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Development of an indirect ELISA using a novel linear epitope at the C-terminal region of the VP2 protein to specifically detect antibodies against Senecavirus A
by
Ma, Zhongyuan
, Zhang, Zhongwang
, Pan, Li
, Lv, Jianliang
in
Accuracy
/ Animals
/ Antibodies
/ Antigen-antibody reactions
/ Antigens
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ C-Terminus
/ Diagnosis
/ diagnostic sensitivity
/ diagnostic specificity
/ ELISA
/ Enzyme-Linked Immunosorbent Assay
/ Epitope
/ Epitope mapping
/ Epitopes
/ Foot & mouth disease
/ foot-and-mouth disease
/ Genetic aspects
/ Genomes
/ Health aspects
/ Hogs
/ Identification and classification
/ Infections
/ Methodology
/ Observations
/ Pathogens
/ Peptide mapping
/ Picornaviridae
/ Picornaviruses
/ Polypeptides
/ Proteins
/ Senecavirus A
/ Serology
/ Stomatitis
/ Swine
/ Vaccines
/ Vesicular stomatitis
/ Viral proteins
/ Virology
/ Viruses
/ VP2
/ VP2 protein
2022
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Development of an indirect ELISA using a novel linear epitope at the C-terminal region of the VP2 protein to specifically detect antibodies against Senecavirus A
by
Ma, Zhongyuan
, Zhang, Zhongwang
, Pan, Li
, Lv, Jianliang
in
Accuracy
/ Animals
/ Antibodies
/ Antigen-antibody reactions
/ Antigens
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ C-Terminus
/ Diagnosis
/ diagnostic sensitivity
/ diagnostic specificity
/ ELISA
/ Enzyme-Linked Immunosorbent Assay
/ Epitope
/ Epitope mapping
/ Epitopes
/ Foot & mouth disease
/ foot-and-mouth disease
/ Genetic aspects
/ Genomes
/ Health aspects
/ Hogs
/ Identification and classification
/ Infections
/ Methodology
/ Observations
/ Pathogens
/ Peptide mapping
/ Picornaviridae
/ Picornaviruses
/ Polypeptides
/ Proteins
/ Senecavirus A
/ Serology
/ Stomatitis
/ Swine
/ Vaccines
/ Vesicular stomatitis
/ Viral proteins
/ Virology
/ Viruses
/ VP2
/ VP2 protein
2022
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Development of an indirect ELISA using a novel linear epitope at the C-terminal region of the VP2 protein to specifically detect antibodies against Senecavirus A
by
Ma, Zhongyuan
, Zhang, Zhongwang
, Pan, Li
, Lv, Jianliang
in
Accuracy
/ Animals
/ Antibodies
/ Antigen-antibody reactions
/ Antigens
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ C-Terminus
/ Diagnosis
/ diagnostic sensitivity
/ diagnostic specificity
/ ELISA
/ Enzyme-Linked Immunosorbent Assay
/ Epitope
/ Epitope mapping
/ Epitopes
/ Foot & mouth disease
/ foot-and-mouth disease
/ Genetic aspects
/ Genomes
/ Health aspects
/ Hogs
/ Identification and classification
/ Infections
/ Methodology
/ Observations
/ Pathogens
/ Peptide mapping
/ Picornaviridae
/ Picornaviruses
/ Polypeptides
/ Proteins
/ Senecavirus A
/ Serology
/ Stomatitis
/ Swine
/ Vaccines
/ Vesicular stomatitis
/ Viral proteins
/ Virology
/ Viruses
/ VP2
/ VP2 protein
2022
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Development of an indirect ELISA using a novel linear epitope at the C-terminal region of the VP2 protein to specifically detect antibodies against Senecavirus A
Journal Article
Development of an indirect ELISA using a novel linear epitope at the C-terminal region of the VP2 protein to specifically detect antibodies against Senecavirus A
2022
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Overview
Background
Senecavirus A (SVA) is a pathogen that has recently caused porcine idiopathic vesicular disease (PIVD). The clinical signs are similar to those of foot-and-mouth disease, porcine vesicular disease, and vesicular stomatitis. Therefore, identification of SVA as a cause of PIVD is important to eliminate this emerging pathogen.
Methods
In this study, an indirect ELISA based on the VP2 epitope (VP2-epitp-ELISA) was developed to detect antibodies directed against SVA.
Results
A novel linear epitope (
271
GLRNRFTTGTDEEQ
284
) was first identified at the C-terminus of the VP2 protein by epitope mapping. The diagnostic performance of VP2-epitp-ELISA was estimated by testing a panel of known background sera from swine. Under the optimum test conditions, when the cutoff value was 37%, the diagnostic sensitivity (Dn) and diagnostic specificity (Dp) of the assay were 91.13% and 91.17%, respectively. The accuracy of VP2-epitp-ELISA was validated and further compared with that of commercial diagnostic kits. The diagnostic results showed that VP2-epitp-ELISA did not cross-react with serum positive for other idiopathic vesicular diseases and had a concordance rate of 90.41% with the Swinecheck
®
SVA bELISA.
Conclusions
These results indicate that VP2-epitp-ELISA is suitable for specific detection of antibodies against SVA in swine.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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