您好，欢迎访问宁夏农林科学院 机构知识库！
宁夏农林科学院机构知识库

全部

  • 全部
  • 标题
  • 学者
  • 机构
  • 关键词

Multiplex one-step RT-qPCR assays for simultaneous detection of BRV, BCoV, Escherichia coli K99+ and Cryptosporidium parvum

文献类型： 外文期刊

作者： Zhao, Xinru 1 ; Li, Min 1 ; Yang, Yingying 1 ; Wang, Yidan 1 ; Zheng, Xiaoru 1 ; Yin, Dehua 2 ; Gao, Haihui 3 ; Li, Huatao 1 ; Fu, Kaiqiang 1 ; Cao, Zhi 1 ;

作者机构： 1.Qingdao Agr Univ, Coll Vet Med, Qingdao, Peoples R China

2.Innovus Solarex Biotech Co Ltd, Qingdao, Peoples R China

3.Ningxia Acad Agr & Forestry Sci, Yinchuan, Ningxia, Peoples R China

关键词： BRV; BCoV; E. coli K99(+); C. parvum; multiplex TaqMan real-time PCR

期刊名称：FRONTIERS IN VETERINARY SCIENCE （ 影响因子：2.9； 五年影响因子：3.3 ）

ISSN：

年卷期： 2025 年 12 卷

页码：

收录情况： SCI

摘要： Introduction Bovine rotavirus (BRV), bovine coronavirus (BCoV), Escherichia coli K99+ (E. coli K99+), and Cryptosporidium parvum (C. parvum) are the most common pathogens involved in calf production. These pathogens can cause calf diarrhea, leading to significant economic losses in the cattle farming industry. These four pathogens have similar clinical symptoms, making them difficult to distinguish. Therefore, we established a one-step quadruple TaqMan fluorescence quantitative PCR method capable of simultaneously and rapidly detecting BRV, BCoV, E. coli K99+, and C. parvum.Methods Specific primers and TaqMan probes were designed for the BRV VP-6 gene, BCoV N gene, E. coli K99+ K99 gene, and C. parvum 18S rRNA gene. Standard positive plasmids were constructed, and the reaction conditions of the method were optimized. The sensitivity, specificity, and repeatability of the method were validated, and clinical samples were tested.Results The minimum detection limits of this method for BRV, BCoV, E. coli K99+, and C. parvum were 5.8 x 101, 2.3 x 101, 4.5 x 102, and 2.6 x 101 copies/mu L, respectively. The intra- and intergroup coefficients of variation were all less than 1.2%. This method has the advantages of strong specificity, reproducibility, low cost, and no cross-reaction with other bovine pathogens. Compared with the commercial reagent kit method were used to analyze clinical samples, and both the diagnostic sensitivity (DSe) and diagnostic specificity (DSp) were above 90%, with kappa values greater than 0.9.Discussion The one-step multiplex RT-qPCR method developed in this study for detecting BRV, BCoV, E. coli K99+, and C. parvum is expected to be an effective tool for the rapid and economical diagnosis and monitoring of diarrhoeal diseases in calves.

  • 相关文献
作者其他论文 更多>>
置顶
购物车
反馈

© 京ICP备09089781号-29 主办单位：宁夏农林科学院

学术资源： 中国农业科学院 农业专业知识服务系统 农科联盟资源共建共享平台 中国农业科技文献与信息服务平台 中国农业期刊集成服务平台