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钩端螺旋体基因组学与发病机制。

Leptospiral Genomics and Pathogenesis.

机构信息

Melbourne Bioinformatics, The University of Melbourne, Carlton, VIC, Australia.

Department of Microbiology, Monash University, Clayton, VIC, Australia.

出版信息

Curr Top Microbiol Immunol. 2018;415:189-214. doi: 10.1007/82_2018_87.

Abstract

Until about 15 years ago, the molecular and cellular basis for pathogenesis in leptospirosis was virtually unknown. The determination of the first full genome sequence in 2003 was followed rapidly by other whole genome sequences, whose availability facilitated the development of transposon mutagenesis and then directed mutagenesis of pathogenic Leptospira spp. The combination of genomics, transcriptomics and mutant construction and characterisation has resulted in major progress in our understanding of the taxonomy and biology of Leptospira. The most recent advances are analysed and discussed in this chapter.

摘要

大约 15 年前,钩端螺旋体病发病机制的分子和细胞基础几乎不为人知。2003 年首次确定了完整基因组序列,随后迅速确定了其他全基因组序列,这些序列的出现促进了转座子诱变的发展,然后对致病性钩端螺旋体进行了定向诱变。基因组学、转录组学和突变体构建与鉴定的结合,使我们对钩端螺旋体的分类学和生物学有了重大的认识进展。本章对最近的进展进行了分析和讨论。

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