Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/50371
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dc.contributor.authorNattawooti Sthitmateeen_US
dc.contributor.authorYasushi Kataokaen_US
dc.contributor.authorTakuo Sawadaen_US
dc.date.accessioned2018-09-04T04:31:20Z-
dc.date.available2018-09-04T04:31:20Z-
dc.date.issued2011-11-01en_US
dc.identifier.issn13477439en_US
dc.identifier.issn09167250en_US
dc.identifier.other2-s2.0-82955251111en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=82955251111&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50371-
dc.description.abstractA mutant strain, PBA322, was constructed by electroporation of a phagemid containing the coding region of antisense RNA of the ompH gene, encoding 39 kDa capsular protein or OmpH, into the parental strain P-1059 (serovar A:3) of Pasteurella multocida, and the pathogenicity was determined in mice and chickens. Grayish colonies of the mutant, indicating loss of capsule synthesis, were observed under a stereomicroscope using obliquely transmitted light, while iridescent colonies were observed for the parental strain. Moreover, strain PBA322 showed a low amount of OmpH compared with the parental strain on SDS-PAGE. Additionally, the capsule of strain PBA322 was thinner than that of the parental strain according to electron microscopy, correlating to the attenuation against chickens. In conclusion, strain PBA322, the mutant of P. multocida strain P-1059, was completely attenuated for chickens.en_US
dc.subjectVeterinaryen_US
dc.titleInhibition of capsular protein synthesis of pasteurella multocida strain P-1059en_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Veterinary Medical Scienceen_US
article.volume73en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsNippon Veterinary and Life Science Universityen_US
article.stream.affiliationsKyoto Biken Laboratoriesen_US
Appears in Collections:CMUL: Journal Articles

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