Poumarat F, Solsona M, Boldini M
Centre National d'Etudes Vétérinaires et Alimentaires-Laboratoire de Pathologie Bovine, Lyon, France.
Vet Microbiol. 1994 Jun;40(3-4):305-21. doi: 10.1016/0378-1135(94)90119-8.
Restriction endonuclease analysis (REA) with three enzymes SmaI, PstI, BamHI- was used to identify 13 different genomic groups among 37 Mycoplasma bovis strains. One genomic group was comprised of 14 strains. Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) patterns for one strain chosen from each genomic group and an international reference strain PG45 were all similar. Antigenic variability in M. bovis species was investigated by immunoblotting, using serum from a calf that had been naturally infected with M. bovis and three M. bovis-specific monoclonal antibodies--mAbs N2, I2 and 5D7. Twenty M. bovis field strains were tested, comprising one from each genomic group, six from the same genomic group and the reference strain. Antigenic profiles obtained with calf serum differed markedly one from the other, the heterogeneity being equally great among the strains belonging to the same genomic group as those coming from different groups. A stable antigen common to 164 out of 168 strains was detected by mAb N2, whilst with mAbs I2 and 5D7, two different membrane antigenic systems were demonstrated that were strikingly variable. These variations in expression occurred not only from one strain to another, but also within the same lineage of clones from a single cell.
使用三种限制性内切酶(SmaI、PstI、BamHI)进行限制性内切酶分析(REA),以鉴定37株牛支原体菌株中的13个不同基因组群。其中一个基因组群由14株菌株组成。从每个基因组群中选取一株菌株以及国际参考菌株PG45的十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)图谱均相似。使用来自自然感染牛支原体的小牛血清和三种牛支原体特异性单克隆抗体——mAb N2、I2和5D7,通过免疫印迹法研究了牛支原体物种的抗原变异性。对20株牛支原体田间菌株进行了检测,其中包括来自每个基因组群的一株、来自同一基因组群的六株以及参考菌株。用小牛血清获得的抗原谱彼此差异显著,同一基因组群内菌株的异质性与来自不同基因组群的菌株一样大。mAb N2检测到168株菌株中有164株存在一种稳定抗原,而mAb I2和5D7则证明了两种不同的膜抗原系统,它们具有显著的变异性。这些表达变化不仅发生在不同菌株之间,也发生在来自单个细胞的同一克隆谱系内。