College of Animal Science and Veterinary Medicine, Jilin University, Xi’an Street 5333#, Changchun, People's Republic of China.
Curr Microbiol. 2011 Oct;63(4):327-31. doi: 10.1007/s00284-011-9986-1. Epub 2011 Jul 20.
The development of serotyping-based diagnostic methods and multivalent vaccines has been significantly hampered due to the limited information available on the genetic differences among the 15 currently known serotypes of Actinobacillus pleuropneumoniae. In this study, using the GenomeComp informatics software, differential genes were screened and identified between the complete genome sequences of the serotypes 5b (L20 strain, highly virulent) and 3 (JL03 strain, weakly virulent), 84 presented uniquely in strain L20, while 57 were only found in JL03 strain. Of these, 75 encode putative proteins and 66 encode hypothetical proteins, including phage-related proteins, Apx toxin, capsular polysaccharide biosynthesis proteins, ATP-binding cassette (ABC) transporters, Clp-like proteases, fimbrial protein (Flp), various glycosyltransferases, methylases, integrases, and other proteins related to virulence. To confirm and further characterize the differential genes, we carefully selected 34 proven or putative virulence genes which were extremely useful on researching into detection and vaccine of A. pleuropneumoniae, and investigated the distribution and transcription of these genes among the 15 serotypes through polymerase chain reaction, reverse transcriptase- polymerase chain reaction and sequencing, and different distribution and transcription patterns of the differential genes in each serotype were first found and described. These information of these differential genes among the 15 serotypes of A. pleuropneumoniae may greatly serve as an indicator for future research on the pathogenic mechanisms of different serotypes, serotyping-based diagnostic methods, and multivalent vaccines.
由于目前已知的 15 种胸膜肺炎放线杆菌血清型之间的遗传差异信息有限,基于血清型的诊断方法和多价疫苗的发展受到了显著阻碍。在这项研究中,使用 GenomeComp 信息学软件,在血清型 5b(L20 株,高致病性)和 3(JL03 株,弱致病性)的全基因组序列之间筛选和鉴定了差异基因,84 个基因仅在 L20 株中存在,而 57 个基因仅在 JL03 株中存在。其中,75 个基因编码假定蛋白,66 个基因编码假定蛋白,包括噬菌体相关蛋白、Apx 毒素、荚膜多糖生物合成蛋白、ATP 结合盒(ABC)转运蛋白、Clp 样蛋白酶、菌毛蛋白(Flp)、各种糖基转移酶、甲基酶、整合酶和其他与毒力相关的蛋白。为了确认和进一步表征差异基因,我们仔细选择了 34 个已证实或假定的毒力基因,这些基因对于胸膜肺炎放线杆菌的检测和疫苗研究非常有用,并通过聚合酶链反应、逆转录聚合酶链反应和测序研究了这些基因在 15 个血清型中的分布和转录情况,首次发现并描述了这些差异基因在每个血清型中的不同分布和转录模式。这些胸膜肺炎放线杆菌 15 个血清型之间的差异基因信息可能极大地为不同血清型的致病机制、基于血清型的诊断方法和多价疫苗的未来研究提供指示。