您好，欢迎访问广东省农业科学院 机构知识库！
广东省农业科学院机构知识库

全部

  • 全部
  • 标题
  • 学者
  • 机构
  • 关键词

A Novel, Cleaved Probe-Based Reverse Transcription Loop-Mediated Isothermal Amplification Method for Specific and Sensitive Detection of Porcine Deltacoronavirus

文献类型： 外文期刊

作者： Shen, Haiyan 1 ; Wang, Songqi 4 ; Huang, Jun 7 ; Lin, Qijie 4 ; Zhang, Chunhong 1 ; Liu, Zhicheng 1 ; Zhang, Jianfeng 1 ; Liao, Ming 1 ;

作者机构： 1.Guangdong Acad Agr Sci, Maoming Branch Ctr Guangdong Lab LingNan Modern Ag, Guangzhou, Peoples R China

2.Guangdong Acad Agr Sci, Key Lab Livestock Dis Prevent Guangdong Prov, Sci Observat & Expt Stn Vet Drugs & Diagnost Tech, Minist Agr & Rural Affairs, Guangzhou, Peoples R China

3.Guangdong Acad Agr Sci, Inst Anim Hlth, Guangzhou, Peoples R China

4.South China Agr Univ, Natl & Reg Joint Engn Lab Medicament Zoonoses Prev, Guangzhou, Peoples R China

5.South China Agr Univ, Key Lab Anim Vaccine Dev, Minist Agr, Guangzhou, Peoples R China

6.South China Agr Univ, Coll Vet Med, Guangzhou, Peoples R China

7.Foshan Univ, Coll Life Sci & Engn, Foshan, Peoples R China

关键词： porcine deltacoronavirus; CP-RT-LAMP; ribonuclease H2; specific and sensitive detection; point-of care testing

期刊名称：FRONTIERS IN VETERINARY SCIENCE （ 影响因子：3.471； 五年影响因子：3.821 ）

ISSN：

年卷期： 2022 年 9 卷

页码：

收录情况： SCI

摘要： Porcine deltacoronavirus (PDCoV) causes watery diarrhea, vomiting, and 30-40% mortality in newborn piglets. A simple, rapid, and sensitive method for PDCoV detection is valuable in its surveillance and control. Here, we developed a novel, cleaved probe-based reverse transcription loop-mediated isothermal amplification (CP-RT-LAMP) method for PDCoV detection. A cleaved probe with a ribonucleotide insertion that targeted the N gene of PDCoV was designed. During the reaction, the enzyme ribonuclease H2 is activated only when the cleaved probe is perfectly complementary to the template, leading to the hydrolytic release of a quencher moiety and signal output. This method can be easily used on a real-time fluorescence quantitative equipment or an on-site isothermal instrument combined with a smartphone. The specificity assay showed no cross-reactivity with other porcine enteric pathogens. This method had a detection limit of 25 copies/mu L, suggesting comparable sensitivity with reverse transcription quantitative PCR (RT-qPCR). In detecting 100 clinical samples (48 fecal swab specimens and 52 intestinal specimens), the detection rate of the CP-RT-LAMP method (26%) was higher than that of RT-qPCR (17%). Thus, it is a highly specific and sensitive diagnostic method for PDCoV, with a great application potential for monitoring PDCoV in the laboratory or point-of-care testing in the field.

  • 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：广东省农业科学院

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