Lalitha M K, Anandi V, Elias L, Kalpana C R
Department of Microbiology, Christian Medical College Hospital, Vellore.
Indian J Med Res. 1991 Mar;93:98-102.
A coagglutination technique using indigenous reagents was applied for the rapid identification of Bacteroides fragilis and the black pigmented bacteroides group, using colony suspensions. All the 58 strains of B. fragilis and 42 strains of black pigmented bacteroides tested could be correctly identified by this method. The specificity of the coagglutination reagent was confirmed by the absence of cross reactivity with the related species of bacteroides, viz., B. distasonis, B. ovatus, B. vulgatus and B. thetaiotaomicron as well as other anaerobic and aerobic bacteria. A panel of four antisera against B. fragilis was required for correct identification of the strains tested, indicating the presence of multiple serotypes. On the other hand, all 42 strains of black pigmented bacteroides tested could be identified, using a single reagent as these strains appeared to have no antigenic type variants.
采用一种使用本地试剂的协同凝集技术,利用菌落悬液对脆弱拟杆菌和产黑色素拟杆菌群进行快速鉴定。所检测的58株脆弱拟杆菌和42株产黑色素拟杆菌均能通过该方法得到正确鉴定。通过与拟杆菌的相关菌种,即狄氏拟杆菌、卵形拟杆菌、普通拟杆菌和嗜麦芽糖拟杆菌以及其他厌氧菌和好氧菌无交叉反应,证实了协同凝集试剂的特异性。正确鉴定所检测的菌株需要一组四种抗脆弱拟杆菌抗血清,这表明存在多种血清型。另一方面,所检测的42株产黑色素拟杆菌均可用单一试剂进行鉴定,因为这些菌株似乎没有抗原型变体。