Mehdizadeh Gohari Iman, Kropinski Andrew M, Weese Scott J, Whitehead Ashley E, Parreira Valeria R, Boerlin Patrick, Prescott John F
Department of Pathobiology, University of Guelph, Guelph, Ontario, Canada.
Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, Calgary, Alberta, Canada.
Infect Genet Evol. 2017 Apr;49:32-38. doi: 10.1016/j.meegid.2016.12.028. Epub 2017 Jan 3.
Clostridium perfringens is an important cause of foal necrotizing enteritis and canine acute hemorrhagic diarrhea. A major virulence determinant of the strains associated with these diseases appears to be a beta-sheet pore-forming toxin, NetF, encoded within a pathogenicity locus (NetF locus) on a large tcp-conjugative plasmid. Strains producing NetF also produce the putative toxin NetE, encoded within the same pathogenicity locus, as well as CPE enterotoxin and CPB2 on a second plasmid, and sometimes the putative toxin NetG within a pathogenicity locus (NetG locus) on another separate large conjugative plasmid. Previous genome sequences of two netF-positive C. perfringens showed that they both shared three similar plasmids, including the NetF/NetE and CPE/CPB2 toxins-encoding plasmids mentioned above and a putative bacteriocin-encoding plasmid. The main purpose of this study was to determine whether all NetF-producing strains share this common plasmid profile and whether their distinct NetF and CPE pathogenicity loci are conserved. To answer this question, 15 equine and 15 canine netF-positive isolates of C. perfringens were sequenced using Illumina Hiseq2000 technology. In addition, the clonal relationships among the NetF-producing strains were evaluated by core genome multilocus sequence typing (cgMLST). The data obtained showed that all NetF-producing strains have a common plasmid profile and that the defined pathogenicity loci on the plasmids are conserved in all these strains. cgMLST analysis showed that the NetF-producing C. perfringens strains belong to two distinct clonal complexes. The pNetG plasmid was absent from isolates of one of the clonal complexes, and there were minor but consistent differences in the NetF/NetE and CPE/CPB2 plasmids between the two clonal complexes.
产气荚膜梭菌是马驹坏死性肠炎和犬急性出血性腹泻的重要病因。与这些疾病相关的菌株的一个主要毒力决定因素似乎是一种β-折叠孔形成毒素NetF,它由一个大型tcp接合质粒上的致病位点(NetF位点)编码。产生NetF的菌株还会产生在同一致病位点编码的假定毒素NetE,以及在第二个质粒上的CPE肠毒素和CPB2,有时还会在另一个单独的大型接合质粒上的致病位点(NetG位点)产生假定毒素NetG。之前两个netF阳性产气荚膜梭菌的基因组序列显示,它们都共享三个相似的质粒,包括上述的NetF/NetE和CPE/CPB2毒素编码质粒以及一个假定的细菌素编码质粒。本研究的主要目的是确定所有产生NetF的菌株是否共享这种共同的质粒图谱,以及它们不同的NetF和CPE致病位点是否保守。为了回答这个问题,使用Illumina Hiseq2000技术对15株马源和15株犬源产气荚膜梭菌netF阳性分离株进行了测序。此外,通过核心基因组多位点序列分型(cgMLST)评估了产生NetF的菌株之间的克隆关系。获得的数据表明,所有产生NetF的菌株都有一个共同的质粒图谱,并且质粒上定义的致病位点在所有这些菌株中都是保守的。cgMLST分析表明,产生NetF的产气荚膜梭菌菌株属于两个不同的克隆复合体。其中一个克隆复合体的分离株中不存在pNetG质粒,并且两个克隆复合体之间的NetF/NetE和CPE/CPB2质粒存在微小但一致的差异。