Johne B, Jarp J, Haaheim L R
National Veterinary Institute, Oslo, Norway.
J Clin Microbiol. 1989 Jul;27(7):1631-5. doi: 10.1128/jcm.27.7.1631-1635.1989.
Staphylococcus aureus strains were separated from mastitis milk samples without cultivation by using monodisperse magnetic polymer particles coated with polyclonal antiserum against an encapsulated S. aureus strain. Exopolysaccharide was verified by transmission electron microscopy and the serum soft-agar culture technique. Capsular polysaccharide was found on virtually all clinical isolates. Surface protein A and S. aureus-specific cell wall components were masked when the strains were cultured on an exopolysaccharide-promoting medium. Masking of surface determinants was dependent on their concentration on the bacterial surface as well as on exopolysaccharide abundance. The polysaccharide layer on in vivo bacteria was reduced markedly after just one transfer from milk to blood agar plates but was reexpressed after culturing was done on a capsule-generating medium.
通过使用包被有针对一株包膜金黄色葡萄球菌的多克隆抗血清的单分散磁性聚合物颗粒,从乳腺炎乳汁样本中分离出金黄色葡萄球菌菌株,无需培养。通过透射电子显微镜和血清软琼脂培养技术验证了胞外多糖。几乎在所有临床分离株中都发现了荚膜多糖。当菌株在促进胞外多糖产生的培养基上培养时,表面蛋白A和金黄色葡萄球菌特异性细胞壁成分被掩盖。表面决定簇的掩盖取决于它们在细菌表面的浓度以及胞外多糖的丰度。从乳汁转移到血琼脂平板仅一代后,体内细菌上的多糖层就显著减少,但在产生荚膜的培养基上培养后又重新表达。