Hall M R, Thoen C O
Am J Vet Res. 1985 Nov;46(11):2249-52.
Extracts of Mycobacterium bovis ATCC 19210 were prepared from cells following treatment with acetone 3 times, ethyl alcohol-ether 3 times (1:1, v/v), and chloroform 3 times. Cells were dried and suspended in 0.05M Tris-HCl (pH 7.5) containing lysozyme (1 mg/50 mg of dried cells). One aliquot of the lysozyme extract was filter-sterilized and 1 aliquot of the lysozyme extract was autoclaved. Delayed-type hypersensitivity responses elicited in sensitized guinea pigs, using the filter-sterilized lysozyme extract, were significantly greater than responses elicited using the autoclaved lysozyme extract (P less than 0.01). The filter-sterilized lysozyme extract and a purified protein derivative (PPD) of M bovis, at equal protein concentrations, elicited comparable delayed-type hypersensitivity responses in sensitized guinea pigs. Significant differences were not detected between the mean enzyme-linked immunosorbent assay (ELISA) values on sera collected from calves before exposure to M bovis, using each of the lysozyme extracts or the M bovis PPD (P greater than 0.05). Significant differences were detected when ELISA values obtained using each of the antigens on post-exposure serum were compared with ELISA values on serum collected from calves before exposure to M bovis (P less than 0.01). Differences were not detected in mean ELISA values on sera from cattle collected 12 months after exposure to M bovis, using each of the lysozyme extracts or M bovis PPD (P greater than 0.05); however, 8 of 8 calves were identified as positive on ELISA, using the filter-sterilized lysozyme extract, 7 of 8 calves were positive, using M bovis PPD, and 7 of 8 calves were positive, using the autoclaved lysozyme extract.
牛分枝杆菌ATCC 19210的提取物是通过以下方式从细胞中制备的:用丙酮处理3次,用乙醇 - 乙醚(1:1,v/v)处理3次,用氯仿处理3次。细胞干燥后,悬浮于含有溶菌酶(1 mg/50 mg干燥细胞)的0.05M Tris - HCl(pH 7.5)中。一份溶菌酶提取物经滤膜除菌,另一份溶菌酶提取物经高压灭菌。用经滤膜除菌的溶菌酶提取物在致敏豚鼠中引发的迟发型超敏反应显著大于用经高压灭菌的溶菌酶提取物引发的反应(P小于0.01)。在致敏豚鼠中,等蛋白浓度的经滤膜除菌的溶菌酶提取物和牛分枝杆菌的纯化蛋白衍生物(PPD)引发了相当的迟发型超敏反应。使用每种溶菌酶提取物或牛分枝杆菌PPD对未接触牛分枝杆菌的犊牛血清进行酶联免疫吸附测定(ELISA),其平均ELISA值之间未检测到显著差异(P大于0.05)。当将每种抗原在接触后血清上获得的ELISA值与未接触牛分枝杆菌的犊牛血清上的ELISA值进行比较时,检测到显著差异(P小于0.01)。使用每种溶菌酶提取物或牛分枝杆菌PPD对接触牛分枝杆菌12个月后的牛血清进行ELISA,其平均ELISA值之间未检测到差异(P大于0.05);然而,使用经滤膜除菌的溶菌酶提取物时,8头犊牛中有8头在ELISA中被鉴定为阳性,使用牛分枝杆菌PPD时,8头犊牛中有7头为阳性,使用经高压灭菌的溶菌酶提取物时,8头犊牛中有7头为阳性。