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首页> 外文期刊>Journal of Veterinary Diagnostic Investigation >Diagnostic performance of fecal quantitative real-time polymerase chain reaction for detection of Lawsonia intracellularis - associated proliferative enteropathy in nursery pigs.
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Diagnostic performance of fecal quantitative real-time polymerase chain reaction for detection of Lawsonia intracellularis - associated proliferative enteropathy in nursery pigs.

机译:粪便定量实时聚合酶链反应对保育猪细胞内劳森菌相关增殖性肠病的诊断性能。

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Quantitative polymerase chain reaction (qPCR) tests for detection and quantification of Lawsonia intracellularis in feces from pigs have been developed. The objective of the current study was to evaluate the diagnostic performance of a fecal qPCR test for detection of nursery pigs with L. intracellularis-associated proliferative enteropathy (PE) under field conditions. Furthermore, the diagnostic performance for different subpopulations of pigs was investigated, including pigs infected or noninfected with Porcine circovirus-2, Brachyspira pilosicoli, and Escherichia coli. The diagnostic performance was evaluated in terms of diagnostic sensitivity and specificity. Data from pigs originating from 20 herds with antibiotic treatment requiring diarrhea outbreaks from a prior study were reused. Before treatment, pigs were randomly selected for histological and immunohistochemical examination of intestinal segments and fecal quantification of L. intracellularis by qPCR. A total of 313 pigs (157 without diarrhea, 156 with diarrhea) were included in the statistical analysis, and 37 pigs (11.8%) were classified as PE positives (defined as proliferative histological lesions in combination with L. intracellularis demonstration by immunohistochemistry). Lawsonia intracellularis was detected by qPCR in feces from 91 pigs (29.1%). A nonparametric receiver operating characteristic (ROC) analysis provided an area under the ROC curve (0.93) and an optimal cutoff value of 4.8 log10 L. intracellularis bacteria/g feces. This cutoff provided a diagnostic sensitivity of 0.84 and diagnostic specificity of 0.93. The diagnostic sensitivity and specificity were significantly different between herds (P<0.0001). Numerically, diagnostic sensitivity and specificity were different between subpopulations of pigs, but no significant differences were demonstrated.Digital Object Identifier http://dx.doi.org/10.1177/1040638713480499
机译:已经开发出用于检测和定量猪粪中胞内劳森菌的定量聚合酶链反应(qPCR)试验。本研究的目的是评估粪便qPCR检测在田间条件下检测胞内劳森氏菌相关增生性肠病(PE)的保育猪的诊断性能。此外,还研究了猪不同亚群的诊断性能,包括感染或未感染猪圆环病毒2,短螺旋体和大肠埃希氏菌的猪。根据诊断敏感性和特异性评估诊断性能。重复使用了来自先前研究的20个猪群的抗生素数据,这些猪使用抗生素治疗需要爆发腹泻。在治疗前,随机选择猪进行肠段的组织学和免疫组化检查,并通过qPCR对细胞内劳森菌进行粪便定量。统计分析中总共包括313头猪(157例没有腹泻,156例有腹泻),并且37头猪(11.8%)被归为PE阳性(通过免疫组织化学结合细胞内劳森氏菌显示为增殖性组织学病变)。通过qPCR在91头猪(29.1%)的粪便中检测到胞内劳森菌。非参数接收器工作特性(ROC)分析提供了ROC曲线下的面积(0.93),最佳临界值为4.8 log 10 胞内劳森氏菌/克粪便。该临界值提供0.84的诊断灵敏度和0.93的诊断特异性。猪群之间的诊断敏感性和特异性显着不同(P <0.0001)。在数字上,猪亚群之间的诊断敏感性和特异性不同,但未显示出显着差异。数字对象标识符http://dx.doi.org/10.1177/1040638713480499

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