Hampson D J, Trott D J, Clarke I L, Mwaniki C G, Robertson I D
School of Veterinary Studies, Murdoch University, Western Australia.
J Clin Microbiol. 1993 Nov;31(11):2895-900. doi: 10.1128/jcm.31.11.2895-2900.1993.
The genetic diversity of 109 isolates of Streptococcus suis, which were recovered mainly from Australian pigs, was examined by multilocus enzyme electrophoresis. The collection was genetically diverse. Sixty-five electrophoretic types (ETs) were recognized, with a mean genetic diversity per enzyme locus of 0.512, or 0.431 when the number of isolates in each ET was considered. Serotype diversity varied, being greatest for isolates of capsular serotype 15 (0.364), and then diminishing in the order of serotypes 9, 1, 4, 1/2, 2, 7, and 3 (0.120). On average, isolates from these eight serotypes represented 4.13 separate clonal groups per serotype. This diversity indicated that serotyping of S. suis for subspecific differentiation is not a reliable technique for identifying specific strains and is not a good predictor of the genetic background of a given isolate. No tendency for isolates recovered from healthy pigs to be genetically distinct from those from diseases animals was found, nor were there consistent differences between isolates recovered from animals with different disease syndromes (meningitis, pneumonia, and septicemia). Danish reference strains of serotypes 1, 2, and 7 each belonged to one of the same clonal groupings of these types found in Australia, but Danish strains of serotypes 3, 4, 6, and 8 and a strain of serotype 1 from the United Kingdom were each genetically distinct from the Australian isolates. Generally, isolates in the same ET belonged to the same serotype, but one ET contained isolates of types 6 and 6/16, and three were made up of isolates of types 2 and 1/2. One isolate of serotype 2, which was recovered from a human with meningitis, belonged to the same ET as two isolates of serotype 2 that were recovered from pigs. The human infection was therefore likely to have been zoonotic.
对主要从澳大利亚猪身上分离出的109株猪链球菌进行多位点酶电泳分析,以检测其遗传多样性。该菌株集合具有遗传多样性。共识别出65种电泳类型(ETs),每个酶位点的平均遗传多样性为0.512,若考虑每个ET中的分离株数量,则为0.431。血清型多样性各不相同,其中荚膜血清型15的分离株多样性最大(0.364),然后按血清型9、1、4、1/2、2、7和3的顺序递减(0.120)。平均而言,这八种血清型的分离株每种血清型代表4.13个独立的克隆群。这种多样性表明,用于亚种分化的猪链球菌血清分型不是鉴定特定菌株的可靠技术,也不是给定分离株遗传背景的良好预测指标。未发现从健康猪身上分离出的菌株在遗传上与患病动物的菌株有明显差异,从患有不同疾病综合征(脑膜炎、肺炎和败血症)的动物身上分离出的菌株之间也没有一致的差异。丹麦血清型1、2和7的参考菌株分别属于在澳大利亚发现的这些类型的相同克隆群之一,但丹麦血清型3、4、6和8的菌株以及一株来自英国的血清型1菌株在遗传上与澳大利亚分离株不同。一般来说,同一ET中的分离株属于同一血清型,但有一个ET包含血清型6和6/16的分离株,还有三个由血清型2和1/2的分离株组成。从一名患有脑膜炎的人类身上分离出的一株血清型2菌株与从猪身上分离出的两株血清型2菌株属于同一ET。因此,该人类感染可能是人畜共患病。