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Detection of Mycoplasma mycoides cluster by indirect immunoperoxidase (IPI) and PCR-REA in the ear canal of bovines

机译:间接免疫过氧化物酶(IPI)和PCR-REA检测牛耳道中的支原体

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Mycoplasma mycoides cluster (MMC) was diagnosed by polimerase chain reaction-restriction endonuclease analysis (PCR-REA) and indirect immunoperoxidase (IPI), both, carried out in flushing from external ear canal, collected from bovine at slaughter time in the State of Rio de Janeiro, southeastern, Brazil. A total of 60 bovines were randomly selected. Sterile syringes (60mL) loaded with buffer solution (PBS, pH 7.2) were used for the ear canal flushing. The obtained samples were stored in glycerol (1:2) and frozen at -20?oC until use. These specimens were diluted up to 10-5, inoculated in liquid and solid modified Hayflick´s media and incubated at 37?oC for 2-3 days. The plates were kept in a microaerophilia condition and examined every two days under a stereomicroscope for the presence of typical colonies “fried-egg”. In this study, 35 strains selected in agreement with their biochemistry and physiologic proprieties, were used. From the 60 cultivated samples, 48 (80.00%) were positive for Mycoplasma spp. Under IPI the prevalence obtained for MMC was 20.0% (12/60) while by PCR-REA it was 41.7% (25/60). The IPI typing of these isolates resulted in 58.3% (7/12) for M.mycoides mycoides LC and 41.7% (5/12) for M. capricolum. PCR-REA for MMC was confirmed by the amplicon size of 785bp, compatible with this group. The Kappa value for the association between these two tests was 0.14 (p0.05). After restriction analysis with AluI in all MMC strains the fragments size obtained were of 81, 98, 186 and 236bp, but not of 370bp that is compatible with Mycoides mycoides mycoides SC of bovine type. The presence of mycoplasmas species in the ear canal of asymptomatic bovines represent a risk of subsequent propagation of Mycoplasma spp. among bovine herds in Brazil. Index
机译:支原体支原体簇(MMC)通过polimerase链反应限制内切核酸酶分析(PCR-REA)和间接免疫过氧化物酶(IPI)进行诊断,二者均从外耳道冲洗后在里约州屠宰时从牛中采集巴西东南部的de Janeiro。总共随机选择了60头牛。装有缓冲溶液(PBS,pH 7.2)的无菌注射器(60mL)用于冲洗耳道。将获得的样品保存在甘油(1:2)中,并在-20℃冷冻直至使用。将这些样品稀释至10-5,接种在液体和固体改良的Hayflick培养基中,并在37°C下孵育2-3天。将板保持在微需氧量条件下,并每两天在体视显微镜下检查典型菌落“煎蛋”的存在。在这项研究中,使用了35株与其生化和生理特性一致的菌株。在60个培养样品中,有48个(80.00%)支原体呈阳性。在IPI下,MMC的患病率为20.0%(12/60),而通过PCR-REA的患病率为41.7%(25/60)。这些分离株的IPI分型导致Mycoides mycoides LC占58.3%(7/12),而癸酸支原体占41.7%(5/12)。通过785bp的扩增子大小证实了MMC的PCR-REA,与该组兼容。这两个测试之间关联的Kappa值为0.14(p> 0.05)。在所有MMC菌株中用AluI进行限制性酶切分析后,获得的片段大小分别为81、98、186和236bp,但不是370bp,与牛型Mycoides mycoides mycoides SC相容。无症状牛的耳道中存在支原体种类,代表了随后传播支原体的风险。在巴西的牛群中。指数

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