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致病性、中间型和非致病性细菌中II型毒素-抗毒素VapBC模块的遗传VapC谱分析

Analysis of Genetic VapC Profiles from the Toxin-Antitoxin Type II VapBC Modules among Pathogenic, Intermediate, and Non-Pathogenic .

作者信息

Lopes Alexandre P Y, Azevedo Bruna O P, Emídio Rebeca C, Damiano Deborah K, Nascimento Ana L T O, Barazzone Giovana C

机构信息

Laboratório Especial de Desenvolvimento de Vacinas-Centro de Biotecnologia, Instituto Butantan, Avenida Vital Brazil, 1500, 05503-900 São Paulo, Brazil.

Programa de Pós-Graduação Interunidades em Biotecnologia, Instituto de Ciências Biomédicas, USP, Avenida Prof. Lineu Prestes, 1730, 05508-900 São Paulo, Brazil.

出版信息

Microorganisms. 2019 Feb 20;7(2):56. doi: 10.3390/microorganisms7020056.

Abstract

Pathogenic spp. is the etiological agent of leptospirosis. The high diversity among species provides an array to look for important mediators involved in pathogenesis. Toxin-antitoxin (TA) systems represent an important survival mechanism on stress conditions. BC modules have been found in nearly one thousand genomes corresponding to about 40% of known TAs. In the present study, we investigated TA profiles of some strains of using a TA database and compared them through protein alignment of VapC toxin sequences among spp. genomes. Our analysis identified significant differences in the number of putative BC modules distributed in pathogenic, saprophytic, and intermediate strains: four in , three in , eight in , and 15 in . The VapC toxins show low identity among amino acid sequences within the species. Some VapC toxins appear to be exclusively conserved in unique species, others appear to be conserved among pathogenic or saprophytic strains, and some appear to be distributed randomly. The data shown here indicate that these modules evolved in a very complex manner, which highlights the strong need to identify and characterize new TAs as well as to understand their regulation networks and the possible roles of TA systems in pathogenic bacteria.

摘要

致病性物种是钩端螺旋体病的病原体。物种间的高度多样性为寻找参与发病机制的重要介质提供了一系列对象。毒素-抗毒素(TA)系统是应激条件下的一种重要生存机制。BC模块已在近一千个基因组中被发现,约占已知TA的40%。在本研究中,我们使用TA数据库研究了某些菌株的TA谱,并通过对致病性物种基因组中VapC毒素序列进行蛋白质比对来比较它们。我们的分析确定了分布在致病、腐生和中间菌株中的假定BC模块数量存在显著差异:致病性菌株中有4个,腐生菌株中有3个,中间菌株中有8个,未提及的菌株中有15个。VapC毒素在物种内的氨基酸序列间显示出低同一性。一些VapC毒素似乎仅在独特物种中保守,另一些似乎在致病或腐生菌株中保守,还有一些似乎是随机分布的。此处所示数据表明这些模块以非常复杂的方式进化,这突出表明迫切需要鉴定和表征新的TA,以及了解它们的调控网络和TA系统在致病细菌中的可能作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7282/6406750/5e0bd999957d/microorganisms-07-00056-g001.jpg

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