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Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells

Mumps viruses show diverse cytopathic effects (CPEs) of infected cells and viral plaque formation (no CPE or no plaque formation in some cases) depending on the viral strain, highlighting the difficulty in mumps laboratory studies. In our previous study, a new sialidase substrate, 2-(benzothiazol-2-...

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Autores principales: Takahashi, Tadanobu, Agarikuchi, Takashi, Kurebayashi, Yuuki, Shibahara, Nona, Suzuki, Chihiro, Kishikawa, Akiko, Fukushima, Keijo, Takano, Maiko, Suzuki, Fumie, Wada, Hirohisa, Otsubo, Tadamune, Ikeda, Kiyoshi, Minami, Akira, Suzuki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668055/
https://www.ncbi.nlm.nih.gov/pubmed/26629699
http://dx.doi.org/10.1371/journal.pone.0144038
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author Takahashi, Tadanobu
Agarikuchi, Takashi
Kurebayashi, Yuuki
Shibahara, Nona
Suzuki, Chihiro
Kishikawa, Akiko
Fukushima, Keijo
Takano, Maiko
Suzuki, Fumie
Wada, Hirohisa
Otsubo, Tadamune
Ikeda, Kiyoshi
Minami, Akira
Suzuki, Takashi
author_facet Takahashi, Tadanobu
Agarikuchi, Takashi
Kurebayashi, Yuuki
Shibahara, Nona
Suzuki, Chihiro
Kishikawa, Akiko
Fukushima, Keijo
Takano, Maiko
Suzuki, Fumie
Wada, Hirohisa
Otsubo, Tadamune
Ikeda, Kiyoshi
Minami, Akira
Suzuki, Takashi
author_sort Takahashi, Tadanobu
collection PubMed
description Mumps viruses show diverse cytopathic effects (CPEs) of infected cells and viral plaque formation (no CPE or no plaque formation in some cases) depending on the viral strain, highlighting the difficulty in mumps laboratory studies. In our previous study, a new sialidase substrate, 2-(benzothiazol-2-yl)-4-bromophenyl 5-acetamido-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosidonic acid (BTP3-Neu5Ac), was developed for visualization of sialidase activity. BTP3-Neu5Ac can easily and rapidly perform histochemical fluorescent visualization of influenza viruses and virus-infected cells without an antiviral antibody and cell fixation. In the present study, the potential utility of BTP3-Neu5Ac for rapid detection of mumps virus was demonstrated. BTP3-Neu5Ac could visualize dot-blotted mumps virus, virus-infected cells, and plaques (plaques should be called focuses due to staining of infected cells in this study), even if a CPE was not observed. Furthermore, virus cultivation was possible by direct pick-up from a fluorescent focus. In conventional methods, visible appearance of the CPE and focuses often requires more than 6 days after infection, but the new method with BTP3-Neu5Ac clearly visualized infected cells after 2 days and focuses after 4 days. The BTP3-Neu5Ac assay is a precise, easy, and rapid assay for confirmation and titration of mumps virus.
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spelling pubmed-46680552015-12-10 Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells Takahashi, Tadanobu Agarikuchi, Takashi Kurebayashi, Yuuki Shibahara, Nona Suzuki, Chihiro Kishikawa, Akiko Fukushima, Keijo Takano, Maiko Suzuki, Fumie Wada, Hirohisa Otsubo, Tadamune Ikeda, Kiyoshi Minami, Akira Suzuki, Takashi PLoS One Research Article Mumps viruses show diverse cytopathic effects (CPEs) of infected cells and viral plaque formation (no CPE or no plaque formation in some cases) depending on the viral strain, highlighting the difficulty in mumps laboratory studies. In our previous study, a new sialidase substrate, 2-(benzothiazol-2-yl)-4-bromophenyl 5-acetamido-3,5-dideoxy-α-D-glycero-D-galacto-2-nonulopyranosidonic acid (BTP3-Neu5Ac), was developed for visualization of sialidase activity. BTP3-Neu5Ac can easily and rapidly perform histochemical fluorescent visualization of influenza viruses and virus-infected cells without an antiviral antibody and cell fixation. In the present study, the potential utility of BTP3-Neu5Ac for rapid detection of mumps virus was demonstrated. BTP3-Neu5Ac could visualize dot-blotted mumps virus, virus-infected cells, and plaques (plaques should be called focuses due to staining of infected cells in this study), even if a CPE was not observed. Furthermore, virus cultivation was possible by direct pick-up from a fluorescent focus. In conventional methods, visible appearance of the CPE and focuses often requires more than 6 days after infection, but the new method with BTP3-Neu5Ac clearly visualized infected cells after 2 days and focuses after 4 days. The BTP3-Neu5Ac assay is a precise, easy, and rapid assay for confirmation and titration of mumps virus. Public Library of Science 2015-12-02 /pmc/articles/PMC4668055/ /pubmed/26629699 http://dx.doi.org/10.1371/journal.pone.0144038 Text en © 2015 Takahashi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Takahashi, Tadanobu
Agarikuchi, Takashi
Kurebayashi, Yuuki
Shibahara, Nona
Suzuki, Chihiro
Kishikawa, Akiko
Fukushima, Keijo
Takano, Maiko
Suzuki, Fumie
Wada, Hirohisa
Otsubo, Tadamune
Ikeda, Kiyoshi
Minami, Akira
Suzuki, Takashi
Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title_full Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title_fullStr Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title_full_unstemmed Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title_short Easy and Rapid Detection of Mumps Virus by Live Fluorescent Visualization of Virus-Infected Cells
title_sort easy and rapid detection of mumps virus by live fluorescent visualization of virus-infected cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668055/
https://www.ncbi.nlm.nih.gov/pubmed/26629699
http://dx.doi.org/10.1371/journal.pone.0144038
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