Cargando…

Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava

Endoparasitoid wasps are important natural enemies of many insect species and are major selective forces on the host immune system. Despite increased interest in insect antiparasitoid immunity, there is sparse information on the evolutionary dynamics of biological pathways and gene regulation involv...

Descripción completa

Detalles Bibliográficos
Autores principales: Yang, Xuyue, Fors, Lisa, Slotte, Tanja, Theopold, Ulrich, Binzer-Panchal, Mahesh, Wheat, Christopher W, Hambäck, Peter A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211424/
https://www.ncbi.nlm.nih.gov/pubmed/32282901
http://dx.doi.org/10.1093/gbe/evaa075
_version_ 1783531454365433856
author Yang, Xuyue
Fors, Lisa
Slotte, Tanja
Theopold, Ulrich
Binzer-Panchal, Mahesh
Wheat, Christopher W
Hambäck, Peter A
author_facet Yang, Xuyue
Fors, Lisa
Slotte, Tanja
Theopold, Ulrich
Binzer-Panchal, Mahesh
Wheat, Christopher W
Hambäck, Peter A
author_sort Yang, Xuyue
collection PubMed
description Endoparasitoid wasps are important natural enemies of many insect species and are major selective forces on the host immune system. Despite increased interest in insect antiparasitoid immunity, there is sparse information on the evolutionary dynamics of biological pathways and gene regulation involved in host immune defense outside Drosophila species. We de novo assembled transcriptomes from two beetle species and used time-course differential expression analysis to investigate gene expression differences in closely related species Galerucella pusilla and G. calmariensis that are, respectively, resistant and susceptible against parasitoid infection by Asecodes parviclava parasitoids. Approximately 271 million and 224 million paired-ended reads were assembled and filtered to form 52,563 and 59,781 transcripts for G. pusilla and G. calmariensis, respectively. In the whole-transcriptome level, an enrichment of functional categories related to energy production, biosynthetic process, and metabolic process was exhibited in both species. The main difference between species appears to be immune response and wound healing process mounted by G. pusilla larvae. Using reciprocal BLAST against the Drosophila melanogaster proteome, 120 and 121 immune-related genes were identified in G. pusilla and G. calmariensis, respectively. More immune genes were differentially expressed in G. pusilla than in G. calmariensis, in particular genes involved in signaling, hematopoiesis, and melanization. In contrast, only one gene was differentially expressed in G. calmariensis. Our study characterizes important genes and pathways involved in different immune functions after parasitoid infection and supports the role of signaling and hematopoiesis genes as key players in host immunity in Galerucella against parasitoid wasps.
format Online
Article
Text
id pubmed-7211424
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-72114242020-05-14 Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava Yang, Xuyue Fors, Lisa Slotte, Tanja Theopold, Ulrich Binzer-Panchal, Mahesh Wheat, Christopher W Hambäck, Peter A Genome Biol Evol Research Article Endoparasitoid wasps are important natural enemies of many insect species and are major selective forces on the host immune system. Despite increased interest in insect antiparasitoid immunity, there is sparse information on the evolutionary dynamics of biological pathways and gene regulation involved in host immune defense outside Drosophila species. We de novo assembled transcriptomes from two beetle species and used time-course differential expression analysis to investigate gene expression differences in closely related species Galerucella pusilla and G. calmariensis that are, respectively, resistant and susceptible against parasitoid infection by Asecodes parviclava parasitoids. Approximately 271 million and 224 million paired-ended reads were assembled and filtered to form 52,563 and 59,781 transcripts for G. pusilla and G. calmariensis, respectively. In the whole-transcriptome level, an enrichment of functional categories related to energy production, biosynthetic process, and metabolic process was exhibited in both species. The main difference between species appears to be immune response and wound healing process mounted by G. pusilla larvae. Using reciprocal BLAST against the Drosophila melanogaster proteome, 120 and 121 immune-related genes were identified in G. pusilla and G. calmariensis, respectively. More immune genes were differentially expressed in G. pusilla than in G. calmariensis, in particular genes involved in signaling, hematopoiesis, and melanization. In contrast, only one gene was differentially expressed in G. calmariensis. Our study characterizes important genes and pathways involved in different immune functions after parasitoid infection and supports the role of signaling and hematopoiesis genes as key players in host immunity in Galerucella against parasitoid wasps. Oxford University Press 2020-04-13 /pmc/articles/PMC7211424/ /pubmed/32282901 http://dx.doi.org/10.1093/gbe/evaa075 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Xuyue
Fors, Lisa
Slotte, Tanja
Theopold, Ulrich
Binzer-Panchal, Mahesh
Wheat, Christopher W
Hambäck, Peter A
Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title_full Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title_fullStr Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title_full_unstemmed Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title_short Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava
title_sort differential expression of immune genes between two closely related beetle species with different immunocompetence following attack by asecodes parviclava
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7211424/
https://www.ncbi.nlm.nih.gov/pubmed/32282901
http://dx.doi.org/10.1093/gbe/evaa075
work_keys_str_mv AT yangxuyue differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT forslisa differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT slottetanja differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT theopoldulrich differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT binzerpanchalmahesh differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT wheatchristopherw differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava
AT hambackpetera differentialexpressionofimmunegenesbetweentwocloselyrelatedbeetlespecieswithdifferentimmunocompetencefollowingattackbyasecodesparviclava