Unite Mycoplasmologie Bacteriologie, CNEVA Ploufragan, Ploufragan, France.
Avian Pathol. 1998;27(1):7-14. doi: 10.1080/03079459808419268.
This review describes some applications of DNA amplification methods for diagnosis or epidemiological investigations of avian mycoplasmosis. Tests for direct detection of pathogenic mycoplasmas have been developed. Moreover, most avian mycoplasma species can be differentiated, according to their unique restriction fragment length polymorphism (RFLP) patterns generated after digestion of PCR products with different restriction enzymes. In order to characterize isolates below the species level, PCR-based subtyping methods have been introduced. One of them, arbitrarily primed-PCR, results in strain-specific arrays of DNA fragments that can distinguish even closely related strains of a given species. This method was successfully used to investigate the molecular epidemiology of vaccine strains and of Mycoplasma gallisepticum conjunctivitis in songbirds. Major issues in the development of DNA-amplification tests concern the selection of the appropriate target, specimen collection, DNA preparation and detection of amplification reaction inhibitors. Careful consideration to the design and work flow of the facility are necessary to avoid false-positive results.
这篇综述描述了 DNA 扩增方法在禽类支原体病诊断或流行病学研究中的一些应用。已经开发出用于直接检测致病性支原体的检测方法。此外,根据用不同的限制性内切酶消化 PCR 产物后产生的独特的限制性片段长度多态性(RFLP)模式,可以区分大多数禽支原体种。为了对种以下的分离株进行特征描述,引入了基于 PCR 的分型方法。其中一种方法,任意引物 PCR,产生菌株特异性的 DNA 片段阵列,甚至可以区分给定种的密切相关菌株。该方法成功地用于调查疫苗株和禽传染性鼻炎的支原体结膜炎在鸣禽中的分子流行病学。DNA 扩增试验开发中的主要问题涉及到合适的目标选择、标本采集、DNA 制备和扩增反应抑制剂的检测。为了避免假阳性结果,需要仔细考虑设施的设计和工作流程。