Cargando…

The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans

The soil bacterium Bacillus thuringiensis is a pathogen of insects and nematodes and is very closely related to, if not the same species as, Bacillus cereus and Bacillus anthracis. The defining characteristic of B. thuringiensis that sets it apart from B. cereus and B. anthracis is the production of...

Descripción completa

Detalles Bibliográficos
Autores principales: Kho, Melanie F., Bellier, Audrey, Balasubramani, Venkatasamy, Hu, Yan, Hsu, Wayne, Nielsen-LeRoux, Christina, McGillivray, Shauna M., Nizet, Victor, Aroian, Raffi V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245237/
https://www.ncbi.nlm.nih.gov/pubmed/22216181
http://dx.doi.org/10.1371/journal.pone.0029122
_version_ 1782219826919374848
author Kho, Melanie F.
Bellier, Audrey
Balasubramani, Venkatasamy
Hu, Yan
Hsu, Wayne
Nielsen-LeRoux, Christina
McGillivray, Shauna M.
Nizet, Victor
Aroian, Raffi V.
author_facet Kho, Melanie F.
Bellier, Audrey
Balasubramani, Venkatasamy
Hu, Yan
Hsu, Wayne
Nielsen-LeRoux, Christina
McGillivray, Shauna M.
Nizet, Victor
Aroian, Raffi V.
author_sort Kho, Melanie F.
collection PubMed
description The soil bacterium Bacillus thuringiensis is a pathogen of insects and nematodes and is very closely related to, if not the same species as, Bacillus cereus and Bacillus anthracis. The defining characteristic of B. thuringiensis that sets it apart from B. cereus and B. anthracis is the production of crystal (Cry) proteins, which are pore-forming toxins or pore-forming proteins (PFPs). Although it is known that PFPs are important virulence factors since their elimination results in reduced virulence of many pathogenic bacteria, the functions by which PFPs promote virulence are incompletely understood. Here we study the effect of Cry proteins in B. thuringiensis pathogenesis of the nematode Caenorhabditis elegans. We find that whereas B. thuringiensis on its own is not able to infect C. elegans, the addition of the PFP Cry protein, Cry5B, results in a robust lethal infection that consumes the nematode host in 1–2 days, leading to a “Bob” or bag-of-bacteria phenotype. Unlike other infections of C. elegans characterized to date, the infection by B. thuringiensis shows dose-dependency based on bacterial inoculum size and based on PFP concentration. Although the infection process takes 1–2 days, the PFP-instigated infection process is irreversibly established within 15 minutes of initial exposure. Remarkably, treatment of C. elegans with Cry5B PFP is able to instigate many other Bacillus species, including B. anthracis and even “non-pathogenic” Bacillus subtilis, to become lethal and infectious agents to C. elegans. Co-culturing of Cry5B-expressing B. thuringiensis with B. anthracis can result in lethal infection of C. elegans by B. anthracis. Our data demonstrate that one potential property of PFPs is to sensitize the host to bacterial infection and further that C. elegans and probably other roundworms can be common hosts for B. cereus-group bacteria, findings with important ecological and research implications.
format Online
Article
Text
id pubmed-3245237
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32452372012-01-03 The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans Kho, Melanie F. Bellier, Audrey Balasubramani, Venkatasamy Hu, Yan Hsu, Wayne Nielsen-LeRoux, Christina McGillivray, Shauna M. Nizet, Victor Aroian, Raffi V. PLoS One Research Article The soil bacterium Bacillus thuringiensis is a pathogen of insects and nematodes and is very closely related to, if not the same species as, Bacillus cereus and Bacillus anthracis. The defining characteristic of B. thuringiensis that sets it apart from B. cereus and B. anthracis is the production of crystal (Cry) proteins, which are pore-forming toxins or pore-forming proteins (PFPs). Although it is known that PFPs are important virulence factors since their elimination results in reduced virulence of many pathogenic bacteria, the functions by which PFPs promote virulence are incompletely understood. Here we study the effect of Cry proteins in B. thuringiensis pathogenesis of the nematode Caenorhabditis elegans. We find that whereas B. thuringiensis on its own is not able to infect C. elegans, the addition of the PFP Cry protein, Cry5B, results in a robust lethal infection that consumes the nematode host in 1–2 days, leading to a “Bob” or bag-of-bacteria phenotype. Unlike other infections of C. elegans characterized to date, the infection by B. thuringiensis shows dose-dependency based on bacterial inoculum size and based on PFP concentration. Although the infection process takes 1–2 days, the PFP-instigated infection process is irreversibly established within 15 minutes of initial exposure. Remarkably, treatment of C. elegans with Cry5B PFP is able to instigate many other Bacillus species, including B. anthracis and even “non-pathogenic” Bacillus subtilis, to become lethal and infectious agents to C. elegans. Co-culturing of Cry5B-expressing B. thuringiensis with B. anthracis can result in lethal infection of C. elegans by B. anthracis. Our data demonstrate that one potential property of PFPs is to sensitize the host to bacterial infection and further that C. elegans and probably other roundworms can be common hosts for B. cereus-group bacteria, findings with important ecological and research implications. Public Library of Science 2011-12-22 /pmc/articles/PMC3245237/ /pubmed/22216181 http://dx.doi.org/10.1371/journal.pone.0029122 Text en Kho 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kho, Melanie F.
Bellier, Audrey
Balasubramani, Venkatasamy
Hu, Yan
Hsu, Wayne
Nielsen-LeRoux, Christina
McGillivray, Shauna M.
Nizet, Victor
Aroian, Raffi V.
The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title_full The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title_fullStr The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title_full_unstemmed The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title_short The Pore-Forming Protein Cry5B Elicits the Pathogenicity of Bacillus sp. against Caenorhabditis elegans
title_sort pore-forming protein cry5b elicits the pathogenicity of bacillus sp. against caenorhabditis elegans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245237/
https://www.ncbi.nlm.nih.gov/pubmed/22216181
http://dx.doi.org/10.1371/journal.pone.0029122
work_keys_str_mv AT khomelanief theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT bellieraudrey theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT balasubramanivenkatasamy theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT huyan theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT hsuwayne theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT nielsenlerouxchristina theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT mcgillivrayshaunam theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT nizetvictor theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT aroianraffiv theporeformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT khomelanief poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT bellieraudrey poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT balasubramanivenkatasamy poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT huyan poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT hsuwayne poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT nielsenlerouxchristina poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT mcgillivrayshaunam poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT nizetvictor poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans
AT aroianraffiv poreformingproteincry5belicitsthepathogenicityofbacillusspagainstcaenorhabditiselegans