Bech-Nielsen S, Burianek L L, Spangler E, Heider L E, Hoffsis G F, Dorn C R
Am J Vet Res. 1985 Nov;46(11):2418-20.
The characterization of a purified antigen from Mycobacterium paratuberculosis, recently made commercially available for use in serodiagnosis by enzyme-linked immunosorbent assay (ELISA), of paratuberculosis in cattle was described. This assay had 89% specificity and 83% sensitivity for M paratuberculosis infection. The protein/polypeptide composition of the purified antigen was compared with that of a crude protoplasmic extract of strain 18 M paratuberculosis used in the agar-gel immunodiffusion test and ELISA and with that of sonicated strain 19698 M paratuberculosis organisms grown on Dorset-Henley synthetic liquid medium. The sonicated M paratuberculosis contained 27 major proteins/polypeptides; the crude protoplasmic extract, 18; and the purified antigen contained 14 proteins/polypeptides, using sodium dodecyl-sulfate polyacrylamide-gel electrophoresis analysis. The serologic reactivity of these proteins/polypeptides were defined, using the enzyme-linked immuno-electrotransfer blot technique. The sonicated M paratuberculosis contained 20 serologically reactive proteins/polypeptides (34,000 to 84,000 daltons); the crude protoplasmic extract contained 3 (37,000 to 45,000 daltons); and the purified extract contained a diffuse polypeptide band (34,000 to 38,000 daltons). Identification by enzyme-linked immuno-electrotransfer blot technique of M paratuberculosis antigens reactive in the ELISA will allow us to further study these antigens in the ELISA to improve sensitivity and specificity of the diagnostic test.
本文描述了一种从副结核分枝杆菌中纯化的抗原,该抗原最近已商业化,可用于牛副结核病的酶联免疫吸附测定(ELISA)血清学诊断。该检测方法对副结核分枝杆菌感染的特异性为89%,敏感性为83%。将纯化抗原的蛋白质/多肽组成与用于琼脂凝胶免疫扩散试验和ELISA的18株副结核分枝杆菌粗原生质提取物以及在多塞特-亨利合成液体培养基上生长的19698株副结核分枝杆菌超声破碎菌体的蛋白质/多肽组成进行了比较。使用十二烷基硫酸钠聚丙烯酰胺凝胶电泳分析,超声破碎的副结核分枝杆菌含有27种主要蛋白质/多肽;粗原生质提取物含有18种;纯化抗原含有14种蛋白质/多肽。使用酶联免疫电转移印迹技术确定了这些蛋白质/多肽的血清学反应性。超声破碎的副结核分枝杆菌含有20种血清学反应性蛋白质/多肽(34,000至8,4000道尔顿);粗原生质提取物含有3种(37,000至45,000道尔顿);纯化提取物含有一条弥散的多肽带(34,000至38,000道尔顿)。通过酶联免疫电转移印迹技术鉴定ELISA中具有反应性的副结核分枝杆菌抗原,将使我们能够在ELISA中进一步研究这些抗原,以提高诊断试验的敏感性和特异性。