Beaudoin M, Harel J, Higgins R, Gottschalk M, Frenette M, MacInnes J I
Groupe de Recherche sur les Maladies Infectieuses du Porc, Faculté de Médecine Vétérinaire, Université de Montréal, Saint-Hyacinthe, Québec, Canada.
J Gen Microbiol. 1992 Dec;138(12):2639-45. doi: 10.1099/00221287-138-12-2639.
This study was undertaken to assess the discriminatory value of restriction endonuclease (RE) digestion patterns of Streptococcus suis chromosomal DNA using polyacrylamide gel electrophoresis (SDS-PAGE) and DNA-rDNA hybridization. For the RE digestion patterns, DNAs were digested separately with the enzymes BamHI and BglII and the resultant fragments were separated by SDS-PAGE. An Escherichia coli rDNA probe derived from pKK3535 was used for the hybridization. Twenty-three S. suis capsular type 2 isolates recovered from diseased and clinically healthy pigs, from a human case, and from a cow were compared in this study. The majority of isolates associated with septicaemia belonged to one restriction endonuclease analysis (REA) profile group. Isolates associated with pneumonia belonged either to the REA profile group of isolates associated with septicaemia or to a second REA profile group. The REA profiles of isolates from clinically healthy animals were more heterogeneous. The REA profile of the type 2 reference strain, S735, which was originally isolated from a pig, was very different from those of the porcine and bovine isolates but similar to the profile of the human isolate. The profiles obtained after rDNA hybridization were more homogeneous. Although different patterns were detected in the 23 isolates, there was no correlation between the source of the isolate and the patterns observed with this technique.
本研究旨在通过聚丙烯酰胺凝胶电泳(SDS-PAGE)和DNA-rDNA杂交技术,评估猪链球菌染色体DNA的限制性内切酶(RE)消化模式的鉴别价值。对于RE消化模式,分别用BamHI和BglII酶消化DNA,所得片段通过SDS-PAGE分离。使用源自pKK3535的大肠杆菌rDNA探针进行杂交。本研究比较了从患病和临床健康猪、1例人类病例以及1头牛中分离出的23株2型猪链球菌。大多数与败血症相关的分离株属于一个限制性内切酶分析(REA)谱型组。与肺炎相关的分离株要么属于与败血症相关的分离株的REA谱型组,要么属于第二个REA谱型组。来自临床健康动物的分离株的REA谱型更为多样。最初从猪分离出的2型参考菌株S735的REA谱型与猪和牛的分离株非常不同,但与人类分离株的谱型相似。rDNA杂交后获得的谱型更为一致。尽管在23株分离株中检测到不同的模式,但分离株的来源与用该技术观察到的模式之间没有相关性。