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首页> 外文期刊>Journal of Clinical Microbiology >Minimum Core Genome Sequence Typing of Bacterial Pathogens: a Unified Approach for Clinical and Public Health Microbiology
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Minimum Core Genome Sequence Typing of Bacterial Pathogens: a Unified Approach for Clinical and Public Health Microbiology

机译:细菌病原体的最小核心基因组序列分型:临床和公共卫生微生物学的统一方法

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Bacterial pathogens impose a heavy health burden worldwide. In the new era of high-throughput sequencing and online bioinformatics, real-time genome typing of infecting agents, and in particular those with potential severe clinical outcomes, holds promise for guiding clinical care to limit the detrimental effects of infections and to prevent potential local or global outbreaks. Here, we sequenced and compared 85 isolates of Streptococcus suis, a zoonotic human and swine pathogen, wherein we analyzed 32 recognized serotypes and 75 sequence types representing the diversity of the species and the human clinical isolates with high public health significance. We found that 1,077 of the 2,469 genes are shared by all isolates. Excluding 201 common but mobile genes, 876 genes were defined as the minimum core genome (MCG) of the species. Of 190,894 single-nucleotide polymorphisms (SNPs) identified, 58,501 were located in the MCG genes and were referred to as MCG SNPs. A population structure analysis of these MCG SNPs classified the 85 isolates into seven MCG groups, of which MCG group 1 includes all isolates from human infections and outbreaks. Our MCG typing system for S. suis provided a clear separation of groups containing human-associated isolates from those containing animal-associated isolates. It also separated the group containing outbreak isolates, including those causing life-threatening streptococcal toxic shock-like syndrome, from sporadic or less severe meningitis or bacteremia-only isolates. The typing system facilitates the application of genome data to the fields of clinical medicine and epidemiology and to the surveillance of S. suis. The MCG groups may also be used as the taxonomical units of S. suis to define bacterial subpopulations with the potential to cause severe clinical infections and large-scale outbreaks.
机译:细菌病原体在世界范围内给健康造成了沉重负担。在高通量测序和在线生物信息学的新时代,感染因子的实时基因组分型,尤其是那些具有严重临床后果的因子,有望指导临床护理以限制感染的有害影响并防止潜在的局部感染。或全球爆发。在这里,我们对人畜共患病的人畜共患病菌猪链球菌的85个分离株进行了测序和比较,其中我们分析了32种公认的血清型和75种序列类型,它们代表了物种的多样性以及具有高度公共卫生意义的人临床分离株。我们发现2,469个基因中的1,077个被所有分离株共有。除201个常见但可移动的基因外,876个基因被定义为该物种的最小核心基因组(MCG)。在确定的190,894个单核苷酸多态性(SNP)中,有58,501个位于MCG基因中,被称为MCG SNP。这些MCG SNP的种群结构分析将85个分离株分为7个MCG组,其中MCG组1包括了来自人类感染和暴发的所有分离株。我们针对猪链球菌的MCG分型系统将含有人相关菌群的组与含有动物相关菌群的组明确分离。它还将包含暴发分离株的组与散发性或程度较轻的脑膜炎分离株或仅菌血症的分离株,包括引起威胁生命的链球菌中毒性休克样综合征的分离株。分型系统有助于将基因组数据应用于临床医学和流行病学领域以及猪链球菌的监测。 MCG组还可以用作猪链球菌的分类单位,以定义可能引起严重临床感染和大规模暴发的细菌亚群。

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