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Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment cultures of swine edema disease clinical samples
To simplify the diagnosis of swine edema disease, overnight culture supernatants of swine clinical samples were assayed using immunochromatographic test strips we developed previously. Small-intestinal contents, mesenteric lymph nodes, and fecal samples were cultured in casamino acid-yeast extract b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762413/ https://www.ncbi.nlm.nih.gov/pubmed/34732609 http://dx.doi.org/10.1292/jvms.21-0387 |
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author | ARIMITSU, Hideyuki KOHDA, Tomoko MUKAMOTO, Masafumi KUSUMOTO, Masahiro |
author_facet | ARIMITSU, Hideyuki KOHDA, Tomoko MUKAMOTO, Masafumi KUSUMOTO, Masahiro |
author_sort | ARIMITSU, Hideyuki |
collection | PubMed |
description | To simplify the diagnosis of swine edema disease, overnight culture supernatants of swine clinical samples were assayed using immunochromatographic test strips we developed previously. Small-intestinal contents, mesenteric lymph nodes, and fecal samples were cultured in casamino acid-yeast extract broth overnight, after which supernatants were loaded onto immunochromatographic test strips to determine whether they could detect Shiga toxin 2e (Stx2e). Among 23 clinical samples in which PCR-identified stx2e-positive E. coli were isolated, samples from seven of ten small-intestinal contents, one of three mesenteric lymph nodes and six of ten fecal samples showed Stx2e-positive reactions in the protein-based immunochromatographic test. Additionally, one small-intestinal content sample, in which stx2e-positive E. coli were not isolated, showed an Stx2e-positive reaction. Furthermore, the immunochromatographic test results of the samples were associated with the toxin concentration determined by sandwich ELISA and cytotoxicity assay results on Vero cells. The toxin concentration range of the samples with positive and negative reactions were 2.1–196.2 ng/ml and 0–12.8 ng/ml, respectively. The sensitivity and specificity of this immunochromatographic test strip calculated from all clinical samples analyzed in this study were 60.9% and 94.4%, respectively. Our immunochromatographic test strip has strong potential for simple and accurate diagnosis for edema disease by detecting toxin expression, complementing the PCR method. |
format | Online Article Text |
id | pubmed-8762413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-87624132022-01-21 Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment cultures of swine edema disease clinical samples ARIMITSU, Hideyuki KOHDA, Tomoko MUKAMOTO, Masafumi KUSUMOTO, Masahiro J Vet Med Sci Bacteriology To simplify the diagnosis of swine edema disease, overnight culture supernatants of swine clinical samples were assayed using immunochromatographic test strips we developed previously. Small-intestinal contents, mesenteric lymph nodes, and fecal samples were cultured in casamino acid-yeast extract broth overnight, after which supernatants were loaded onto immunochromatographic test strips to determine whether they could detect Shiga toxin 2e (Stx2e). Among 23 clinical samples in which PCR-identified stx2e-positive E. coli were isolated, samples from seven of ten small-intestinal contents, one of three mesenteric lymph nodes and six of ten fecal samples showed Stx2e-positive reactions in the protein-based immunochromatographic test. Additionally, one small-intestinal content sample, in which stx2e-positive E. coli were not isolated, showed an Stx2e-positive reaction. Furthermore, the immunochromatographic test results of the samples were associated with the toxin concentration determined by sandwich ELISA and cytotoxicity assay results on Vero cells. The toxin concentration range of the samples with positive and negative reactions were 2.1–196.2 ng/ml and 0–12.8 ng/ml, respectively. The sensitivity and specificity of this immunochromatographic test strip calculated from all clinical samples analyzed in this study were 60.9% and 94.4%, respectively. Our immunochromatographic test strip has strong potential for simple and accurate diagnosis for edema disease by detecting toxin expression, complementing the PCR method. The Japanese Society of Veterinary Science 2021-11-04 2021-12 /pmc/articles/PMC8762413/ /pubmed/34732609 http://dx.doi.org/10.1292/jvms.21-0387 Text en ©2021 The Japanese Society of Veterinary Science https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Bacteriology ARIMITSU, Hideyuki KOHDA, Tomoko MUKAMOTO, Masafumi KUSUMOTO, Masahiro Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment cultures of swine edema disease clinical samples |
title | Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
title_full | Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
title_fullStr | Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
title_full_unstemmed | Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
title_short | Evaluation of immunochromatographic test of Shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
title_sort | evaluation of immunochromatographic test of shiga toxin 2e in enrichment
cultures of swine edema disease clinical samples |
topic | Bacteriology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762413/ https://www.ncbi.nlm.nih.gov/pubmed/34732609 http://dx.doi.org/10.1292/jvms.21-0387 |
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