Suksai Parut, Sangkachai Nareerat, Chatsiriwech Jarin, Kanthasaewee Oraphan, Sariya Ladawan, Chaichoun Kridsada
The Monitoring and Surveillance Center of Zoonotic Diseases in Wildlife and Exotic Animals, Faculty of Veterinery Science, Mahidol University, Nakhon Pathom, Thailand.
Southeast Asian J Trop Med Public Health. 2010 Nov;41(6):1447-53.
A multiplex polymerase chain reaction (PCR) was developed for the detection of feline hemotropic mycoplasmas which simultaneously differentiates infections of Mycoplasma haemofelis (Mhf), Candidatus Mycoplasma haemominutum (CMhm) and Candidatus Mycoplasma turicensis (CMtc) in feline blood and spleen. These organisms are responsible for the cause of various pathogenicity of feline infectious anemia. These infections are difficult to be detected by microscopic examination, the most commonly used method for general laboratory diagnoses. Specific primers were designed by selected consensus 16S rDNA sequences of three distinct species. The multiplex PCR assay developed in this study was sensitive and specific with detection limit 100 copies/microl DNA of Mhf and CMhm and 10 copies/microl DNA of CMtc. No amplicons could be amplified for other blood parasites or bacterial pathogens. This multiplex PCR will allow studies of pathogenicity and the monitoring of clinical treatment.
开发了一种多重聚合酶链反应(PCR)用于检测猫血支原体,该反应可同时鉴别猫血液和脾脏中溶血支原体(Mhf)、溶血微小支原体(CMhm)和苏黎世支原体(CMtc)的感染情况。这些病原体是猫传染性贫血各种致病性的病因。这些感染难以通过显微镜检查检测出来,而显微镜检查是一般实验室诊断中最常用的方法。通过选择三个不同物种的共有16S rDNA序列设计了特异性引物。本研究开发的多重PCR检测方法灵敏且特异,检测限为Mhf和CMhm的DNA为100拷贝/微升,CMtc的DNA为10拷贝/微升。对于其他血液寄生虫或细菌病原体,未扩增出扩增子。这种多重PCR将有助于致病性研究和临床治疗监测。