Athey Taryn B T, Teatero Sarah, Takamatsu Daisuke, Wasserscheid Jessica, Dewar Ken, Gottschalk Marcelo, Fittipaldi Nahuel
Public Health Ontario, Toronto, ON, Canada.
Bacterial and Parasitic Diseases Research Division, National Institute of Animal Health, National Agriculture and Food Research Organization, Tsukuba, Japan.
PLoS One. 2016 Mar 8;11(3):e0150908. doi: 10.1371/journal.pone.0150908. eCollection 2016.
Strains of serotype 2 Streptococcus suis are responsible for swine and human infections. Different serotype 2 genetic backgrounds have been defined using multilocus sequence typing (MLST). However, little is known about the genetic diversity within each MLST sequence type (ST). Here, we used whole-genome sequencing to test the hypothesis that S. suis serotype 2 strains of the ST25 lineage are genetically heterogeneous. We evaluated 51 serotype 2 ST25 S. suis strains isolated from diseased pigs and humans in Canada, the United States of America, and Thailand. Whole-genome sequencing revealed numerous large-scale rearrangements in the ST25 genome, compared to the genomes of ST1 and ST28 S. suis strains, which result, among other changes, in disruption of a pilus island locus. We report that recombination and lateral gene transfer contribute to ST25 genetic diversity. Phylogenetic analysis identified two main and distinct Thai and North American clades grouping most strains investigated. These clades also possessed distinct patterns of antimicrobial resistance genes, which correlated with acquisition of different integrative and conjugative elements (ICEs). Some of these ICEs were found to be integrated at a recombination hot spot, previously identified as the site of integration of the 89K pathogenicity island in serotype 2 ST7 S. suis strains. Our results highlight the limitations of MLST for phylogenetic analysis of S. suis, and the importance of lateral gene transfer and recombination as drivers of diversity in this swine pathogen and zoonotic agent.
2型猪链球菌菌株可导致猪和人类感染。已使用多位点序列分型(MLST)定义了不同的2型遗传背景。然而,对于每个MLST序列类型(ST)内的遗传多样性知之甚少。在此,我们使用全基因组测序来检验ST25谱系的2型猪链球菌菌株在遗传上具有异质性这一假设。我们评估了从加拿大、美国和泰国的患病猪和人类中分离出的51株2型ST25猪链球菌菌株。与ST1和ST28猪链球菌菌株的基因组相比,全基因组测序揭示了ST25基因组中存在大量大规模重排,这除了其他变化外,还导致菌毛岛位点的破坏。我们报告重组和横向基因转移有助于ST25的遗传多样性。系统发育分析确定了两个主要且不同的泰国和北美分支,大多数被研究菌株归为这两个分支。这些分支还具有不同的抗菌抗性基因模式,这与获得不同的整合和接合元件(ICE)相关。其中一些ICE被发现整合在一个重组热点处,该热点先前被确定为2型ST7猪链球菌菌株中89K致病岛的整合位点。我们的结果突出了MLST在猪链球菌系统发育分析中的局限性,以及横向基因转移和重组作为这种猪病原体和人畜共患病原体多样性驱动因素的重要性。