<?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">OALibJ</journal-id><journal-title-group><journal-title>Open Access Library Journal</journal-title></journal-title-group><issn pub-type="epub">2333-9705</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/oalib.1101808</article-id><article-id pub-id-type="publisher-id">OALibJ-68589</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> Business&amp;Economics</subject><subject> Chemistry&amp;Materials Science</subject><subject> Computer Science&amp;Communications</subject><subject> Earth&amp;Environmental Sciences</subject><subject> Engineering</subject><subject> Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject><subject> Social Sciences&amp;Humanities</subject></subj-group></article-categories><title-group><article-title>
 
 
  Bacteria Isolated from the Oropharynxs of Apparently Healthy Chickens in Jos, Nigeria
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yakubu</surname><given-names>G. Dashe</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>Moshood</surname><given-names>A. Raji</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>Paul</surname><given-names>A. Abdu</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Blessing</surname><given-names>S. Oladele</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lola</surname><given-names>Oluwadare</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Department of Veterinary Microbiology, Ahmadu Bello University, Zaria, Nigeria</addr-line></aff><aff id="aff4"><addr-line>Department of Veterinary Pathology, Ahmadu Bello University, Zaria, Nigeria</addr-line></aff><aff id="aff3"><addr-line>Department of Veterinary Medicine, Ahmadu Bello University, Zaria, Nigeria</addr-line></aff><aff id="aff1"><addr-line>National Veterinary Research Institute, Akure Zonal Office, State Veterinary Hospital, Akure, Nigeria</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>yakubudashe@yahoo.co.uk(YGD)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>30</day><month>09</month><year>2015</year></pub-date><volume>02</volume><issue>09</issue><fpage>1</fpage><lpage>5</lpage><history><date date-type="received"><day>10</day>	<month>August</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>26</month>	<year>August</year>	</date><date date-type="accepted"><day>1</day>	<month>September</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>
 
 
   
   There are concerns that apparently healthy chickens may transmit potentially pathogenic pathogens that could threaten not only poultry industry, but also public health. This investigative study was carried out in Jos, Nigeria to determine the prevalent bacterial agents in the oropharynxs of apparently healthy chickens. Four hundred (400) oropharyngeal swabs were collected from 400 apparently healthy chickens for bacteriological analysis. Swab from each sample was cultured on 7% defibrinated sheep blood, Casein Sucrose Yeast (CSY) agar and MacConkey. Oropharyngeal swabs were cultured indirectly by inoculating into 5 ml of brain heart infusion broth (BHI), incubated at 37℃ for 24 h and then streaked unto Casein Sucrose Yeast (CSY) agar, MacConkey agar and Blood agar. Presumptive colonies of bacterial agents were subjected to conventional biochemical characterization. The result of biochemical test identified the following bacteria: 
   Staphylococcus aureus 
   82 (20.5%),
    Escherichia coli 
   53 (13.3%),
    Klebsiella pneumonia 
   35 (8.8%) and
    Proteus species 
   26 (6.6%), 
   Pasteurella multocida
    5 (1.3%)
    
   among others. 
   Staphylococcus aureus 
   (20.5%) was the highest followed by
    Escherichia coli 
   (13.3%), 
   Klebsiella pneumoniae
    (8.8%) and 
   Pasteurella multocida 
   (1.3%) was the least. It was concluded that the oropharynxs of apparently healthy chickens harbored a lot of bacterial agents which could cause infections when the immune system was compromised. 
  
 
</p></abstract><kwd-group><kwd>Aerobic</kwd><kwd> Bacteria</kwd><kwd> Chicken</kwd><kwd> Jos</kwd><kwd> Nigeria</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Bacteria are known to be associated with a variety of poultry diseases. Escherichia coli is a common avian pathogen which contributes to enormous losses in poultry industry. Bacillus subtilis produces serine proteinase (trypsin and chymotrypsin) which contributes to causing mortality in affected birds [<xref ref-type="bibr" rid="scirp.68589-ref1">1</xref>] . Staphylococcus species cause acute death in laying birds and seem to be prevalent in tropical environment. E. coli and Staphylococcus species can also act as secondary bacteria to exacerbate clinical conditions leading to high mortality [<xref ref-type="bibr" rid="scirp.68589-ref2">2</xref>] . Klebsiella pneumoniae can occasionally cause embryonic mortality and severe losses in young chickens and turkeys [<xref ref-type="bibr" rid="scirp.68589-ref3">3</xref>] . Aeromonas hydrophila alone or concurrently with other organisms can cause localized and systemic infections in avian species including poultry [<xref ref-type="bibr" rid="scirp.68589-ref4">4</xref>] . Proteus species occasionally cause embryonic death, yolk sac infections, and mortality in young chickens, turkeys and ducks [<xref ref-type="bibr" rid="scirp.68589-ref5">5</xref>] .</p><p>Despite the established roles of bacteria in causing opportunistic infections in poultry, there is a paucity of information on the prevalent bacteria in the oropharynxs of chickens in Jos, Nigeria. This study is therefore aimed at determining the prevalent bacterial agents in the oropharynxs of apparently healthy chickens in Jos, Nigeria.</p></sec><sec id="s2"><title>2. Materials and Methods</title><sec id="s2_1"><title>2.1. Study Area</title><p>The study was conducted in Jos North and South Local Government Areas of Plateau state, which is located between latitudes 8.50˚N - 100.46˚N and longitudes 8.20˚E - 10.36˚E in the North-Central geopolitical zone of Nigeria. Plateau state shares common borders with four of the 36 states of the country. To the South-West is Nasarawa, while to the North-West and North-East are Kaduna and Bauchi respectively and to the South-East is Taraba state. The Jos terrain consists of a flat land resembling a table top, from which the name “Plateau” of the state is derived. According to the report of [<xref ref-type="bibr" rid="scirp.68589-ref6">6</xref>] , at Jos, the average monthly temperature ranges between 21˚C and 25˚C (69˚F and 77˚F), the average humidity is 60% and the average annual rainfall is 1400 mm (56&quot;). Owing to its high altitude placement, Jos has a much cooler weather when compared with most other parts of Nigeria. The vegetation of the area is extensive highland savannah with short grasses interspersed with very few trees. There are two major seasons on the Jos Plateau: A long dry season that commences at about the middle of October and ends in March. Jos receives an average of 1351 mm of precipitation annually, and up to 96 percent of the rainfall occurs between April and September of each year [<xref ref-type="bibr" rid="scirp.68589-ref7">7</xref>] . According to 2006 national Census of Nigeria Report [<xref ref-type="bibr" rid="scirp.68589-ref8">8</xref>] , Jos North LGA has a land area of 291 km<sup>2</sup> and a population of 429,300, while Jos South LGA has a land area of 510 km<sup>2</sup> and a population of 306,716. The study area was purposively chosen for this study because of the availability of veterinary hospitals and clinics, high concentration of poultry farms and willingness of poultry owners and clinicians to cooperate with the researchers.</p></sec><sec id="s2_2"><title>2.2. Collection of Samples</title><p>Poultry clinics, poultry farms and live birds markets were identified in Jos North (Railway-terminus and Yan Kaji) and South Local Government Areas (National Veterinary Research Institute canteen and Poultry Division Vom, Kugiya in Bukuru) for sample collection.</p></sec><sec id="s2_3"><title>2.3. Sampling Method</title><p>Systematic random sampling method (one in five; every 5<sup>th</sup> bird on each visit) was applied for the selection of 400 apparently healthy chickens between November, 2010 and October, 2011 (8 chickens/week).</p></sec><sec id="s2_4"><title>2.4. Sampling Locations</title><p>Sampling of apparently healthy chickens</p><p>Notable areas in Jos South such as National Veterinary Research Institute canteen and Poultry Division Vom and Jos North (Kugiya in Bukuru, Railway-terminus and Yan Kaji) were used for the collection of four hundred oro-pharyngeal swabs from apparently healthy chickens. Eighty oro-pharyngeal swabs were collected at each of the five locations.</p></sec><sec id="s2_5"><title>2.5. Transportation of Samples</title><p>The samples collected were transported on ice to the Bacteriology Unit of the Central Diagnostic Laboratory, NVRI, Vom for culture and microbiological examination as described by [<xref ref-type="bibr" rid="scirp.68589-ref9">9</xref>] .</p></sec><sec id="s2_6"><title>2.6. Culture and Isolation of Organism</title><p>Oro-pharyngeal swabs were cultured indirectly by first inoculating each sample into 5 ml of brain heart infusion broth (BHI), followed by incubation of the broth mixture at 37˚C for 24 h and then streaking loop samples of the broth culture unto media such as Casein Sucrose Yeast (CSY) agar, Blood and MacConkey agar. Colonies representing each bacteria species were identified and characterized according to the methods described by [<xref ref-type="bibr" rid="scirp.68589-ref10">10</xref>] , while organisms belonging to the Enterobacteriaceace were identified using standard biochemical methods described by [<xref ref-type="bibr" rid="scirp.68589-ref10">10</xref>] . Presumptive Pasteurella multocida colonies were subjected to Gram and methylene blue staining for cellular morphology. Cultural and morphological examinations were conducted as described by [<xref ref-type="bibr" rid="scirp.68589-ref10">10</xref>] . Capsular and bipolar organisms were further confirmed as Pasteurella multocida by biochemical tests according to [<xref ref-type="bibr" rid="scirp.68589-ref9">9</xref>] . The biochemical reagents and tests used included: Triple sugar iron agar, urease, Simmons citrate, nitrate, indole, motility, methyl red and Voges Proskauer. Catalase, and coagulase tests were performed on presumed Staphylococcus aureus isolates.</p></sec><sec id="s2_7"><title>2.7. Microbact Test</title><p>All Pasteurella multocida, Escherichia coli, Aeromonas hydrophila isolates recovered by biochemical tests were further subjected to additional analytical profile test using Oxoid<sup>TM</sup> Microbact GNB 24E kit (a commercially available biochemical test kit in microplate format for identifying Enterobacteriaceae and miscellaneous Gram negative bacilli) and this was done according to the manufacturer’s instruction.</p></sec><sec id="s2_8"><title>2.8. Statistical Analysis</title><p>Data generated was entered and processed using Microsoft Excel 2010. Descriptive statistical analysis was conducted using [<xref ref-type="bibr" rid="scirp.68589-ref11">11</xref>] and the results were summarized as percentages in a table.</p></sec></sec><sec id="s3"><title>3. Results</title><p>From the 400 oro-pharyngeal swabs collected, a total of 7 aerobic bacterial species were isolated from 250 (62.5%) samples, while the remaining 150 (37.5%) yielded no bacteria. Of the bacteria isolated, 3 (42.8%) were gram positive, while 4 (57.1%) gram negative. Bacterial isolated from the apparently healthy chickens indicated that Staphylococcus aureus 82 (20.5%) was the highest followed by Escherichia coli 53 (13.3%), Klebsiella pneumoniae 35 (8.8%) and Pasteurella multocida 5 (1.3%) was the least (<xref ref-type="table" rid="table1">Table 1</xref>). Microbact test identified Pasteurella multocida (1.0%) and Escherichia coli (7.5%) from the oro-pharyngeal swabs apparently healthy chickens.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Bacteria isolated from oropharynxs of apparently healthy chickens in Jos, Nigeria</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Bacteria</th><th align="center" valign="middle" >Number of bacteria isolated</th><th align="center" valign="middle" >Percentage (%)</th></tr></thead><tr><td align="center" valign="middle" >Staphylococcus aureus</td><td align="center" valign="middle" >82</td><td align="center" valign="middle" >20.5</td></tr><tr><td align="center" valign="middle" >Escherichia coli</td><td align="center" valign="middle" >53</td><td align="center" valign="middle" >13.3</td></tr><tr><td align="center" valign="middle" >Klebsiella pneumoniae</td><td align="center" valign="middle" >35</td><td align="center" valign="middle" >8.8</td></tr><tr><td align="center" valign="middle" >E. coli and Staphylococcus aureus</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >4</td></tr><tr><td align="center" valign="middle" >Pasteurella multocida</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >1.3</td></tr><tr><td align="center" valign="middle" >Streptococcus pneumoniae</td><td align="center" valign="middle" >18</td><td align="center" valign="middle" >4.5</td></tr><tr><td align="center" valign="middle" >Bacillus species</td><td align="center" valign="middle" >15</td><td align="center" valign="middle" >3.8</td></tr><tr><td align="center" valign="middle" >Proteus species</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >6.5</td></tr><tr><td align="center" valign="middle" >No bacterial growth</td><td align="center" valign="middle" >150</td><td align="center" valign="middle" >37.5</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >400</td><td align="center" valign="middle" >100</td></tr></tbody></table></table-wrap></sec><sec id="s4"><title>4. Discussion</title><p>Bacterial agents have been reported to contribute immensely to economic losses incurred in poultry production in Nigeria [<xref ref-type="bibr" rid="scirp.68589-ref12">12</xref>] . Some of the bacterial species isolated in the present study such as S. aureus and Proteus species are considered to be opportunistic invaders from environmental sources, while others (E. coli, Klebsiella species) are normal intestinal flora of poultry, but could cause infections whenever the immune system of affected bird is compromised [<xref ref-type="bibr" rid="scirp.68589-ref13">13</xref>] . It was observed that none of the chickens from which oro-pharyngeal swab was taken showed any clinical signs of disease, suggesting that the pathogens were present as subclinical infections, or as commensals in the chickens. Though the chickens appeared to be apparently healthy, the high prevalence of potentially pathogenic bacteria species isolated from their oro-pharynx could signify that they could possibly act as reservoirs for the bacterial species detected, with the potential risk of transmitting these pathogens to other poultry. The preponderance of these bacterial agents in apparently healthy poultry could possibly be responsible for their worldwide association with various disease conditions in a broad range of host including domestic and wild birds. This study also indicated that there were predominantly gram negative bacteria compared to gram positive. This finding is concurred to the report of [<xref ref-type="bibr" rid="scirp.68589-ref14">14</xref>] . The reflection of bacteria type identified in this study could have a significant impact on the chickens based on the severity of diseases they caused when the immune system was compromised. [<xref ref-type="bibr" rid="scirp.68589-ref2">2</xref>] reported that the activities of some aerobic bacteria, such as E. coli, Staphylococcus species and others could exacerbate clinical conditions leading to high mortality. The high isolation rate of E. coli in the oropharynx could probably be attributed to the ability of the organism to be acquired from the environment within the few days after hatching. This bacterium has also been reported to be one of the commonest bacteria that complicate both bacterial and viral diseases of poultry [<xref ref-type="bibr" rid="scirp.68589-ref15">15</xref>] .</p><p>Despite the fact that the isolation rate of P. multocida was low, the implication of the isolation of this organism was that it could act as secondary invader during other diseases. These findings have also revealed that apparently healthy chickens can be carriers of P. multocida. [<xref ref-type="bibr" rid="scirp.68589-ref16">16</xref>] reported that P. multocida had been consistently recovered in the upper respiratory tract of apparently and clinically sick birds. This suggests that this bacterium might have played a significant role in the fulminating and high mortality encountered during fowl cholera outbreaks. The finding of this study conformed to the previous report of [<xref ref-type="bibr" rid="scirp.68589-ref17">17</xref>] who opined that in their study on relationship of Pasteurella isolated from free ranging chickens and contact animals that healthy chickens could be carriers of P. multocida which caused clinical disease when the immune system was compromised. In a similar study conducted by [<xref ref-type="bibr" rid="scirp.68589-ref18">18</xref>] also indicated that carriers of P. multocida might exist within poultry flocks with no history of previous outbreaks of fowl cholera and they might play a dominant role in the transmission of the disease. [<xref ref-type="bibr" rid="scirp.68589-ref19">19</xref>] asserted that the pathogenicity P. multocida increased by bird-to-bird passage over a short period of time; this may indicate that natural passage of P. multocida between the birds may enhance the virulence of a normally avirulent strain, leading to clinical disease in a flock of carriers. The isolation of these micro-organisms in the present study suggests their probable role in the epizootiology and source of infections to susceptible domestic birds, since oro-pharyngeal carriage contribute to the shedding of these bacteria, which may add to the rapid spread of infections for other domestic poultry.</p><p>The finding of this study has shown that aerobic bacterial agents were present in the oro-pharynx of apparently healthy chickens in Jos metropolis. Further study to elucidate the role and associated economic impact of these organisms during outbreaks is recommended.</p></sec><sec id="s5"><title>Acknowledgements</title><p>The authors acknowledge the assistance of the Executive Director Veterinary Research, Vom, staff of Molecular Biology Department, National Veterinary Research Institute, Vom and Central Diagnostic Laboratory.</p></sec><sec id="s6"><title>Cite this paper</title><p>Yakubu G. Dashe,Moshood A. Raji,Paul A. Abdu,Blessing S. Oladele,Lola Oluwadare, (2015) Bacteria Isolated from the Oropharynxs of Apparently Healthy Chickens in Jos, Nigeria. Open Access Library Journal,02,1-5. doi: 10.4236/oalib.1101808</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.68589-ref1"><label>1</label><mixed-citation publication-type="book" xlink:type="simple">Glisson, J.R., Hofacre, C.L. and Christensen, J.P. (2003) Avian Pasteurellosis. 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