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

被引:4
|
作者
Memon, Atta Muhammad [1 ]
Chen, Fangzhou [1 ]
Khan, Sher Bahadar [1 ]
Guo, Xiaozhen [1 ]
Khan, Rajwali [2 ]
Khan, Farhan Anwar [1 ]
Zhu, Yinxing [1 ]
He, Qigai [1 ]
机构
[1] Huazhong Agr Univ, Coll Vet Med, State Key Lab Agr Microbiol, Wuhan, Peoples R China
[2] Univ Agr Peshawar, Dept Livestock Management Breeding & Genet, Peshawar, Pakistan
关键词
Porcine rotavirus; VP6; polyclonal antibodies; AC-ELISA; POTENTIALLY ZOONOTIC VIRUSES; GROUP-A; DIARRHEA; PIGS; ANIMALS; FECES;
D O I
10.1080/10495398.2022.2052304
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Rotaviruses 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 (kappa -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 STATEMENT In 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.
引用
收藏
页码:1807 / 1814
页数:8
相关论文
共 50 条
  • [21] Indirect sandwich ELISA for antigen detection of African swine fever virus: Comparison of polyclonal and monoclonal antibodies
    Hutchings, GH
    Ferris, NP
    JOURNAL OF VIROLOGICAL METHODS, 2006, 131 (02) : 213 - 217
  • [22] Development of an Antigen Capture Enzyme-Linked Immunosorbent Assay for Virus Detection Based on Porcine Epidemic Diarrhea Virus Monoclonal Antibodies
    Wang, Zanyu
    Yin Jiyuan
    Su, Chen
    Qiao Xinyuan
    Tang Lijie
    Li Yijing
    VIRAL IMMUNOLOGY, 2015, 28 (03) : 184 - 189
  • [23] EVALUATION OF RECOMBINANT LIG ANTIGEN-BASED ELISA FOR DETECTION OF LEPTOSPIRAL ANTIBODIES IN CANINE SERA
    La-ard, Anchalee
    Amavisit, Patamaporn
    Sukpuaram, Thavajchai
    Wajjwalku, Worawidh
    SOUTHEAST ASIAN JOURNAL OF TROPICAL MEDICINE AND PUBLIC HEALTH, 2011, 42 (01) : 128 - 137
  • [24] Development of an ELISA based on a multi-fragment antigen of infectious bronchitis virus for antibodies detection
    Meng-die Ding
    Xin Yang
    Hong-ning Wang
    An-yun Zhang
    Zhi-kun Zhang
    Wen-qiao Fan
    Hai-peng Cao
    Biotechnology Letters, 2015, 37 : 2453 - 2459
  • [25] Development of Monoclonal Antibodies and Antigen-Capture ELISA for Human Parechovirus Type 3
    Goto, Keiko
    Yamaoka, Yutaro
    Khatun, Hajera
    Miyakawa, Kei
    Nishi, Mayuko
    Nagata, Noriko
    Yanaoka, Toshikazu
    Kimura, Hirokazu
    Ryo, Akihide
    MICROORGANISMS, 2020, 8 (09) : 1 - 12
  • [26] Development of an ELISA based on a multi-fragment antigen of infectious bronchitis virus for antibodies detection
    Ding, Meng-die
    Yang, Xin
    Wang, Hong-ning
    Zhang, An-yun
    Zhang, Zhi-kun
    Fan, Wen-qiao
    Cao, Hai-peng
    BIOTECHNOLOGY LETTERS, 2015, 37 (12) : 2453 - 2459
  • [27] ELISA detection of Francisella tularensis using polyclonal and monoclonal antibodies
    Pohanka, Miroslav
    Pavlis, Oto
    Kroca, Michal
    DEFENCE SCIENCE JOURNAL, 2008, 58 (05) : 698 - 702
  • [28] Generation of monospecific antibodies based on affinity capture of polyclonal antibodies
    Hjelm, Barbara
    Forsstrom, Bjorn
    Igel, Ulrika
    Johannesson, Henrik
    Stadler, Charlotte
    Lundberg, Emma
    Ponten, Fredrik
    Sjoberg, Anna
    Rockberg, Johan
    Schwenk, Jochen M.
    Nilsson, Peter
    Johansson, Christine
    Uhlen, Mathias
    PROTEIN SCIENCE, 2011, 20 (11) : 1824 - 1835
  • [29] Development of an antigen-capture ELISA for the detection of equine influenza virus nucleoprotein
    Ji, Yuanyuan
    Guo, Wei
    Zhao, Liping
    Li, Hongmei
    Lu, Gang
    Wang, Zheng
    Wang, Guibin
    Liu, Cuiyun
    Xiang, Wenhua
    JOURNAL OF VIROLOGICAL METHODS, 2011, 175 (01) : 120 - 124
  • [30] DEVELOPMENT OF POLYCLONAL ANTIBODIES AND EVALUATION OF A SENSITIVE RADIOIMMUNOASSAY FOR DETECTION AND MEASUREMENT OF SYNAPTOPHYSIN
    STRIDSBERG, M
    LUNDQVIST, G
    ENGSTROM, U
    WILANDER, E
    SU, H
    GOBL, A
    OBERG, K
    ACTA NEUROPATHOLOGICA, 1994, 87 (06) : 635 - 641