| Literature DB >> 26059519 |
Fei Zhang1, Yangyi Zhang1, Xintian Wen1, Xiaobo Huang1, Yiping Wen1, Rui Wu1, Qigui Yan1, Yong Huang1, Xiaoping Ma1, Qin Zhao1, Sanjie Cao1.
Abstract
Porcine pleuropneumonia is an infectious disease caused by Actinobacillus pleuropneumoniae. The identification of A. pleuropneumoniae genes, specially expressed in vivo, is a useful tool to reveal the mechanism of infection. IVIAT was used in this work to identify antigens expressed in vivo during A. pleuropneumoniae infection, using sera from individuals with chronic porcine pleuropneumonia. Sequencing of DNA inserts from positive clones showed 11 open reading frames with high homology to A. pleuropneumoniae genes. Based on sequence analysis, proteins encoded by these genes were involved in metabolism, replication, transcription regulation, and signal transduction. Moreover, three function-unknown proteins were also indentified in this work. Expression analysis using quantitative real-time PCR showed that most of the genes tested were up-regulated in vivo relative to their expression levels in vitro. IVI (in vivoinduced) genes that were amplified by PCR in different A. pleuropneumoniae strains showed that these genes could be detected in almost all of the strains. It is demonstrated that the identified IVI antigen may have important roles in the infection of A. pleuropneumoniae.Entities:
Keywords: Actinobacillus pleuropneumoniae; Differential expression; In vivo-induced genes
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Year: 2015 PMID: 26059519 DOI: 10.4014/jmb.1504.04007
Source DB: PubMed Journal: J Microbiol Biotechnol ISSN: 1017-7825 Impact factor: 2.351