Cargando…

Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles

BACKGROUND: Horizontal gene transfer (HGT) has been documented in many herbivorous insects, conferring the ability to digest plant material and promoting their remarkable ecological diversification. Previous reports suggest HGT of antibacterial enzymes may have contributed to the insect immune respo...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Hao-Sen, Tang, Xue-Fei, Huang, Yu-Hao, Xu, Ze-Yu, Chen, Mei-Lan, Du, Xue-Yong, Qiu, Bo-Yuan, Chen, Pei-Tao, Zhang, Wei, Ślipiński, Adam, Escalona, Hermes E., Waterhouse, Robert M., Zwick, Andreas, Pang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807722/
https://www.ncbi.nlm.nih.gov/pubmed/33446206
http://dx.doi.org/10.1186/s12915-020-00945-7
_version_ 1783636803425665024
author Li, Hao-Sen
Tang, Xue-Fei
Huang, Yu-Hao
Xu, Ze-Yu
Chen, Mei-Lan
Du, Xue-Yong
Qiu, Bo-Yuan
Chen, Pei-Tao
Zhang, Wei
Ślipiński, Adam
Escalona, Hermes E.
Waterhouse, Robert M.
Zwick, Andreas
Pang, Hong
author_facet Li, Hao-Sen
Tang, Xue-Fei
Huang, Yu-Hao
Xu, Ze-Yu
Chen, Mei-Lan
Du, Xue-Yong
Qiu, Bo-Yuan
Chen, Pei-Tao
Zhang, Wei
Ślipiński, Adam
Escalona, Hermes E.
Waterhouse, Robert M.
Zwick, Andreas
Pang, Hong
author_sort Li, Hao-Sen
collection PubMed
description BACKGROUND: Horizontal gene transfer (HGT) has been documented in many herbivorous insects, conferring the ability to digest plant material and promoting their remarkable ecological diversification. Previous reports suggest HGT of antibacterial enzymes may have contributed to the insect immune response and limit bacterial growth. Carnivorous insects also display many evolutionary successful lineages, but in contrast to the plant feeders, the potential role of HGTs has been less well-studied. RESULTS: Using genomic and transcriptomic data from 38 species of ladybird beetles, we identified a set of bacterial cell wall hydrolase (cwh) genes acquired by this group of beetles. Infection with Bacillus subtilis led to upregulated expression of these ladybird cwh genes, and their recombinantly produced proteins limited bacterial proliferation. Moreover, RNAi-mediated cwh knockdown led to downregulation of other antibacterial genes, indicating a role in antibacterial immune defense. cwh genes are rare in eukaryotes, but have been maintained in all tested Coccinellinae species, suggesting that this putative immune-related HGT event played a role in the evolution of this speciose subfamily of predominant predatory ladybirds. CONCLUSION: Our work demonstrates that, in a manner analogous to HGT-facilitated plant feeding, enhanced immunity through HGT might have played a key role in the prey adaptation and niche expansion that promoted the diversification of carnivorous beetle lineages. We believe that this represents the first example of immune-related HGT in carnivorous insects with an association with a subsequent successful species radiation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00945-7.
format Online
Article
Text
id pubmed-7807722
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-78077222021-01-15 Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles Li, Hao-Sen Tang, Xue-Fei Huang, Yu-Hao Xu, Ze-Yu Chen, Mei-Lan Du, Xue-Yong Qiu, Bo-Yuan Chen, Pei-Tao Zhang, Wei Ślipiński, Adam Escalona, Hermes E. Waterhouse, Robert M. Zwick, Andreas Pang, Hong BMC Biol Research Article BACKGROUND: Horizontal gene transfer (HGT) has been documented in many herbivorous insects, conferring the ability to digest plant material and promoting their remarkable ecological diversification. Previous reports suggest HGT of antibacterial enzymes may have contributed to the insect immune response and limit bacterial growth. Carnivorous insects also display many evolutionary successful lineages, but in contrast to the plant feeders, the potential role of HGTs has been less well-studied. RESULTS: Using genomic and transcriptomic data from 38 species of ladybird beetles, we identified a set of bacterial cell wall hydrolase (cwh) genes acquired by this group of beetles. Infection with Bacillus subtilis led to upregulated expression of these ladybird cwh genes, and their recombinantly produced proteins limited bacterial proliferation. Moreover, RNAi-mediated cwh knockdown led to downregulation of other antibacterial genes, indicating a role in antibacterial immune defense. cwh genes are rare in eukaryotes, but have been maintained in all tested Coccinellinae species, suggesting that this putative immune-related HGT event played a role in the evolution of this speciose subfamily of predominant predatory ladybirds. CONCLUSION: Our work demonstrates that, in a manner analogous to HGT-facilitated plant feeding, enhanced immunity through HGT might have played a key role in the prey adaptation and niche expansion that promoted the diversification of carnivorous beetle lineages. We believe that this represents the first example of immune-related HGT in carnivorous insects with an association with a subsequent successful species radiation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00945-7. BioMed Central 2021-01-14 /pmc/articles/PMC7807722/ /pubmed/33446206 http://dx.doi.org/10.1186/s12915-020-00945-7 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Li, Hao-Sen
Tang, Xue-Fei
Huang, Yu-Hao
Xu, Ze-Yu
Chen, Mei-Lan
Du, Xue-Yong
Qiu, Bo-Yuan
Chen, Pei-Tao
Zhang, Wei
Ślipiński, Adam
Escalona, Hermes E.
Waterhouse, Robert M.
Zwick, Andreas
Pang, Hong
Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title_full Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title_fullStr Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title_full_unstemmed Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title_short Horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
title_sort horizontally acquired antibacterial genes associated with adaptive radiation of ladybird beetles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807722/
https://www.ncbi.nlm.nih.gov/pubmed/33446206
http://dx.doi.org/10.1186/s12915-020-00945-7
work_keys_str_mv AT lihaosen horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT tangxuefei horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT huangyuhao horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT xuzeyu horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT chenmeilan horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT duxueyong horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT qiuboyuan horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT chenpeitao horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT zhangwei horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT slipinskiadam horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT escalonahermese horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT waterhouserobertm horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT zwickandreas horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles
AT panghong horizontallyacquiredantibacterialgenesassociatedwithadaptiveradiationofladybirdbeetles