Center for Food Safety and Applied Nutrition, US Food and Drug Administration, Laurel, Maryland, United States of America.
Public Health Microbiology Laboratory, Queensland Health Forensic and Scientific Services, Queensland, Australia.
PLoS One. 2014 Feb 19;9(2):e89024. doi: 10.1371/journal.pone.0089024. eCollection 2014.
Over 90% of the human listeriosis cases are caused by Listeria monocytogenes serotypes 1/2a, 1/2b and 4b strains. As an alternative to antigen-antibody based serotyping, a PCR-based method for serogrouping has been developed and validated. In this communication, we report an in-depth analysis of five 4b variant strains, four clinical isolates from Australia and one environmental isolate from USA. Although these five strains were serotype 4b by classical serotyping method, the serogrouping PCR profiles of these strains show the presence of a 1/2a-3a specific amplicon in addition to the standard 4b-4d-4e specific amplicons. These strains were further analyzed by pulsed field gel electrophoresis, binary gene typing, multi-locus variable-number-tandem-repeat analysis and a high density pan-genomic Listeria microarray. Using these sub-typing results, the clinical isolates were grouped into two distinct genomic groups- one of which could be part of an unidentified outbreak. The microarray results when compared with our database of other 4b outbreak isolates indicated that the serotype 4b variant strains represent very different genotypic profiles than the known reported 4b outbreak strains representing major epidemic clones. The acquisition of serotype 1/2a gene clusters by the 4b variant strains appears to be independent in origin, spanning large areas of geographical and temporal space and may indicate predisposition of some 4b strains towards accepting DNA from related organisms.
超过 90%的人类李斯特菌病病例是由李斯特菌血清型 1/2a、1/2b 和 4b 菌株引起的。作为基于抗原-抗体的血清分型的替代方法,已经开发并验证了一种基于 PCR 的血清群分型方法。在本通讯中,我们报告了对五个 4b 变体菌株的深入分析,其中四个是来自澳大利亚的临床分离株,一个是来自美国的环境分离株。尽管这五个菌株通过经典血清分型方法被鉴定为血清型 4b,但这些菌株的血清群 PCR 图谱显示除了标准的 4b-4d-4e 特异性扩增子之外,还存在 1/2a-3a 特异性扩增子。这些菌株进一步通过脉冲场凝胶电泳、二元基因分型、多位点可变数串联重复分析和高密度李斯特菌全基因组微阵列进行分析。使用这些亚分型结果,临床分离株被分为两个不同的基因组群,其中一个可能是未识别的暴发的一部分。与我们的其他 4b 暴发分离株数据库相比,微阵列结果表明,血清型 4b 变体菌株的基因型与已知的报告的 4b 暴发菌株代表主要流行克隆的基因型有很大不同。4b 变体菌株获得 1/2a 基因簇似乎是独立起源的,跨越了很大的地理和时间空间范围,可能表明一些 4b 菌株具有接受来自相关生物的 DNA 的倾向。