpon, H., Hounmanou, G., Amadou, A., Fabiyi, K., Assogba, P., Hounsa, E., Aniambossou, A., Deguenon, E., de Souza, M., Bankole, H.S. and Baba-Moussa, L. (2018) Utilisation des plantes du Sud-Bénin dans le traitement des fièvres typhoides et para-typhoides: role des herboristes. Ethnopharmacologia, 60, 20-29.</mixed-citation></ref><ref id="scirp.103205-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Legba, B., Dougnon, V., Ahoyo, A., Agbankpè, J., Hounmanou, G., Aniambossou, A., et al. (2018) Exploration of the Antibacterial and Chemical Potential of Some Beninese Pharmacopoiea Traditional Plants. Journal of Medical Microbiology, 32, 149-157. https://doi.org/10.4081/mm.2017.6998</mixed-citation></ref><ref id="scirp.103205-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Dahiru, D., Malgwi, A.R. and Sambo, H.S. (2013) Growth Inhibitory Effect of Senna siamea Leaf Extracts on Selected Microorganisms. The American Journal of the Medical Sciences, 3, 103-107.</mixed-citation></ref><ref id="scirp.103205-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Doughari, J.H. and Okafor, N.B. (2008) Antibacterial Activity of Senna siamae Leaf Extracts on Salmonella typhi. African Journal of Microbiology Research, 2, 42-46.</mixed-citation></ref><ref id="scirp.103205-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Bolou, G.E.K., Attioua, B., N’Guessan, C.A., Coulibaly, A., N’Guessan, D.J. and Djaman, J.A. (2011) évaluation in vitro de l’activité antibactérienne des extraits de Terminalia glaucescens planch. sur Salmonella typhi et Salmonella typhimurium. Bulletin de la Société Royale des Sciences de Liège, 80, 772-790</mixed-citation></ref><ref id="scirp.103205-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Legba, B., Dougnon, V., Chabi, Y., Gbaguidi, C., Aniambossou, A., Deguenon, E., et al. (2020) Evaluation of In-Vivo Anti-Salmonella Activity of Uvaria chamae, Lantana camara and Phyllantus amarus Used in Benin, West Africa. BMC Veterinary Research, 16, Article No. 49. https://doi.org/10.1186/s12917-020-2266-1</mixed-citation></ref><ref id="scirp.103205-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Organisation Mondiale de la Santé (2002) L’utilisation des antimicrobiens en dehors de la médecine humaine et les résistances qui en résultent chez l’homme. Aide-Mémoire N°268. Genève.</mixed-citation></ref><ref id="scirp.103205-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Nas, F.S., Oyeyi, T.I. and Ali, M. (2018) Antibacterial Efficacy and Phytochemical Screening of Senna siamea Leaves Extracts on Some Pathogenic Bacteria. Journal of Microbiology &amp; Experimentation, 6, 159-163. https://doi.org/10.15406/jmen.2018.06.00208</mixed-citation></ref><ref id="scirp.103205-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Abdulrasheed, M., Isiaka, I.H. and Siddan, I.A. (2015) Determining the Phytochemical Constituents and the Antimicrobial Activity of Ethanolic Extract of Acassia Leaf (Senna siamea) on Some Enterobacteriaceae. IOSR Journal of Pharmacy, 5, 18-22.</mixed-citation></ref><ref id="scirp.103205-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Nsonde Ntandou, G.F., Banzouzi, J.T., Mbatchi, B., Elion-Itou, R.D.G., Etou-Ossibi, A.W., Ramos, S., et al. (2010) Analgesic and Anti-Inflammatory Effects of Cassia siamea Lam. stem bark extracts. Journal of Ethnopharmacology, 127, 108-111.https://doi.org/10.1016/j.jep.2009.09.040</mixed-citation></ref><ref id="scirp.103205-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Wiam, I.M., Jacks, T.W. and Zongoma, Y.A. (2005) Acute Toxicity and Phytochemical Studies of Cassia siamea Extract in Rats. Pakistan Journal of Biological Sciences, 8, 586-588. https://doi.org/10.3923/pjbs.2005.586.588</mixed-citation></ref><ref id="scirp.103205-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Thongsaard, W., Deachapunya, C., Pongsakorn, S., Boyd, E.A., Bennett, G.W. and Marsden, C.A. (1996) Barakol: A Potential Anxiolytic Extracted from Cassia siamea. Pharmacology Biochemistry and Behavior, 53, 753-758. https://doi.org/10.1016/0091-3057(95)02088-8</mixed-citation></ref></ref-list></back></article>