Surujballi O P, Marenger R M, Eaglesome M D, Sugden E A
Agriculture and Agri-Food Canada, Animal Diseases Research Institute, Nepean, Ontario.
Can J Vet Res. 1997 Oct;61(4):260-6.
Outer sheath antigen from Leptospira interrogans serovar hardjo type hardjoprajitno and acetic acid extracted antigens from serovar hardjo types hardjoprajitno and hardjobovis were evaluated in an immunoassay for ability to detect hyperimmune rabbit serum to serovar hardjo. The degree of cross-reactivity with hyperimmune rabbit sera to L. interrogans serovars pomona, copenhageni, grippotyphosa, canicola and sejroe, and Leptospira biflexa serovar patoc was also measured for each antigen. All of the antigens reacted with the antiserum to L. interrogans serovar hardjo. The outer sheath antigen however, also showed wide cross-reactivity with the antisera to all of the serovars of L. interrogans tested and with the antiserum to L. biflexa serovar patoc. The acetic acid extracted antigen from either type hardjoprajitno, or type hardjobovis, showed a high degree of specificity for serovar hardjo antiserum. The hardjobovis acetic acid extracted antigen was characterized by sodium dodecyl sulfate polyacrylamide gel electrophoresis and immunoblotting, and was incorporated into an indirect ELISA for detection of anti-serovar hardjo antibodies in bovine serum. This ELISA showed a relative specificity of 100% with 156 bovine sera which were negative at a dilution of 1:100 in the microscopic agglutination test (MAT) for L. interrogans serovars hardjo, pomona, sejroe, icterohaemorrhagiae, copenhageni, canicola, and grippotyphosa. The relative sensitivity of this assay with 192 bovine sera which had serovar hardjo MAT titres of > or = 100 was 95.3% (95% confidence limit = 2.99%). The degree of cross-reactivity with 289 bovine sera which had serovar pomona MAT titres of > or = 100 (with no detectable serovar hardjo MAT titres) was approximately 1.0%. This assay was: easily standardized, scored objectively, repeatable, semi-automated and used a non-hazardous antigen that can be routinely prepared in gram amounts.
对问号钩端螺旋体哈焦型哈焦普拉吉特纳的外膜抗原以及哈焦型哈焦普拉吉特纳和哈焦博维斯型的乙酸提取抗原进行了免疫分析,以评估其检测针对哈焦型的超免疫兔血清的能力。还测定了每种抗原与针对波摩那型、哥本哈根型、七日热型、犬型和爪哇型问号钩端螺旋体以及双曲钩端螺旋体帕托型的超免疫兔血清的交叉反应程度。所有抗原均与针对问号钩端螺旋体哈焦型的抗血清发生反应。然而,外膜抗原还与针对所检测的所有问号钩端螺旋体血清型的抗血清以及针对双曲钩端螺旋体帕托型的抗血清表现出广泛的交叉反应。来自哈焦普拉吉特纳型或哈焦博维斯型的乙酸提取抗原对哈焦型抗血清表现出高度特异性。对哈焦博维斯型乙酸提取抗原进行了十二烷基硫酸钠聚丙烯酰胺凝胶电泳和免疫印迹分析,并将其用于间接酶联免疫吸附测定(ELISA),以检测牛血清中抗哈焦型抗体。该ELISA对156份牛血清显示出100%的相对特异性,这些牛血清在针对问号钩端螺旋体哈焦型、波摩那型、爪哇型、黄疸出血型、哥本哈根型、犬型和七日热型的显微镜凝集试验(MAT)中以1:100稀释度呈阴性。该测定对192份哈焦型MAT效价≥100的牛血清的相对敏感性为95.3%(95%置信限=2.99%)。与289份波摩那型MAT效价≥100(无可检测到的哈焦型MAT效价)的牛血清的交叉反应程度约为1.0%。该测定方法:易于标准化、客观评分、可重复、半自动,并且使用了一种可常规制备克级量的无危害抗原。