Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1782425371575058432 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4820269 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chuzhenjian genomewidehostpathogeninteractionunveiledbytranscriptomicresponseofdiamondbackmothtofungalinfection AT wangyujun genomewidehostpathogeninteractionunveiledbytranscriptomicresponseofdiamondbackmothtofungalinfection AT yingshenghua genomewidehostpathogeninteractionunveiledbytranscriptomicresponseofdiamondbackmothtofungalinfection AT wangxiaowei genomewidehostpathogeninteractionunveiledbytranscriptomicresponseofdiamondbackmothtofungalinfection AT fengmingguang genomewidehostpathogeninteractionunveiledbytranscriptomicresponseofdiamondbackmothtofungalinfection |