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志贺毒素阳性和阴性O157:H7菌株TT12A和TT12B的病原体基因组:使用封闭基因组的综合系统发育基因组分析

Pathogenomes of Shiga Toxin Positive and Negative O157:H7 Strains TT12A and TT12B: Comprehensive Phylogenomic Analysis Using Closed Genomes.

作者信息

Kalalah Anwar A, Koenig Sara S K, Feng Peter, Bosilevac Joseph M, Bono James L, Eppinger Mark

机构信息

Department of Molecular Microbiology and Immunology, University of Texas at San Antonio, San Antonio, TX 78249, USA.

South Texas Center for Emerging Infectious Diseases (STCEID), San Antonio, TX 78249, USA.

出版信息

Microorganisms. 2024 Mar 29;12(4):699. doi: 10.3390/microorganisms12040699.

Abstract

Shiga toxin-producing are zoonotic pathogens that cause food-borne human disease. Among these, the O157:H7 serotype has evolved from an enteropathogenic O55:H7 ancestor through the displacement of the somatic gene cluster and recurrent toxigenic conversion by Shiga toxin-converting bacteriophages. However, atypical strains that lack the Shiga toxin, the characteristic virulence hallmark, are circulating in this lineage. For this study, we analyzed the pathogenome and virulence inventories of the + strain, TT12A, isolated from a patient with hemorrhagic colitis, and its respective co-isolated - strain, TT12B. Sequencing the genomes to closure proved critical to the cataloguing of subtle strain differentiating sequence and structural polymorphisms at a high-level of phylogenetic accuracy and resolution. Phylogenomic profiling revealed SNP and MLST profiles similar to the near clonal outbreak isolates. Their prophage inventories, however, were notably different. The attenuated atypical non-shigatoxigenic status of TT12B is explained by the absence of both the ΦStx- and ΦStx-prophages carried by TT12A, and we also recorded further alterations in the non-Stx prophage complement. Phenotypic characterization indicated that culture growth was directly impacted by the strains' distinct lytic phage complement. Altogether, our phylogenomic and phenotypic analyses show that these intimately related isogenic strains are on divergent Stx(+/stx-) evolutionary paths.

摘要

产志贺毒素菌是引起食源性人类疾病的人畜共患病原体。其中,O157:H7血清型是由肠致病性O55:H7祖先通过体细胞基因簇的置换和志贺毒素转换噬菌体的反复产毒转化而进化而来。然而,缺乏志贺毒素这一特征性毒力标志的非典型菌株也在这一谱系中传播。在本研究中,我们分析了从一名出血性结肠炎患者分离出的+菌株TT12A及其共同分离出的-菌株TT12B的病原体基因组和毒力库。将基因组测序至封闭对于在高系统发育准确性和分辨率水平上对细微的菌株分化序列和结构多态性进行编目至关重要。系统发育基因组分析揭示了与近乎克隆爆发分离株相似的单核苷酸多态性(SNP)和多位点序列分型(MLST)图谱。然而,它们的前噬菌体库却明显不同。TT12B的减毒非典型非产志贺毒素状态可以通过TT12A携带 的ΦStx-和ΦStx-前噬菌体的缺失来解释,并且我们还记录了非Stx前噬菌体互补的进一步改变。表型特征表明,菌株不同的裂解性噬菌体互补直接影响了培养物的生长。总之,我们的系统发育基因组和表型分析表明,这些密切相关的同基因菌株正处于不同的Stx(+/stx-)进化路径上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85f6/11052207/928685d1ebc8/microorganisms-12-00699-g001.jpg

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