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Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay

Rapid and simple serologic tests that require only a small amount of blood without the euthanization of animals are valuable for microbial control in colonies of laboratory animals. In this study, we developed a multiplex immunochromatographic assay (ICA) for detection of antibodies to Sendai virus...

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Autores principales: Tosa, Noriko, Ishida, Tomoko, Yoshimatsu, Kumiko, Hayashimoto, Nobuhito, Shiokawa, Kanae, Takakura, Akira, Arikawa, Jiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150241/
https://www.ncbi.nlm.nih.gov/pubmed/33177250
http://dx.doi.org/10.1538/expanim.20-0099
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author Tosa, Noriko
Ishida, Tomoko
Yoshimatsu, Kumiko
Hayashimoto, Nobuhito
Shiokawa, Kanae
Takakura, Akira
Arikawa, Jiro
author_facet Tosa, Noriko
Ishida, Tomoko
Yoshimatsu, Kumiko
Hayashimoto, Nobuhito
Shiokawa, Kanae
Takakura, Akira
Arikawa, Jiro
author_sort Tosa, Noriko
collection PubMed
description Rapid and simple serologic tests that require only a small amount of blood without the euthanization of animals are valuable for microbial control in colonies of laboratory animals. In this study, we developed a multiplex immunochromatographic assay (ICA) for detection of antibodies to Sendai virus (also known as hemagglutinating virus of Japan), hantavirus, and sialodacryoadenitis virus, which are causative agents of major infectious diseases in rats. For this assay, an ICA strip was placed into a microtube containing 150 µl PBS and either 0.75 µl of rat serum or 1.5 µl of whole blood. Binding antibodies were visualized by using anti-rat IgG antibody-conjugated colloidal gold. Under these conditions, the multiplex ICA simultaneously and specifically detected antibodies to multiple antigens. Positive serum samples for each infectious disease were used to evaluate the sensitivity and specificity of the multiplex ICA. The sensitivities of the multiplex ICA for Sendai virus, hantavirus, and sialodacryoadenitis virus were 100%, 100%, and 81%, respectively. No nonspecific reactions were observed in any of the 52 positive sera against heterologous antigens. In addition, 10 samples of uninfected sera did not show any bands except for the control line. These observations indicate high specificity of the multiplex ICA. Moreover, the multiplex ICA could be applied to diluted blood. These results indicate that the multiplex ICA is appropriate for rapid and simple serological testing of laboratory rats.
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spelling pubmed-81502412021-05-28 Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay Tosa, Noriko Ishida, Tomoko Yoshimatsu, Kumiko Hayashimoto, Nobuhito Shiokawa, Kanae Takakura, Akira Arikawa, Jiro Exp Anim Original Rapid and simple serologic tests that require only a small amount of blood without the euthanization of animals are valuable for microbial control in colonies of laboratory animals. In this study, we developed a multiplex immunochromatographic assay (ICA) for detection of antibodies to Sendai virus (also known as hemagglutinating virus of Japan), hantavirus, and sialodacryoadenitis virus, which are causative agents of major infectious diseases in rats. For this assay, an ICA strip was placed into a microtube containing 150 µl PBS and either 0.75 µl of rat serum or 1.5 µl of whole blood. Binding antibodies were visualized by using anti-rat IgG antibody-conjugated colloidal gold. Under these conditions, the multiplex ICA simultaneously and specifically detected antibodies to multiple antigens. Positive serum samples for each infectious disease were used to evaluate the sensitivity and specificity of the multiplex ICA. The sensitivities of the multiplex ICA for Sendai virus, hantavirus, and sialodacryoadenitis virus were 100%, 100%, and 81%, respectively. No nonspecific reactions were observed in any of the 52 positive sera against heterologous antigens. In addition, 10 samples of uninfected sera did not show any bands except for the control line. These observations indicate high specificity of the multiplex ICA. Moreover, the multiplex ICA could be applied to diluted blood. These results indicate that the multiplex ICA is appropriate for rapid and simple serological testing of laboratory rats. Japanese Association for Laboratory Animal Science 2020-11-12 2021 /pmc/articles/PMC8150241/ /pubmed/33177250 http://dx.doi.org/10.1538/expanim.20-0099 Text en ©2021 Japanese Association for Laboratory Animal Science https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License.
spellingShingle Original
Tosa, Noriko
Ishida, Tomoko
Yoshimatsu, Kumiko
Hayashimoto, Nobuhito
Shiokawa, Kanae
Takakura, Akira
Arikawa, Jiro
Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title_full Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title_fullStr Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title_full_unstemmed Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title_short Simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
title_sort simultaneous serodetection of major rat infectious pathogens by a multiplex immunochromatographic assay
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150241/
https://www.ncbi.nlm.nih.gov/pubmed/33177250
http://dx.doi.org/10.1538/expanim.20-0099
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