Woubit S, Manso-Silván L, Lorenzon S, Gaurivaud P, Poumarat F, Pellet M-P, Singh V P, Thiaucourt F
CIRAD UPR 15 Contrôle des maladies animales exotiques et émergentes, TA A-15/G Campus International de Baillarguet, 34398 Montpellier Cedex 5, France.
Mol Cell Probes. 2007 Oct-Dec;21(5-6):391-9. doi: 10.1016/j.mcp.2007.05.008. Epub 2007 Jun 7.
Contagious agalactia is a mycoplasmal infection caused by Mycoplasma agalactiae, Mycoplasma mycoides subsp. mycoides LC, M. mycoides subsp. capri, Mycoplasma capricolum subsp. capricolum and Mycoplasma putrefaciens. Identification of the causative organisms is usually performed by isolation and classical biochemical and serological tests, though this is a lengthy and cumbersome process for mycoplasmas. Specific PCR assays have been developed for the identification of Mycoplasma agalactiae and M. putrefaciens. For members of the M. mycoides cluster existing PCR tests are based on the amplification of highly conserved genes coding for ribosomal proteins, hence a possibility of cross-reactions. The gene glk, coding for a glucokinase, that is found in this cluster is very distantly related to any other bacterial glucokinase described so far. It was therefore chosen as target to design a new PCR test. The validation was performed independently in three laboratories in France and India using over 100 mycoplasma strains of various geographical origins. All strains belonging to the M. mycoides cluster were detected by amplification of the expected PCR product (428 bp) while no amplification was obtained from M. agalactiae strains. Our results demonstrate the universality of this PCR in spite of the great heterogeneity found within this cluster. This new tool may be of great help for the implementation of control measures directed towards contagious agalactia.
传染性无乳症是由无乳支原体、丝状支原体丝状亚种、丝状支原体山羊亚种、山羊支原体山羊亚种和腐败支原体引起的支原体感染。通常通过分离以及经典的生化和血清学检测来鉴定病原体,不过对于支原体而言,这是一个漫长且繁琐的过程。已经开发出特异性PCR检测方法用于鉴定无乳支原体和腐败支原体。对于丝状支原体菌群的成员,现有的PCR检测基于编码核糖体蛋白的高度保守基因的扩增,因此存在交叉反应的可能性。在该菌群中发现的编码葡萄糖激酶的glk基因,与迄今为止描述的任何其他细菌葡萄糖激酶的亲缘关系都非常远。因此,它被选作设计新PCR检测的靶标。在法国和印度的三个实验室中,使用来自不同地理来源的100多种支原体菌株独立进行了验证。通过扩增预期的PCR产物(428 bp)检测到所有属于丝状支原体菌群的菌株,而无乳支原体菌株未获得扩增。我们的结果表明,尽管该菌群内存在很大的异质性,但这种PCR具有通用性。这种新工具可能对实施针对传染性无乳症的控制措施有很大帮助。