鸡败血症支原体
生物
抗血清
血清转化
拉伤
凝胶电泳
微生物学
抗原
分子质量
聚丙烯酰胺凝胶电泳
血清学
病毒学
分子生物学
支原体
抗体
病毒
生物化学
免疫学
解剖
酶
作者
A P Avakian,David H. Ley,Mary Ann T. McBride
出处
期刊:PubMed
[National Institutes of Health]
日期:1992-01-01
卷期号:36 (1): 69-77
被引量:14
摘要
Two putative variant Mycoplasma gallisepticum (MG) strains (M876 and M35), originally isolated from commercial turkeys, were compared with eight well-characterized MG strains by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). SDS-PAGE protein profiles indicated that the variant strains were correctly classified as MG based on homologous patterns in species-specific regions of the electrophoretic profiles. However, differences in protein profiles also indicated that variant strains M876 and M35 were different from each other and the other MG strains tested. Immunoblotting was used to assess the humoral immune response of turkeys to infection with the S6 reference strain or M876 variant strain of MG. Immunoblots using antisera to M876 showed that seroconversion to this isolate was slower, and to fewer MG proteins when compared with immunoblots using antisera to S6. Immunoblot analyses further indicated that pooled antisera from turkeys inoculated with either S6 or M876 reacted with each of 10 MG strains tested. However, pooled S6 antisera reacted with greater intensity and with more MG proteins than did pooled M876 antisera. The species-specific immunodominant proteins with the greatest potential for use as antigens in serologic tests appeared to be those of 64 (p64) and 56 (p56) kilodaltons molecular mass.
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