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Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population
RNA viruses typically occur in genetically diverse populations due to their error-prone genome replication. Genetic diversity is thought to be important in allowing RNA viruses to explore sequence space, facilitating adaptation to changing environments and hosts. Some arboviruses that infect both a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441635/ https://www.ncbi.nlm.nih.gov/pubmed/23028310 http://dx.doi.org/10.1371/journal.ppat.1002897 |
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author | Forrester, Naomi L. Guerbois, Mathilde Seymour, Robert L. Spratt, Heidi Weaver, Scott C. |
author_facet | Forrester, Naomi L. Guerbois, Mathilde Seymour, Robert L. Spratt, Heidi Weaver, Scott C. |
author_sort | Forrester, Naomi L. |
collection | PubMed |
description | RNA viruses typically occur in genetically diverse populations due to their error-prone genome replication. Genetic diversity is thought to be important in allowing RNA viruses to explore sequence space, facilitating adaptation to changing environments and hosts. Some arboviruses that infect both a mosquito vector and a mammalian host are known to experience population bottlenecks in their vectors, which may constrain their genetic diversity and could potentially lead to extinction events via Muller's ratchet. To examine this potential challenge of bottlenecks for arbovirus perpetuation, we studied Venezuelan equine encephalitis virus (VEEV) enzootic subtype IE and its natural vector Culex (Melanoconion) taeniopus, as an example of a virus-vector interaction with a long evolutionary history. Using a mixture of marked VEEV clones to infect C. taeniopus and real-time RT-PCR to track these clones during mosquito infection and dissemination, we observed severe bottleneck events that resulted in a significant drop in the number of clones present. At higher initial doses, the midgut was readily infected and there was a severe bottleneck at the midgut escape. Following a lower initial dose, the major bottleneck occurred at initial midgut infection. A second, less severe bottleneck was identified at the salivary gland infection stage following intrathoracic inoculation. Our results suggest that VEEV consistently encounters bottlenecks during infection, dissemination and transmission by its natural enzootic vector. The potential impacts of these bottlenecks on viral fitness and transmission, and the viral mechanisms that prevent genetic drift leading to extinction, deserve further study. |
format | Online Article Text |
id | pubmed-3441635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34416352012-10-01 Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population Forrester, Naomi L. Guerbois, Mathilde Seymour, Robert L. Spratt, Heidi Weaver, Scott C. PLoS Pathog Research Article RNA viruses typically occur in genetically diverse populations due to their error-prone genome replication. Genetic diversity is thought to be important in allowing RNA viruses to explore sequence space, facilitating adaptation to changing environments and hosts. Some arboviruses that infect both a mosquito vector and a mammalian host are known to experience population bottlenecks in their vectors, which may constrain their genetic diversity and could potentially lead to extinction events via Muller's ratchet. To examine this potential challenge of bottlenecks for arbovirus perpetuation, we studied Venezuelan equine encephalitis virus (VEEV) enzootic subtype IE and its natural vector Culex (Melanoconion) taeniopus, as an example of a virus-vector interaction with a long evolutionary history. Using a mixture of marked VEEV clones to infect C. taeniopus and real-time RT-PCR to track these clones during mosquito infection and dissemination, we observed severe bottleneck events that resulted in a significant drop in the number of clones present. At higher initial doses, the midgut was readily infected and there was a severe bottleneck at the midgut escape. Following a lower initial dose, the major bottleneck occurred at initial midgut infection. A second, less severe bottleneck was identified at the salivary gland infection stage following intrathoracic inoculation. Our results suggest that VEEV consistently encounters bottlenecks during infection, dissemination and transmission by its natural enzootic vector. The potential impacts of these bottlenecks on viral fitness and transmission, and the viral mechanisms that prevent genetic drift leading to extinction, deserve further study. Public Library of Science 2012-09-13 /pmc/articles/PMC3441635/ /pubmed/23028310 http://dx.doi.org/10.1371/journal.ppat.1002897 Text en © 2012 Forrester 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 Forrester, Naomi L. Guerbois, Mathilde Seymour, Robert L. Spratt, Heidi Weaver, Scott C. Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title | Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title_full | Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title_fullStr | Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title_full_unstemmed | Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title_short | Vector-Borne Transmission Imposes a Severe Bottleneck on an RNA Virus Population |
title_sort | vector-borne transmission imposes a severe bottleneck on an rna virus population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3441635/ https://www.ncbi.nlm.nih.gov/pubmed/23028310 http://dx.doi.org/10.1371/journal.ppat.1002897 |
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