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Finished genome of the fungal wheat pathogen Mycosphaerella graminicola reveals dispensome structure, chromosome plasticity, and stealth pathogenesis.

Authors :
Stephen B Goodwin
Sarrah Ben M'barek
Braham Dhillon
Alexander H J Wittenberg
Charles F Crane
James K Hane
Andrew J Foster
Theo A J Van der Lee
Jane Grimwood
Andrea Aerts
John Antoniw
Andy Bailey
Burt Bluhm
Judith Bowler
Jim Bristow
Ate van der Burgt
Blondy Canto-Canché
Alice C L Churchill
Laura Conde-Ferràez
Hans J Cools
Pedro M Coutinho
Michael Csukai
Paramvir Dehal
Pierre De Wit
Bruno Donzelli
Henri C van de Geest
Roeland C H J van Ham
Kim E Hammond-Kosack
Bernard Henrissat
Andrzej Kilian
Adilson K Kobayashi
Edda Koopmann
Yiannis Kourmpetis
Arnold Kuzniar
Erika Lindquist
Vincent Lombard
Chris Maliepaard
Natalia Martins
Rahim Mehrabi
Jan P H Nap
Alisa Ponomarenko
Jason J Rudd
Asaf Salamov
Jeremy Schmutz
Henk J Schouten
Harris Shapiro
Ioannis Stergiopoulos
Stefano F F Torriani
Hank Tu
Ronald P de Vries
Cees Waalwijk
Sarah B Ware
Ad Wiebenga
Lute-Harm Zwiers
Richard P Oliver
Igor V Grigoriev
Gert H J Kema
Source :
PLoS Genetics, Vol 7, Iss 6, p e1002070 (2011)
Publication Year :
2011
Publisher :
Public Library of Science (PLoS), 2011.

Abstract

The plant-pathogenic fungus Mycosphaerella graminicola (asexual stage: Septoria tritici) causes septoria tritici blotch, a disease that greatly reduces the yield and quality of wheat. This disease is economically important in most wheat-growing areas worldwide and threatens global food production. Control of the disease has been hampered by a limited understanding of the genetic and biochemical bases of pathogenicity, including mechanisms of infection and of resistance in the host. Unlike most other plant pathogens, M. graminicola has a long latent period during which it evades host defenses. Although this type of stealth pathogenicity occurs commonly in Mycosphaerella and other Dothideomycetes, the largest class of plant-pathogenic fungi, its genetic basis is not known. To address this problem, the genome of M. graminicola was sequenced completely. The finished genome contains 21 chromosomes, eight of which could be lost with no visible effect on the fungus and thus are dispensable. This eight-chromosome dispensome is dynamic in field and progeny isolates, is different from the core genome in gene and repeat content, and appears to have originated by ancient horizontal transfer from an unknown donor. Synteny plots of the M. graminicola chromosomes versus those of the only other sequenced Dothideomycete, Stagonospora nodorum, revealed conservation of gene content but not order or orientation, suggesting a high rate of intra-chromosomal rearrangement in one or both species. This observed "mesosynteny" is very different from synteny seen between other organisms. A surprising feature of the M. graminicola genome compared to other sequenced plant pathogens was that it contained very few genes for enzymes that break down plant cell walls, which was more similar to endophytes than to pathogens. The stealth pathogenesis of M. graminicola probably involves degradation of proteins rather than carbohydrates to evade host defenses during the biotrophic stage of infection and may have evolved from endophytic ancestors.

Subjects

Subjects :
Genetics
QH426-470

Details

Language :
English
ISSN :
15537390 and 15537404
Volume :
7
Issue :
6
Database :
Directory of Open Access Journals
Journal :
PLoS Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.810b8a63930e4e278d2fbf622f1808d3
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pgen.1002070