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Development and evaluation of polyclonal antibodies based antigen capture ELISA for detection of porcine rotavirus

多克隆抗体 病毒学 猪流行性腹泻病毒 轮状病毒 生物 抗体 猪圆环病毒 抗原 病毒 塔克曼 分子生物学 检出限 实时聚合酶链反应 化学 免疫学 基因 生物化学 色谱法
作者
Atta Muhammad Memon,Fangzhou Chen,Sher Bahadar Khan,Xiaozhen Guo,Rajwali Khan,Farhan Anwar Khan,Yinxing Zhu,Qigai He
出处
期刊:Animal Biotechnology [Taylor & Francis]
卷期号:34 (5): 1807-1814 被引量:2
标识
DOI:10.1080/10495398.2022.2052304
摘要

AbstractRotaviruses are rising as zoonotic viruses worldwide, causing the lethal dehydrating diarrhea in children, piglets, and other livestock of economic importance. A simple, swift, cost-effective, highly specific, and sensitive antigen-capture enzyme–linked immunosorbent assay (AC-ELISA) was developed for detection of porcine rotavirus-A (PoRVA) by employing rabbit (capture antibody) and murine polyclonal antibodies (detector antibody) produced against VP6 of PoRVA (RVA/Pig-tc/CHN/TM-a/2009/G9P23). Reactivity of the both polyclonal antibodies was confirmed by using an indirect ELISA, western-blot analysis and indirect fluorescence assay against rVP6 protein and PoRVA. The detection limit of AC-ELISA was found 50 ng/ml of PoRVA protein. The relative sensitivity and specificity of this in-house AC-ELISA were evaluated for detection of PoRVA from 295 porcine diarrhea samples, and results were compared with that of RT-PCR and TaqMan RT-qPCR. The relative sensitivity and specificity of AC-ELISA compared with those of TaqMan RT-qPCR were found as 94.4 and 99.2%, respectively, with the strong agreement (κ −0.58) between these two techniques. Furthermore, AC-ELISA could not detect any cross-reactivity with porcine epidemic diarrhea virus, transmissible gastro-enteritis virus, pseudo rabies virus and porcine circovirus-2. This in-house AC-ELISA efficiently detected PoRVA from clinical samples, which suggests that this technique can be used for large-scale surveillance and timely detection of rotavirus infection in the porcine farms.NOVELTY STATEMENTIn this study, we used a Chinese porcine rotavirus-A (PoRVA) strain containing the I5, a dominant VP6-genotype in pigs, for production of VP6 (most conserved) protein based polyclonal antibodies (pAb) in rabbits (as capture Ab) and mouse (as detector Ab) for development of simple, cost effective, highly specific and sensitive AC-ELISA for detection of PoRVA. Furthermore, there is no any previous published report on application of rabbit and mouse pAb against VP6 for developing an AC-ELISA against PoRVA.Keywords: Porcine rotavirusVP6polyclonal antibodiesAC-ELISA Disclosure statementNo potential conflict of interest was reported by the author(s).Author contributionsAMM and QGH were involved in conception, designing the study and drafted the manuscript. FAK, XZG established the method and co-drafted the manuscript. SBK, RWK, YXZ and FZC assisted in the development of assay. All authors produced both the murine, as well as rabbit polyclonal antibodies, reviewed the manuscript and validated the developed assay. All authors read and approved the final manuscript.Additional informationFundingThis work was supported by the China Agricultural Research System (CARS) of Ministry of Finance (MOF) and Ministry of Agriculture and Rural Affairs (MARA). This work was also supported by Fundamental Research Funds for the Central Universities; National Swine Industry Research System.
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