Sharma G, Singh S V, Sevilla I, Singh A V, Whittington R J, Juste R A, Kumar S, Gupta V K, Singh P K, Sohal J S, Vihan V S
Central Institute for Research on Goats, Makhdoom, 281 122 Farah, Mathura District, UP, India.
Res Vet Sci. 2008 Feb;84(1):30-7. doi: 10.1016/j.rvsc.2007.03.014. Epub 2007 Jun 1.
Present study is the first attempt to evaluate an indigenous milk ELISA with milk culture, standardize milk PCR, estimate lacto-prevalence of Map and genotype Map DNA from milk samples in few Indian dairy herds. In all 115 cows were sampled from 669 lactating cows in six dairy herds from three districts of North India. Fifty milk samples (four herds) were screened by three tests (milk culture, m-ELISA and m-PCR). Lacto-prevalence of Map in four dairy herds was 84.0% (50.0% in fat and 62.0% in sediment). Screening of both fat and sediment increased the sensitivity of culture. Colonies appeared between 45 and 120 DPI. In indigenous m-ELISA, protoplasmic antigen derived from native Map 'Bison type' strain of goat origin was used. Screening of 115 lactating cows by m-ELISA ('herd screening test') detected 32.1% positive lactating cows (lacto-prevalence). Sensitivity of ELISA was 28.5% and 42.8% in single point cutoff and S/P ratio, respectively. Lacto-prevalence of JD was high in dairy herds (66.6-100.0% by culture and 20.0-50.0% by m-ELISA). DDD farm, Mathura had very high (95.8%) and moderate prevalence of Map and lacto-antibodies, respectively. All cows were clinically suffering from JD. Specific IS 900 PCR was standardized in decontaminated fat and sediment of milk samples. DNA isolated from decontaminated pellets was amplified and characteristic 229 bp band was confirmatory for Map. Of the 50 milk samples, 6.0% were positive in m-PCR. The test needs further standardization. Map DNA were genotyped as Map 'Bison type' by IS 1311 PCR-REA. Of the three tests, milk culture was most sensitive followed by m-ELISA and m-PCR. Map DNA isolated from milk samples of dairy cattle were first time genotyped as Map, 'Bison type' in India. High prevalence of Map in milk of dairy herds, posed major health hazard for calves and human beings.
本研究首次尝试将本土牛奶酶联免疫吸附测定法(ELISA)与牛奶培养法相结合,对牛奶聚合酶链反应(PCR)进行标准化,估算印度少数奶牛场牛奶样本中副结核分枝杆菌(Map)的乳糖患病率以及Map DNA的基因型。从印度北部三个地区六个奶牛场的669头泌乳奶牛中总共采集了115份奶牛样本。对50份牛奶样本(来自四个牛群)进行了三项检测(牛奶培养、牛奶ELISA和牛奶PCR)。四个奶牛场中Map的乳糖患病率为84.0%(脂肪中为50.0%,沉淀物中为62.0%)。对脂肪和沉淀物进行筛查提高了培养的灵敏度。菌落出现在接种后45至120天。在本土牛奶ELISA中,使用了源自山羊源本土Map“野牛型”菌株的原生质体抗原。通过牛奶ELISA(“牛群筛查试验”)对115头泌乳奶牛进行筛查,检测出32.1%的泌乳奶牛呈阳性(乳糖患病率)。ELISA在单点截断值和S/P比值下的灵敏度分别为28.5%和42.8%。奶牛场中约内氏分枝杆菌(JD)的乳糖患病率很高(培养法为66.6 - 100.0%,牛奶ELISA法为20.0 - 50.0%)。马图拉的DDD农场中Map和乳糖抗体的患病率分别非常高(95.8%)和中等。所有奶牛临床上都患有JD。在牛奶样本经净化处理的脂肪和沉淀物中对特异性IS 900 PCR进行了标准化。从净化后的沉淀中分离出的DNA进行扩增,特征性的229 bp条带可确认为Map。在50份牛奶样本中,6.0%在牛奶PCR中呈阳性。该检测需要进一步标准化。通过IS 1311 PCR - REA将Map DNA基因型鉴定为Map“野牛型”。在这三项检测中,牛奶培养最敏感,其次是牛奶ELISA和牛奶PCR。从奶牛牛奶样本中分离出的Map DNA在印度首次被基因型鉴定为Map“野牛型”。奶牛场牛奶中Map的高患病率对犊牛和人类构成了重大健康危害。