Cargando…

Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts

Understanding the genetic basis of host shifts is a key genomic question for pathogen and parasite biology. The Bacillus cereus group, which encompasses Bacillus thuringiensis and Bacillus anthracis, contains pathogens that can infect insects, nematodes, and vertebrates. Since the target range of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Zheng, Jinshui, Gao, Qiuling, Liu, Linlin, Liu, Hualin, Wang, Yueying, Peng, Donghai, Ruan, Lifang, Raymond, Ben, Sun, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550751/
https://www.ncbi.nlm.nih.gov/pubmed/28790205
http://dx.doi.org/10.1128/mBio.00822-17
_version_ 1783256177901043712
author Zheng, Jinshui
Gao, Qiuling
Liu, Linlin
Liu, Hualin
Wang, Yueying
Peng, Donghai
Ruan, Lifang
Raymond, Ben
Sun, Ming
author_facet Zheng, Jinshui
Gao, Qiuling
Liu, Linlin
Liu, Hualin
Wang, Yueying
Peng, Donghai
Ruan, Lifang
Raymond, Ben
Sun, Ming
author_sort Zheng, Jinshui
collection PubMed
description Understanding the genetic basis of host shifts is a key genomic question for pathogen and parasite biology. The Bacillus cereus group, which encompasses Bacillus thuringiensis and Bacillus anthracis, contains pathogens that can infect insects, nematodes, and vertebrates. Since the target range of the essential virulence factors (Cry toxins) and many isolates is well known, this group presents a powerful system for investigating how pathogens can diversify and adapt to phylogenetically distant hosts. Specialization to exploit insects occurs at the level of the major clade and is associated with substantial changes in the core genome, and host switching between insect orders has occurred repeatedly within subclades. The transfer of plasmids with linked cry genes may account for much of the adaptation to particular insect orders, and network analysis implies that host specialization has produced strong associations between key toxin genes with similar targets. Analysis of the distribution of plasmid minireplicons shows that plasmids with orf156 and orf157, which carry genes encoding toxins against Lepidoptera or Diptera, were contained only by B. thuringiensis in the specialized insect clade (clade 2), indicating that tight genome/plasmid associations have been important in adaptation to invertebrate hosts. Moreover, the accumulation of multiple virulence factors on transposable elements suggests that cotransfer of diverse virulence factors is advantageous in terms of expanding the insecticidal spectrum, overcoming insect resistance, or through gains in pathogenicity via synergistic interactions between toxins.
format Online
Article
Text
id pubmed-5550751
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-55507512017-08-14 Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts Zheng, Jinshui Gao, Qiuling Liu, Linlin Liu, Hualin Wang, Yueying Peng, Donghai Ruan, Lifang Raymond, Ben Sun, Ming mBio Research Article Understanding the genetic basis of host shifts is a key genomic question for pathogen and parasite biology. The Bacillus cereus group, which encompasses Bacillus thuringiensis and Bacillus anthracis, contains pathogens that can infect insects, nematodes, and vertebrates. Since the target range of the essential virulence factors (Cry toxins) and many isolates is well known, this group presents a powerful system for investigating how pathogens can diversify and adapt to phylogenetically distant hosts. Specialization to exploit insects occurs at the level of the major clade and is associated with substantial changes in the core genome, and host switching between insect orders has occurred repeatedly within subclades. The transfer of plasmids with linked cry genes may account for much of the adaptation to particular insect orders, and network analysis implies that host specialization has produced strong associations between key toxin genes with similar targets. Analysis of the distribution of plasmid minireplicons shows that plasmids with orf156 and orf157, which carry genes encoding toxins against Lepidoptera or Diptera, were contained only by B. thuringiensis in the specialized insect clade (clade 2), indicating that tight genome/plasmid associations have been important in adaptation to invertebrate hosts. Moreover, the accumulation of multiple virulence factors on transposable elements suggests that cotransfer of diverse virulence factors is advantageous in terms of expanding the insecticidal spectrum, overcoming insect resistance, or through gains in pathogenicity via synergistic interactions between toxins. American Society for Microbiology 2017-08-08 /pmc/articles/PMC5550751/ /pubmed/28790205 http://dx.doi.org/10.1128/mBio.00822-17 Text en Copyright © 2017 Zheng et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Zheng, Jinshui
Gao, Qiuling
Liu, Linlin
Liu, Hualin
Wang, Yueying
Peng, Donghai
Ruan, Lifang
Raymond, Ben
Sun, Ming
Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title_full Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title_fullStr Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title_full_unstemmed Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title_short Comparative Genomics of Bacillus thuringiensis Reveals a Path to Specialized Exploitation of Multiple Invertebrate Hosts
title_sort comparative genomics of bacillus thuringiensis reveals a path to specialized exploitation of multiple invertebrate hosts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550751/
https://www.ncbi.nlm.nih.gov/pubmed/28790205
http://dx.doi.org/10.1128/mBio.00822-17
work_keys_str_mv AT zhengjinshui comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT gaoqiuling comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT liulinlin comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT liuhualin comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT wangyueying comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT pengdonghai comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT ruanlifang comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT raymondben comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts
AT sunming comparativegenomicsofbacillusthuringiensisrevealsapathtospecializedexploitationofmultipleinvertebratehosts