Nehra K, Rana R, Viswas K N, Arun T R, Singh V P, Singh A P, Prabhu S N
Graduated from Indian Veterinary Research Institute, Izatnagar, 243122, Bareilly, Uttar Pradesh, India;
Referral Lab on Mycoplasma, Division Bacteriology & Mycology, Indian Veterinary Research Institute, Izatnagar, 243122, Bareilly, Uttar Pradesh, India;
Iran J Vet Res. 2015 Spring;16(2):176-81.
Although Mycoplasma equigenitalium has been implicated in equine reproductive problems, its prevalence is largely unexplored due to the lack of specific diagnostic tests. To address this limitation, the authors developed and optimized species-specific primer pairs that target M. eguigenitalium rpoB (RNA polymerase B subunit) gene sequences. The specificity of the PCR assay developed in this study was determined using 12 field isolates including the type strain of M. equigenitalium and other Mycoplasma species. In the field study, a total of 122 mare and stallion samples comprising of 50 clinical and 72 random samples were subjected to species-specific PCR assay to detect M. equigenitalium in equine genital tracts. Mycoplasma equigenitalium (MEG) species-specific PCR detected 22.13% positive samples; however, only 9.01% of the samples were found to be positive using the conventional culture technique. The PCR established in this study could be used for rapid, specific and accurate diagnosis of M. equigenitalium strains. To the authors' knowledge, this is the first report addressing the development and evaluation of species-specific PCR to detect M. equigenitalium.
虽然马生殖支原体与马的繁殖问题有关,但由于缺乏特异性诊断测试,其流行情况在很大程度上尚未得到充分研究。为解决这一局限性,作者开发并优化了针对马生殖支原体rpoB(RNA聚合酶B亚基)基因序列的种特异性引物对。本研究中开发的PCR检测方法的特异性是使用12株现场分离株确定的,包括马生殖支原体的模式菌株和其他支原体物种。在现场研究中,总共122份母马和种马样本(包括50份临床样本和72份随机样本)接受了种特异性PCR检测,以检测马生殖道中的马生殖支原体。马生殖支原体(MEG)种特异性PCR检测到22.13%的阳性样本;然而,使用传统培养技术仅发现9.01%的样本呈阳性。本研究中建立的PCR可用于快速、特异性和准确地诊断马生殖支原体菌株。据作者所知,这是第一份关于开发和评估用于检测马生殖支原体的种特异性PCR的报告。