属于 Bdellovibrionota 门的强制性捕食细菌的比较基因组学突显了特定品系蛋白质家族的分布和预测功能。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
mSphere Pub Date : 2024-11-13 DOI:10.1128/msphere.00680-24
Sidney C Davis, Joseph Cerra, Laura E Williams
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引用次数: 0

摘要

食肉细菌的比较基因组学对于了解其生态学和进化以及探索其治疗耐药性感染的潜力非常重要。我们比较了 Bdellovibrionota 门 18 种必须捕食细菌(16 种质粒内捕食细菌,2 种外捕食细菌)和 15 种非捕食细菌的染色体。保守单拷贝基因的系统发生学和全基因组平均氨基酸同一性分析提供了至少 5 种 Bdellovibrio 的证据,并支持了最近对掠食性类群的重新分类。为了确定共享和差异基因组内容,我们根据序列相似性将预测的蛋白质序列归入基因簇。所有 33 种细菌或所有 18 种捕食性细菌共享的基因簇很少;但是,我们发现了一些在各系(如质内双胞杆菌)中保守的基因簇,而这些基因簇在其他细菌中并不存在。其中许多基因被认为具有细胞膜生物发生、信号转导和其他对掠食性生活方式很重要的功能。在质膜内布氏嗜血杆菌中,我们发现了高丰度的基因簇,这些基因簇被预测为编码转糖苷酶、内肽酶和溶菌酶,我们还发现了六个基因簇(酰胺酶、L,D-转肽酶、四个转糖苷酶),这些基因簇都有近期基因复制和基因家族扩展的证据。以肽聚糖代谢为重点,我们定义了一套基因簇,其中包括肽聚糖降解酶和修饰酶,而且只出现在捕食性细菌中,这表明这些蛋白质可能进化出了捕食性细菌特有的活动。我们的分析突显了强制性捕食细菌与非捕食性近缘细菌之间的关键基因组内容差异,并确定了可能编码适应捕食性生活方式的酶的基因簇。重要意义捕食作为一种细菌生活方式的进化涉及对有助于杀死和消化猎物细菌的酶的选择性压力和适应,在某些情况下,这些酶来自猎物本身。这种酶是属于细菌门(Bdellovibrionota)的强制性捕食细菌的标志,其中包括研究得很清楚的捕食者 Bdellovibrio。通过比较强制性捕食细菌及其非捕食性近亲的蛋白质序列,我们确定了区别细菌捕食者的关键基因组内容差异,并鉴定了可能由于与捕食性生活方式相关的选择性压力而进化出独特活性的特异性酶。除了为捕食性细菌的生态学和进化提供见解之外,类似的比较基因组学研究还能为开发捕食性细菌和/或其酶作为潜在生物控制剂以对抗耐药性细菌感染提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative genomics of obligate predatory bacteria belonging to phylum Bdellovibrionota highlights distribution and predicted functions of lineage-specific protein families.

Comparative genomics of predatory bacteria is important to understand their ecology and evolution and explore their potential to treat drug-resistant infections. We compared chromosomes of 18 obligate predators from phylum Bdellovibrionota (16 intraperiplasmic, two epibiotic) and 15 non-predatory bacteria. Phylogenetics of conserved single-copy genes and analysis of genome-wide average amino acid identity provide evidence for at least five Bdellovibrio species and support recent reclassifications of predatory taxa. To define shared and differential genome content, we grouped predicted protein sequences into gene clusters based on sequence similarity. Few gene clusters are shared by all 33 bacteria or all 18 predatory bacteria; however, we identified gene clusters conserved within lineages, such as intraperiplasmic Bdellovibrio, and not found in other bacteria. Many of these are predicted to function in cell envelope biogenesis, signal transduction, and other roles important for predatory lifestyles. Among intraperiplasmic Bdellovibrio, we detected high abundance of gene clusters predicted to encode transglycosylases, endopeptidases, and lysozymes, and we identified six gene clusters (amidase, L,D-transpeptidase, four transglycosylases) with evidence of recent gene duplication and gene family expansion. Focusing on peptidoglycan metabolism, we defined a suite of gene clusters that include peptidoglycan-degrading and -modifying enzymes and occur only in predatory bacteria, suggesting these proteins may have evolved activities specific to predation. Our analyses highlight key genome content differences between obligate predatory bacteria and non-predatory relatives and identify gene clusters that may encode enzymes adapted to predatory lifestyles. These lineage-specific proteins are strong candidates for functional characterization to clarify their role in predation.IMPORTANCEEvolution of predation as a bacterial lifestyle involves selective pressure on and adaptation of enzymes that contribute to killing and digestion of prey bacteria, in some cases from within the prey itself. Such enzymes are a hallmark of obligate predatory bacteria belonging to phylum Bdellovibrionota, which includes the well-studied predator Bdellovibrio. By comparing protein sequences of obligate predatory bacteria and their non-predatory relatives, we define key genome content differences that distinguish bacterial predators and identify lineage-specific enzymes that may have evolved unique activities due to selective pressures related to a predatory lifestyle. In addition to providing insights into the ecology and evolution of predatory bacteria, comparative genomics studies, like this, can inform efforts to develop predatory bacteria and/or their enzymes as potential biocontrol agents to combat drug-resistant bacterial infections.

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来源期刊
mSphere
mSphere Immunology and Microbiology-Microbiology
CiteScore
8.50
自引率
2.10%
发文量
192
审稿时长
11 weeks
期刊介绍: mSphere™ is a multi-disciplinary open-access journal that will focus on rapid publication of fundamental contributions to our understanding of microbiology. Its scope will reflect the immense range of fields within the microbial sciences, creating new opportunities for researchers to share findings that are transforming our understanding of human health and disease, ecosystems, neuroscience, agriculture, energy production, climate change, evolution, biogeochemical cycling, and food and drug production. Submissions will be encouraged of all high-quality work that makes fundamental contributions to our understanding of microbiology. mSphere™ will provide streamlined decisions, while carrying on ASM''s tradition for rigorous peer review.
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