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Detection of porcine parainfluenza virus type-1 antibody in swine serum using whole-virus ELISA, indirect fluorescence antibody and virus neutralizing assays
by
Zhang, Jianqiang
, Gauger, Phillip
, Magtoto, Ronaldo
, Strait, Erin
, Welch, Michael
, Giménez-Lirola, Luis
, Wang, Chong
, Krueger, Karen
, Mogler, Mark
, Piñeyro, Pablo
in
Antibodies
/ Assaying
/ blood serum
/ Bovine respirovirus 3
/ Enzyme linked immunosorbent assay
/ family
/ fluorescence
/ genus
/ humans
/ Identification and classification
/ Immunization
/ Indirect fluorescence antibody
/ Laboratories
/ Medicine
/ Medicine & Public Health
/ Methods
/ Murine respirovirus
/ neutralization
/ neutralization tests
/ Parainfluenza
/ Paramyxoviruses
/ Physiological aspects
/ Porcine parainfluenza virus 1
/ Seroconversion
/ Serology
/ seroprevalence
/ Serum virus neutralization
/ Strains (organisms)
/ Swine
/ Transgenics
/ Vaccine efficacy
/ Vaccines
/ Validation
/ Veterinary Medicine/Veterinary Science
/ Viruses
/ Zoology
2022
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Detection of porcine parainfluenza virus type-1 antibody in swine serum using whole-virus ELISA, indirect fluorescence antibody and virus neutralizing assays
by
Zhang, Jianqiang
, Gauger, Phillip
, Magtoto, Ronaldo
, Strait, Erin
, Welch, Michael
, Giménez-Lirola, Luis
, Wang, Chong
, Krueger, Karen
, Mogler, Mark
, Piñeyro, Pablo
in
Antibodies
/ Assaying
/ blood serum
/ Bovine respirovirus 3
/ Enzyme linked immunosorbent assay
/ family
/ fluorescence
/ genus
/ humans
/ Identification and classification
/ Immunization
/ Indirect fluorescence antibody
/ Laboratories
/ Medicine
/ Medicine & Public Health
/ Methods
/ Murine respirovirus
/ neutralization
/ neutralization tests
/ Parainfluenza
/ Paramyxoviruses
/ Physiological aspects
/ Porcine parainfluenza virus 1
/ Seroconversion
/ Serology
/ seroprevalence
/ Serum virus neutralization
/ Strains (organisms)
/ Swine
/ Transgenics
/ Vaccine efficacy
/ Vaccines
/ Validation
/ Veterinary Medicine/Veterinary Science
/ Viruses
/ Zoology
2022
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Detection of porcine parainfluenza virus type-1 antibody in swine serum using whole-virus ELISA, indirect fluorescence antibody and virus neutralizing assays
by
Zhang, Jianqiang
, Gauger, Phillip
, Magtoto, Ronaldo
, Strait, Erin
, Welch, Michael
, Giménez-Lirola, Luis
, Wang, Chong
, Krueger, Karen
, Mogler, Mark
, Piñeyro, Pablo
in
Antibodies
/ Assaying
/ blood serum
/ Bovine respirovirus 3
/ Enzyme linked immunosorbent assay
/ family
/ fluorescence
/ genus
/ humans
/ Identification and classification
/ Immunization
/ Indirect fluorescence antibody
/ Laboratories
/ Medicine
/ Medicine & Public Health
/ Methods
/ Murine respirovirus
/ neutralization
/ neutralization tests
/ Parainfluenza
/ Paramyxoviruses
/ Physiological aspects
/ Porcine parainfluenza virus 1
/ Seroconversion
/ Serology
/ seroprevalence
/ Serum virus neutralization
/ Strains (organisms)
/ Swine
/ Transgenics
/ Vaccine efficacy
/ Vaccines
/ Validation
/ Veterinary Medicine/Veterinary Science
/ Viruses
/ Zoology
2022
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Detection of porcine parainfluenza virus type-1 antibody in swine serum using whole-virus ELISA, indirect fluorescence antibody and virus neutralizing assays
Journal Article
Detection of porcine parainfluenza virus type-1 antibody in swine serum using whole-virus ELISA, indirect fluorescence antibody and virus neutralizing assays
2022
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Overview
Background
Porcine parainfluenza virus 1 (PPIV-1) is a respiratory virus in the family
Paramyxoviridae
and genus
Respirovirus
. It is closely related to bovine parainfluenza virus 3, human parainfluenza virus 1, and Sendai virus. Recent reports suggest PPIV-1 is widespread in swine herds in the United States and abroad. However, seroprevalence studies and the ability to evaluate cross neutralization between heterologous strains is not possible without validated antibody assays. This study describes the development of an indirect fluorescence antibody (IFA) assay, a whole virus enzyme-linked immunosorbent assay (wv-ELISA) and a serum virus neutralization (SVN) assay for the detection of PPIV-1 antibodies using 521 serum samples collected from three longitudinal studies and two different challenge strains in swine.
Results
The area under the curve (AUC) of the wv-ELISA (95% CI, 0.93–0.98) was significantly higher (
p
= 0.03) compared to the IFA (95% CI, 0.90–0.96). However, no significant difference was observed between the IFA and wv-ELISA when compared to the SVN (95% CI, 0.92–0.97). All three assays demonstrated relatively uniform results at a 99% true negative rate, with only 11 disagreements observed between the IFA, wv-ELISA and SVN.
Conclusions
All three serology assays detected PPIV-1 antibody in swine serum of known status that was collected from experimental studies. The SVN detected seroconversion earlier compared to the IFA and the wv-ELISA. Both the wv-ELISA and the SVN had similar diagnostic performance, while the IFA was not as sensitive as the wv-ELISA. All three assays are considered valid for routine diagnostic use. These assays will be important for future studies to screen seronegative swine for research, determine PPIV-1 seroprevalence, and to evaluate vaccine efficacy against PPIV-1 under experimental and field conditions.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
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