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Genome Biology of Actinobacillus pleuropneumoniae JL03 an Isolate of Serotype 3 Prevalent in China

机译:中国流行的3型血清分离株胸膜肺炎放线杆菌JL03的基因组生物学

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摘要

Actinobacillus pleuropneumoniae is the etiologic agent of porcine contagious pleuropneumonia, a cause of considerable world wide economic losses in the swine industry. We sequenced the complete genome of A. pleuropneumoniae, JL03, an isolate of serotype 3 prevalent in China. Its genome is a single chromosome of 2,242,062 base pairs containing 2,097 predicted protein-coding sequences, six ribosomal rRNA operons, and 63 tRNA genes. Preliminary analysis of the genomic sequence and the functions of the encoded proteins not only confirmed the present physiological and pathological knowledge but also offered new insights into the metabolic and virulence characteristics of this important pathogen. We identified a full spectrum of genes related to its characteristic chemoheterotrophic catabolism of fermentation and respiration with an incomplete TCA system for anabolism. In addition to confirming the lack of ApxI toxin, identification of a nonsense mutation in apxIVA and a 5′-proximal truncation of the flp operon deleting both its promoter and the flp1flp2tadV genes have provided convincing scenarios for the low virulence property of JL03. Comparative genomic analysis using the available sequences of other serotypes, probable strain (serotype)-specific genomic islands related to capsular polysaccharides and lipopolysaccharide O-antigen biosyntheses were identified in JL03, which provides a foundation for future research into the mechanisms of serotypic diversity of A. pleuropneumoniae.
机译:胸膜肺炎放线杆菌是猪传染性胸膜肺炎的病原体,是猪业在世界范围内造成巨大经济损失的原因。我们对胸膜肺炎链球菌JL03(在中国流行的血清型3的分离株)的完整基因组进行了测序。它的基因组是一个具有2,242,062个碱基对的单染色体,其中包含2,097个预测的蛋白质编码序列,六个核糖体rRNA操纵子和63个tRNA基因。对基因组序列和编码蛋白功能的初步分析不仅证实了目前的生理和病理学知识,而且还提供了对该重要病原体的代谢和毒力特性的新见解。我们确定了一个与不完整的TCA系统合成代谢相关的全谱基因,这些基因与其发酵和呼吸的特征性化学营养分解代谢有关。除了确认缺乏ApxI毒素外,鉴定apxIVA中的无意义突变以及flp操纵子的5'-近端截短都删除了其启动子和flp1flp2tadV基因,这为JL03的低毒力特性提供了令人信服的方案。在JL03中鉴定了使用其他血清型的可用序列进行的比较基因组分析,与荚膜多糖和脂多糖O抗原生物合成有关的可能的菌株(血清型)特异性基因岛,这为将来研究A的血清型多样性机制提供了基础胸膜肺炎

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