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Evaluation of PCR and multiplex PCR in relation to nested PCR for diagnosing Theileria equi

机译:嵌套PCR与嵌套PCR诊断中的PCR和多重PCR评价

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Conventional PCR (PCRTeq) for diagnosing Theileria equi and multiplex PCR (M/PCRTeq-Bc) for diagnosing T. equi and Babesia caballi were comparatively evaluated with nested PCR (N/PCR-Teq) for diagnosing equine piroplasmosis. In DNA sensitivity determinations, in multiple dilutions of equine blood that had tested positive for T. equi, PCR-Teq and N/PCR-Teq detected hemoparasite DNA in the larger dilutions (1:128), but did not differ significantly from the M/PCRTeq-Bc (1:64). In analyses on equine serum tested by ELISA, there was high agreement between this serological test and PCR-Teq (k = 0.780) and moderate agreement with N/PCR-Teq (k = 0.562) and M/PCRTeq-Bc (k = 0.488). PCR-Teq found a higher frequency of T. equi both in extensively and intensively reared horses, but this was not significant in relation to N/PCR-Teq (P0.05), and both PCRs indicated that there was an endemic situation regarding T. equi in the population of horses of this sample. PCR-Teq was only significantly different from M/PCR-Teq-Bc (P
机译:用于诊断用于诊断T. Equi和Babesia Caballi的鉴定肠杆菌和多重PCR(M / PCRTEQ-BC)的常规PCR(PCRTEQ)对嵌套的PCR(N / PCR-TEQ)进行鉴别进行评估,用于诊断标牌粒子菌病。在DNA敏感性测定中,在较大稀释液(1:128)中检测到均为T.Equi,PCR-TEQ和N / PCR-TEQ检测到的血液卤化物DNA的多种稀释液中,但从M中没有显着差异/ pcrteq-bc(1:64)。在ELISA测试的马血清分析中,该血清学试验和PCR-TEQ(k = 0.780)之间的高度协议和与N / PCR-TEQ(k = 0.562)和M / PCRTEQ-BC(k = 0.488 )。 PCR-TEQ在广泛和集中的马匹中发现了较高的T.Equi的频率,但这与N / PCR-TEQ相关(P> 0.05)并不重要,并且两种PCR都表明存在有关T的流行情况。在这个样本的马匹中的equi。 PCR-TEQ与M / PCR-TEQ-BC显着不同(P

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