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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of a Fecal Shedding Test To Detect Badger Social Groups Infected with Mycobacterium bovis
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Evaluation of a Fecal Shedding Test To Detect Badger Social Groups Infected with Mycobacterium bovis

机译:评估粪便脱落测试,以检测感染<命名内容型=“Genus-incies”> Mycobacterium Bovis 的獾社会群体

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摘要

Bovine tuberculosis (bTB) is an economically important disease affecting the cattle industry in England and Wales. bTB, caused by Mycobacterium bovis , also causes disease in the Eurasian badger ( Meles meles ), a secondary maintenance host. Disease transmission between these two species is bidirectional. Infected badgers shed M. bovis in their feces. The Animal and Plant Health Agency (APHA) of the United Kingdom organized a comparative trial to determine the performance of tests in detecting M. bovis in badger feces for the Department for Environment, Food, and Rural Affairs (DEFRA). ABSTRACT Bovine tuberculosis (bTB) is an economically important disease affecting the cattle industry in England and Wales. bTB, caused by Mycobacterium bovis , also causes disease in the Eurasian badger ( Meles meles ), a secondary maintenance host. Disease transmission between these two species is bidirectional. Infected badgers shed M. bovis in their feces. The Animal and Plant Health Agency (APHA) of the United Kingdom organized a comparative trial to determine the performance of tests in detecting M. bovis in badger feces for the Department for Environment, Food, and Rural Affairs (DEFRA). Here, we assessed the performance of the existing Warwick Fast24-qPCR test and its modified version based on a high-throughput DNA extraction method (Fast96-qPCR). We found Fast24-qPCR to have a sensitivity of 96.7% (95% confidence interval [CI], 94.5 to 99%; n ?=?244) and a specificity of 99% (95% CI, 97.8 to 100%; n ?=?292). Fast96-qPCR requires further optimization. Determining the disease status of badger social groups requires multiple tests per group. Therefore, to increase specificity further, we independently repeated the Fast24-qPCR test on positive samples, increasing stringency by requiring a second positive result. Fast24-qPCR with repeat testing had a sensitivity of 87.3% (95% CI, 83.1 to 91.5%; n ?=?244), and a specificity of 100% (95% CI, 100 to 100; n ?=?201) on an individual-sample level. At the social-group level, this repeat testing gives Fast24-qPCR high herd specificity, while testing multiple samples per group provides high herd sensitivity. With Fast24-qPCR, we provide a social-group-level test with sufficient specificity and sensitivity to monitor shedding in badgers via latrine sampling, delivering a potentially valuable tool to measure the impacts of bTB control measures.
机译:牛结核病(BTB)是一种影响英格兰和威尔士养牛行业的经济上重要的疾病。 BTB由BOVIS引起的,也引起欧亚獾(MELES MELES)的疾病,是二级维护主持人。这两个物种之间的疾病传输是双向的。被感染的獾在他们的粪便中脱落。联合王国的动物和植物卫生机构(APHA)组织了一个比较审判,以确定测试在獾粪便中饲养环境,食品和农村事务部(DECRA)的獾粪便。摘要牛结核病(BTB)是一种影响英格兰和威尔士养牛行业的经济上重要的疾病。 BTB由BOVIS引起的,也引起欧亚獾(MELES MELES)的疾病,是二级维护主持人。这两个物种之间的疾病传输是双向的。被感染的獾在他们的粪便中脱落。联合王国的动物和植物卫生机构(APHA)组织了一个比较审判,以确定测试在獾粪便中饲养环境,食品和农村事务部(DECRA)的獾粪便。在这里,我们根据高通量DNA提取方法(FAST96-QPCR)评估了现有的Warwick Fast24-QPCR测试及其改进版本的性能。我们发现FAST24-QPCR具有96.7%的敏感性(95%置信区间[CI],94.5至99%; n?=Δ244)和99%的特异性(95%CI,97.8至100%; n? =?292)。 FAST96-QPCR需要进一步优化。确定獾社会群体的疾病状况需要每组多次测试。因此,为了进一步增加特异性,我们独立地重复了阳性样本的FAST24-QPCR测试,通过需要第二阳性结果来增加严格性。 FAST24-QPCR具有重复检测的敏感性为87.3%(95%CI,83.1至91.5%; N?=Δ244),1.100%(95%CI,100至100; n?=?201)在个人样本水平上。在社交群级别,这种重复测试提供了Fast24-QPCR高牛群特异性,同时测试每组多个样本提供高群敏感性。使用FAST24-QPCR,我们提供了一种社交群体级测试,具有足够的特异性和敏感性,可以通过Latrine采样监测獾在獾中,提供潜在有价值的工具来衡量BTB控制措施的影响。

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