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Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D
End-point and real-time avian metapneumovirus (AMPV) RT-PCRs have been developed to detect one or two of the four recognized subgroups (A,B,C, and D) simultaneously or for broad range AMPV detection. Current subgroup specific tests target variable areas of the genome which makes these PCRs sensitive...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705331/ https://www.ncbi.nlm.nih.gov/pubmed/36458056 http://dx.doi.org/10.3389/fvets.2022.1058294 |
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author | Lemaitre, Evelyne Bougeard, Stéphanie Allée, Chantal Eterradossi, Nicolas Courtillon, Céline Brown, Paul Alun |
author_facet | Lemaitre, Evelyne Bougeard, Stéphanie Allée, Chantal Eterradossi, Nicolas Courtillon, Céline Brown, Paul Alun |
author_sort | Lemaitre, Evelyne |
collection | PubMed |
description | End-point and real-time avian metapneumovirus (AMPV) RT-PCRs have been developed to detect one or two of the four recognized subgroups (A,B,C, and D) simultaneously or for broad range AMPV detection. Current subgroup specific tests target variable areas of the genome which makes these PCRs sensitive to specificity defects as recently documented. In the current study, a single five-plex digital droplet RT-PCR targeting the conserved viral polymerase gene of AMPV, which is less prone to genetic drift, has been designed. This digital droplet RT-PCR was capable of identifying each of the four AMPV subgroups. Each subgroup was identified according to a specifically assigned fluorescent amplitude. Specificity, which was tested including 31 AMPV strains, non-AMPV avian viruses and closely related human respiratory viruses, was 100%. The specific limit of detection for extracted viral RNA was estimated between 1 and 3 copies/μl. This tool simplifies the number of tests required for AMPV genotype diagnostics and should be theoretically less effected by viral genome evolution due to its target region. Ultimately, application of this test will contribute to an improved understanding of the global geographic distribution and subgroup host range of field strains. |
format | Online Article Text |
id | pubmed-9705331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97053312022-11-30 Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D Lemaitre, Evelyne Bougeard, Stéphanie Allée, Chantal Eterradossi, Nicolas Courtillon, Céline Brown, Paul Alun Front Vet Sci Veterinary Science End-point and real-time avian metapneumovirus (AMPV) RT-PCRs have been developed to detect one or two of the four recognized subgroups (A,B,C, and D) simultaneously or for broad range AMPV detection. Current subgroup specific tests target variable areas of the genome which makes these PCRs sensitive to specificity defects as recently documented. In the current study, a single five-plex digital droplet RT-PCR targeting the conserved viral polymerase gene of AMPV, which is less prone to genetic drift, has been designed. This digital droplet RT-PCR was capable of identifying each of the four AMPV subgroups. Each subgroup was identified according to a specifically assigned fluorescent amplitude. Specificity, which was tested including 31 AMPV strains, non-AMPV avian viruses and closely related human respiratory viruses, was 100%. The specific limit of detection for extracted viral RNA was estimated between 1 and 3 copies/μl. This tool simplifies the number of tests required for AMPV genotype diagnostics and should be theoretically less effected by viral genome evolution due to its target region. Ultimately, application of this test will contribute to an improved understanding of the global geographic distribution and subgroup host range of field strains. Frontiers Media S.A. 2022-11-15 /pmc/articles/PMC9705331/ /pubmed/36458056 http://dx.doi.org/10.3389/fvets.2022.1058294 Text en Copyright © 2022 Lemaitre, Bougeard, Allée, Eterradossi, Courtillon and Brown. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Veterinary Science Lemaitre, Evelyne Bougeard, Stéphanie Allée, Chantal Eterradossi, Nicolas Courtillon, Céline Brown, Paul Alun Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title | Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title_full | Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title_fullStr | Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title_full_unstemmed | Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title_short | Avian metapneumovirus: A five-plex digital droplet RT-PCR method for identification of subgroups A, B, C, and D |
title_sort | avian metapneumovirus: a five-plex digital droplet rt-pcr method for identification of subgroups a, b, c, and d |
topic | Veterinary Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705331/ https://www.ncbi.nlm.nih.gov/pubmed/36458056 http://dx.doi.org/10.3389/fvets.2022.1058294 |
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