Cargando…
Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection
Necrotrophic fungi are unable to occupy living plant cells. How such pathogens survive first contact with living host tissue and initiate infection is therefore unclear. Here, we show that the necrotrophic grey mold fungus Botrytis cinerea undergoes massive apoptotic-like programmed cell death (PCD)...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158046/ https://www.ncbi.nlm.nih.gov/pubmed/21876671 http://dx.doi.org/10.1371/journal.ppat.1002185 |
_version_ | 1782210349993295872 |
---|---|
author | Shlezinger, Neta Minz, Anna Gur, Yonatan Hatam, Ido Dagdas, Yasin F. Talbot, Nicholas J. Sharon, Amir |
author_facet | Shlezinger, Neta Minz, Anna Gur, Yonatan Hatam, Ido Dagdas, Yasin F. Talbot, Nicholas J. Sharon, Amir |
author_sort | Shlezinger, Neta |
collection | PubMed |
description | Necrotrophic fungi are unable to occupy living plant cells. How such pathogens survive first contact with living host tissue and initiate infection is therefore unclear. Here, we show that the necrotrophic grey mold fungus Botrytis cinerea undergoes massive apoptotic-like programmed cell death (PCD) following germination on the host plant. Manipulation of an anti-apoptotic gene BcBIR1 modified fungal response to PCD-inducing conditions. As a consequence, strains with reduced sensitivity to PCD were hyper virulent, while strains in which PCD was over-stimulated showed reduced pathogenicity. Similarly, reduced levels of PCD in the fungus were recorded following infection of Arabidopsis mutants that show enhanced susceptibility to B. cinerea. When considered together, these results suggest that Botrytis PCD machinery is targeted by plant defense molecules, and that the fungal anti-apoptotic machinery is essential for overcoming this host-induced PCD and hence, for establishment of infection. As such, fungal PCD machinery represents a novel target for fungicides and antifungal drugs. |
format | Online Article Text |
id | pubmed-3158046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31580462011-08-29 Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection Shlezinger, Neta Minz, Anna Gur, Yonatan Hatam, Ido Dagdas, Yasin F. Talbot, Nicholas J. Sharon, Amir PLoS Pathog Research Article Necrotrophic fungi are unable to occupy living plant cells. How such pathogens survive first contact with living host tissue and initiate infection is therefore unclear. Here, we show that the necrotrophic grey mold fungus Botrytis cinerea undergoes massive apoptotic-like programmed cell death (PCD) following germination on the host plant. Manipulation of an anti-apoptotic gene BcBIR1 modified fungal response to PCD-inducing conditions. As a consequence, strains with reduced sensitivity to PCD were hyper virulent, while strains in which PCD was over-stimulated showed reduced pathogenicity. Similarly, reduced levels of PCD in the fungus were recorded following infection of Arabidopsis mutants that show enhanced susceptibility to B. cinerea. When considered together, these results suggest that Botrytis PCD machinery is targeted by plant defense molecules, and that the fungal anti-apoptotic machinery is essential for overcoming this host-induced PCD and hence, for establishment of infection. As such, fungal PCD machinery represents a novel target for fungicides and antifungal drugs. Public Library of Science 2011-08-18 /pmc/articles/PMC3158046/ /pubmed/21876671 http://dx.doi.org/10.1371/journal.ppat.1002185 Text en Shlezinger 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 Shlezinger, Neta Minz, Anna Gur, Yonatan Hatam, Ido Dagdas, Yasin F. Talbot, Nicholas J. Sharon, Amir Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title | Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title_full | Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title_fullStr | Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title_full_unstemmed | Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title_short | Anti-Apoptotic Machinery Protects the Necrotrophic Fungus Botrytis cinerea from Host-Induced Apoptotic-Like Cell Death during Plant Infection |
title_sort | anti-apoptotic machinery protects the necrotrophic fungus botrytis cinerea from host-induced apoptotic-like cell death during plant infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3158046/ https://www.ncbi.nlm.nih.gov/pubmed/21876671 http://dx.doi.org/10.1371/journal.ppat.1002185 |
work_keys_str_mv | AT shlezingerneta antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT minzanna antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT guryonatan antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT hatamido antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT dagdasyasinf antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT talbotnicholasj antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection AT sharonamir antiapoptoticmachineryprotectsthenecrotrophicfungusbotrytiscinereafromhostinducedapoptoticlikecelldeathduringplantinfection |