College of Food Science and Engineering, Yangzhou University, Yangzhou, Jiangsu 225127, China; College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu 225009, China.
College of Food Science and Engineering, Yangzhou University, Yangzhou, Jiangsu 225127, China.
Microbiol Res. 2023 Oct;275:127461. doi: 10.1016/j.micres.2023.127461. Epub 2023 Jul 22.
Owing to the threats that Salmonella poses to public health and the abuse of antimicrobials, bacteriophage therapy against Salmonella is experiencing a resurgence. Although several phages have been reported as safe and efficient for controlling Salmonella, the genetic diversity and relatedness among Salmonella phages remain poorly understood. In this study, whole-genome sequences of 91 Salmonella bacteriophages were obtained from the National Center for Biological Information genome database. Phylogenetic analysis, mosaic structure comparisons, gene content analysis, and orthologue group clustering were performed. Phylogenetic analysis revealed four singletons and two major lineages (I-II), including five subdividing clades, of which Salmonella phages belonging to morphologically distinct families were clustered in the same clade. Chimeric structures (n = 31), holin genes (n = 18), lysin genes (n = 66), DNA packaging genes (n = 55), and DNA metabolism genes (n = 24) were present in these phages. Moreover, phages from different subdivided clusters harboured distinct genes associated with host cell lysis, DNA packaging, and DNA metabolism. Notably, phages belonging to morphologically distinct families shared common orthologue groups. Although several functional modules of phages SS1 and SE16 shared > 99% nucleotide sequence identity with phages SI2 and SI23, the major differences between these phages were the absence and replication of functional modules. The data obtained herein revealed the genetic diversity of Salmonella phages at genomic, structural, and gene content levels. The genetic diversity of Salmonella phages is likely owing to the acquisition, loss, and replication of functional modules.
由于沙门氏菌对公共健康构成的威胁以及抗菌药物的滥用,针对沙门氏菌的噬菌体疗法正在复兴。尽管已经有几种噬菌体被报道可安全有效地控制沙门氏菌,但沙门氏菌噬菌体的遗传多样性和相关性仍知之甚少。在本研究中,从国家生物技术信息中心基因组数据库中获得了 91 株沙门氏菌噬菌体的全基因组序列。进行了系统发育分析、马赛克结构比较、基因内容分析和直系同源物聚类。系统发育分析显示,有四个单倍体和两个主要谱系(I-II),包括五个细分分支,其中属于不同形态家族的沙门氏菌噬菌体聚集在同一分支中。嵌合结构(n=31)、溶菌基因(n=18)、溶素基因(n=66)、DNA 包装基因(n=55)和 DNA 代谢基因(n=24)存在于这些噬菌体中。此外,来自不同细分群的噬菌体具有不同的与宿主细胞裂解、DNA 包装和 DNA 代谢相关的基因。值得注意的是,属于不同形态家族的噬菌体共享与宿主细胞裂解、DNA 包装和 DNA 代谢相关的共同直系同源物。尽管噬菌体 SS1 和 SE16 的几个功能模块与噬菌体 SI2 和 SI23 的核苷酸序列同一性>99%,但这些噬菌体之间的主要区别是功能模块的缺失和复制。本文获得的数据揭示了沙门氏菌噬菌体在基因组、结构和基因内容水平上的遗传多样性。沙门氏菌噬菌体的遗传多样性可能是由于功能模块的获得、丢失和复制所致。