Cocito C, Gilot P, Coene M, de Kesel M, Poupart P, Vannuffel P
Microbiology and Genetics Unit, University of Louvain, Medical School, Brussels, Belgium.
Clin Microbiol Rev. 1994 Jul;7(3):328-45. doi: 10.1128/CMR.7.3.328.
Paratuberculosis (Johne's disease) is a chronic, wasting, widespread mycobacteriosis of ruminants. It involves extensive mycobacterial shedding, which accounts for the high contagiousness, and ends with a fatal enteritis. Decreases in weight, milk production, and fertility produce severe economic loss. The DNA of the etiological agent (Mycobacterium paratuberculosis) has a base composition (66 to 67% G+C) within the range of that of mycobacteria (62 to 70% G+C), a size (4.4 x 10(6) to 4.7 x 10(6) bp) larger than that of most pathogenic mycobacteria (2.0 x 10(6) to 4.2 x 10(6) bp), and a high relatedness (> 90%) to Mycobacterium avium DNA. However, the DNAs of the two organisms can be distinguished by restriction fragment length polymorphism analysis. M. paratuberculosis genes coding for a transposase, a cell wall-associated protein (P34), and two heat shock proteins have been cloned and sequenced. Nucleic acid probes (two of which are species specific) are used, after PCR amplification, for M. paratuberculosis identification in stools and milk. As in leprosy, with disease progression, cellular immune reactions decrease and humoral immune reactions increase. Cutaneous testing with sensitins, lymphocyte proliferation assays, and cytokine tests are used to monitor cellular immune reactions in paratuberculosis, but these tests lack specificity. Complement fixation, immunodiffusion, and enzymometric tests based on antibodies to M. paratuberculosis extracts, to mycobacterial antigen complex A36, to glycolipids, and to proteins help identify affected cattle but are not species specific. The carboxyl-terminal portion of the 34-kDa cell wall-associated A36 protein (P34) carries species-specific B-cell epitopes and is the basis for an enzyme-linked immunosorbent assay. Diagnostic tests for paratuberculosis are also used in Crohn's disease, a chronic human ileitis mimicking Johne's disease, in which isolates identified as M. paratuberculosis have been found.
副结核病(约翰氏病)是反刍动物的一种慢性、消耗性、广泛传播的分枝杆菌病。它涉及大量分枝杆菌排出,这导致了高传染性,最终以致命性肠炎告终。体重减轻、产奶量下降和繁殖力降低会造成严重的经济损失。病原体(副结核分枝杆菌)的DNA碱基组成(66%至67%的G+C)在分枝杆菌的范围内(62%至70%的G+C),大小(4.4×10⁶至4.7×10⁶碱基对)比大多数致病性分枝杆菌(2.0×10⁶至4.2×10⁶碱基对)大,并且与鸟分枝杆菌DNA有高度相关性(>90%)。然而,这两种生物体的DNA可通过限制性片段长度多态性分析加以区分。编码转座酶、一种细胞壁相关蛋白(P34)和两种热休克蛋白的副结核分枝杆菌基因已被克隆和测序。核酸探针(其中两种是种特异性的)在PCR扩增后用于粪便和牛奶中副结核分枝杆菌的鉴定。与麻风病一样,随着疾病进展,细胞免疫反应降低而体液免疫反应增加。用致敏素进行皮肤试验、淋巴细胞增殖测定和细胞因子检测用于监测副结核病中的细胞免疫反应,但这些检测缺乏特异性。基于针对副结核分枝杆菌提取物、分枝杆菌抗原复合物A36、糖脂和蛋白质的抗体的补体结合、免疫扩散和酶学检测有助于识别受感染的牛,但不是种特异性的。34 kDa细胞壁相关A36蛋白(P34)羧基末端部分携带种特异性B细胞表位,是酶联免疫吸附测定的基础。副结核病的诊断检测也用于克罗恩病,一种模拟约翰氏病的慢性人类回肠炎,在其中已发现被鉴定为副结核分枝杆菌的分离株。