Septuagintavirus的分离和特征;Vequintavirinae亚科大肠杆菌噬菌体的一个新支系。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-08-05 DOI:10.1128/spectrum.00592-24
Adrián Cortés-Martín, Colin Buttimer, Nadiia Pozhydaieva, Frank Hille, Hiba Shareefdeen, Andrei S Bolocan, Lorraine A Draper, Andrey N Shkoporov, Charles M A P Franz, Katharina Höfer, R Paul Ross, Colin Hill
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引用次数: 0

摘要

大肠埃希氏菌是哺乳动物肠道微生物群中的共生菌,经常与各种胃肠道疾病相关。人们越来越有兴趣了解针对这种细菌的各种噬菌体(噬菌体),因为了解这些噬菌体可以为它们在治疗中的潜在应用铺平道路。在此,我们报告了新发现的四种感染大肠杆菌的有尾噬菌体(W70、A7-1、A5-4 和 A73)的分离和特征描述,发现它们构成了 Vequintavirinae 亚科中的一个新属--Septuagintavirus。这些噬菌体的基因组大小从 137 kbp 到 145 kbp 不等,GC 含量为 41 mol%。它们与系统发育最接近的噬菌体属 Certrevirus 的最大核苷酸相似度为 30%,而与 Vequintavirinae 科其他属的同源性有限。宿主范围分析表明,这些噬菌体对一组大肠杆菌菌株具有有限的活性,在 16 个受测分离株中,无论其系统型如何,都能感染其中的 6 个。对噬菌体 W70 的病毒体进行了电喷雾离子化-串联质谱分析(ESI-MS/MS),鉴定出 28 种结构蛋白,其中 19 种与 Vequintavirinae 家族其他属的噬菌体共享。形成尾纤结构的蛋白质具有最大的多样性,这可能表明该亚科中每个噬菌体属的病毒都能识别宿主细胞上的目标受体。本研究的发现使人们对 Vequintavirinae 亚科噬菌体有了更深入的了解,有助于丰富目前有关这些噬菌体的知识:大肠杆菌是一种众所周知的细菌,栖息于不同的生态位,包括哺乳动物的肠道微生物群。某些菌株与胃肠道疾病有关,人们对利用噬菌体(感染细菌的病毒)来对抗细菌感染的兴趣与日俱增。在这里,我们描述了四种新型大肠杆菌噬菌体的分离和特征,它们构成了 Vequintavirinae 亚科中的一个新属--Septuagintavirus。我们对这一新支系中具有代表性的噬菌体的病毒进行了质谱分析,并将其与该亚科中的其他噬菌体进行了比较。我们的分析表明,除了与宿主范围有关的尾纤结构相关的蛋白质外,所有噬菌体的病毒结构都是高度保守的。这些发现使我们对 Vequintavirinae 亚科噬菌体有了更深入的了解,有助于丰富现有的关于这些噬菌体的知识库。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation and characterization of Septuagintavirus; a novel clade of Escherichia coli phages within the subfamily Vequintavirinae.

Escherichia coli is a commensal inhabitant of the mammalian gut microbiota, frequently associated with various gastrointestinal diseases. There is increasing interest in comprehending the variety of bacteriophages (phages) that target this bacterium, as such insights could pave the way for their potential use in therapeutic applications. Here, we report the isolation and characterization of four newly identified E. coli infecting tailed phages (W70, A7-1, A5-4, and A73) that were found to constitute a novel genus, Septuagintavirus, within the subfamily Vequintavirinae. Genomes of these phages ranged from 137 kbp to 145 kbp, with a GC content of 41 mol%. They possess a maximum nucleotide similarity of 30% with phages of the closest phylogenetic genus, Certrevirus, while displaying limited homology to other genera of the Vequintavirinae family. Host range analysis showed that these phages have limited activity against a panel of E. coli strains, infecting 6 out of 16 tested isolates, regardless of their phylotype. Electrospray ionization-tandem mass spectrometry (ESI-MS/MS) was performed on the virion of phage W70, allowing the identification of 28 structural proteins, 19 of which were shared with phages of other genera of Vequintavirinae family. The greatest diversity was identified with proteins forming tail fiber structures, likely indicating the adaptation of virions of each phage genus of this subfamily for the recognition of their target receptor on host cells. The findings of this study provide greater insights into the phages of the subfamily Vequintavirinae, contributing to the pool of knowledge currently known about these phages.

Importance: Escherichia coli is a well-known bacterium that inhabits diverse ecological niches, including the mammalian gut microbiota. Certain strains are associated with gastrointestinal diseases, and there is a growing interest in using bacteriophages, viruses that infect bacteria, to combat bacterial infections. Here, we describe the isolation and characterization of four novel E. coli bacteriophages that constitute a new genus, Septuagintavirus, within the subfamily Vequintavirinae. We conducted mass spectrometry on virions of a representative phage of this novel clade and compared it to other phages within the subfamily. Our analysis shows that virion structure is highly conserved among all phages, except for proteins related to tail fiber structures implicated in the host range. These findings provide greater insights into the phages of the subfamily Vequintavirinae, contributing to the existing pool of knowledge about these phages.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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