Office of Applied Research and Safety Assessment, Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, Laurel, Maryland, United States of America.
PLoS One. 2012;7(3):e32896. doi: 10.1371/journal.pone.0032896. Epub 2012 Mar 21.
Listeria monocytogenes, a foodborne bacterial pathogen, causes invasive and febrile gastroenteritis forms of listeriosis in humans. Both invasive and febrile gastroenteritis listeriosis is caused mostly by serotypes 1/2a, 1/2b and 4b strains. The outbreak strains of serotype 1/2a and 4b could be further classified into several epidemic clones but the genetic bases for the diverse pathophysiology have been unsuccessful. DNA microarray provides an important tool to scan the entire genome for genetic signatures that may distinguish the L. monocytogenes strains belonging to different outbreaks. We have designed a pan-genomic microarray chip (Listeria GeneChip) containing sequences from 24 L. monocytogenes strains. The chip was designed to identify the presence/absence of genomic sequences, analyze transcription profiles and identify SNPs. Analysis of the genomic profiles of 38 outbreak strains representing 1/2a, 1/2b and 4b serotypes, revealed that the strains formed distinct genetic clusters adhering to their serotypes and epidemic clone types. Although serologically 1/2a and 1/b strains share common antigenic markers microarray analysis revealed that 1/2a strains are further apart from the closely related 1/2b and 4b strains. Within any given serotype and epidemic clone type the febrile gastroenteritis and invasive strains can be further distinguished based on several genetic markers including large numbers of phage genome, and intergenic sequences. Our results showed that the microarray-based data can be an important tool in characterization of L. monocytogenes strains involved in both invasive and gastroenteritis outbreaks. The results for the first time showed that the serotypes and epidemic clones are based on extensive pan-genomic variability and the 1/2b and 4bstrains are more closely related to each other than the 1/2a strains. The data also supported the hypothesis that the strains causing these two diverse outbreaks are genotypically different and this finding might be important in understanding the pathophysiology of this organism.
产单核李斯特菌是一种食源性病原体,可引起侵袭性和发热性肠胃炎形式的李斯特菌病。侵袭性和发热性肠胃炎李斯特菌病主要由血清型 1/2a、1/2b 和 4b 菌株引起。血清型 1/2a 和 4b 的暴发菌株可进一步分为几种流行克隆,但导致不同病理生理学的遗传基础尚未成功。DNA 微阵列提供了一种重要的工具,可以扫描整个基因组,寻找可能区分不同暴发的李斯特菌菌株的遗传特征。我们设计了一种包含 24 株李斯特菌序列的泛基因组微阵列芯片(李斯特菌基因芯片)。该芯片旨在识别基因组序列的存在/缺失、分析转录谱和识别 SNP。对代表 1/2a、1/2b 和 4b 血清型的 38 株暴发菌株的基因组图谱进行分析,结果表明这些菌株形成了与其血清型和流行克隆类型相符的独特遗传簇。尽管 1/2a 和 1/2b 菌株在血清学上具有共同的抗原标记,但微阵列分析表明,1/2a 菌株与密切相关的 1/2b 和 4b 菌株相距更远。在任何给定的血清型和流行克隆类型中,基于噬菌体基因组和基因间序列等多种遗传标记,可以进一步区分发热性肠胃炎和侵袭性菌株。我们的结果表明,基于微阵列的数据分析可以成为描述涉及侵袭性和肠胃炎暴发的李斯特菌菌株的重要工具。结果首次表明,血清型和流行克隆基于广泛的泛基因组变异性,1/2b 和 4b 菌株彼此之间的亲缘关系比 1/2a 菌株更密切。该数据还支持了这样一种假说,即引起这两种不同暴发的菌株在基因型上存在差异,这一发现可能对理解该生物体的病理生理学具有重要意义。