Lytsy Birgitta, Engstrand Lars, Gustafsson Åke, Kaden Rene
Uppsala University, Department of Medical Sciences, Uppsala, Sweden.
Uppsala University, Department of Medical Sciences, Uppsala, Sweden; Karolinska Institute Solna, Sweden; Science for Life Laboratory Solna, Sweden.
Infect Genet Evol. 2017 Oct;54:74-80. doi: 10.1016/j.meegid.2017.06.010. Epub 2017 Jun 15.
Vancomycin-resistant enterococci (VRE) are a challenge to the health-care system regarding transmission rate and treatment of infections. VRE outbreaks have to be controlled from the first cases which means that appropriate and sensitive genotyping methods are needed. The aim of this study was to investigate the applicability of whole genome sequencing based analysis compared to Pulsed-Field Gel Electrophoresis (PFGE) and Multi-Locus Sequence Typing (MLST) in epidemiological investigations as well as the development of a user friendly method for daily laboratory use. Out of 14,000 VRE - screening samples, a total of 60 isolates positive for either vanA or vanB gene were isolated of which 38 were from patients with epidemiological links from three suspected outbreaks at Uppsala University Hospital. The isolates were genotypically characterised with PFGE, MLST, and WGS based core genome Average Nucleotide Identity analysis (cgANI). PFGE was compared to WGS and MLST regarding reliability, resolution, and applicability capacity. The PFGE analysis of the 38 isolates confirmed the epidemiological investigation that three outbreaks had occurred but gave an unclear picture for the largest cluster. The WGS analysis could clearly distinguish six ANI clusters for those 38 isolates. As result of the comparison of the investigated methods, we recommend WGS-ANI analysis for epidemiological issues with VRE. The recommended threshold for Enterococcus faecium VRE outbreak strain delineation with core genome based ANI is 98.5%. All referred sequences of this study are available from the NCBI BioProject number PRJNA301929.
耐万古霉素肠球菌(VRE)在感染传播率和治疗方面对医疗保健系统构成挑战。VRE暴发必须从首例病例开始控制,这意味着需要合适且灵敏的基因分型方法。本研究的目的是调查基于全基因组测序的分析与脉冲场凝胶电泳(PFGE)和多位点序列分型(MLST)相比在流行病学调查中的适用性,以及开发一种便于日常实验室使用的用户友好方法。在14000份VRE筛查样本中,共分离出60株vanA或vanB基因阳性的菌株,其中38株来自乌普萨拉大学医院三起疑似暴发且有流行病学关联的患者。采用PFGE、MLST以及基于全基因组测序的核心基因组平均核苷酸同一性分析(cgANI)对分离株进行基因分型。在可靠性、分辨率和适用能力方面,将PFGE与全基因组测序和MLST进行比较。对38株分离株的PFGE分析证实了流行病学调查结果,即已发生三起暴发,但对于最大的簇给出的情况不清晰。全基因组测序分析能够清晰地区分这38株分离株的六个ANI簇。作为所研究方法比较的结果,我们推荐将全基因组测序 - ANI分析用于VRE的流行病学问题。基于核心基因组ANI划定屎肠球菌VRE暴发菌株的推荐阈值为98.5%。本研究所有提及的序列可从NCBI生物项目编号PRJNA301929获取。