Cargando…

Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps

BACKGROUND: Polydnaviruses, double-stranded DNA viruses with segmented genomes, have evolved as obligate endosymbionts of parasitoid wasps. Virus particles are replication deficient and produced by female wasps from proviral sequences integrated into the wasp genome. These particles are co-injected...

Descripción completa

Detalles Bibliográficos
Autores principales: Desjardins, Christopher A, Gundersen-Rindal, Dawn E, Hostetler, Jessica B, Tallon, Luke J, Fadrosh, Douglas W, Fuester, Roger W, Pedroni, Monica J, Haas, Brian J, Schatz, Michael C, Jones, Kristine M, Crabtree, Jonathan, Forberger, Heather, Nene, Vishvanath
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646287/
https://www.ncbi.nlm.nih.gov/pubmed/19116010
http://dx.doi.org/10.1186/gb-2008-9-12-r183
_version_ 1782164838292652032
author Desjardins, Christopher A
Gundersen-Rindal, Dawn E
Hostetler, Jessica B
Tallon, Luke J
Fadrosh, Douglas W
Fuester, Roger W
Pedroni, Monica J
Haas, Brian J
Schatz, Michael C
Jones, Kristine M
Crabtree, Jonathan
Forberger, Heather
Nene, Vishvanath
author_facet Desjardins, Christopher A
Gundersen-Rindal, Dawn E
Hostetler, Jessica B
Tallon, Luke J
Fadrosh, Douglas W
Fuester, Roger W
Pedroni, Monica J
Haas, Brian J
Schatz, Michael C
Jones, Kristine M
Crabtree, Jonathan
Forberger, Heather
Nene, Vishvanath
author_sort Desjardins, Christopher A
collection PubMed
description BACKGROUND: Polydnaviruses, double-stranded DNA viruses with segmented genomes, have evolved as obligate endosymbionts of parasitoid wasps. Virus particles are replication deficient and produced by female wasps from proviral sequences integrated into the wasp genome. These particles are co-injected with eggs into caterpillar hosts, where viral gene expression facilitates parasitoid survival and, thereby, survival of proviral DNA. Here we characterize and compare the encapsidated viral genome sequences of bracoviruses in the family Polydnaviridae associated with Glyptapanteles gypsy moth parasitoids, along with near complete proviral sequences from which both viral genomes are derived. RESULTS: The encapsidated Glyptapanteles indiensis and Glyptapanteles flavicoxis bracoviral genomes, each composed of 29 different size segments, total approximately 517 and 594 kbp, respectively. They are generated from a minimum of seven distinct loci in the wasp genome. Annotation of these sequences revealed numerous novel features for polydnaviruses, including insect-like sugar transporter genes and transposable elements. Evolutionary analyses suggest that positive selection is widespread among bracoviral genes. CONCLUSIONS: The structure and organization of G. indiensis and G. flavicoxis bracovirus proviral segments as multiple loci containing one to many viral segments, flanked and separated by wasp gene-encoding DNA, is confirmed. Rapid evolution of bracovirus genes supports the hypothesis of bracovirus genes in an 'arms race' between bracovirus and caterpillar. Phylogenetic analyses of the bracoviral genes encoding sugar transporters provides the first robust evidence of a wasp origin for some polydnavirus genes. We hypothesize transposable elements, such as those described here, could facilitate transfer of genes between proviral segments and host DNA.
format Text
id pubmed-2646287
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26462872009-02-23 Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps Desjardins, Christopher A Gundersen-Rindal, Dawn E Hostetler, Jessica B Tallon, Luke J Fadrosh, Douglas W Fuester, Roger W Pedroni, Monica J Haas, Brian J Schatz, Michael C Jones, Kristine M Crabtree, Jonathan Forberger, Heather Nene, Vishvanath Genome Biol Research BACKGROUND: Polydnaviruses, double-stranded DNA viruses with segmented genomes, have evolved as obligate endosymbionts of parasitoid wasps. Virus particles are replication deficient and produced by female wasps from proviral sequences integrated into the wasp genome. These particles are co-injected with eggs into caterpillar hosts, where viral gene expression facilitates parasitoid survival and, thereby, survival of proviral DNA. Here we characterize and compare the encapsidated viral genome sequences of bracoviruses in the family Polydnaviridae associated with Glyptapanteles gypsy moth parasitoids, along with near complete proviral sequences from which both viral genomes are derived. RESULTS: The encapsidated Glyptapanteles indiensis and Glyptapanteles flavicoxis bracoviral genomes, each composed of 29 different size segments, total approximately 517 and 594 kbp, respectively. They are generated from a minimum of seven distinct loci in the wasp genome. Annotation of these sequences revealed numerous novel features for polydnaviruses, including insect-like sugar transporter genes and transposable elements. Evolutionary analyses suggest that positive selection is widespread among bracoviral genes. CONCLUSIONS: The structure and organization of G. indiensis and G. flavicoxis bracovirus proviral segments as multiple loci containing one to many viral segments, flanked and separated by wasp gene-encoding DNA, is confirmed. Rapid evolution of bracovirus genes supports the hypothesis of bracovirus genes in an 'arms race' between bracovirus and caterpillar. Phylogenetic analyses of the bracoviral genes encoding sugar transporters provides the first robust evidence of a wasp origin for some polydnavirus genes. We hypothesize transposable elements, such as those described here, could facilitate transfer of genes between proviral segments and host DNA. BioMed Central 2008 2008-12-30 /pmc/articles/PMC2646287/ /pubmed/19116010 http://dx.doi.org/10.1186/gb-2008-9-12-r183 Text en Copyright © 2008 Desjardins et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Desjardins, Christopher A
Gundersen-Rindal, Dawn E
Hostetler, Jessica B
Tallon, Luke J
Fadrosh, Douglas W
Fuester, Roger W
Pedroni, Monica J
Haas, Brian J
Schatz, Michael C
Jones, Kristine M
Crabtree, Jonathan
Forberger, Heather
Nene, Vishvanath
Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title_full Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title_fullStr Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title_full_unstemmed Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title_short Comparative genomics of mutualistic viruses of Glyptapanteles parasitic wasps
title_sort comparative genomics of mutualistic viruses of glyptapanteles parasitic wasps
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2646287/
https://www.ncbi.nlm.nih.gov/pubmed/19116010
http://dx.doi.org/10.1186/gb-2008-9-12-r183
work_keys_str_mv AT desjardinschristophera comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT gundersenrindaldawne comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT hostetlerjessicab comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT tallonlukej comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT fadroshdouglasw comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT fuesterrogerw comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT pedronimonicaj comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT haasbrianj comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT schatzmichaelc comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT joneskristinem comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT crabtreejonathan comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT forbergerheather comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps
AT nenevishvanath comparativegenomicsofmutualisticvirusesofglyptapantelesparasiticwasps