剖析金黄色葡萄球菌序列 88 型的遗传特征和进化:全球视角。

IF 5 2区 生物学 Q1 MICROBIOLOGY
mSystems Pub Date : 2024-11-12 DOI:10.1128/msystems.01142-24
Ye Jin, Chenyang Gao, Gaoqin Teng, Zhenchao Zhou, Wangxiao Zhou, Man Huang
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引用次数: 0

摘要

金黄色葡萄球菌序列类型(ST)88 包括耐甲氧西林金黄色葡萄球菌(MRSA)和甲氧西林敏感金黄色葡萄球菌(MSSA)两种表型,在全球普遍存在,通常与皮肤和软组织感染有关。尽管其广泛存在,但对该克隆的全面基因组研究仍然很少。在本研究中,我们对 130 个来自严重血流感染的 ST88 分离物和 275 个公开的 ST88 序列进行了详细的基因组分析。我们的系统进化分析确定了四个不同的支系,有证据表明 ST88 在中国有独立的进化和显著的支系扩展,尤其是在支系 I 中,该支系似乎出现于 1964 年前后。我们记录了 ST88 分离物在地区间、国际间甚至洲际间的显著传播。在不同支系中,SCCmec 和 spa 类型的分布存在差异。我们的硅学分析表明,各支系之间的抗性基因、毒力基因和移动遗传因子的分布具有不同的模式,其中支系 I 的完整 sraP 基因和独立获得的新型噬菌体 φST88-1 的流行率最高。体外实验证实,虽然各支系的溶血和细胞毒性水平相似,但支系 I 分离物的生物膜形成能力更强。全基因组关联研究显示,核心 SNPs 而非附属基因组是 ST88 支链多样化的主要因素。重要意义由于金黄色葡萄球菌 ST88 克隆在食品、医院和社区环境中传播,导致严重的健康问题,因此了解金黄色葡萄球菌 ST88 克隆的进化和传播至关重要。尽管金黄色葡萄球菌 ST88 普遍存在,但人们一直缺乏对其基因组的详细了解,尤其是对其多样性和进化动态的了解。我们对来自严重血流感染的 130 株 ST88 分离物以及来自公共数据库的 275 个序列进行了全面的基因组分析,大大加深了我们对这种病原体的了解。我们发现了四个不同的进化支系,证明了 ST88 在中国的独立进化和大量克隆扩增,以及跨地区和跨大陆传播的能力。分离株之间的多样性体现在它们独特的 SCCmec 基因、抗生素耐药基因、毒力基因和移动遗传因子上。我们的发现强调了核心基因组变异比附属元件在驱动 ST88 多样化中的关键作用。这种进一步的了解提供了新的见解,可以为更有效的控制策略提供依据,这对制定干预措施以遏制这种可怕病原体的全球传播至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dissecting the genetic features and evolution of Staphylococcus aureus sequence type 88: a global perspective.

Staphylococcus aureus sequence type (ST) 88, encompassing both methicillin-resistant S. aureus (MRSA) and methicillin-sensitive S. aureus (MSSA) phenotypes, is globally prevalent and commonly associated with skin and soft tissue infections. Despite its widespread occurrence, comprehensive genomic studies on this clone remain scarce. In this study, we performed detailed genomic analyses on 130 ST88 isolates derived from severe bloodstream infections alongside 275 publicly available ST88 sequences. Our phylogenetic analysis identified four distinct clades, with evidence suggesting independent evolution and significant clonal expansion of ST88 in China, particularly within clade I, which appeared to have emerged circa 1964. We documented notable interregional, international, and even intercontinental transmission of ST88 isolates. Variability in the distribution of SCCmec and spa types was observed across clades. Our in silico analyses indicated distinct patterns in the distribution of resistance genes, virulence genes, and mobile genetic elements among the clades, with clade I notably harboring the highest prevalence of the intact sraP gene and an independently acquired novel prophage, φST88-1. Conversely, clade IV exhibited deletions within the sasC gene, with certain sub-clades lacking the sdrDE and fnbB genes, underscoring the superior adhesive capabilities of clade I. In vitro experiments confirmed enhanced biofilm formation in clade I isolates, although the levels of hemolysis and cytotoxicity were similar across clades. Pan-genome-wide association study revealed that core SNPs, rather than the accessory genome, are the primary contributors to the diversification of the ST88 clades. These findings enrich our understanding of the genetic foundations underpinning the transmission dynamics and phenotypic diversity of ST88 clones globally.IMPORTANCEUnderstanding the evolution and transmission of Staphylococcus aureus ST88 clones is critically important due to their spread within food, hospital, and community environments, leading to significant health issues. Despite its prevalence, detailed genomic insights into ST88, particularly regarding its diversity and evolutionary dynamics, have been lacking. Our comprehensive genomic analysis of 130 ST88 isolates from severe bloodstream infections, alongside 275 sequences from public databases, significantly advances our understanding of this pathogen. We identified four distinct evolutionary clades, demonstrating the independent evolution and substantial clonal expansion of ST88 in China, as well as its ability to spread across regions and continents. The diversity among the isolates was evident in their unique profiles of SCCmec elements, antibiotic resistance genes, virulence genes, and mobile genetic elements. Our findings underscore the critical role of core genomic variations over accessory elements in driving the diversification of ST88. This enhanced understanding provides new insights that could inform more effective control strategies, crucial for developing interventions to combat the global spread of this formidable pathogen.

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来源期刊
mSystems
mSystems Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
10.50
自引率
3.10%
发文量
308
审稿时长
13 weeks
期刊介绍: mSystems™ will publish preeminent work that stems from applying technologies for high-throughput analyses to achieve insights into the metabolic and regulatory systems at the scale of both the single cell and microbial communities. The scope of mSystems™ encompasses all important biological and biochemical findings drawn from analyses of large data sets, as well as new computational approaches for deriving these insights. mSystems™ will welcome submissions from researchers who focus on the microbiome, genomics, metagenomics, transcriptomics, metabolomics, proteomics, glycomics, bioinformatics, and computational microbiology. mSystems™ will provide streamlined decisions, while carrying on ASM''s tradition of rigorous peer review.
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