<?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">OJMM</journal-id><journal-title-group><journal-title>Open Journal of Medical Microbiology</journal-title></journal-title-group><issn pub-type="epub">2165-3372</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojmm.2018.83007</article-id><article-id pub-id-type="publisher-id">OJMM-87370</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Prevalence, Identification and Antibiotic Susceptibility of &lt;i&gt;Enterococcus&lt;/i&gt; Species Isolated from Chicken and Pigeon Meat in Gazipur Area of Bangladesh
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Avijit</surname><given-names>Banik</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>Noor</surname><given-names>Mohammad</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>Tanzina</surname><given-names>Akter</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>Kaniz</surname><given-names>Fatema</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>Maruf</surname><given-names>Abony</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Microbiology, Primeasia University, HBR Tower, Dhaka, Bangladesh</addr-line></aff><pub-date pub-type="epub"><day>04</day><month>07</month><year>2018</year></pub-date><volume>08</volume><issue>03</issue><fpage>74</fpage><lpage>83</lpage><history><date date-type="received"><day>9,</day>	<month>August</month>	<year>2018</year></date><date date-type="rev-recd"><day>15,</day>	<month>September</month>	<year>2018</year>	</date><date date-type="accepted"><day>18,</day>	<month>September</month>	<year>2018</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>
 
 
  <b>Aims:</b> The aims of this work undertaken to investigate and identify the prevalence of 
  Enterococcus spp isolated from Chicken and pigeon meat and determine the using antibiotics sensitivity against isolates for human safety. This study was conducted in center of excellence lab in Microbiology Department of Primeasia University, Banani, Dhaka-1213, Bangladesh during August, 2017 to March, 2018. 
  <b>Methodology and Results:</b> Twenty four samples were collected in pre-sterilized zip-lock bags from different Gazipur area in different local meat vendors. All samples were transported to the Microbiology Laboratory of Primeasia University and analyzed according to standard analysis methods. Total viable count (TVC) and Total Enterocooci count (TEC) were estimated by using plate count agar (PCA) and Bile Esculineagar plates respectively. Various Selective media and Biochemical tests were used for presumptive isolation and identification. Kirby-Bauer disc diffusion method on Mueller Hinton agar media was used for the determination of sensitivity of the isolated strains to commonly prescribe antibiotics. A total of 24 meat samples were examined of which 92% were positive to 
  Enterococcus spp whereas 62.5% were Chicken and 32.5% pigeon. The counts of 
  enterococci range of 0 - 6.49 log CFU/gm in chicken and 4.4 - 6.4 log CFU/gm in pigeon. 22 isolates of 
  enterococci, 77.27% were resistance to Azithromycin, 54.55% to Nalidixic acid and 50% to Sulfamethoxazole. We found high sensitivity of antimicrobial agent against to Imipenem (100%), Ciprofloxacin (81.81%) and (77.27%) both Tetracycline and Erythromycin. 
  <b>Conclusion: Significance and Impact of the study:</b> The study result expressed that awareness of the meat pathogen and when consumption of meat was well cooked of our daily life.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Enterococcus&lt;/i&gt;</kwd><kwd> &lt;i&gt;Enterococci&lt;/i&gt; from Chicken and Pigeon</kwd><kwd> Antibiotic Sensitivity</kwd><kwd> Gazipur Area in Bangladesh</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Enterococcus spp. are representative of the key genera of lactic acid bacteria (LAB), with a wide distribution in the environment and also found in a variety of food sources, such as meat, vegetables, milk, Cheese, water surface and plants [<xref ref-type="bibr" rid="scirp.87370-ref1">1</xref>] . They are gram positive, non spore forming facultative anaerobes and also lack catalase activity, having tolerance of a high restrictive condition, such as temperature (10˚C - 45˚C), <sub>P</sub>H (9.6), hyperosmolarity (6.5% NaCl) and prolonged desiccation [<xref ref-type="bibr" rid="scirp.87370-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.87370-ref3">3</xref>] . Enterococci are mostly inhabitants in gastrointestinal tract (GIT) of humans and animals, but recent reports have suggested their presence in wide distribution in environment and diverse ecological niches [<xref ref-type="bibr" rid="scirp.87370-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.87370-ref5">5</xref>] . A wide variety of human infections are occurring by the most frequent causative agents Enterococcus spp which are infect Blood stream, heart, abdomen, urinary tract etc, with 70% - 80% of the responsible for being Enterococcus faecalis of the cases [<xref ref-type="bibr" rid="scirp.87370-ref6">6</xref>] and also as an infected nosocomial infection like ear and eyes infections, meningitis, burns wounds and abscess, paranasal sinuses etc. [<xref ref-type="bibr" rid="scirp.87370-ref7">7</xref>] . The key contributor for acquiring and disseminating antibiotic resistance against Enterococcus spp. has been isolated from poultry meat, feed and other food-chain stuffs [<xref ref-type="bibr" rid="scirp.87370-ref8">8</xref>] . Poultry, which are infected by wide range of Enterococcus spp. such as Ent. cecorum causes arthritis, spondylitis, femoral head necrosis, osteomyelitis, lameness and paralysis of broilers [<xref ref-type="bibr" rid="scirp.87370-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.87370-ref10">10</xref>] .</p><p>Bangladesh is one of the key players in the South Asian livestock industry; especially in poultry industry [<xref ref-type="bibr" rid="scirp.87370-ref11">11</xref>] . Poultry industries play an important role in poverty alleviation and economic development of Bangladesh. In Bangladesh, out of a total animal protein supplies approximately 37% comes from poultry meat [<xref ref-type="bibr" rid="scirp.87370-ref12">12</xref>] . According to WHO-FAO joint survey, people in Bangladesh consume 15.23 kg meat per person in a year and poultry provided 35.25% of total meat supply [<xref ref-type="bibr" rid="scirp.87370-ref13">13</xref>] .</p><p>In 2015 to 2016, Enterococcus faecalis and Enterococcus faecium were isolated from clinical infection (Urine, Pus and wound swab) in Mymensingh medical college hospital [<xref ref-type="bibr" rid="scirp.87370-ref14">14</xref>] . In most cases, the birds are not sick and the production is not affected. The degree of illness depends on factors of both the host and the bacteria. However, No surveillance data of Enterococcus spp. associated with poultry have been made in Bangladesh.</p><p>Thus, our present study was designed to comprehensive microbial status on Enterococcus spp. associated with livestock (poultry and pigeon meat) and their drug sensitivity status against enterococci in Gazipur district, Bangladesh. Our results indisputably indicate that a serious promise is required to deal with pathogenic enterococci associated with poultry and pigeon meat for preventing transmission of infectious agent to humans.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Sample Collection and Enrichment Procedure</title><p>A total of 24 meat Samples were collected different location of Gazipur areas. Samples included 15 poultry chicken and 9 pigeon meat samples, which were purchased from the different local meat shops at Gazipur area during August, 2017 to March, 2018.Gazipur area is the most poultry (chicken and pigeon) supplying area around Dhaka city, mymensingh and nearest area in Gazipur. Samples were collected the different location of the Gazipur areas based on following some citrate such as area most repeated customer shop, wholesales farms and most customers gathering market. Using sample in this experiment, chicken weight were almost (1 - 1.5) kg and pigeon (300 - 500) gm. All samples were kill by butcher in the meat shop and washed and clean the outer layer of feather in samples and other dirt matters. After that sample were washed by the fresh water and clean blood. All Samples meat were collected in pre-sterilized Stomacher bags (165 mm &#215; 150 mm &#215; 0.55 mm) and all samples were transported to the Microbiology (Centre of Excellence) Laboratory of Primeasia University at the earliest convenience for processing and further assessment as <xref ref-type="table" rid="table1">Table 1</xref>.</p></sec><sec id="s2_2"><title>2.2. Microbiological Analysis</title><p>After taking sample in laboratory for further analysis, each sample were transferred 10 g in 90 ml sterile Nutrient broth media (Oxoid Ltd, Hampshire, England) in sterile Borosilicate Media Bottles and incubated 37˚C for 4 hours. Every 30 minutes later, the incubated bottle was shaken for homogenized in manually by head in 5 min. Total Viable Count (TVC) and Total Enterococcus count (TEC) of samples were counted on plate count agar and Bile Esculine Agar media respectively (Oxoid Ltd, Hampshire, UK &amp; HiMedia Laboratories, Mumbai, India). According to manufacturer’s instruction media were prepared. All media were sterilized by autoclave at 121˚C for 15 minutes. One ml of incubated sample was diluted in 9 ml sterile normal saline water (0.85% NaCl). After dilution, Decimal dilutions were prepared up to 10<sup>−6</sup> and after appropriate dilution, 100 &#181;l homogenate of each samples was inoculated in respective media and using spread method by sterile glass spreader. Inoculated plates were kept in an incubator at 37˚C for overnight growth. After incubation the number of visible colonies upon media surface were counted and expressed as logarithm of colony forming unit (log CFU) per gram of samples.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Name of the location area and sample size in Gazipur area</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Name of the area in Gazipur</th><th align="center" valign="middle" >Chicken sample</th><th align="center" valign="middle" >Name of the area in Gazipur</th><th align="center" valign="middle" >Pigeon Sample</th></tr></thead><tr><td align="center" valign="middle" >Gazipur Chowrasta area</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >Kanabari bazar area</td><td align="center" valign="middle" >3</td></tr><tr><td align="center" valign="middle" >Joydepur area</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >Salna bazaar area</td><td align="center" valign="middle" >6</td></tr><tr><td align="center" valign="middle" >Tongi Bazar area</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap></sec><sec id="s2_3"><title>2.3. Isolation and Identification of Enterococcus sp</title><p>Isolated Enterococcus Count of sample in Bile Esculine Agar media respectively than collected pure colony the count plate and again using four way streaking method in fresh Bile Esculine Agar media (HiMedia Laboratories, Mumbai, India) for isolated Enterococcus spp and was incubated at 37˚C for 20 to 24 hours and after incubation period isolated was showing Black colony. Enterococcus spp were given black colony in BEA medium and presumptive identification of each colony came from biochemical tests and Microscopic profiling (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p></sec><sec id="s2_4"><title>2.4. Biochemical Test</title><p>Pure colonies from nutrient agar (NA) plates were subjected for biochemical tests such as Triple sugar iron agar (TSI), Simmons citrate agar media, MR-VP media for Methyl red and Voges-Proskeur test, SIM media for Indole and motility test, Oxidase, Catalase test were done [<xref ref-type="bibr" rid="scirp.87370-ref15">15</xref>] .</p></sec><sec id="s2_5"><title>2.5. Antibiotics Susceptibility Test</title><p>Susceptibility of Isolated Enterococcus spp. was tested to different antimicrobial agents was measured in vitro by the Kirby-Bauer method [<xref ref-type="bibr" rid="scirp.87370-ref16">16</xref>] . It allowed determination of the efficiency of antibiotic by measuring the diameter of the zone of inhibition that outcome from diffusion of the antimicrobial agent into the medium surrounding the disc. The ranges of susceptible antibiotic of the isolates were measured using commercially purchased discs (Oxoid Ltd, Hampshire, England) on Muller-Hinton Agar (Oxoid Ltd, Hampshire, England). Commercially available antibiotics used in this experiment included Tetracyclin 30 &#181;g (TE), Azithromycin 15 &#181;g (AZM), Sulphamethoxazole 25 &#181;g (SXT), Ciprofloxacin 5 &#181;g (CIP), Erythromycin 15 &#181;g (E), Nalidixic Acid 30 &#181;g (NA), Chloramphenicol 30 &#181;g (C), Imipenem 10 &#181;g (IMI) [<xref ref-type="bibr" rid="scirp.87370-ref17">17</xref>] .</p></sec><sec id="s2_6"><title>2.6. Statistical Analysis</title><p>Microbiological data were transformed into logarithms of number of colony forming units (CFU/gm) and were subjected to analysis of variance (ANOVA). Means and standard deviations were calculated, and, when F-values were significant</p><p>at the P &lt; 0.05 level, mean differences were Significant by the Least Significant Differences (LSD) procedure [<xref ref-type="bibr" rid="scirp.87370-ref18">18</xref>] .</p></sec></sec><sec id="s3"><title>3. Result</title><p>In this study, all most all Samples were showed positive Enterococcus spp. in the lower levels of contamination found in meat. There were 13 chicken and 9 pigeon meat found the positive result in 24 meat samples in the different location in Gazipur area <xref ref-type="fig" rid="fig2">Figure 2</xref>.</p><p>It is probably related with different sampling areas of poultry and Pigeon. The total bacterial count (TBC) and count of enterococci presented by plotting the log10 value of CFU/gm in poultry and pigeon are showed in <xref ref-type="table" rid="table2">Table 2</xref>. Poultry and pigeon had significantly (p &lt; 0.05) higher number of TBC than enterococci count. The differences among TBC in both meat from different abattoirs were collection statistically significant (P &lt; 0.05), which could be explained by relevant pre-slaughter conditions which include those condition (shower, transport distance, sanitary and chilling conditions). In this slaughter condition of the abattoirs increase the total bacterial load in samples.</p><p>After slaughtering the both samples (Chicken and pigeon) washed to clean them of dirt and fecal matters. Such matter as well as contaminant present in water may affect the bacteriological load on the meat sample. Based on the transport distance after slaughter TBC of meat sample will Change.</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> The total bacterial count and count of enterococci in different meat samples</title></caption><table><tbody><thead><tr><th align="center" valign="middle"  rowspan="3"  ></th><th align="center" valign="middle"  colspan="4"  >Count (CFU/gm)</th></tr></thead><tr><td align="center" valign="middle"  colspan="2"  >Total Bacterial count</td><td align="center" valign="middle"  colspan="2"  >Total Enterococcus spp. count</td></tr><tr><td align="center" valign="middle" >Poultry</td><td align="center" valign="middle" >Pigeon</td><td align="center" valign="middle" >Poultry</td><td align="center" valign="middle" >Pigeon</td></tr><tr><td align="center" valign="middle" >X</td><td align="center" valign="middle" >6.34</td><td align="center" valign="middle" >6.18</td><td align="center" valign="middle" >4.83</td><td align="center" valign="middle" >5.25</td></tr><tr><td align="center" valign="middle" >MIN</td><td align="center" valign="middle" >5.96</td><td align="center" valign="middle" >5.85</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >4.44</td></tr><tr><td align="center" valign="middle" >MAX</td><td align="center" valign="middle" >6.78</td><td align="center" valign="middle" >6.45</td><td align="center" valign="middle" >6.49</td><td align="center" valign="middle" >6.4</td></tr><tr><td align="center" valign="middle" >S</td><td align="center" valign="middle" >0.87</td><td align="center" valign="middle" >0.85</td><td align="center" valign="middle" >1.08</td><td align="center" valign="middle" >0.98</td></tr></tbody></table></table-wrap><p>Note: X = values of means, MIN = Minimum, MAX = Maximum, S = Standard deviation.</p><p>Sanitary condition of the poultry slaughter house has significant on the TBC. It may be caused by the unhygienic condition of the butcher, cutting instruments, surrounding environment of the slaughter house, without clean and washed knife slaughter the samples repeatedly. It chilling condition and temperature imbalances are not maintain properly reservation of the samples; it may impact on the increase if the bacterial load counts. E. faecalis predominated in the Gram-positive cocci isolated from chicken samples collected at poultry abattoirs in found FRANZ et al. [<xref ref-type="bibr" rid="scirp.87370-ref19">19</xref>] .</p><p>In the present study, Enterococcus spp was found in almost 92% of the chicken and pigeon carcasses analyzed. A total of 22 strains were isolated and indentified. Only 2 isolates were not identified to Enterococcus spp. The total bacterial count (TBC) records 6.78 CFU/gm in joydepur Bazar and 5.85 CFU/gm in pigeon in Konabari Bazar area. Maximum counts of Enterococci of chicken were similar place on TBC and salna Bazar area pigeon showed the maximum Enterocooci count. After the colony morphology in selective media, the presumptive isolation was indicating in target microorganisms. Presence of Black colonies on Bile Esculine agar indicated presumptive Enterococcus spp. isolates on a both meat samples. Most of the isolate showed cocci and diplococci shape in violet positive color in gram straining. Triple sugar iron (TSI) showed carbohydrate fermentation with gas production and H<sub>2</sub>S from the isolates, whereas IMViC (Indole, Methyl-red, Voges-Proskeur, Citrate) test and also oxidase, catalase and motility indicated identifying for Enterococcus spp (<xref ref-type="table" rid="table3">Table 3</xref>).</p><p>Finally the antibiotic susceptibility patterns of the isolates indicated. In using of Kirby-Bauer method, to determine sensitivity inculcated Muller-Hinton Agar plates were observed. Isolates from meat products identified as Enterococcus spp introduced against eight antibiotics for their susceptibility test. Among the isolates, antibiotics of resistance were detected mainly in Enterococcus spp significantly prevalence of resistant isolates from Azithromycin (78%), Nalidixic acid (55%) and Sulfomethoxazole (50%) detected. Sensitivity pattern of Enterococcus spp. from meat samples as <xref ref-type="fig" rid="fig3">Figure 3</xref>.</p><p>Isolated enterococci from poultry and pigeon showed resistance to two or more antibiotics such as Azithromycin 84.62%, Sulfomethoxazole 53.84% in poultry and 66.67% in Azithromycin, 55.56% in Nalidixic acid resistance in pigeon</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Biochemical profile of bacterial isolates from meat samples</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Gram straining</th><th align="center" valign="middle" >TSI Butt Slant Gas</th><th align="center" valign="middle" >H<sub>2</sub>S Test</th><th align="center" valign="middle" >Citrate Test</th><th align="center" valign="middle" >MIU Test</th><th align="center" valign="middle" >MR Test</th><th align="center" valign="middle" >VP Test</th><th align="center" valign="middle" >Catalase Test</th><th align="center" valign="middle" >Oxidase Test</th><th align="center" valign="middle" >Presumptive organism</th></tr></thead><tr><td align="center" valign="middle" >Violet, cocci</td><td align="center" valign="middle" >B- Red S- Red G: (-)</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >M- (-) I- (-) U- (-)</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" >Enterococcus spp</td></tr><tr><td align="center" valign="middle" >Violet, Diplococci</td><td align="center" valign="middle" >B- Yellow S- Yellow G- (-)</td><td align="center" valign="middle" >-</td><td align="center" valign="middle" >+</td><td align="center" valign="middle" >M- (-) I- (-) U- (-)</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" >Enterococcus spp</td></tr></tbody></table></table-wrap><p>Note: TSI = Triple Sugar Iron; MIU = Motility, Indole, Urea, MR = Methyl red; VP = Voges-Proskeur.</p><p>isolates. Of 24 isolates of enterococci, 100% were sensitive in imipenem in both meat samples.88.89% and 76.92% were sensitive in ciprofloxacin in pigeon and poultry isolates showed by <xref ref-type="fig" rid="fig4">Figure 4</xref> &amp; <xref ref-type="fig" rid="fig5">Figure 5</xref>.</p></sec><sec id="s4"><title>4. Discussion</title><p>In the growing and developing industry in Bangladesh, poultry is one of them. In recent decades, poultry industry faces lots of old and new infection of poultry animals in Bangladesh. In recent times, Enterococci are emerged as important pathogens responsible for occurred a serious infection in hospital and also as community acquired infection, whereas it’s normally found of the normal intestinal flora of human and animals. In Labadie presented that, the slaughtering</p><p>process, storage condition, temperature and different type of packing of meat spoilage flora is influenced singularly [<xref ref-type="bibr" rid="scirp.87370-ref20">20</xref>] . The average of the TBC in poultry was 6.34 log CFU/gm and the enterococci were 4.83 log CFU/gm. Comparative results of TBC in log CFU∙cm<sup>−2</sup> were present 4.11 log CFU∙cm<sup>−2</sup> and 4.98 log CFU∙cm<sup>−2</sup> in previous work [<xref ref-type="bibr" rid="scirp.87370-ref21">21</xref>] [<xref ref-type="bibr" rid="scirp.87370-ref22">22</xref>] .</p><p>In-vitro antibiotic sensitivity pattern of isolated enteroccus spp. was accomplished against 8 commonly used antibiotics in different groups. After incubation, Zone of inhibition (ZOI) in diameter were measured for individual antibiotics agents which one were highly sensitive, moderately sensitive, less sensitive and resistant (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>Among the isolates poultry and pigeon meat samples, Imipenem and Ciprofloxacin wee highly sensitive. Tetracycline, Erythromycin and chloramphenicol were showed moderately sensitive range 80% to 60% in isolates. Nalidixic acid was seen less sensitivity against both meats isolates 55% to 45%. Azithromycin were presented resistance in isolates showed (<xref ref-type="fig" rid="fig3">Figure 3</xref> &amp; <xref ref-type="fig" rid="fig4">Figure 4</xref>). One antibiotic, sulfamethoxazole were showed less sensitive in poultry but showed more sensitivity pattern in pigeon isolates. Rest of the antibiotics exhibited high antimicrobial activity against the isolates.</p><p>In 21<sup>st</sup> century, development and use of antibiotic has been one of the most important steps towards controlling of infectious bacterial disease. The reveals the emergences of the finding antibiotics against Enterococcus spp infection are great suggested in human and environment.</p></sec><sec id="s5"><title>5. Conclusion</title><p>It is concluded from the present study that public health safety and awareness should be developed to reduce the incidence of Enterococci infection among the people in order to avoid illness. To successfully increasing number of drug sensitive and multi drug sensitive bacteria, extensive knowledge of the molecular mechanisms of acquiring antibiotic and updated information is required.</p></sec><sec id="s6"><title>6. Limitation of This Study</title><p>Finding in this study indicates Enterococcus can cause food-borne illness in undercooked meat product. Molecular study of isolates needs to be conducted for better understanding of drug resistance mechanism. Also, analysis of meat samples from different location of different district may be helpful for determining of drug resistance pattern. Poultry feed used in farm and comparison of farm raised poultry with home raised one may also exhibit contrast in resistance between isolates.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>Authors have declared that no competing interests exist.</p></sec><sec id="s8"><title>Authors Contributions</title><p>This work was carried out in collaboration between all authors. Authors KF designed the study. Author NM and AB managed the experimental process and analyses of the raw data. Authors AB and KF wrote the protocol and the first draft of the manuscript. Author TA managed the literature searches. All authors read and approved the final manuscript.</p></sec><sec id="s9"><title>Cite this paper</title><p>Banik, A., Mohammad, N., Akter, T., Fatema, K. and Abony, M. (2018) Prevalence, Identification and Antibiotic Susceptibility of Enterococcus Species Isolated from Chicken and Pigeon Meat in Gazipur Area of Bangladesh. Open Journal of Medical Microbiology, 8, 74-83. https://doi.org/10.4236/ojmm.2018.83007</p></sec></body><back><ref-list><title>References</title><ref id="scirp.87370-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Frankenberg, L., Brugna, M. and Hederstedt, L. (2002) Enterococcus faecalisheme-Dependent Catalase. Journal of Bacteriology, 184, 6351-6356. https://doi.org/10.1128/JB.184.22.6351-6356.2002</mixed-citation></ref><ref id="scirp.87370-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Foulquié Moreno, M.R., Sarantinopoulos, P., Tsakalidou, E. and De Vuyst, L. (2006) The Role and Application of Enterococci in Food and Health. International Journal of Food Microbiology, 106, 1-24. https://doi.org/10.1016/j.ijfoodmicro.2005.06.026</mixed-citation></ref><ref id="scirp.87370-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Kayser, F.H. (2003) Safety Aspects of Enterococci from the Medicinal Point of View. International Journal of Food Microbiology, 88, 255-262. https://doi.org/10.1016/S0168-1605(03)00188-0</mixed-citation></ref><ref id="scirp.87370-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Poulsen, L.L., Bisgaard, M., Son, N.T., Trung, N.V., An, H.M. and Dalsgaard, A. (2012) Enterococcus faecalis Clones in Poultry and in Humans with Urinary Tract Infections, Vietnam. Emerging Infectious Diseases, 18, 1096-1100. https://doi.org/10.3201/eid1807.111754</mixed-citation></ref><ref id="scirp.87370-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Kapoor, L., Randhawa, V.S. and Deb, M. (2005) Antimicrobial Resistance of Enterococcal Blood Isolates at a Pediatric Care Hospital in India. Japanese Journal of Infectious Diseases, 58, 101-103.</mixed-citation></ref><ref id="scirp.87370-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Kaszanyitzky, E.J., Tenk, M., Ghidan, A., Fehervari, G.Y. and Papp, M. (2005) Antimicrobial Susceptibility of Enterococci Strains Isolated from Slaughter Animals on the Data of Hungary Resistance Monitoring System from 2001 to 2004. International Journal of Food Microbiology, 115, 119-123. https://doi.org/10.1016/j.ijfoodmicro.2006.10.004</mixed-citation></ref><ref id="scirp.87370-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Stalker, M.J., Brash, M.L., Weisz, A., Ouckama, R.M. and Slavic, D. (2010) Arthritis and Osteomyelitis Associated with Enterococcus cecorum Infection in Broiler and Broiler Breeder Chickens In Ontario, Canada. Journal of Veterinary Diagnostic Investigation, 22, 643-645. https://doi.org/10.1177/104063871002200426</mixed-citation></ref><ref id="scirp.87370-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Velkers, F.C., van de Graaf-Bloois, L., Wagenaar, J.A., Westendorp, S.T., van Bergen, M.A., Dwars, R.M. and Landman, W.J.M. (2011) Enterococcus hirae-Associated Endocarditis Outbreaks in Broiler Flocks. Clinical and Pathological Characteristics and Molecular Epidemiology, 31, 3-17.</mixed-citation></ref><ref id="scirp.87370-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Mongkolchavivat, L. (2011) Bangladesh Remains a Strong Player in Poultry. Outlook Bright despite Effects of Bird-Flu: Experts. Star Business Report. The Daily Star Newspaper. https://www.thedailystar.net/news-detail-188204</mixed-citation></ref><ref id="scirp.87370-ref10"><label>10</label><mixed-citation publication-type="book" xlink:type="simple">Rahman, M.M. and Rahman, A. (1998) Cattle and Poultry Development Activities. In: Karjakrom, K.O., Ed., Directorate of Livestock Services (DLS), Bangladesh, 1, 31-55.</mixed-citation></ref><ref id="scirp.87370-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Akbar, M.A., Amin, M.R., Ali, M.A., Bhuiyan, M.S.A. and Kabir, A.K.M.A. (2013) Animal Husbandry—A Business Education for Today or Tomorrow. 3rd Annual Conference and Seminar-2013, Bangladesh Society for Animal Production Education and Research (BSAPER), Savar, 26 October 2013, 21-34.</mixed-citation></ref><ref id="scirp.87370-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Boby, F., Ahmed, S., Paul, S.K., Nasreen, S.A. and Haque, N. (2016) Antimicrobial Susceptibility Pattern of Enterococci Isolated from Clinical Specimens at Mymensingh Medical College Hospital, Mymensingh, Bangladesh. Journal of Bacteriology &amp; Mycology Open Access, 3, Article Title: 00061.</mixed-citation></ref><ref id="scirp.87370-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Cappuccino, J.G. and Sherman, N. (2010) Microbiology A Laboratory Manual. 7th Edition, Pearson Education in South Asia, Singapore, Part 5, 143-203.</mixed-citation></ref><ref id="scirp.87370-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Bauer, A.W., Kirby, W.M., Sherris, J.C. and Turck, M. (1966) Antibiotic Susceptibility Testing by a Standardized Single Disk Method. American Journal of Clinical Pathology, 45, 493-496. https://doi.org/10.1093/ajcp/45.4_ts.493</mixed-citation></ref><ref id="scirp.87370-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">(1999) Approved Standard M31-A. NCCLS Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated from Animals. National Committee for Clinical Laboratory Standards, Wayne, 86 p.</mixed-citation></ref><ref id="scirp.87370-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Vaidya, V.M., Paturkar, A.M., Wakar, V.S., Zende, R.J. and Rawool, D.B. (2005) Detection of Indicator Organisms on Poultry Carcass Sites in an Organized Slaughterhouse. Journal of Muscle Foods, 16, 289-297. https://doi.org/10.1111/j.1745-4573.2005.00021.x</mixed-citation></ref><ref id="scirp.87370-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">Krocko, M., Canigova, M. and Duckova, V. (2007) Occurrence, Isolation and Antibiotic Resistance of Enterococcus Species Isolated from Raw Pork, Beef and Poultry. Journal of Food and Nutrition Research, 46, 91-95.</mixed-citation></ref><ref id="scirp.87370-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">Labadie, J. (1999) Consequences of Packaging on Bacterial Growth. Meat Is an Ecological Niche. Meat Science, 52, 299-305. https://doi.org/10.1016/S0309-1740(99)00006-6</mixed-citation></ref><ref id="scirp.87370-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Franz, C.M.A.P., Stiles, M.E., Schleifer, K.H. and Holzapfel, W.H. (2003) Enterococci in Foods—A Conundrum for Food Safety. International Journal of Food Microbiology, 88, 105-122. https://doi.org/10.1016/S0168-1605(03)00174-0</mixed-citation></ref><ref id="scirp.87370-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Steel, R.O.D. and Torrie, J.H. (1980) Principles and Procedures of Statistics. A Biometrical Approach. McGraw-Hill, New York, 633 p.</mixed-citation></ref><ref id="scirp.87370-ref21"><label>21</label><mixed-citation publication-type="other" xlink:type="simple">Moraes, P.M., Perin, L.M., Todorov, S.D., Silva Jr., A., Franco, B.D. and Nero, L.A. (2012) Bacteriocinogenic and Virulence Potential of Enterococcus Isolates Obtained from Raw Milk and Cheese. Journal of Applied Microbiology, 113, 318-328. https://doi.org/10.1111/j.1365-2672.2012.05341.x</mixed-citation></ref><ref id="scirp.87370-ref22"><label>22</label><mixed-citation publication-type="other" xlink:type="simple">Jamet, E., Akary, E., Poisson, A.A.J.F., Bertrand-Chamba, X. and Serror, P. (2012) Prevalence and Characterization of Antibiotic-Resistant Enterococcus faecalis in French Cheeses. Food Microbiology, 31, 191-198. https://doi.org/10.1016/j.fm.2012.03.009</mixed-citation></ref></ref-list></back></article>