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转座原噬菌体在钩端螺旋体中的分布:一种古老而多样的群体,在韦尔氏病病原体中占主导地位。

Transposable Prophages in Leptospira: An Ancient, Now Diverse, Group Predominant in Causative Agents of Weil's Disease.

机构信息

Laboratoire Microorganismes: Genome Environment (LMGE), Université Clermont Auvergne, CNRS, F-63000 Clermont-Ferrand, France.

Microbiologie Cellulaire et Moléculaire, Université Libre de Bruxelles, IBMM-DBM, 12 Rue des Professeurs Jeneer et Brachet, B-6041 Gosselies, Belgium.

出版信息

Int J Mol Sci. 2021 Dec 14;22(24):13434. doi: 10.3390/ijms222413434.

DOI:10.3390/ijms222413434
PMID:34948244
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8705779/
Abstract

The virome associated with the corkscrew shaped bacterium Leptospira, responsible for Weil's disease, is scarcely known, and genetic tools available for these bacteria remain limited. To reduce these two issues, potential transposable prophages were searched in genomes. The 236 predicted transposable prophages were particularly abundant in the most pathogenic leptospiral clade, being potentially involved in the acquisition of virulent traits. According to genomic similarities and phylogenies, these prophages are distantly related to known transposable phages and are organized into six groups, one of them encompassing prophages with unusual TA-TA ends. Interestingly, structural and transposition proteins reconstruct different relationships between groups, suggesting ancestral recombinations. Based on the baseplate phylogeny, two large clades emerge, with specific gene-contents and high sequence divergence reflecting their ancient origin. Despite their high divergence, the size and overall genomic organization of all prophages are very conserved, a testimony to the highly constrained nature of their genomes. Finally, similarities between these prophages and the three known non-transposable phages infecting , suggest gene transfer between different Caudovirales inside their leptospiral host, and the possibility to use some of the transposable prophages in that model strain.

摘要

与导致韦尔病的旋体菌(Leptospira)相关的病毒组几乎不为人知,这些细菌可用的遗传工具仍然有限。为了减少这两个问题,在基因组中搜索了潜在的可移动原噬菌体。在最具致病性的钩端螺旋体菌目中,预测的 236 个可移动原噬菌体特别丰富,可能参与了毒力性状的获得。根据基因组的相似性和系统发育,这些原噬菌体与已知的可移动噬菌体关系较远,分为六个组,其中一个组包含具有不寻常 TA-TA 末端的原噬菌体。有趣的是,结构和转位蛋白在组之间重建了不同的关系,表明存在祖先重组。基于基板系统发育,出现了两个大的分支,具有特定的基因含量和高序列差异,反映了它们的古老起源。尽管存在高度的分化,但所有原噬菌体的大小和整体基因组组织都非常保守,证明了它们基因组的高度约束性。最后,这些原噬菌体与感染的三种已知非可移动噬菌体之间的相似性表明,不同的长尾病毒目之间在其螺旋体宿主中发生了基因转移,并且有可能在该模式菌株中使用一些可移动原噬菌体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/e4a958217568/ijms-22-13434-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/9e7444a4ab65/ijms-22-13434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/df408758d33a/ijms-22-13434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/d25738d811b2/ijms-22-13434-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/e4a958217568/ijms-22-13434-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/9e7444a4ab65/ijms-22-13434-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/df408758d33a/ijms-22-13434-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/d25738d811b2/ijms-22-13434-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ac/8705779/e4a958217568/ijms-22-13434-g004.jpg

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