Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk

Abstract Background Porcine epidemic diarrhea (PED), caused by PED virus (PEDV), is a severe enteric disease burdening the global swine industry in recent years. Especially, the mortality of PED in neonatal piglets approaches 100%. Maternal antibodies in milk, particularly immunoglobulin A (IgA) ant...

Full description

Bibliographic Details
Main Authors: Rui Li, Ying Wen, Lei Yang, Qi-sheng Qian, Xin-xin Chen, Jia-qing Zhang, Xuewu Li, Bao-song Xing, Songlin Qiao, Gaiping Zhang
Format: Article
Language:English
Published: BMC 2023-02-01
Series:BMC Veterinary Research
Subjects:
Online Access:https://doi.org/10.1186/s12917-023-03605-4
_version_ 1811165876779483136
author Rui Li
Ying Wen
Lei Yang
Qi-sheng Qian
Xin-xin Chen
Jia-qing Zhang
Xuewu Li
Bao-song Xing
Songlin Qiao
Gaiping Zhang
author_facet Rui Li
Ying Wen
Lei Yang
Qi-sheng Qian
Xin-xin Chen
Jia-qing Zhang
Xuewu Li
Bao-song Xing
Songlin Qiao
Gaiping Zhang
author_sort Rui Li
collection DOAJ
description Abstract Background Porcine epidemic diarrhea (PED), caused by PED virus (PEDV), is a severe enteric disease burdening the global swine industry in recent years. Especially, the mortality of PED in neonatal piglets approaches 100%. Maternal antibodies in milk, particularly immunoglobulin A (IgA) antibodies, are of great importance for protection neonatal suckling piglets against PEDV infection as passive lactogenic immunity. Therefore, appropriate detection methods are required for detecting PEDV IgA antibodies in milk. In the current study, we prepared monoclonal antibodies (mAbs) against PEDV spike (S) glycoprotein. An enzyme-linked immunosorbent assay (ELISA) was subsequently developed based on PEDV antigen capture by a specific anti-S mAb. Results The developed ELISA showed high sensitivity (the maximum dilution of milk samples up to 1:1280) and repeatability (coefficient of variation values < 10%) in detecting PEDV IgA antibody positive and negative milk samples. More importantly, the developed ELISA showed a high coincidence rate with a commercial ELISA kit for PEDV IgA antibody detection in clinical milk samples. Conclusions The developed ELISA in the current study is applicable for PEDV IgA antibody detection in milk samples, which is beneficial for evaluating vaccination efficacies and neonate immune status against the virus.
first_indexed 2024-04-10T15:43:30Z
format Article
id doaj.art-bf33f8a000814bf3a84154df64fe7a1a
institution Directory Open Access Journal
issn 1746-6148
language English
last_indexed 2024-04-10T15:43:30Z
publishDate 2023-02-01
publisher BMC
record_format Article
series BMC Veterinary Research
spelling doaj.art-bf33f8a000814bf3a84154df64fe7a1a2023-02-12T12:14:57ZengBMCBMC Veterinary Research1746-61482023-02-0119111110.1186/s12917-023-03605-4Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milkRui Li0Ying Wen1Lei Yang2Qi-sheng Qian3Xin-xin Chen4Jia-qing Zhang5Xuewu Li6Bao-song Xing7Songlin Qiao8Gaiping Zhang9Key Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesInstitute of Animal Husbandry and Veterinary Science, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesInstitute of Animal Husbandry and Veterinary Science, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesKey Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural SciencesAbstract Background Porcine epidemic diarrhea (PED), caused by PED virus (PEDV), is a severe enteric disease burdening the global swine industry in recent years. Especially, the mortality of PED in neonatal piglets approaches 100%. Maternal antibodies in milk, particularly immunoglobulin A (IgA) antibodies, are of great importance for protection neonatal suckling piglets against PEDV infection as passive lactogenic immunity. Therefore, appropriate detection methods are required for detecting PEDV IgA antibodies in milk. In the current study, we prepared monoclonal antibodies (mAbs) against PEDV spike (S) glycoprotein. An enzyme-linked immunosorbent assay (ELISA) was subsequently developed based on PEDV antigen capture by a specific anti-S mAb. Results The developed ELISA showed high sensitivity (the maximum dilution of milk samples up to 1:1280) and repeatability (coefficient of variation values < 10%) in detecting PEDV IgA antibody positive and negative milk samples. More importantly, the developed ELISA showed a high coincidence rate with a commercial ELISA kit for PEDV IgA antibody detection in clinical milk samples. Conclusions The developed ELISA in the current study is applicable for PEDV IgA antibody detection in milk samples, which is beneficial for evaluating vaccination efficacies and neonate immune status against the virus.https://doi.org/10.1186/s12917-023-03605-4PEDVIgA antibody detectionELISAS proteinmAb
spellingShingle Rui Li
Ying Wen
Lei Yang
Qi-sheng Qian
Xin-xin Chen
Jia-qing Zhang
Xuewu Li
Bao-song Xing
Songlin Qiao
Gaiping Zhang
Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
BMC Veterinary Research
PEDV
IgA antibody detection
ELISA
S protein
mAb
title Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
title_full Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
title_fullStr Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
title_full_unstemmed Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
title_short Development of an enzyme-linked immunosorbent assay based on viral antigen capture by anti-spike glycoprotein monoclonal antibody for detecting immunoglobulin A antibodies against porcine epidemic diarrhea virus in milk
title_sort development of an enzyme linked immunosorbent assay based on viral antigen capture by anti spike glycoprotein monoclonal antibody for detecting immunoglobulin a antibodies against porcine epidemic diarrhea virus in milk
topic PEDV
IgA antibody detection
ELISA
S protein
mAb
url https://doi.org/10.1186/s12917-023-03605-4
work_keys_str_mv AT ruili developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT yingwen developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT leiyang developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT qishengqian developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT xinxinchen developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT jiaqingzhang developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT xuewuli developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT baosongxing developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT songlinqiao developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk
AT gaipingzhang developmentofanenzymelinkedimmunosorbentassaybasedonviralantigencapturebyantispikeglycoproteinmonoclonalantibodyfordetectingimmunoglobulinaantibodiesagainstporcineepidemicdiarrheavirusinmilk