Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/6435
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dc.contributor.authorShivachandra, S B-
dc.contributor.authorKumar, A A-
dc.contributor.authorGautam, R-
dc.contributor.authorJoseph, S-
dc.contributor.authorChaudhuri, P-
dc.contributor.authorSaxena, M K-
dc.contributor.authorSrivastava, S K-
dc.contributor.authorSingh, Nem-
dc.date.accessioned2009-11-05T06:35:32Z-
dc.date.available2009-11-05T06:35:32Z-
dc.date.issued2006-04-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/6435-
dc.description321-324en_US
dc.description.abstractApplicability of polymerase chain reaction (PCR) assay to detect Pasteurella multocida in experimentally infected embryonated chicken egg was assessed in the present study. PCR assay rapidly and specifically detected the genome of P. multocida in amniotic fluid, allantoic fluid and homogenates of infected embryo and its membranes. The sensitivity of detection was as low as 20 bacterial cells/ml of allantoic or amniotic fluids. Detection of P. multocida in dead embryos by PCR was possible up to 6 and 30 days or more following storage of dead embryos at 37oC, and at 4oC as well as at -20oC, respectively. The study revealed that PCR assays could be employed directly for detection and confirmation of P. multocida infection in experimentally infected chicken embryos.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.sourceIJEB Vol.44(04) [April 2006]en_US
dc.subjectChick embryoen_US
dc.subjectPasteurella multocidaen_US
dc.subjectPCRen_US
dc.titleDetection of Pasteurella multocida in experimentally infected embryonated chicken eggs by PCR assayen_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.44(04) [April 2006]

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