Cargando…

Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors

Viruses are usually thought to form parasitic associations with hosts, but all members of the family Polydnaviridae are obligate mutualists of insects called parasitoid wasps. Phylogenetic data founded on sequence comparisons of viral genes indicate that polydnaviruses in the genus Bracovirus (BV) a...

Descripción completa

Detalles Bibliográficos
Autores principales: Burke, Gaelen R., Thomas, Sarah A., Eum, Jai H., Strand, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649998/
https://www.ncbi.nlm.nih.gov/pubmed/23671417
http://dx.doi.org/10.1371/journal.ppat.1003348
_version_ 1782269055299747840
author Burke, Gaelen R.
Thomas, Sarah A.
Eum, Jai H.
Strand, Michael R.
author_facet Burke, Gaelen R.
Thomas, Sarah A.
Eum, Jai H.
Strand, Michael R.
author_sort Burke, Gaelen R.
collection PubMed
description Viruses are usually thought to form parasitic associations with hosts, but all members of the family Polydnaviridae are obligate mutualists of insects called parasitoid wasps. Phylogenetic data founded on sequence comparisons of viral genes indicate that polydnaviruses in the genus Bracovirus (BV) are closely related to pathogenic nudiviruses and baculoviruses. However, pronounced differences in the biology of BVs and baculoviruses together with high divergence of many shared genes make it unclear whether BV homologs still retain baculovirus-like functions. Here we report that virions from Microplitis demolitor bracovirus (MdBV) contain multiple baculovirus-like and nudivirus-like conserved gene products. We further show that RNA interference effectively and specifically knocks down MdBV gene expression. Coupling RNAi knockdown methods with functional assays, we examined the activity of six genes in the MdBV conserved gene set that are known to have essential roles in transcription (lef-4, lef-9), capsid assembly (vp39, vlf-1), and envelope formation (p74, pif-1) during baculovirus replication. Our results indicated that MdBV produces a baculovirus-like RNA polymerase that transcribes virus structural genes. Our results also supported a conserved role for vp39, vlf-1, p74, and pif-1 as structural components of MdBV virions. Additional experiments suggested that vlf-1 together with the nudivirus-like gene int-1 also have novel functions in regulating excision of MdBV proviral DNAs for packaging into virions. Overall, these data provide the first experimental insights into the function of BV genes in virion formation.
format Online
Article
Text
id pubmed-3649998
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36499982013-05-13 Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors Burke, Gaelen R. Thomas, Sarah A. Eum, Jai H. Strand, Michael R. PLoS Pathog Research Article Viruses are usually thought to form parasitic associations with hosts, but all members of the family Polydnaviridae are obligate mutualists of insects called parasitoid wasps. Phylogenetic data founded on sequence comparisons of viral genes indicate that polydnaviruses in the genus Bracovirus (BV) are closely related to pathogenic nudiviruses and baculoviruses. However, pronounced differences in the biology of BVs and baculoviruses together with high divergence of many shared genes make it unclear whether BV homologs still retain baculovirus-like functions. Here we report that virions from Microplitis demolitor bracovirus (MdBV) contain multiple baculovirus-like and nudivirus-like conserved gene products. We further show that RNA interference effectively and specifically knocks down MdBV gene expression. Coupling RNAi knockdown methods with functional assays, we examined the activity of six genes in the MdBV conserved gene set that are known to have essential roles in transcription (lef-4, lef-9), capsid assembly (vp39, vlf-1), and envelope formation (p74, pif-1) during baculovirus replication. Our results indicated that MdBV produces a baculovirus-like RNA polymerase that transcribes virus structural genes. Our results also supported a conserved role for vp39, vlf-1, p74, and pif-1 as structural components of MdBV virions. Additional experiments suggested that vlf-1 together with the nudivirus-like gene int-1 also have novel functions in regulating excision of MdBV proviral DNAs for packaging into virions. Overall, these data provide the first experimental insights into the function of BV genes in virion formation. Public Library of Science 2013-05-09 /pmc/articles/PMC3649998/ /pubmed/23671417 http://dx.doi.org/10.1371/journal.ppat.1003348 Text en © 2013 Burke 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
Burke, Gaelen R.
Thomas, Sarah A.
Eum, Jai H.
Strand, Michael R.
Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title_full Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title_fullStr Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title_full_unstemmed Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title_short Mutualistic Polydnaviruses Share Essential Replication Gene Functions with Pathogenic Ancestors
title_sort mutualistic polydnaviruses share essential replication gene functions with pathogenic ancestors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3649998/
https://www.ncbi.nlm.nih.gov/pubmed/23671417
http://dx.doi.org/10.1371/journal.ppat.1003348
work_keys_str_mv AT burkegaelenr mutualisticpolydnavirusesshareessentialreplicationgenefunctionswithpathogenicancestors
AT thomassaraha mutualisticpolydnavirusesshareessentialreplicationgenefunctionswithpathogenicancestors
AT eumjaih mutualisticpolydnavirusesshareessentialreplicationgenefunctionswithpathogenicancestors
AT strandmichaelr mutualisticpolydnavirusesshareessentialreplicationgenefunctionswithpathogenicancestors