Abshire R L, Lombard G L, Dowell V R
J Clin Microbiol. 1977 Oct;6(4):425-32. doi: 10.1128/jcm.6.4.425-432.1977.
Antisera against seven strains of Bacteroides fragilis subspecies fragilis were produced from dense suspensions of whole cells. These sera exhibited high agglutination titers with homologous antigens. Reciprocal cross-reactions in agglutination tests with each immunizing strain yielded lower titers. Both the indirect and direct fluorescent-antibody techniques were used to evaluate these reagents in the serological identification of 24 defined strains of B. fragilis subspecies fragilis. Subspecies and even strain specificities were noted with particular antisera. A pooled antiserum and conjugate were prepared and studied. Study results showed that specific and high-titered antisera against strains within this subspecies can be produced by the methods described herein and that possibly more than one serotype exists within the seven strains studied. The development of more antibody pools will be necessary to encompass a wider antigenic coverage before the fluorescent-antibody technique can be relied upon altogether for serologically identifying isolates of B. fragilis subspecies fragilis. Test data showed that the indirect method of fluorescent-antibody staining with whole antiserum is an excellent means of identifying strains of this organism.
用脆弱拟杆菌脆弱亚种的7个菌株的全细胞浓悬液制备了抗血清。这些血清与同源抗原呈现出高凝集效价。在与每种免疫菌株的凝集试验中,相互交叉反应产生的效价较低。间接和直接荧光抗体技术都用于评估这些试剂在24株已明确的脆弱拟杆菌脆弱亚种血清学鉴定中的作用。用特定抗血清可观察到亚种甚至菌株特异性。制备并研究了一种混合抗血清和结合物。研究结果表明,通过本文所述方法可制备针对该亚种内菌株的特异性、高效价抗血清,且在所研究的7个菌株中可能存在不止一种血清型。在完全依靠荧光抗体技术进行脆弱拟杆菌脆弱亚种分离株的血清学鉴定之前,有必要开发更多抗体池以涵盖更广泛的抗原范围。试验数据表明,用全抗血清进行荧光抗体染色的间接方法是鉴定该菌菌株的极佳手段。