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  <titleInfo>
    <title>Bacteria associated with respiratory tract infections in rabbits</title>
  </titleInfo>
  <name type="personal">
    <namePart>Jini Jeorge</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Koshy John (Guide)</namePart>
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    <place>
      <placeTerm type="text">Mannuthy</placeTerm>
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    <publisher>Department of Veterinary Microbiology, College of Veterinary and Animal Sciences</publisher>
    <dateIssued>2009</dateIssued>
    <dateIssued encoding="marc">9999</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">und</languageTerm>
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    <extent>104</extent>
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  <abstract>A study was undertaken to isolate the bacteria associated with respiratory tract infections in rabbits. In this study, isolation, identification and antibiotic susceptibility of the isolates as well as determination of their pathogenicity to mice were carried out. Samples were collected from ailing and dead rabbits. Nasal  swabs from the ailing rabbits showing clinical signs such as nasal discharge and  respiratory distress, tracheal and  lung samples of the  dead rabbits  with post mortem lesions such as pneumonia, congestion of lungs  and  haemorrhages of   trachea were collected for the isolation trials. These samples were collected from rabbit farm attached to Kerala Agricultural University, commercial farms in Malapuram district, dead rabbits brought to Centre of Excellence in Pathology for post mortem and ailing animals brought for microbiological examination   to the Department of Veterinary Microbiology. A total of 62 samples were collected, comprising of 30 nasal swabs, 25 lung samples and 7 tracheal swabs, for the isolation of the organisms.

Brain Heart Infusion Agar (BHIA) and Blood Agar were used for the primary isolation   of the organisms. In the present study 32 isolates were obtained in which Staphylococcus sp. contributed 59.56 per cent  of the total isolates,  E. coli contributed 25  per cent,  Klebsiella sp.  9.43 per cent, Streptococcus uberis 3.31 per cent and Pasteurella multocida 3.13 per cent. The bacteria were isolated and identified based on morphology, cultural and biochemical tests. In Staphylococcus sp. 19 isolates were obtained, comprising of Staphylococcus aureus-11, Staphylococcus scuri -2 , Staphylococcus xylosus- 1, Staphylococcus intermedius-2, Staphylococcus cohnii -2 and  Staphylococcus lentus-  1. Other isolates were Streptococcus uberis -1, Pasteurella multocida -1, E. coli -8, Klebsiella pneumoniae -2 and Klebsiella ozaenae-1.

Most of the Staphylococcus sp. showed resistance to sulphadiazine, polymyxin B, co-trimoxazole, amoxycillin and oxytetracycline. The antimicrobial susceptibility pattern shown by the isolates exhibited multi-drug resistance. Multi drug resistance was also observed for E. coli isolates to amoxycillin, cefuroxime, gentamicin, carbenicillin, methicillin, chloramphenicol, enrofloxacin, oxytetracycline, penicillin G, nitrofurantoin, cefotaxime, oxacillin, streptomycin and erythromycin.  Klebsiella sp. only showed sensitivity to enrofloxacin, gentamicin, cefotaxime, streptomycin and ciprofloxacin and highly resistant  to  amoxycillin,  carbenicillin, methicilin, oxytetracycline, co-trimoxazole, penicillin G, nitrofurantoin,  sulphadiazine, polymyxin B, bacitracin, erythromycin and ciprofloxacin. 

On pathogenicity testing in mice only four isolates of S. aureus, five isolates of E. coli, two isolates of K.  pneumoniae and   one isolate of Pasteurella multocida caused death of the mice. The other isolates of  S. aureus didn’t cause  death of mice but could be   re-isolated  from the sacrificed mice after completion of the observation period. The S.scuri, S. xylosus,  S. intermedius, S. cohnii and S. lentus isolates didn’t cause death in mice and the organisms were not  re -isolated from lungs, liver, spleen and heart of the mice on sacrifice after 14 days observation period. The Streptococcus uberis isolate also didn’t cause death in mice and the organisms could not be re-isolated from lungs, liver, spleen and heart   of the sacrificed mice.</abstract>
  <note>MVSc</note>
  <classification authority="ddc">636.0896 JIN/BA PG</classification>
  <identifier type="uri">http://krishikosh.egranth.ac.in/handle/1/5810027756</identifier>
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