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Accueil Tous les numéros Volume 207 / Numéro 4 (2013) Biologie Aujourd'hui, 207 4 (2013) 277-290 Références
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Numéro
Biologie Aujourd'hui
Volume 207, Numéro 4, 2013
Page(s) 277 - 290
DOI https://doi.org/10.1051/jbio/2013026
Publié en ligne 5 mars 2014
  • Anderson P.K., Cunningham A.A., Patel N.G., Morales F.J., Epstein P.R., Daszak P., Emerging infectious diseases of plants: pathogen pollution, climate change and agrotechnology drivers. Trends Evol Ecol, 2004, 19, 535–544. [Google Scholar]
  • Biffen R.H., The inheritance of sterility in the barleys. J Agric Sci, 1905, 1, 250–257. [CrossRef] [Google Scholar]
  • Blaise F., Rémy E., Meyer M., Zhou L., Narcy J.P., Roux J., Balesdent M.H., Rouxel T., A critical assessment of Agrobacterium tumefaciens-mediated transformation as a tool for pathogenicity gene discovery in the phytopathogenic fungus Leptosphaeria maculans. Fungal Genet Biol, 2007, 44, 123–138. [CrossRef] [PubMed] [Google Scholar]
  • Chuma I., Isobe C., Hotta Y., Ibaragi K., Futamata N., Kusaba M., Yoshida K., Terauchi R., Fujita Y., Nakayashiki H., Valent B., Tosa Y., Multiple translocation of the AVR-Pita effector gene among chromosomes of the rice blast fungus Magnaporthe oryzae and related species. PloS Pathog, 2011, 7, e1002147. [CrossRef] [PubMed] [Google Scholar]
  • Condon B.J., Leng Y., Wu D., Bushley K.E., Ohm R.A., Otillar R., Martin J., Schackwitz W., Grimwood J., MohdZainudin N., Xue C., Wang R., Manning V.A., Dhillon B., Tu Z.J., Steffenson B.J., Salamov A., Sun H., Lowry S., LaButti K., Han J., Copeland A., Lindquist E., Barry K., Schmutz J., Baker S.E., Ciuffetti L.M., Grigoriev I.V., Zhong S., Turgeon B.G., Comparative genome structure, secondary metabolite, and effector coding capacity across Cochliobolus pathogens. PloS Genet, 2013, 9, e1003233. [CrossRef] [PubMed] [Google Scholar]
  • Cuomo C.A., Güldener U., Xu J.R., Trail F., Turgeon B.G., Di Pietro A., Walton J.D., Ma L.J., Baker S.E., Rep M., Adam G., Antoniw J., Baldwin T., Calvo S., Chang Y.L., Decaprio D., Gale L.R., Gnerre S., Goswami R.S., Hammond-Kosack K., Harris L.J., Hilburn K., Kennell J.C., Kroken S., Magnuson J.K., Mannhaupt G., Mauceli E., Mewes H.W., Mitterbauer R., Muehlbauer G., Münsterkötter M., Nelson D., O’Donnell K., Ouellet T., Qi W., Quesneville H., Roncero M.I., Seong K.Y., Tetko I.V., Urban M., Waalwijk C., Ward T.J., Yao J., Birren B.W., Kistler H.C., The Fusarium graminearum genome reveals a link between localized polymorphism and pathogen specialization. Science, 2007, 317, 1400–1402. [CrossRef] [PubMed] [Google Scholar]
  • Daverdin G., Rouxel T., Gout L., Aubertot J.N., Fudal I., Meyer M., Parlange F., Carpezat J., Balesdent M.H., Genome structure and reproductive behaviour influence the evolutionary potential of a fungal phytopathogen. PloS Pathog, 2012, 8, e1003020. [CrossRef] [PubMed] [Google Scholar]
  • Dean R.A., Talbot N.J., Ebbole D.J., Farman M.L., Mitchell T.K., Orbach M.J., Thon M., Kulkarni R., Xu J.R., Pan H., Read N.D., Lee Y.H., Carbone I., Brown D., Oh Y.Y., Donofrio N., Jeong J.S., Soanes D.M., Djonovic S., Kolomiets E., Rehmeyer C., Li W., Harding M., Kim S., Lebrun M.H., Bohnert H., Coughlan S., Butler J., Calvo S., Ma L.J., Nicol R., Purcell S., Nusbaum C., Galagan J.E., Birren B.W., The genome sequence of the rice blast fungus Magnaporthe grisea. Nature, 2005, 434, 980–986. [CrossRef] [PubMed] [Google Scholar]
  • De Jonge R., Bolton M.D., Kombrink A., van den Berg G.C., Yadeta K.A., Thomma B.P., Extensive chromosomal reshuffling drives evolution of virulence in an asexual pathogen. Genome Res, 2013, 23, doi:10.1101/gr.152660.112. [PubMed] [Google Scholar]
  • De Wit P.J., van der Burgt A., Ökmen B., Stergiopoulos I., Abd-Elsalam K.A., Aerts A.L., Bahkali A.H., Beenen H.G., Chettri P., Cox M.P., Datema E., de Vries R.P., Dhillon B., Ganley A.R., Griffiths S.A., Guo Y., Hamelin R.C., Henrissat B., Kabir M.S., Jashni M.K., Kema G., Klaubauf S., Lapidus A., Levasseur A., Lindquist E., Mehrabi R., Ohm R.A., Owen T.J., Salamov A., Schwelm A., Schijlen E., Sun H., van den Burg H.A., van Ham R.C., Zhang S., Goodwin S.B., Grigoriev I.V., Collemare J., Bradshaw R.E., The genomes of the fungal plant pathogens Cladosporium fulvum and Dothistroma septosporum reveal adaptation to different hosts and lifestyles but also signatures of common ancestry. PloS Genet, 2012, 8, e1003088. [CrossRef] [PubMed] [Google Scholar]
  • Duplessis S., Cuomo C.A., Lin Y.C., Aerts A., Tisserant E., Veneault-Fourrey C., Joly D.L., Hacquard S., Amselem J., Cantarel B.L., Chiu R., Coutinho P.M., Feau N., Field M., Frey P., Gelhaye E., Goldberg J., Grabherr M.G., Kodira C.D., Kohler A., Kües U., Lindquist E.A., Lucas S.M., Mago R., Mauceli E., Morin E., Murat C., Pangilinan J.L., Park R., Pearson M., Quesneville H., Rouhier N., Sakthikumar S., Salamov A.A., Schmutz J., Selles B., Shapiro H., Tanguay P., Tuskan G.A., Henrissat B., Van de Peer Y., Rouzé P., Ellis J.G., Dodds P.N., Schein J.E., Zhong S., Hamelin R.C., Grigoriev I.V., Szabo L.J., Martin F., Obligate biotrophy features unraveled by the genomic analysis of rust fungi. Proc Natl Acad Sci USA., 2011, 108, 9166–9171. [CrossRef] [Google Scholar]
  • Farman M.L., Telomeres in the rice blast fungus Magnaporthe oryzae: the world of the end as we know it. FEMS Microbiol Lett, 2007, 273, 125–132. [CrossRef] [PubMed] [Google Scholar]
  • Fisher M.C., Henk D.A., Briggs C.J., Brownstein J.S., Madoff L.C., McCraw S.L., Gurr S.J., Emerging fungal threats to animal, plant and ecosystem health. Nature, 2012, 484, 186–194. [CrossRef] [PubMed] [Google Scholar]
  • Fudal I., Böhnert H.U., Tharreau D., Lebrun M.H., Transposition of MINE, a composite retrotransposon, in the avirulence gene ACE1 of the rice blast fungus Magnaporthe grisea. Fungal Genet Biol, 2005, 42, 761–772. [CrossRef] [PubMed] [Google Scholar]
  • Fudal I., Ross S., Brun H., Besnard A.L., Ermel M., Kuhn M.L., Balesdent M.H., Rouxel T., Repeat-induced point mutation (RIP) as an alternative mechanism of evolution toward virulence in Leptosphaeria maculans. Mol Plant Microbe Interact, 2009, 22, 932–941. [CrossRef] [PubMed] [Google Scholar]
  • Galagan J.E., Calvo S.E., Borkovich K.A., Selker E.U., Read N.D., Jaffe D., FitzHugh W., Ma L.J., Smirnov S., Purcell S., Rehman B., Elkins T., Engels R., Wang S., Nielsen C.B., Butler J., Endrizzi M., Qui D., Ianakiev P., Bell-Pedersen D., Nelson M.A., Werner-Washburne M., Selitrennikoff C.P., Kinsey J.A., Braun E.L., Zelter A., Schulte U., Kothe G.O., Jedd G., Mewes W., Staben C., Marcotte E., Greenberg D., Roy A., Foley K., Naylor J., Stange-Thomann N., Barrett R., Gnerre S., Kamal M., Kamvysselis M., Mauceli E., Bielke C., Rudd S., Frishman D., Krystofova S., Rasmussen C., Metzenberg R.L., Perkins D.D., Kroken S., Cogoni C., Macino G., Catcheside D., Li W., Pratt R.J., Osmani S.A., DeSouza C.P., Glass L., Orbach M.J., Berglund J.A., Voelker R., Yarden O., Plamann M., Seiler S., Dunlap J., Radford A., Aramayo R., Natvig D.O., Alex L.A., Mannhaupt G., Ebbole D.J., Freitag M., Paulsen I., Sachs M.S., Lander E.S., Nusbaum C., Birren B.W., The genome sequence of the filamentous fungus Neurospora crassa. Nature, 2003, 422, 859–868. [CrossRef] [PubMed] [Google Scholar]
  • Gan P., Ikeda K., Irieda H., Narusaka M., O’Connell R.J., Narusaka Y., Takano Y., Kubo Y., Shirasu K. Comparative genomic and transcriptomic analyses reveal the hemibiotrophic stage shift of Colletotrichum fungi. New Phytol, 2013, 197, 1236–1249. [CrossRef] [PubMed] [Google Scholar]
  • Giraud T., Gladieux P., Gavrilets S., Linking the emergence of fungal plant diseases with ecological speciation. Trends Ecol Evol, 2010, 25, 387–395. [CrossRef] [PubMed] [Google Scholar]
  • Gout L., Kuhn M.L., Vincenot L., Bernard-Samain S., Cattolico L., Barbetti M., Moreno-Rico O., Balesdent M.H., Rouxel T. Genome structure impacts molecular evolution at the AvrLm1 avirulence locus of the plant pathogen Leptosphaeria maculans. Environ Microbiol, 2007, 9, 2978–2992. [CrossRef] [PubMed] [Google Scholar]
  • Haas B.J., Kamoun S., Zody M.C., Jiang R.H., Handsaker R.E., Cano L.M., Grabherr M., Kodira C.D., Raffaele S., Torto-Alalibo T., Bozkurt T.O., Ah-Fong A.M., Alvarado L., Anderson V.L., Armstrong M.R., Avrova A., Baxter L., Beynon J., Boevink P.C., Bollmann S.R., Bos J.I., Bulone V., Cai G., Cakir C., Carrington J.C., Chawner M., Conti L., Costanzo S., Ewan R., Fahlgren N., Fischbach M.A., Fugelstad J., Gilroy E.M., Gnerre S., Green P.J., Grenville-Briggs L.J., Griffith J., Grünwald N.J., Horn K., Horner N.R., Hu C.H., Huitema E., Jeong D.H., Jones A.M., Jones J.D., Jones R.W., Karlsson E.K., Kunjeti S.G., Lamour K., Liu Z., Ma L., Maclean D., Chibucos M.C., McDonald H., McWalters J., Meijer H.J., Morgan W., Morris P.F., Munro C.A., O’Neill K., Ospina-Giraldo M., Pinzón A., Pritchard L., Ramsahoye B., Ren Q., Restrepo S., Roy S., Sadanandom A., Savidor A., Schornack S., Schwartz D.C., Schumann U.D., Schwessinger B., Seyer L., Sharpe T., Silvar C., Song J., Studholme D.J., Sykes S., Thines M., van de Vondervoort P.J., Phuntumart V., Wawra S., Weide R., Win J., Young C., Zhou S., Fry W., Meyers B.C., van West P., Ristaino J., Govers F., Birch P.R., Whisson S.C., Judelson H.S., Nusbaum C., Genome sequence and analysis of the Irish potato famine pathogen Phytophthora infestans. Nature, 2009, 461, 393–398. [CrossRef] [PubMed] [Google Scholar]
  • Hacquard S., Kracher B., Maekawa T., Vernaldi S., Schulze-Lefert P., Ver Loren van Themaat E., Mosaic genome structure of the barley powdery mildew pathogen and conservation of transcriptional programs in divergent hosts. Proc Natl Acad Sci USA, 2013, 110, 2219–22828. [CrossRef] [Google Scholar]
  • Hane J.K., Lowe R.G.T., Solomon P.S., Tan K.C., Schoch C.L., Spatafora J.W., Crous P.W., Kodira C., Birren B.W., Galagan J.E., Torriani S.F.F., McDonald B.A., Oliver R.P., Dothideomycete-plant interactions illuminated by genome sequencing and EST analysis of the wheat pathogen Stagonospora nodorum. Plant Cell, 2007, 19, 3347–3368. [CrossRef] [PubMed] [Google Scholar]
  • Hane J.K., Rouxel T., Howlett B.J., Kema G.H., Goodwin S.B., Oliver R.P., A novel mode of chromosomal evolution peculiar to filamentous Ascomycete fungi. Genome Biol, 2011, 12, R45. [CrossRef] [PubMed] [Google Scholar]
  • Kämper J., Kahmann R., Bölker M., Ma L.J., Brefort T., Saville B.J., Banuett F., Kronstad J.W., Gold S.E., Müller O., Perlin M.H., Wösten H.A., de Vries R., Ruiz-Herrera J., Reynaga-Peña C.G., Snetselaar K., McCann M., Pérez-Martín J., Feldbrügge M., Basse CW., Steinberg G., Ibeas J.I., Holloman W., Guzman P., Farman M., Stajich J.E., Sentandreu R., González-Prieto J.M., Kennell J.C., Molina L., Schirawski J., Mendoza-Mendoza A., Greilinger D., Münch K., Rössel N., Scherer M., Vranes M., Ladendorf O., Vincon V., Fuchs U., Sandrock B., Meng S., Ho E.C., Cahill M.J., Boyce K.J., Klose J., Klosterman S.J., Deelstra H.J., Ortiz-Castellanos L., Li W., Sanchez-Alonso P., Schreier P.H., Häuser-Hahn I., Vaupel M., Koopmann E., Friedrich G., Voss H., Schlüter T., Margolis J., Platt D., Swimmer C., Gnirke A., Chen F., Vysotskaia V., Mannhaupt G., Güldener U., Münsterkötter M., Haase D., Oesterheld M., Mewes H.W., Mauceli E.W., DeCaprio D., Wade C.M., Butler J., Young S., Jaffe D.B., Calvo S., Nusbaum C., Galagan J., Birren B.W., Insights from the genome of the biotrophic fungal plant pathogen Ustilago maydis. Nature, 2006, 444, 97–101. [CrossRef] [PubMed] [Google Scholar]
  • Kang S., Lebrun M.H., Farrall L., Valent B., Gain of virulence caused by insertion of a Pot3 transposon in a Magnaporthe grisea avirulence gene. Mol Plant Microbe Interact, 2001, 14, 671–674. [CrossRef] [PubMed] [Google Scholar]
  • Kupferschmidt, K., Mycology Attack of the clones. Science, 2012, 337, 636–638. [CrossRef] [PubMed] [Google Scholar]
  • Ma L.J., van der Does H.C., Borkovich K.A., Coleman J.J., Daboussi M.J., Di Pietro A., Dufresne M., Freitag M., Grabherr M., Henrissat B., Houterman P.M., Kang S., Shim W.B., Woloshuk C., Xie X., Xu J.R., Antoniw J., Baker S.E., Bluhm B.H., Breakspear A., Brown D.W., Butchko R.A., Chapman S., Coulson R., Coutinho P.M., Danchin E.G., Diener A., Gale L.R., Gardiner D.M., Goff S., Hammond-Kosack K.E., Hilburn K., Hua-Van A., Jonkers W., Kazan K., Kodira C.D., Koehrsen M., Kumar L., Lee Y.H., Li L., Manners J.M., Miranda-Saavedra D., Mukherjee M., Park G., Park J., Park S.Y., Proctor R.H., Regev A., Ruiz-Roldan M.C., Sain D., Sakthikumar S., Sykes S., Schwartz D.C., Turgeon B.G., Wapinski I., Yoder O., Young S., Zeng Q., Zhou S., Galagan J., Cuomo C.A., Kistler H.C., Rep M., Comparative genomics reveals mobile pathogenicity chromosomes in Fusarium. Nature, 2010, 464, 367–373. [CrossRef] [PubMed] [Google Scholar]
  • Machida M., Asai K., Sano M., Tanaka T., Kumagai T., Terai G., Kusumoto K., Arima T., Akita O., Kashiwagi Y., Abe K., Gomi K., Horiuchi H., Kitamoto K., Kobayashi T., Takeuchi M., Denning D.W., Galagan J.E., Nierman W.C., Yu J., Archer D.B., Bennett J.W., Bhatnagar D., Cleveland T.E., Fedorova N.D., Gotoh O., Horikawa H., Hosoyama A., Ichinomiya M., Igarashi R., Iwashita K., Juvvadi P.R., Kato M., Kato Y., Kin T., Kokubun A., Maeda H., Maeyama N., Maruyama J., Nagasaki H., Nakajima T., Oda K., Okada K., Paulsen I., Sakamoto K., Sawano T., Takahashi M., Takase K., Terabayashi Y., Wortman J.R., Yamada O., Yamagata Y., Anazawa H., Hata Y., Koide Y., Komori T., Koyama Y., Minetoki T., Suharnan S., Tanaka A., Isono K., Kuhara S., Ogasawara N., Kikuchi H., Genome sequencing and analysis of Aspergillus oryzae. Nature, 2005, 438, 1157–1161. [Google Scholar]
  • Manning V.A., Pandelova I., Dhillon B., Wilhelm L.J., Goodwin S.B., Berlin A.M., Figueroa M., Freitag M., Hane J.K., Henrissat B., Holman W.H., Kodira C.D., Martin J., Oliver R.P., Robbertse B., Schackwitz W., Schwartz D.C., Spatafora J.W., Turgeon B.G., Yandava C., Young S., Zhou S., Zeng Q., Grigoriev I.V., Ma L.J., Ciuffetti L.M., Comparative genomics of a plant-pathogenic fungus, Pyrenophora tritici-repentis, reveals transduplication and the impact of repeat elements on pathogenicity and population divergence. G3, 2013, 3, 41–63. [CrossRef] [Google Scholar]
  • McDonald B.A., Linde C., Pathogen population genetics, evolutionary potential and durable resistance. Annu Rev Phytopathol, 2002, 40, 349–379. [CrossRef] [PubMed] [Google Scholar]
  • Mendes-Pereira E., Balesdent M.H., Brun H., Rouxel T., Molecular phylogeny of the Leptosphaeria maculans-L. biglobosa species complex. Mycol Res, 2003, 107, 1287–1304. [CrossRef] [PubMed] [Google Scholar]
  • Ohm R.A., Feau N., Henrissat B., Schoch C.L., Horwitz B.A., Barry K.W., Condon B.J., Copeland A.C., Dhillon B., Glaser F., Hesse C.N., Kosti I., LaButti K., Lindquist E.A., Lucas S., Salamov A.A., Bradshaw R.E., Ciuffetti L., Hamelin R.C., Kema G.H., Lawrence C., Scott J.A., Spatafora J.W., Turgeon B.G., de Wit P.J., Zhong S., Goodwin S.B., Grigoriev I.V., Diverse lifestyles and strategies of plant pathogenesis encoded in the genomes of eighteen Dothideomycetes fungi. PloS Pathog, 2012, 8, e1003037. [CrossRef] [PubMed] [Google Scholar]
  • Olsen L.A., Choffnes E.R., Relman D.A., Pray L., Fungal diseases: an emerging threat to human, animal, and plant health: Workshop Summary. 2011, The National Academies Press, Washington DC, USA, http://www.nap.edu/catalog.php?record˙id=13147. [Google Scholar]
  • Orbach M.J., Farrall L., Sweigard J.A., Chumley F.G., Valent B. A telomeric avirulence gene determines efficacy for the rice blast resistance gene Pi-ta. Plant Cell, 2000, 12, 2019–2032. [CrossRef] [PubMed] [Google Scholar]
  • Parlange F., Daverdin G., Fudal I., Kuhn M.L., Balesdent M.H., Blaise F., Grezes-Besset B., Rouxel T., Leptosphaeria maculans avirulence gene AvrLm4-7 confers a dual recognition specificity by the Rlm4 and Rlm7 resistance genes of oilseed rape, and circumvents Rlm4-mediated recognition through a single amino-acid change. Mol Microbiol, 2009, 71, 851–863. [CrossRef] [PubMed] [Google Scholar]
  • Pennisi E., Armed and dangerous. Science, 2010, 327, 804–805. [CrossRef] [PubMed] [Google Scholar]
  • Raffaele S., Win J., Cano L.M., Kamoun S. Analyses of genome architecture and gene expression reveal novel candidate virulence factors in the secretome of Phytophthora infestans. BMC Genomics, 2010, 11, 637. [CrossRef] [PubMed] [Google Scholar]
  • Raffaele S., Kamoun S., Genome evolution in filamentous plant pathogens: why bigger can be better. Nat Rev Microbiol, 2012, 10, 417–430. [PubMed] [Google Scholar]
  • Rebollo R., Horard B., Hubert B., Vieira C., Jumping genes and epigenetics: Towards new species. Gene, 2010, 454, 1–7. [CrossRef] [PubMed] [Google Scholar]
  • Rep M., Meijer M., Houterman P.M., van der Does H.C., Cornelissen B.J., A small, cysteine-rich protein secreted by Fusarium oxysporum during colonization of xylem vessels is required for I-3-mediated resistance in tomato. Mol Microbiol, 2004, 53, 1373–1383. [CrossRef] [PubMed] [Google Scholar]
  • Rouxel T., Balesdent M.H., The stem canker (blackleg) fungus, Leptosphaeria maculans, enters the genomic era. Mol Plant Pathol, 2005, 6, 225–241. [CrossRef] [PubMed] [Google Scholar]
  • Rouxel T., Penaud A., Pinochet X., Brun H., Gout L., Delourme R., Schmit J., Balesdent, M. H., A 10-year survey of populations of Leptosphaeria maculans in France indicates a rapid adaptation towards the Rlm1 resistance gene of oilseed rape. Eur J Plant Pathol, 2003, 109, 871–881. [CrossRef] [Google Scholar]
  • Rouxel T., Grandaubert J., Hane J.K., Hoede C., van de Wouw A.P., Couloux A., Dominguez V., Anthouard V., Bally P., Bourras S., Cozijnsen A.J., Ciuffetti L.M., Degrave A., Dilmaghani A., Duret L., Fudal I., Goodwin S.B., Gout L., Glaser N., Linglin J., Kema G.H., Lapalu N., Lawrence C.B., May K., Meyer M., Ollivier B., Poulain J., Schoch C.L., Simon A., Spatafora J.W., Stachowiak A., Turgeon B.G., Tyler B.M., Vincent D., Weissenbach J., Amselem J., Quesneville H., Oliver R.P., Wincker P., Balesdent M.H., Howlett B.J., Effector diversification within compartments of the Leptosphaeria maculans genome affected by Repeat-Induced Point Mutations. Nat Commun 2011, 2, 202-1. [CrossRef] [PubMed] [Google Scholar]
  • Schardl C.L., Young C.A., Hesse U., Amyotte S.G., Andreeva K., Calie P.J., Fleetwood D.J., Haws D.C., Moore N., Oeser B., Panaccione D.G., Schweri K.K., Voisey C.R., Farman M.L., Jaromczyk J.W., Roe B.A., O’Sullivan D.M., Scott B., Tudzynski P., An Z., Arnaoudova E.G., Bullock C.T., Charlton N.D., Chen L., Cox M., Dinkins R.D., Florea S., Glenn A.E., Gordon A., Güldener U., Harris D.R., Hollin W., Jaromczyk J., Johnson R.D., Khan A.K., Leistner E., Leuchtmann A., Li C., Liu J., Liu J., Liu M., Mace W., Machado C., Nagabhyru P., Pan J., Schmid J., Sugawara K., Steiner U., Takach J.E., Tanaka E., Webb J.S., Wilson E.V., Wiseman J.L., Yoshida R., Zeng Z., Plant-symbiotic fungi as chemical engineers: multi-genome analysis of the Clavicipitaceae reveals dynamics of alkaloid loci. PloS Genet, 2013, 9, e1003323. [CrossRef] [PubMed] [Google Scholar]
  • Schirawski J., Mannhaupt G., Münch K., Brefort T., Schipper K., Doehlemann G., Di Stasio M., Rössel N., Mendoza-Mendoza A., Pester D., Müller O., Winterberg B., Meyer E., Ghareeb H., Wollenberg T., Münsterkötter M., Wong P., Walter M., Stukenbrock E., Güldener U., Kahmann R., Pathogenicity determinants in smut fungi revealed by genome comparison. Science, 2010, 330, 1546–1548. [CrossRef] [PubMed] [Google Scholar]
  • Shoemaker R.A., Brun H., The telemorph of the weakly aggressive segregate of Leptosphaeria maculans. Can J Bot, 2001, 79, 412–419. [Google Scholar]
  • Silar P., La mycologie au début du 21e siècle : crise et renouveau. Biol Auj, 2013, 207, n° 4. [Google Scholar]
  • Spanu P.D., The genomics of obligate (and nonobligate) biotrophs. Annu Rev Phytopathol, 2012, 50, 91–109. [CrossRef] [PubMed] [Google Scholar]
  • Spanu P.D., Abbott J.C., Amselem J., Burgis T.A., Soanes D.M., Stüber K., Ver Loren van Themaat E., Brown J.K., Butcher S.A., Gurr S.J., Lebrun M.H., Ridout C.J., Schulze-Lefert P., Talbot N.J., Ahmadinejad N., Ametz C., Barton G.R., Benjdia M., Bidzinski P., Bindschedler L.V., Both M., Brewer M.T., Cadle-Davidson L., Cadle-Davidson M.M., Collemare J., Cramer R., Frenkel O., Godfrey D., Harriman J., Hoede C., King B.C., Klages S., Kleemann J., Knoll D., Koti P.S., Kreplak J., López-Ruiz F.J., Lu X., Maekawa T., Mahanil S., Micali C., Milgroom M.G., Montana G., Noir S., O’Connell R.J., Oberhaensli S., Parlange F., Pedersen C., Quesneville H., Reinhardt R., Rott M., Sacristán S., Schmidt S.M., Schön M., Skamnioti P., Sommer H., Stephens A., Takahara H., Thordal-Christensen H., Vigouroux M., Wessling R., Wicker T., Panstruga R., Genome expansion and gene loss in powdery mildew fungi reveal tradeoffs in extreme parasitism. Science, 2010, 330, 1543–1546. [CrossRef] [PubMed] [Google Scholar]
  • Stergiopoulos I., De Kock M.J., Lindhout P., De Wit P.J., Allelic variation in the effector genes of the tomato pathogen Cladosporium fulvum reveals different modes of adaptive evolution. Mol Plant Microbe Interact, 2007, 20, 1271–1283. [CrossRef] [PubMed] [Google Scholar]
  • Strange R.N., Scott P.R., Plant disease: a threat to global food security. Annu Rev Phytopathol, 2005, 43, 83–116. [CrossRef] [PubMed] [Google Scholar]
  • Stukenbrock E.H., McDonald B.A., The origins of plant pathogens in agro-ecosystems. Annu Rev Phytopathol, 2008, 46, 75–100. [CrossRef] [PubMed] [Google Scholar]
  • Stukenbrock E.H., Bataillon T., A population genomics perspective on the emergence and adaptation of new plant pathogens in agro-ecosystems. PloS Pathog, 2012, 8, e1002893. [CrossRef] [PubMed] [Google Scholar]
  • Syme R.A., Hane J.K., Friesen T.L., Oliver R.P., Resequencing and Comparative Genomics of Stagonospora nodorum: Sectional Gene Absence and Effector Discovery. G3, 2013, 3, 959–969. [CrossRef] [Google Scholar]
  • Vincenot L., Balesdent M.H., Li H., Barbetti M.J., Sivasithamparam K., Gout L., Rouxel T., Occurrence of a new subclade of Leptosphaeria biglobosa in Western Australia. Phytopathology, 2008, 98, 321–329. [CrossRef] [PubMed] [Google Scholar]
  • West J.S., Fitt B.D.L., Leech P.K., Biddulph J.E., Balesdent M.H., Huang Y.J., Effects of timing of Leptosphaeria maculans ascospore release and fungicide regime on phoma leaf spot and phoma stem canker development on winter oilseed rape Brassica napus in southern England. Plant Pathol, 2002, 51, 454–463. [CrossRef] [Google Scholar]
  • Zhou E., Jia Y., Singh P., Correll J.C., Lee F.N., Instability of the Magnaporthe oryzae avirulence gene AVR-Pita alters virulence. Fungal Genet Biol, 2007, 44, 1024–1034. [CrossRef] [PubMed] [Google Scholar]
  • Zolan M.E., Chromosome-length polymorphism in fungi. Microbiol Rev, 1995, 59, 686–698. [PubMed] [Google Scholar]
  • http://www.thesundaytimes.co.uk/sto/news/uk˙news/Environment/article1238345.ece [Google Scholar]
  • https://www.youtube.com/watch?v=HIll-˙blL5c&list=UU˙iFLW6c8oHkYuWnc8hzTqA [Google Scholar]
  • http://news.bbc.co.uk/2/hi/programmes/newsnight/8912727.stm [Google Scholar]
  • http://www.miamiherald.com/2013/05/19/3405435/colombias-fight-against-coffee.html [Google Scholar]
  • http://genome.jgi.doe.gov/programs/fungi/index.jsf [Google Scholar]

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