Veterinary Research Institute, Brno 621 00, Czech Republic; Department of Experimental Biology, Faculty of Science, Masaryk University, Brno 625 00, Czech Republic.
GREMIP and CRIPA, Faculty of Veterinary Medicine, University of Montreal, Saint-Hyacinthe, QC J2S 2M2, Canada.
Vet Microbiol. 2024 Nov;298:110265. doi: 10.1016/j.vetmic.2024.110265. Epub 2024 Sep 26.
Streptococcus suis (S. suis) causes serious diseases in pigs, and certain serotypes also pose a risk to humans. The expression of capsular polysaccharides (CPS) is considered an important virulence property of the pathogen. Recently, some serotypes have been reclassified as other organisms, while novel S. suis serotypes are being described. Although the CPS can be typed by serological methods using antisera, the presence of unique sequences for each capsular polysaccharide synthesis locus (cps locus) enables convenient PCR-based serotyping. In this study, we characterized 33 non-serotypeable S. suis strains obtained from diseased pigs in the Czech Republic by sequencing and analyzing the cps locus. Phylogenetic analysis of cpn60 confirmed that all isolates belong to the S. suis species. Four isolates had cps loci similar to the previously described reference S. suis serotypes. Eleven isolates were classified as recently described novel cps loci (NCLs). Nine isolates had substitutions, insertions and/or deletions in their cps loci and showed only partial similarity to the already described NCLs. Another eight isolates had previously undescribed cps locus structures and were proposed as novel NCLs. One isolate had lost the genes encoding capsule biosynthesis. Only four sequence types (ST) had two isolates each; the rest had unique STs. Two isolates harbored the classical virulence associated genes (VAGs) mrp and sly. Another isolate had only the mrp gene, while a different isolate harbored only the sly gene. This study provides insight into untypeable isolates in the Czech Republic, highlighting the genetic diversity and potential for novel serotype identification.
猪链球菌(S. suis)可引起猪的严重疾病,某些血清型也对人类构成威胁。荚膜多糖(CPS)的表达被认为是病原体重要的毒力特性。最近,一些血清型已被重新归类为其他生物体,同时也在描述新的 S. suis 血清型。尽管可以使用抗血清通过血清学方法对 CPS 进行分型,但每个荚膜多糖合成基因座(cps 基因座)的独特序列的存在使得基于 PCR 的分型变得方便。在这项研究中,我们通过测序和分析 cps 基因座对从捷克共和国患病猪中获得的 33 株无法定型的 S. suis 菌株进行了表征。cpn60 的系统发育分析证实所有分离株均属于 S. suis 种。四个分离株的 cps 基因座与先前描述的参考 S. suis 血清型相似。11 个分离株被归类为最近描述的新型 cps 基因座(NCL)。九个分离株的 cps 基因座发生了取代、插入和/或缺失,与已描述的 NCL 只有部分相似。另 8 个分离株的 cps 基因座结构以前未被描述,被提议为新型 NCL。一个分离株失去了编码荚膜生物合成的基因。只有四个序列型(ST)各有两个分离株;其余的分离株具有独特的 ST。两个分离株携带经典的毒力相关基因(VAGs)mrp 和 sly。另一个分离株仅携带 mrp 基因,而另一个分离株仅携带 sly 基因。本研究深入了解了捷克共和国的不可分型分离株,突出了遗传多样性和新型血清型鉴定的潜力。