Eamens Graeme J, Whittington Richard J, Turner Mark J, Austin Susan L, Fell Shayne A, Marsh Ian B
Elizabeth Macarthur Agricultural Institute, NSW Department of Primary Industries, Menangle, NSW, Australia.
Vet Microbiol. 2007 Nov 15;125(1-2):22-35. doi: 10.1016/j.vetmic.2007.04.043. Epub 2007 May 5.
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.
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。