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两株猪链球菌2型突变株的构建与特性分析

Production and characterization of two Streptococcus suis capsular type 2 mutants.

作者信息

Gottschalk M, Higgins R, Jacques M, Dubreuil D

机构信息

Groupe de Recherche sur les Maladies Infectieuses du Porc. Faculté de médecine vétérinaire, Université de Montréal, St-Hyacinthe, Québec, Canada.

出版信息

Vet Microbiol. 1992 Jan;30(1):59-71. doi: 10.1016/0378-1135(92)90094-a.

Abstract

Two avirulent mutants of Streptococcus suis capsular type 2 (M2 and M42) were produced from a highly virulent strain. Mutant M2, obtained after serial subcultures of the parent strain in the presence of rabbit anti-capsular type 2 serum, no longer possessed the type-specific capsular antigen, as demonstrated by serotyping methods and immunoelectron microscopy. The Lancefield group D antigen could not be detected on the cell surface of this mutant using the immunogold labelling technique. SDS-PAGE of lysozyme treated cells demonstrated that a 44 kDa protein which was present in the parent strain, was absent in mutant M2. Immunoblotting using rabbit whole cell homologous anti-serum revealed that the protein was strongly immunogenic. Mutant M2 was totally avirulent in mice, and the homologous antiserum completely failed to protect mice against challenge with the parent strain. However, mutant M42, obtained after passages of the parent strain at 42 degrees C, remained capsulated but lacked the same 44 kDa protein as mutant M2. The quantity of sialic acid present in the capsule was similar to that of the parent strain. Despite the presence of antibodies against the capsule, antiserum prepared against M42 only partially protected mice against a challenge with the parent strain. The 44 kDa cell wall protein could act as a virulence factor as well as an important immunogen of S. suis capsular type 2.

摘要

从一株高毒力猪链球菌2型菌株获得了两个无毒突变体(M2和M42)。突变体M2是在亲本菌株于兔抗2型荚膜血清存在下连续传代培养后获得的,血清分型方法和免疫电子显微镜显示其不再具有型特异性荚膜抗原。使用免疫金标记技术在该突变体细胞表面未检测到兰斯菲尔德D群抗原。经溶菌酶处理的细胞的SDS-PAGE表明,亲本菌株中存在的一种44 kDa蛋白在突变体M2中缺失。使用兔全细胞同源抗血清进行免疫印迹显示该蛋白具有强免疫原性。突变体M2在小鼠中完全无毒,其同源抗血清完全无法保护小鼠免受亲本菌株的攻击。然而,亲本菌株在42℃传代后获得的突变体M42仍有荚膜,但与突变体M2一样缺乏相同的44 kDa蛋白。荚膜中唾液酸的含量与亲本菌株相似。尽管存在针对荚膜的抗体,但用M42制备的抗血清仅部分保护小鼠免受亲本菌株的攻击。44 kDa细胞壁蛋白可作为猪链球菌2型的毒力因子和重要免疫原。

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