Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.

It has been hypothesized that horizontal gene/chromosome transfer and parasexual recombination following hyphal fusion between different strains may contribute to the emergence of wide genetic variability in plant pathogenic and other fungi. However, the significance of vegetative (heterokaryon) inc...

Full description

Bibliographic Details
Main Authors: Francine H Ishikawa, Elaine A Souza, Jun-Ya Shoji, Lanelle Connolly, Michael Freitag, Nick D Read, M Gabriela Roca
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3271119?pdf=render
id doaj-a84aa67d75d64f61bf164adf69b7edf6
record_format Article
spelling doaj-a84aa67d75d64f61bf164adf69b7edf62020-11-25T01:46:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0172e3117510.1371/journal.pone.0031175Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.Francine H IshikawaElaine A SouzaJun-Ya ShojiLanelle ConnollyMichael FreitagNick D ReadM Gabriela RocaIt has been hypothesized that horizontal gene/chromosome transfer and parasexual recombination following hyphal fusion between different strains may contribute to the emergence of wide genetic variability in plant pathogenic and other fungi. However, the significance of vegetative (heterokaryon) incompatibility responses, which commonly result in cell death, in preventing these processes is not known. In this study, we have assessed this issue following different types of hyphal fusion during colony initiation and in the mature colony. We used vegetatively compatible and incompatible strains of the common bean pathogen Colletotrichum lindemuthianum in which nuclei were labelled with either a green or red fluorescent protein in order to microscopically monitor the fates of nuclei and heterokaryotic cells following hyphal fusion. As opposed to fusion of hyphae in mature colonies that resulted in cell death within 3 h, fusions by conidial anastomosis tubes (CAT) between two incompatible strains during colony initiation did not induce the vegetative incompatibility response. Instead, fused conidia and germlings survived and formed heterokaryotic colonies that in turn produced uninucleate conidia that germinated to form colonies with phenotypic features different to those of either parental strain. Our results demonstrate that the vegetative incompatibility response is suppressed during colony initiation in C. lindemuthianum. Thus, CAT fusion may allow asexual fungi to increase their genetic diversity, and to acquire new pathogenic traits.http://europepmc.org/articles/PMC3271119?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Francine H Ishikawa
Elaine A Souza
Jun-Ya Shoji
Lanelle Connolly
Michael Freitag
Nick D Read
M Gabriela Roca
spellingShingle Francine H Ishikawa
Elaine A Souza
Jun-Ya Shoji
Lanelle Connolly
Michael Freitag
Nick D Read
M Gabriela Roca
Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
PLoS ONE
author_facet Francine H Ishikawa
Elaine A Souza
Jun-Ya Shoji
Lanelle Connolly
Michael Freitag
Nick D Read
M Gabriela Roca
author_sort Francine H Ishikawa
title Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
title_short Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
title_full Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
title_fullStr Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
title_full_unstemmed Heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
title_sort heterokaryon incompatibility is suppressed following conidial anastomosis tube fusion in a fungal plant pathogen.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description It has been hypothesized that horizontal gene/chromosome transfer and parasexual recombination following hyphal fusion between different strains may contribute to the emergence of wide genetic variability in plant pathogenic and other fungi. However, the significance of vegetative (heterokaryon) incompatibility responses, which commonly result in cell death, in preventing these processes is not known. In this study, we have assessed this issue following different types of hyphal fusion during colony initiation and in the mature colony. We used vegetatively compatible and incompatible strains of the common bean pathogen Colletotrichum lindemuthianum in which nuclei were labelled with either a green or red fluorescent protein in order to microscopically monitor the fates of nuclei and heterokaryotic cells following hyphal fusion. As opposed to fusion of hyphae in mature colonies that resulted in cell death within 3 h, fusions by conidial anastomosis tubes (CAT) between two incompatible strains during colony initiation did not induce the vegetative incompatibility response. Instead, fused conidia and germlings survived and formed heterokaryotic colonies that in turn produced uninucleate conidia that germinated to form colonies with phenotypic features different to those of either parental strain. Our results demonstrate that the vegetative incompatibility response is suppressed during colony initiation in C. lindemuthianum. Thus, CAT fusion may allow asexual fungi to increase their genetic diversity, and to acquire new pathogenic traits.
url http://europepmc.org/articles/PMC3271119?pdf=render
work_keys_str_mv AT francinehishikawa heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT elaineasouza heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT junyashoji heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT lanelleconnolly heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT michaelfreitag heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT nickdread heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
AT mgabrielaroca heterokaryonincompatibilityissuppressedfollowingconidialanastomosistubefusioninafungalplantpathogen
_version_ 1725019289793069056