Birdsell Dawn N, Vogler Amy J, Buchhagen Jordan, Clare Ashley, Kaufman Emily, Naumann Amber, Driebe Elizabeth, Wagner David M, Keim Paul S
Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America.
Center for Microbial Genetics and Genomics, Northern Arizona University, Flagstaff, Arizona, United States of America; Translational Genomics Research Institute, Flagstaff, Arizona, United States of America.
PLoS One. 2014 Sep 19;9(9):e107964. doi: 10.1371/journal.pone.0107964. eCollection 2014.
Francisella tularensis, the etiologic agent of tularemia and a Class A Select Agent, is divided into three subspecies and multiple subpopulations that differ in virulence and geographic distribution. Given these differences, there is a need to rapidly and accurately determine if a strain is F. tularensis and, if it is, assign it to subspecies and subpopulation. We designed TaqMan real-time PCR genotyping assays using eleven single nucleotide polymorphisms (SNPs) that were potentially specific to closely related groups within the genus Francisella, including numerous subpopulations within F. tularensis species. We performed extensive validation studies to test the specificity of these SNPs to particular populations by screening the assays across a set of 565 genetically and geographically diverse F. tularensis isolates and an additional 21 genetic near-neighbor (outgroup) isolates. All eleven assays correctly determined the genetic groups of all 565 F. tularensis isolates. One assay differentiates F. tularensis, F. novicida, and F. hispaniensis from the more genetically distant F. philomiragia and Francisella-like endosymbionts. Another assay differentiates F. tularensis isolates from near neighbors. The remaining nine assays classify F. tularensis-confirmed isolates into F. tularensis subspecies and subpopulations. The genotyping accuracy of these nine assays diminished when tested on outgroup isolates (i.e. non F. tularensis), therefore a hierarchical approach of assay usage is recommended wherein the F. tularensis-specific assay is used before the nine downstream assays. Among F. tularensis isolates, all eleven assays were highly sensitive, consistently amplifying very low concentrations of DNA. Altogether, these eleven TaqMan real-time PCR assays represent a highly accurate, rapid, and sensitive means of identifying the species, subspecies, and subpopulation of any F. tularensis isolate if used in a step-wise hierarchical scheme. These assays would be very useful in clinical, epidemiological, and/or forensic investigations involving F. tularensis.
土拉弗朗西斯菌是兔热病的病原体,属于A类生物制剂,可分为三个亚种和多个亚群,它们在毒力和地理分布上存在差异。鉴于这些差异,需要快速准确地确定一个菌株是否为土拉弗朗西斯菌,如果是,则将其归为相应的亚种和亚群。我们利用11个单核苷酸多态性(SNP)设计了TaqMan实时荧光定量PCR基因分型检测方法,这些SNP可能对弗朗西斯菌属内密切相关的群体具有特异性,包括土拉弗朗西斯菌种内的众多亚群。我们进行了广泛的验证研究,通过对一组565株遗传和地理分布多样的土拉弗朗西斯菌分离株以及另外21株遗传近邻(外群)分离株进行检测,来测试这些SNP对特定群体的特异性。所有11种检测方法都正确地确定了所有565株土拉弗朗西斯菌分离株的遗传群体。一种检测方法可将土拉弗朗西斯菌、新凶手弗朗西斯菌和西班牙弗朗西斯菌与遗传关系较远的嗜肺弗朗西斯菌和类弗朗西斯菌内共生体区分开来。另一种检测方法可将土拉弗朗西斯菌分离株与近邻区分开来。其余9种检测方法可将已确认的土拉弗朗西斯菌分离株分类到土拉弗朗西斯菌的亚种和亚群中。当在外群分离株(即非土拉弗朗西斯菌)上进行测试时,这9种检测方法的基因分型准确性会降低,因此建议采用分层检测方法,即在使用9种下游检测方法之前先使用土拉弗朗西斯菌特异性检测方法。在土拉弗朗西斯菌分离株中,所有11种检测方法都具有高度敏感性,能够持续扩增极低浓度的DNA。总之,如果按照逐步分层方案使用,这11种TaqMan实时荧光定量PCR检测方法是鉴定任何土拉弗朗西斯菌分离株的物种、亚种和亚群的高度准确、快速且灵敏的方法。这些检测方法在涉及土拉弗朗西斯菌病的临床、流行病学和/或法医调查中非常有用。