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Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus
Both mosquito species-specific differences and virus strain -specific differences impact vector competence. Previous results in our laboratory with individual populations of N. American mosquitoes support studies suggesting Aedes aegypti are more competent than Ae. albopictus for American Zika virus...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588074/ https://www.ncbi.nlm.nih.gov/pubmed/33052957 http://dx.doi.org/10.1371/journal.ppat.1008951 |
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author | Kuo, Lili Jaeger, Anna S. Banker, Elyse M. Bialosuknia, Sean M. Mathias, Nicholas Payne, Anne F. Kramer, Laura D. Aliota, Matthew T. Ciota, Alexander T. |
author_facet | Kuo, Lili Jaeger, Anna S. Banker, Elyse M. Bialosuknia, Sean M. Mathias, Nicholas Payne, Anne F. Kramer, Laura D. Aliota, Matthew T. Ciota, Alexander T. |
author_sort | Kuo, Lili |
collection | PubMed |
description | Both mosquito species-specific differences and virus strain -specific differences impact vector competence. Previous results in our laboratory with individual populations of N. American mosquitoes support studies suggesting Aedes aegypti are more competent than Ae. albopictus for American Zika virus (ZIKV) strains and demonstrate that U.S. Ae. albopictus have higher competence for an ancestral Asian ZIKV strain. A982V, an amino acid substitution in the NS1 gene acquired prior to the American outbreak, has been shown to increase competence in Ae. aegypti. We hypothesized that variability in the NS1 could therefore contribute to species-specific differences and developed a reverse genetics system based on a 2016 ZIKV isolate from Honduras (ZIKV-WTic) to evaluate the phenotypic correlates of individual amino acid substitutions. In addition to A982V, we evaluated G894A, which was acquired during circulation in the Americas. Reversion of 982 and 894 to ancestral residues increased infectivity, transmissibility and viral loads in Ae. albopictus but had no effect on competence or replication in Ae. aegypti. In addition, while host cell-specific differences in NS1 secretion were measured, with significantly higher secretion in mammalian cells relative to mosquito cells, strain-specific differences in secretion were not detected, despite previous reports. These results demonstrate that individual mutations in NS1 can influence competence in a species-specific manner independent of differences in NS1 secretion and further indicate that ancestral NS1 residues confer increased competence in Ae. albopictus. Lastly, experimental infections of Ifnar1(-/-) mice demonstrated that these NS1 substitutions can influence viral replication in the host and, specifically, that G894A could represent a compensatory change following a fitness loss from A982V with some viral genetic backgrounds. Together these data suggest a possible role for epistatic interactions in ZIKV fitness in invertebrate and vertebrate hosts and demonstrate that strains with increased transmission potential in U.S. Ae. albopictus could emerge. |
format | Online Article Text |
id | pubmed-7588074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75880742020-10-30 Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus Kuo, Lili Jaeger, Anna S. Banker, Elyse M. Bialosuknia, Sean M. Mathias, Nicholas Payne, Anne F. Kramer, Laura D. Aliota, Matthew T. Ciota, Alexander T. PLoS Pathog Research Article Both mosquito species-specific differences and virus strain -specific differences impact vector competence. Previous results in our laboratory with individual populations of N. American mosquitoes support studies suggesting Aedes aegypti are more competent than Ae. albopictus for American Zika virus (ZIKV) strains and demonstrate that U.S. Ae. albopictus have higher competence for an ancestral Asian ZIKV strain. A982V, an amino acid substitution in the NS1 gene acquired prior to the American outbreak, has been shown to increase competence in Ae. aegypti. We hypothesized that variability in the NS1 could therefore contribute to species-specific differences and developed a reverse genetics system based on a 2016 ZIKV isolate from Honduras (ZIKV-WTic) to evaluate the phenotypic correlates of individual amino acid substitutions. In addition to A982V, we evaluated G894A, which was acquired during circulation in the Americas. Reversion of 982 and 894 to ancestral residues increased infectivity, transmissibility and viral loads in Ae. albopictus but had no effect on competence or replication in Ae. aegypti. In addition, while host cell-specific differences in NS1 secretion were measured, with significantly higher secretion in mammalian cells relative to mosquito cells, strain-specific differences in secretion were not detected, despite previous reports. These results demonstrate that individual mutations in NS1 can influence competence in a species-specific manner independent of differences in NS1 secretion and further indicate that ancestral NS1 residues confer increased competence in Ae. albopictus. Lastly, experimental infections of Ifnar1(-/-) mice demonstrated that these NS1 substitutions can influence viral replication in the host and, specifically, that G894A could represent a compensatory change following a fitness loss from A982V with some viral genetic backgrounds. Together these data suggest a possible role for epistatic interactions in ZIKV fitness in invertebrate and vertebrate hosts and demonstrate that strains with increased transmission potential in U.S. Ae. albopictus could emerge. Public Library of Science 2020-10-14 /pmc/articles/PMC7588074/ /pubmed/33052957 http://dx.doi.org/10.1371/journal.ppat.1008951 Text en © 2020 Kuo 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kuo, Lili Jaeger, Anna S. Banker, Elyse M. Bialosuknia, Sean M. Mathias, Nicholas Payne, Anne F. Kramer, Laura D. Aliota, Matthew T. Ciota, Alexander T. Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title | Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title_full | Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title_fullStr | Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title_full_unstemmed | Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title_short | Reversion to ancestral Zika virus NS1 residues increases competence of Aedes albopictus |
title_sort | reversion to ancestral zika virus ns1 residues increases competence of aedes albopictus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588074/ https://www.ncbi.nlm.nih.gov/pubmed/33052957 http://dx.doi.org/10.1371/journal.ppat.1008951 |
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