巴尔通体属宿主限制性病原体的基因组学研究。

Genome dynamics Pub Date : 2009-01-01 Epub Date: 2009-08-19 DOI:10.1159/000235769
P Engel, C Dehio
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引用次数: 28

摘要

巴尔通体属由许多节肢动物传播的病原体组成,它们具有共同的宿主受限生活方式,其特点是在其特定的哺乳动物宿主中长期存在红细胞内感染,并通过吸血节肢动物传播。在没有红细胞内感染的情况下,偶然感染宿主(如人感染人畜共患病种)可引起疾病。已知四种巴尔通体的基因组序列,即人类特异性病原体杆菌状巴尔通体和金氏巴尔通体,也引起人类偶然感染的猫特异性母鸡巴尔通体,以及大鼠特异性物种tribocorum巴尔通体。这些巴尔通体的圆形染色体大小从1.44 Mb(编码1,283个基因)到2.62 Mb(编码2,136个基因)不等。它们共享一个主要由959个基因组成的合成核心基因组,具有宿主整合代谢的特征。多样的辅助基因组突出了物种水平上的动态基因组进化,从tribocorum中由于基因复制和前噬菌体和基因组岛(如在宿主适应和特异性中发挥重要作用的IV型分泌系统)的显著基因组扩增到B. quintana的大量次级基因组减少。此外,对天然居群的分析显示,在品系水平上存在明显的基因组动力学,基因组重排、缺失和扩增。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genomics of host-restricted pathogens of the genus bartonella.

The alpha-proteobacterial genus Bartonella comprises numerous arthropod-borne pathogens that share a common host-restricted life-style, which is characterized by long-lasting intraerythrocytic infections in their specific mammalian reservoirs and transmission by blood-sucking arthropods. Infection of an incidental host (e.g. humans by a zoonotic species) may cause disease in the absence of intra-erythrocytic infection. The genome sequences of four Bartonella species are known, i.e. those of the human-specific pathogens Bartonella bacilliformis and Bartonella quintana, the feline-specific Bartonella henselae also causing incidental human infections, and the rat-specific species Bartonella tribocorum. The circular chromosomes of these bartonellae range in size from 1.44 Mb (encoding1,283 genes) to 2.62 Mb (encoding 2,136 genes). They share a mostly synthenic core genome of 959 genes that features characteristics of a host-integrated metabolism. The diverse accessory genomes highlight dynamic genome evolution at the species level, ranging from significant genome expansion in B. tribocorum due to gene duplication and lateral acquisition of prophages and genomic islands (such as type IV secretion systems that adopted prominent roles in host adaptation and specificity) to massive secondary genome reduction in B. quintana. Moreover, analysis of natural populations of B. henselae revealed genomic rearrangements, deletions and amplifications, evidencing marked genome dynamics at the strain level.

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