Cargando…
Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection
BACKGROUND: Rift Valley fever virus is an arthropod-borne human and animal pathogen responsible for large outbreaks of acute and febrile illness throughout Africa and the Arabian Peninsula. Reverse genetics technology has been used to develop deletion mutants of the virus that lack the NSs and/or NS...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341344/ https://www.ncbi.nlm.nih.gov/pubmed/22563517 http://dx.doi.org/10.1371/journal.pntd.0001639 |
_version_ | 1782231529651437568 |
---|---|
author | Crabtree, Mary B. Kent Crockett, Rebekah J. Bird, Brian H. Nichol, Stuart T. Erickson, Bobbie Rae Biggerstaff, Brad J. Horiuchi, Kalanthe Miller, Barry R. |
author_facet | Crabtree, Mary B. Kent Crockett, Rebekah J. Bird, Brian H. Nichol, Stuart T. Erickson, Bobbie Rae Biggerstaff, Brad J. Horiuchi, Kalanthe Miller, Barry R. |
author_sort | Crabtree, Mary B. |
collection | PubMed |
description | BACKGROUND: Rift Valley fever virus is an arthropod-borne human and animal pathogen responsible for large outbreaks of acute and febrile illness throughout Africa and the Arabian Peninsula. Reverse genetics technology has been used to develop deletion mutants of the virus that lack the NSs and/or NSm virulence genes and have been shown to be stable, immunogenic and protective against Rift Valley fever virus infection in animals. We assessed the potential for these deletion mutant viruses to infect and be transmitted by Aedes mosquitoes, which are the principal vectors for maintenance of the virus in nature and emergence of virus initiating disease outbreaks, and by Culex mosquitoes which are important amplification vectors. METHODOLOGY AND PRINCIPAL FINDINGS: Aedes aegypti and Culex quinquefasciatus mosquitoes were fed bloodmeals containing the deletion mutant viruses. Two weeks post-exposure mosquitoes were assayed for infection, dissemination, and transmission. In Ae. aegypti, infection and transmission rates of the NSs deletion virus were similar to wild type virus while dissemination rates were significantly reduced. Infection and dissemination rates for the NSm deletion virus were lower compared to wild type. Virus lacking both NSs and NSm failed to infect Ae. aegypti. In Cx. quinquefasciatus, infection rates for viruses lacking NSm or both NSs and NSm were lower than for wild type virus. CONCLUSIONS/SIGNIFICANCE: In both species, deletion of NSm or both NSs and NSm reduced the infection and transmission potential of the virus. Deletion of both NSs and NSm resulted in the highest level of attenuation of virus replication. Deletion of NSm alone was sufficient to nearly abolish infection in Aedes aegypti mosquitoes, indicating an important role for this protein. The double deleted viruses represent an ideal vaccine profile in terms of environmental containment due to lack of ability to efficiently infect and be transmitted by mosquitoes. |
format | Online Article Text |
id | pubmed-3341344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33413442012-05-04 Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection Crabtree, Mary B. Kent Crockett, Rebekah J. Bird, Brian H. Nichol, Stuart T. Erickson, Bobbie Rae Biggerstaff, Brad J. Horiuchi, Kalanthe Miller, Barry R. PLoS Negl Trop Dis Research Article BACKGROUND: Rift Valley fever virus is an arthropod-borne human and animal pathogen responsible for large outbreaks of acute and febrile illness throughout Africa and the Arabian Peninsula. Reverse genetics technology has been used to develop deletion mutants of the virus that lack the NSs and/or NSm virulence genes and have been shown to be stable, immunogenic and protective against Rift Valley fever virus infection in animals. We assessed the potential for these deletion mutant viruses to infect and be transmitted by Aedes mosquitoes, which are the principal vectors for maintenance of the virus in nature and emergence of virus initiating disease outbreaks, and by Culex mosquitoes which are important amplification vectors. METHODOLOGY AND PRINCIPAL FINDINGS: Aedes aegypti and Culex quinquefasciatus mosquitoes were fed bloodmeals containing the deletion mutant viruses. Two weeks post-exposure mosquitoes were assayed for infection, dissemination, and transmission. In Ae. aegypti, infection and transmission rates of the NSs deletion virus were similar to wild type virus while dissemination rates were significantly reduced. Infection and dissemination rates for the NSm deletion virus were lower compared to wild type. Virus lacking both NSs and NSm failed to infect Ae. aegypti. In Cx. quinquefasciatus, infection rates for viruses lacking NSm or both NSs and NSm were lower than for wild type virus. CONCLUSIONS/SIGNIFICANCE: In both species, deletion of NSm or both NSs and NSm reduced the infection and transmission potential of the virus. Deletion of both NSs and NSm resulted in the highest level of attenuation of virus replication. Deletion of NSm alone was sufficient to nearly abolish infection in Aedes aegypti mosquitoes, indicating an important role for this protein. The double deleted viruses represent an ideal vaccine profile in terms of environmental containment due to lack of ability to efficiently infect and be transmitted by mosquitoes. Public Library of Science 2012-05-01 /pmc/articles/PMC3341344/ /pubmed/22563517 http://dx.doi.org/10.1371/journal.pntd.0001639 Text en This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Crabtree, Mary B. Kent Crockett, Rebekah J. Bird, Brian H. Nichol, Stuart T. Erickson, Bobbie Rae Biggerstaff, Brad J. Horiuchi, Kalanthe Miller, Barry R. Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title | Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title_full | Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title_fullStr | Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title_full_unstemmed | Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title_short | Infection and Transmission of Rift Valley Fever Viruses Lacking the NSs and/or NSm Genes in Mosquitoes: Potential Role for NSm in Mosquito Infection |
title_sort | infection and transmission of rift valley fever viruses lacking the nss and/or nsm genes in mosquitoes: potential role for nsm in mosquito infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341344/ https://www.ncbi.nlm.nih.gov/pubmed/22563517 http://dx.doi.org/10.1371/journal.pntd.0001639 |
work_keys_str_mv | AT crabtreemaryb infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT kentcrockettrebekahj infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT birdbrianh infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT nicholstuartt infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT ericksonbobbierae infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT biggerstaffbradj infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT horiuchikalanthe infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection AT millerbarryr infectionandtransmissionofriftvalleyfeverviruseslackingthenssandornsmgenesinmosquitoespotentialrolefornsminmosquitoinfection |