Cargando…

Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection

Thrips palmi is a widely distributed major agricultural pest in the tropics and subtropics, causing significant losses in cucurbit and solanaceous crops through feeding damage and transmission of tospoviruses. Thrips palmi is a vector of capsicum chlorosis virus (CaCV) in Australia. The present unde...

Descripción completa

Detalles Bibliográficos
Autores principales: Widana Gamage, Shirani M. K., Rotenberg, Dorith, Schneweis, Derek J., Tsai, Chi-Wei, Dietzgen, Ralf G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286046/
https://www.ncbi.nlm.nih.gov/pubmed/30532222
http://dx.doi.org/10.1371/journal.pone.0208538
_version_ 1783379403383767040
author Widana Gamage, Shirani M. K.
Rotenberg, Dorith
Schneweis, Derek J.
Tsai, Chi-Wei
Dietzgen, Ralf G.
author_facet Widana Gamage, Shirani M. K.
Rotenberg, Dorith
Schneweis, Derek J.
Tsai, Chi-Wei
Dietzgen, Ralf G.
author_sort Widana Gamage, Shirani M. K.
collection PubMed
description Thrips palmi is a widely distributed major agricultural pest in the tropics and subtropics, causing significant losses in cucurbit and solanaceous crops through feeding damage and transmission of tospoviruses. Thrips palmi is a vector of capsicum chlorosis virus (CaCV) in Australia. The present understanding of transmission biology and potential effects of CaCV on T. palmi is limited. To gain insights into molecular responses to CaCV infection, we performed RNA-Seq to identify thrips transcripts that are differentially-abundant during virus infection of adults. De-novo assembly of the transcriptome generated from whole bodies of T. palmi adults generated 166,445 contigs, of which ~24% contained a predicted open reading frame. We identified 1,389 differentially-expressed (DE) transcripts, with comparable numbers up- (708) and down-regulated (681) in virus-exposed thrips compared to non-exposed thrips. Approximately 59% of these DE transcripts had significant matches to NCBI non-redundant proteins (Blastx) and Blast2GO identified provisional functional categories among the up-regulated transcripts in virus-exposed thrips including innate immune response-related genes, salivary gland and/or gut-associated genes and vitellogenin genes. The majority of the immune-related proteins are known to serve functions in lysosome activity and melanisation in insects. Most of the up-regulated oral and extra-oral digestion-associated genes appear to be involved in digestion of proteins, lipids and plant cell wall components which may indirectly enhance the likelihood or frequency of virus transmission or may be involved in the regulation of host defence responses. Most of the down-regulated transcripts fell into the gene ontology functional category of ‘structural constituent of cuticle’. Comparison to DE genes responsive to tomato spotted wilt virus in Frankliniella occidentalis indicates conservation of some thrips molecular responses to infection by different tospoviruses. This study assembled the first transcriptome in the genus Thrips and provides important data to broaden our understanding of networks of molecular interactions between thrips and tospoviruses.
format Online
Article
Text
id pubmed-6286046
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-62860462018-12-28 Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection Widana Gamage, Shirani M. K. Rotenberg, Dorith Schneweis, Derek J. Tsai, Chi-Wei Dietzgen, Ralf G. PLoS One Research Article Thrips palmi is a widely distributed major agricultural pest in the tropics and subtropics, causing significant losses in cucurbit and solanaceous crops through feeding damage and transmission of tospoviruses. Thrips palmi is a vector of capsicum chlorosis virus (CaCV) in Australia. The present understanding of transmission biology and potential effects of CaCV on T. palmi is limited. To gain insights into molecular responses to CaCV infection, we performed RNA-Seq to identify thrips transcripts that are differentially-abundant during virus infection of adults. De-novo assembly of the transcriptome generated from whole bodies of T. palmi adults generated 166,445 contigs, of which ~24% contained a predicted open reading frame. We identified 1,389 differentially-expressed (DE) transcripts, with comparable numbers up- (708) and down-regulated (681) in virus-exposed thrips compared to non-exposed thrips. Approximately 59% of these DE transcripts had significant matches to NCBI non-redundant proteins (Blastx) and Blast2GO identified provisional functional categories among the up-regulated transcripts in virus-exposed thrips including innate immune response-related genes, salivary gland and/or gut-associated genes and vitellogenin genes. The majority of the immune-related proteins are known to serve functions in lysosome activity and melanisation in insects. Most of the up-regulated oral and extra-oral digestion-associated genes appear to be involved in digestion of proteins, lipids and plant cell wall components which may indirectly enhance the likelihood or frequency of virus transmission or may be involved in the regulation of host defence responses. Most of the down-regulated transcripts fell into the gene ontology functional category of ‘structural constituent of cuticle’. Comparison to DE genes responsive to tomato spotted wilt virus in Frankliniella occidentalis indicates conservation of some thrips molecular responses to infection by different tospoviruses. This study assembled the first transcriptome in the genus Thrips and provides important data to broaden our understanding of networks of molecular interactions between thrips and tospoviruses. Public Library of Science 2018-12-07 /pmc/articles/PMC6286046/ /pubmed/30532222 http://dx.doi.org/10.1371/journal.pone.0208538 Text en © 2018 Widana Gamage 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
Widana Gamage, Shirani M. K.
Rotenberg, Dorith
Schneweis, Derek J.
Tsai, Chi-Wei
Dietzgen, Ralf G.
Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title_full Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title_fullStr Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title_full_unstemmed Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title_short Transcriptome-wide responses of adult melon thrips (Thrips palmi) associated with capsicum chlorosis virus infection
title_sort transcriptome-wide responses of adult melon thrips (thrips palmi) associated with capsicum chlorosis virus infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286046/
https://www.ncbi.nlm.nih.gov/pubmed/30532222
http://dx.doi.org/10.1371/journal.pone.0208538
work_keys_str_mv AT widanagamageshiranimk transcriptomewideresponsesofadultmelonthripsthripspalmiassociatedwithcapsicumchlorosisvirusinfection
AT rotenbergdorith transcriptomewideresponsesofadultmelonthripsthripspalmiassociatedwithcapsicumchlorosisvirusinfection
AT schneweisderekj transcriptomewideresponsesofadultmelonthripsthripspalmiassociatedwithcapsicumchlorosisvirusinfection
AT tsaichiwei transcriptomewideresponsesofadultmelonthripsthripspalmiassociatedwithcapsicumchlorosisvirusinfection
AT dietzgenralfg transcriptomewideresponsesofadultmelonthripsthripspalmiassociatedwithcapsicumchlorosisvirusinfection