Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.

<h4>Background</h4>The rice blast fungus Magnaporthe oryzae elaborates a specialized infection structure called an appressorium to breach the rice leaf surface and gain access to plant tissue. Appressorium development is controlled by cell cycle progression, and a single round of nuclear...

Full description

Saved in:
Bibliographic Details
Main Authors: Min He, Michael J Kershaw, Darren M Soanes, Yuxian Xia, Nicholas J Talbot
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033270&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850119766674505728
author Min He
Michael J Kershaw
Darren M Soanes
Yuxian Xia
Nicholas J Talbot
author_facet Min He
Michael J Kershaw
Darren M Soanes
Yuxian Xia
Nicholas J Talbot
author_sort Min He
collection DOAJ
description <h4>Background</h4>The rice blast fungus Magnaporthe oryzae elaborates a specialized infection structure called an appressorium to breach the rice leaf surface and gain access to plant tissue. Appressorium development is controlled by cell cycle progression, and a single round of nuclear division occurs prior to appressorium formation. Mitosis is always followed by programmed cell death of the spore from which the appressorium develops. Nuclear degeneration in the spore is known to be essential for plant infection, but the precise mechanism by which it occurs is not known.<h4>Methodology/principal findings</h4>In yeast, nuclear breakdown requires a specific form of autophagy, known as piecemeal microautophagy of the nucleus (PMN), and we therefore investigated whether this process occurs in the rice blast fungus. Here, we report that M. oryzae possesses two conserved components of a putative PMN pathway, MoVac8 and MoTsc13, but that both are dispensable for nuclear breakdown during plant infection. MoVAC8 encodes a vacuolar membrane protein and MoTSC13 a peri-nuclear and peripheral ER protein.<h4>Conclusions/significance</h4>We show that MoVAC8 is necessary for caffeine resistance, but dispensable for pathogenicity of M. oryzae, while MoTSC13 is involved in cell wall stress responses and is an important virulence determinant. By functional analysis of ΔMoatg1 and ΔMoatg4 mutants, we demonstrate that infection-associated nuclear degeneration in M. oryzae instead occurs by non-selective macroautophagy, which is necessary for rice blast disease.
format Article
id doaj-art-2b3b24f2e36f4d52858cf4efeddbe38e
institution OA Journals
issn 1932-6203
language English
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-2b3b24f2e36f4d52858cf4efeddbe38e2025-08-20T02:35:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3327010.1371/journal.pone.0033270Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.Min HeMichael J KershawDarren M SoanesYuxian XiaNicholas J Talbot<h4>Background</h4>The rice blast fungus Magnaporthe oryzae elaborates a specialized infection structure called an appressorium to breach the rice leaf surface and gain access to plant tissue. Appressorium development is controlled by cell cycle progression, and a single round of nuclear division occurs prior to appressorium formation. Mitosis is always followed by programmed cell death of the spore from which the appressorium develops. Nuclear degeneration in the spore is known to be essential for plant infection, but the precise mechanism by which it occurs is not known.<h4>Methodology/principal findings</h4>In yeast, nuclear breakdown requires a specific form of autophagy, known as piecemeal microautophagy of the nucleus (PMN), and we therefore investigated whether this process occurs in the rice blast fungus. Here, we report that M. oryzae possesses two conserved components of a putative PMN pathway, MoVac8 and MoTsc13, but that both are dispensable for nuclear breakdown during plant infection. MoVAC8 encodes a vacuolar membrane protein and MoTSC13 a peri-nuclear and peripheral ER protein.<h4>Conclusions/significance</h4>We show that MoVAC8 is necessary for caffeine resistance, but dispensable for pathogenicity of M. oryzae, while MoTSC13 is involved in cell wall stress responses and is an important virulence determinant. By functional analysis of ΔMoatg1 and ΔMoatg4 mutants, we demonstrate that infection-associated nuclear degeneration in M. oryzae instead occurs by non-selective macroautophagy, which is necessary for rice blast disease.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033270&type=printable
spellingShingle Min He
Michael J Kershaw
Darren M Soanes
Yuxian Xia
Nicholas J Talbot
Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
PLoS ONE
title Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
title_full Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
title_fullStr Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
title_full_unstemmed Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
title_short Infection-associated nuclear degeneration in the rice blast fungus Magnaporthe oryzae requires non-selective macro-autophagy.
title_sort infection associated nuclear degeneration in the rice blast fungus magnaporthe oryzae requires non selective macro autophagy
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0033270&type=printable
work_keys_str_mv AT minhe infectionassociatednucleardegenerationinthericeblastfungusmagnaportheoryzaerequiresnonselectivemacroautophagy
AT michaeljkershaw infectionassociatednucleardegenerationinthericeblastfungusmagnaportheoryzaerequiresnonselectivemacroautophagy
AT darrenmsoanes infectionassociatednucleardegenerationinthericeblastfungusmagnaportheoryzaerequiresnonselectivemacroautophagy
AT yuxianxia infectionassociatednucleardegenerationinthericeblastfungusmagnaportheoryzaerequiresnonselectivemacroautophagy
AT nicholasjtalbot infectionassociatednucleardegenerationinthericeblastfungusmagnaportheoryzaerequiresnonselectivemacroautophagy