Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059

A 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...

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Main Authors: Sthitmatee N., Kataoka Y., Sawada T.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-82955251111&partnerID=40&md5=e41cb22858fcff790daa6023d043abba
http://www.ncbi.nlm.nih.gov/pubmed/21747216
http://cmuir.cmu.ac.th/handle/6653943832/7500
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-75002014-08-30T04:11:40Z Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059 Sthitmatee N. Kataoka Y. Sawada T. A 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. 2014-08-30T04:11:40Z 2014-08-30T04:11:40Z 2011 Article 9167250 http://www.scopus.com/inward/record.url?eid=2-s2.0-82955251111&partnerID=40&md5=e41cb22858fcff790daa6023d043abba http://www.ncbi.nlm.nih.gov/pubmed/21747216 http://cmuir.cmu.ac.th/handle/6653943832/7500 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description A 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.
format Article
author Sthitmatee N.
Kataoka Y.
Sawada T.
spellingShingle Sthitmatee N.
Kataoka Y.
Sawada T.
Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
author_facet Sthitmatee N.
Kataoka Y.
Sawada T.
author_sort Sthitmatee N.
title Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
title_short Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
title_full Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
title_fullStr Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
title_full_unstemmed Inhibition of capsular protein synthesis of pasteurella multocida strain P-1059
title_sort inhibition of capsular protein synthesis of pasteurella multocida strain p-1059
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-82955251111&partnerID=40&md5=e41cb22858fcff790daa6023d043abba
http://www.ncbi.nlm.nih.gov/pubmed/21747216
http://cmuir.cmu.ac.th/handle/6653943832/7500
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