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Whole genome SNP typing to investigate methicillin-resistant Staphylococcus aureus carriage in a health-care provider as the source of multiple surgical site infections

机译:全基因组SNP分型以调查在医疗保健提供者中耐甲氧西林的金黄色葡萄球菌的携带情况,作为多种手术部位感染的来源

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Prevention of nosocomial transmission of infections is a central responsibility in the healthcare environment, and accurate identification of transmission events presents the first challenge. Phylogenetic analysis based on whole genome sequencing provides a high-resolution approach for accurately relating isolates to one another, allowing precise identification or exclusion of transmission events and sources for nearly all cases. We sequenced 24 methicillin-resistant Staphylococcus aureus (MRSA) genomes to retrospectively investigate a suspected point source of three surgical site infections (SSIs) that occurred over a one-year period. The source of transmission was believed to be a surgical team member colonized with MRSA, involved in all surgeries preceding the SSI cases, who was subsequently decolonized. Genetic relatedness among isolates was determined using whole genome single nucleotide polymorphism (SNP) data. Whole genome SNP typing (WGST) revealed 283 informative SNPs between the surgical team member’s isolate and the closest SSI isolate. The second isolate was 286 and the third was thousands of SNPs different, indicating the nasal carriage strain from the surgical team member was not the source of the SSIs. Given the mutation rates estimated for S. aureus, none of the SSI isolates share a common ancestor within the past 16?years, further discounting any common point source for these infections. The decolonization procedures and resources spent on the point source infection control could have been prevented if WGST was performed at the time of the suspected transmission, instead of retrospectively. Whole genome sequence analysis is an ideal method to exclude isolates involved in transmission events and nosocomial outbreaks, and coupling this method with epidemiological data can determine if a transmission event occurred. These methods promise to direct infection control resources more appropriately.
机译:预防医院感染的传播是医疗环境中的核心职责,准确识别传播事件是第一个挑战。基于全基因组测序的系统发育分析提供了一种高分辨率的方法,可将分离株彼此准确关联,从而几乎可以在所有情况下准确鉴定或排除传播事件和来源。我们对耐甲氧西林的金黄色葡萄球菌(MRSA)基因组进行了测序,以回顾性调查一年内发生的三种手术部位感染(SSI)的可疑点源。据认为,传播源是由MRSA定植的外科小组成员,参与了SSI病例之前的所有手术,随后被非殖民化。使用全基因组单核苷酸多态性(SNP)数据确定了分离株之间的遗传相关性。全基因组SNP分型(WGST)显示了手术组成员的分离株和最接近的SSI分离株之间的283种信息性SNP。第二个隔离群是286个,第三个隔离群是数千个不同的SNP,这表明来自外科手术团队成员的鼻支架拉伤不是SSI的来源。根据估计的金黄色葡萄球菌突变率,在过去的16年中,没有一个SSI分离株具有共同的祖先,进一步降低了这些感染的任何共同点来源。如果在疑似传播时而不是追溯地进行WGST,则可以避免在点源感染控制上花费的非殖民化程序和资源。全基因组序列分析是排除涉及传播事件和医院内暴发的分离株的理想方法,将该方法与流行病学数据结合可以确定是否发生传播事件。这些方法有望更适当地指导感染控制资源。

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