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Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection

Genome-wide insight into insect pest response to the infection of Beauveria bassiana (fungal insect pathogen) is critical for genetic improvement of fungal insecticides but has been poorly explored. We constructed three pairs of transcriptomes of Plutella xylostella larvae at 24, 36 and 48 hours pos...

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Autores principales: Chu, Zhen-Jian, Wang, Yu-Jun, Ying, Sheng-Hua, Wang, Xiao-Wei, Feng, Ming-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820269/
https://www.ncbi.nlm.nih.gov/pubmed/27043942
http://dx.doi.org/10.1371/journal.pone.0152908
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author Chu, Zhen-Jian
Wang, Yu-Jun
Ying, Sheng-Hua
Wang, Xiao-Wei
Feng, Ming-Guang
author_facet Chu, Zhen-Jian
Wang, Yu-Jun
Ying, Sheng-Hua
Wang, Xiao-Wei
Feng, Ming-Guang
author_sort Chu, Zhen-Jian
collection PubMed
description Genome-wide insight into insect pest response to the infection of Beauveria bassiana (fungal insect pathogen) is critical for genetic improvement of fungal insecticides but has been poorly explored. We constructed three pairs of transcriptomes of Plutella xylostella larvae at 24, 36 and 48 hours post treatment of infection (hpt(I)) and of control (hpt(C)) for insight into the host-pathogen interaction at genomic level. There were 2143, 3200 and 2967 host genes differentially expressed at 24, 36 and 48 hpt(I)/hpt(C) respectively. These infection-responsive genes (~15% of the host genome) were enriched in various immune processes, such as complement and coagulation cascades, protein digestion and absorption, and drug metabolism-cytochrome P450. Fungal penetration into cuticle and host defense reaction began at 24 hpt(I), followed by most intensive host immune response at 36 hpt(I) and attenuated immunity at 48 hpt(I). Contrastingly, 44% of fungal genes were differentially expressed in the infection course and enriched in several biological processes, such as antioxidant activity, peroxidase activity and proteolysis. There were 1636 fungal genes co-expressed during 24–48 hpt(I), including 116 encoding putative secretion proteins. Our results provide novel insights into the insect-pathogen interaction and help to probe molecular mechanisms involved in the fungal infection to the global pest.
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spelling pubmed-48202692016-04-22 Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection Chu, Zhen-Jian Wang, Yu-Jun Ying, Sheng-Hua Wang, Xiao-Wei Feng, Ming-Guang PLoS One Research Article Genome-wide insight into insect pest response to the infection of Beauveria bassiana (fungal insect pathogen) is critical for genetic improvement of fungal insecticides but has been poorly explored. We constructed three pairs of transcriptomes of Plutella xylostella larvae at 24, 36 and 48 hours post treatment of infection (hpt(I)) and of control (hpt(C)) for insight into the host-pathogen interaction at genomic level. There were 2143, 3200 and 2967 host genes differentially expressed at 24, 36 and 48 hpt(I)/hpt(C) respectively. These infection-responsive genes (~15% of the host genome) were enriched in various immune processes, such as complement and coagulation cascades, protein digestion and absorption, and drug metabolism-cytochrome P450. Fungal penetration into cuticle and host defense reaction began at 24 hpt(I), followed by most intensive host immune response at 36 hpt(I) and attenuated immunity at 48 hpt(I). Contrastingly, 44% of fungal genes were differentially expressed in the infection course and enriched in several biological processes, such as antioxidant activity, peroxidase activity and proteolysis. There were 1636 fungal genes co-expressed during 24–48 hpt(I), including 116 encoding putative secretion proteins. Our results provide novel insights into the insect-pathogen interaction and help to probe molecular mechanisms involved in the fungal infection to the global pest. Public Library of Science 2016-04-04 /pmc/articles/PMC4820269/ /pubmed/27043942 http://dx.doi.org/10.1371/journal.pone.0152908 Text en © 2016 Chu 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
Chu, Zhen-Jian
Wang, Yu-Jun
Ying, Sheng-Hua
Wang, Xiao-Wei
Feng, Ming-Guang
Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title_full Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title_fullStr Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title_full_unstemmed Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title_short Genome-Wide Host-Pathogen Interaction Unveiled by Transcriptomic Response of Diamondback Moth to Fungal Infection
title_sort genome-wide host-pathogen interaction unveiled by transcriptomic response of diamondback moth to fungal infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820269/
https://www.ncbi.nlm.nih.gov/pubmed/27043942
http://dx.doi.org/10.1371/journal.pone.0152908
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