Yachison Chris A, Yoshida Catherine, Robertson James, Nash John H E, Kruczkiewicz Peter, Taboada Eduardo N, Walker Matthew, Reimer Aleisha, Christianson Sara, Nichani Anil, Nadon Celine
National Microbiology Laboratory, Public Health Agency of Canada, WinnipegMB, Canada.
Department of Medical Microbiology, University of Manitoba, WinnipegMB, Canada.
Front Microbiol. 2017 Jun 9;8:1044. doi: 10.3389/fmicb.2017.01044. eCollection 2017.
serotyping remains the gold-standard tool for the classification of isolates and forms the basis of Canada's national surveillance program for this priority foodborne pathogen. Public health officials have been increasingly looking toward whole genome sequencing (WGS) to provide a large set of data from which all the relevant information about an isolate can be mined. However, rigorous validation and careful consideration of potential implications in the replacement of traditional surveillance methodologies with WGS data analysis tools is needed. Two tools for serotyping have been developed, the Typing Resource (SISTR) and SeqSero, while seven gene MLST for serovar prediction can be adapted for analysis. All three analysis methods were assessed and compared to traditional serotyping techniques using a set of 813 verified clinical and laboratory isolates, including 492 Canadian clinical isolates and 321 isolates of human and non-human sources. Successful results were obtained for 94.8, 88.2, and 88.3% of the isolates tested using SISTR, SeqSero, and MLST, respectively, indicating all would be suitable for maintaining historical records, surveillance systems, and communication structures currently in place and the choice of the platform used will ultimately depend on the users need. Results also pointed to the need to reframe serotyping in the genomic era as a test to understand the genes that are carried by an isolate, one which is not necessarily congruent with what is antigenically expressed. The adoption of WGS for serotyping will provide the simultaneous collection of information that can be used by multiple programs within the current surveillance paradigm; however, this does not negate the importance of the various programs or the role of serotyping going forward.
血清分型仍然是分离株分类的金标准工具,也是加拿大针对这种重点食源性病原体的国家监测计划的基础。公共卫生官员越来越倾向于使用全基因组测序(WGS)来提供大量数据,从中挖掘出关于分离株的所有相关信息。然而,需要对用WGS数据分析工具取代传统监测方法进行严格验证并仔细考虑其潜在影响。已经开发了两种血清分型工具,即分型资源(SISTR)和SeqSero,同时可以采用七种基因的多位点序列分型(MLST)进行血清型预测分析。使用一组813株经过验证的临床和实验室分离株,包括492株加拿大临床分离株以及321株来自人类和非人类来源的分离株,对这三种分析方法进行了评估,并与传统血清分型技术进行了比较。使用SISTR、SeqSero和MLST分别对94.8%、88.2%和88.3%的测试分离株获得了成功结果,这表明所有这些方法都适用于维护现有的历史记录、监测系统和通信结构,最终使用平台的选择将取决于用户需求。结果还表明,在基因组时代需要重新将血清分型定义为一种了解分离株携带基因的测试,这种测试不一定与抗原表达情况一致。采用WGS进行血清分型将在当前监测范式内同时收集多个项目可使用的信息;然而,这并不否定各个项目的重要性以及血清分型未来的作用。