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Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks
Vector competence (VC) refers to the efficiency of pathogen transmission by vectors. Each step in the infection of a mosquito vector constitutes a barrier to transmission that may impose bottlenecks on virus populations. West Nile virus (WNV) is maintained by multiple mosquito species with varying V...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494182/ https://www.ncbi.nlm.nih.gov/pubmed/37701570 http://dx.doi.org/10.1016/j.isci.2023.107711 |
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author | Fitzmeyer, Emily A. Gallichotte, Emily N. Weger-Lucarelli, James Kapuscinski, Marylee L. Abdo, Zaid Pyron, Kyra Young, Michael C. Ebel, Gregory D. |
author_facet | Fitzmeyer, Emily A. Gallichotte, Emily N. Weger-Lucarelli, James Kapuscinski, Marylee L. Abdo, Zaid Pyron, Kyra Young, Michael C. Ebel, Gregory D. |
author_sort | Fitzmeyer, Emily A. |
collection | PubMed |
description | Vector competence (VC) refers to the efficiency of pathogen transmission by vectors. Each step in the infection of a mosquito vector constitutes a barrier to transmission that may impose bottlenecks on virus populations. West Nile virus (WNV) is maintained by multiple mosquito species with varying VC. However, the extent to which bottlenecks and VC are linked is poorly understood. Similarly, quantitative analyses of mosquito-imposed bottlenecks on virus populations are limited. We used molecularly barcoded WNV to quantify tissue-associated population bottlenecks in three variably competent WNV vectors. Our results confirm strong population bottlenecks during mosquito infection that are capable of dramatically reshaping virus population structure in a non-selective manner. In addition, we found that mosquitoes with differing VC uniquely shape WNV population structure: highly competent vectors are more likely to contribute to the maintenance of rare viral genotypes. These findings have important implications for arbovirus emergence and evolution. |
format | Online Article Text |
id | pubmed-10494182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-104941822023-09-12 Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks Fitzmeyer, Emily A. Gallichotte, Emily N. Weger-Lucarelli, James Kapuscinski, Marylee L. Abdo, Zaid Pyron, Kyra Young, Michael C. Ebel, Gregory D. iScience Article Vector competence (VC) refers to the efficiency of pathogen transmission by vectors. Each step in the infection of a mosquito vector constitutes a barrier to transmission that may impose bottlenecks on virus populations. West Nile virus (WNV) is maintained by multiple mosquito species with varying VC. However, the extent to which bottlenecks and VC are linked is poorly understood. Similarly, quantitative analyses of mosquito-imposed bottlenecks on virus populations are limited. We used molecularly barcoded WNV to quantify tissue-associated population bottlenecks in three variably competent WNV vectors. Our results confirm strong population bottlenecks during mosquito infection that are capable of dramatically reshaping virus population structure in a non-selective manner. In addition, we found that mosquitoes with differing VC uniquely shape WNV population structure: highly competent vectors are more likely to contribute to the maintenance of rare viral genotypes. These findings have important implications for arbovirus emergence and evolution. Elsevier 2023-08-25 /pmc/articles/PMC10494182/ /pubmed/37701570 http://dx.doi.org/10.1016/j.isci.2023.107711 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Fitzmeyer, Emily A. Gallichotte, Emily N. Weger-Lucarelli, James Kapuscinski, Marylee L. Abdo, Zaid Pyron, Kyra Young, Michael C. Ebel, Gregory D. Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title | Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title_full | Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title_fullStr | Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title_full_unstemmed | Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title_short | Loss of West Nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
title_sort | loss of west nile virus genetic diversity during mosquito infection due to species-dependent population bottlenecks |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494182/ https://www.ncbi.nlm.nih.gov/pubmed/37701570 http://dx.doi.org/10.1016/j.isci.2023.107711 |
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