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对牛粪便样本进行放射性粪便培养和直接聚合酶链反应(PCR)检测副结核分枝杆菌的评估。

Evaluation of radiometric faecal culture and direct PCR on pooled faeces for detection of Mycobacterium avium subsp. paratuberculosis in cattle.

作者信息

Eamens Graeme J, Whittington Richard J, Turner Mark J, Austin Susan L, Fell Shayne A, Marsh Ian B

机构信息

Elizabeth Macarthur Agricultural Institute, NSW Department of Primary Industries, Menangle, NSW, Australia.

出版信息

Vet Microbiol. 2007 Nov 15;125(1-2):22-35. doi: 10.1016/j.vetmic.2007.04.043. Epub 2007 May 5.

Abstract

Dilution rates for pooled faecal culture (PFC) and direct IS900 polymerase chain reaction (D-PCR) tests were evaluated on faecal samples from infected cows mixed with uninfected faeces in dilutions from 1 in 5 to 1 in 50. PFC was performed by radiometric culture, with confirmation by IS900 PCR and restriction endonuclease analysis (PCR/REA) on growth, and by mycobactin dependency testing on solid medium. Using 37 culture positive faecal samples from 12 subclinical cows, 83.8% and 94.6% of samples were confirmed positive in the PFC assay at dilutions of 1 in 50 and 1 in 30, respectively. Lower dilutions (1 in 5 to 1 in 20) provided only marginally better sensitivity, and confirmation of PFC growth by PCR/REA was significantly more sensitive than mycobactin dependency. D-PCR had significantly lower sensitivity than PFC confirmed by PCR/REA, with pools of 1 in 50, 30, 10 and 5 yielding positive results in 64.9%, 70.3%, 78.4% and 83.8% of samples, respectively. Cattle considered to be shedding 1.5 x 10(6) viable M. avium subsp. paratuberculosis (Map)/g faeces (on the basis of estimated losses in processing and growth rates in radiometric broth) were positive at dilutions up to 1 in 50 in the PFC and D-PCR. Those shedding 5 x 10(5) viable Map/g were positive in the PFC at dilutions up to 1 in 40, but required a 1 in 10 dilution or less for D-PCR. The results suggest that for cattle shedding relatively high concentrations of Map in faeces (>2 x 10(5) viable Map/g), maximal dilutions of 1 in 30 for PFC and 1 in 10 for D-PCR would be applicable.

摘要

对来自感染奶牛的粪便样本与未感染粪便按1:5至1:50的比例进行稀释,评估混合粪便培养(PFC)和直接IS900聚合酶链反应(D-PCR)检测的稀释率。PFC通过放射性培养进行,通过对生长物进行IS900 PCR和限制性内切酶分析(PCR/REA)以及在固体培养基上进行分枝杆菌素依赖性测试来确认。使用来自12头亚临床奶牛的37份培养阳性粪便样本,在PFC检测中,分别在1:50和1:30的稀释度下,83.8%和94.6%的样本被确认为阳性。较低的稀释度(1:5至1:20)仅略微提高了敏感性,并且通过PCR/REA确认PFC生长比分枝杆菌素依赖性更敏感。D-PCR的敏感性明显低于通过PCR/REA确认的PFC,在1:50、1:30、1:10和1:5的混合样本中,分别有64.9%、70.3%、78.4%和83.8%的样本产生阳性结果。根据放射性肉汤中的处理损失和生长速率估计,被认为每克粪便排出1.5×10⁶ 存活副结核分枝杆菌(Map)的牛,在PFC和D-PCR中,稀释度高达1:50时呈阳性。每克粪便排出5×10⁵ 存活Map的牛,在PFC中,稀释度高达1:40时呈阳性,但D-PCR需要1:10或更低的稀释度。结果表明,对于粪便中排出相对高浓度Map(>2×10⁵ 存活Map/g)的牛,PFC的最大稀释度为1:30,D-PCR的最大稀释度为1:10适用。

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