Origins of Host-Specific Populations of the Blast Pathogen Magnaporthe oryzae in Crop Domestication With Subsequent Expansion of Pandemic Clones on Rice and Weeds of Rice

Rice, as a widely and intensively cultivated crop, should be a target for parasite host shifts and a source for shifts to co-occurring weeds. Magnaporthe oryzae, of the M. grisea species complex, is the most important fungal pathogen of rice, with a high degree of host specificity. On the basis of 10 loci from six of its seven linkage groups, 37 multilocus haplotypes among 497 isolates of M. oryzae from rice and other grasses were identified. Phylogenetic relationships among isolates from rice (Oryza sativa), millet (Setaria spp.), cutgrass (Leersia hexandra), and torpedo grass (Panicum repens) were predominantly tree like, consistent with a lack of recombination, but from other hosts were reticulate, consistent with recombination. The single origin of rice-infecting M. oryzae followed a host shift from a Setaria millet and was closely followed by additional shifts to weeds of rice, cutgrass, and torpedo grass. Two independent estimators of divergence time indicate that these host shifts predate the Green Revolution and could be associated with rice domestication. The rice-infecting lineage is characterized by high copy number of the transposable element MGR586 (Pot3) and, except in two haplotypes, by a loss of AVR-Co39. Both mating types have been retained in ancestral, well-distributed rice-infecting haplotypes 10 (mainly temperate) and 14 (mainly tropical), but only one mating type was recovered from several derived, geographically restricted haplotypes. There is evidence of a common origin of both ACE1 virulence genotypes in haplotype 14. Host-haplotype association is evidenced by low pathogenicity on hosts associated with other haplotypes.

[1]  J. Correll,et al.  Rice Blast Epidemics Initiated by Infested Rice Grain on the Soil Surface. , 2001, Plant disease.

[2]  T. Sekiya,et al.  Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction. , 1989, Genomics.

[3]  DNA Fingerprinting with a Dispersed Repeated Sequence Resolves Pathotype Diversity in the Rice Blast Fungus. , 1991, The Plant cell.

[4]  F. Chumley,et al.  A Mechanism for Surface Attachment in Spores of a Plant Pathogenic Fungus , 1988, Science.

[5]  G. Crawford,et al.  The origins of rice agriculture: recent progress in East Asia , 1998, Antiquity.

[6]  Yo-ichiro Sato,et al.  Dual origin of the cultivated rice based on molecular markers of newly collected annual and perennial strains of wild rice species, Oryza nivara and O. rufipogon , 2003, Genetic Resources and Crop Evolution.

[7]  H. Nakayashiki,et al.  Characterization of an Avena isolate of Magnaporthe grisea and identification of a locus conditioning its specificity on oat , 2002 .

[8]  J. D. Fry The Evolution of Host Specialization: Are Trade-Offs Overrated? , 1996, The American Naturalist.

[9]  P. Ronald The molecular basis of disease resistance in rice , 1997, Plant Molecular Biology.

[10]  W. Uddin,et al.  Pyricularia grisea Causing Gray Leaf Spot of Perennial Ryegrass Turf: Population Structure and Host Specificity. , 2001, Plant disease.

[11]  R. Motohashi,et al.  Polyphyletic origin of cultivated rice: based on the interspersion pattern of SINEs. , 2003, Molecular biology and evolution.

[12]  Bruce D. Smith,et al.  The origins of agriculture : an international perspective , 1993 .

[13]  N. Hayashi,et al.  Distribution of Fertile Magnaporthe grisea Fungus Pathogenic to Rice in Yunnan Province, China , 1997 .

[14]  P. Landschoot,et al.  Gray leaf spot of perennial ryegrass turf in Pennsylvania , 1992 .

[15]  James B. Anderson,et al.  PATTERNS OF DESCENT IN CLONAL LINEAGES AND THEIR MULTILOCUS FINGERPRINTS ARE RESOLVED WITH COMBINED GENE GENEALOGIES , 1999, Evolution; international journal of organic evolution.

[16]  F. Chumley,et al.  Identification, cloning, and characterization of PWL2, a gene for host species specificity in the rice blast fungus. , 1995, The Plant cell.

[17]  M. Hood,et al.  The Ecology and Genetics of a Host Shift: Microbotryum as a Model System , 2002, The American Naturalist.

[18]  D. Rhoads,et al.  DNA fingerprinting to examine microgeographic variation in the Magnaporthe grisea (Pyricularia grisea) population in two rice fields in Arkansas , 1993 .

[19]  R. May,et al.  Infectious disease dynamics: What characterizes a successful invader? , 2001, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[20]  R. Nelson,et al.  Population structure and dynamics of Magnaporthe grisea in the Indian Himalayas. , 1999, Genetics.

[21]  F. Tajima,et al.  Simple methods for testing the molecular evolutionary clock hypothesis. , 1993, Genetics.

[22]  G. Sécond Origin of the genic diversity of cultivated rice (Oryza spp.): study of the polymorphism scored at 40 isozyme loci , 1982 .

[23]  C. N. Bollich,et al.  Inheritance of resistance to Pyricularia oryzae in rice cultivars grown in the United States , 1987 .

[24]  E. Selker,et al.  Repeat-induced G-C to A-T mutations in Neurospora. , 1989, Science.

[25]  J. M. Smith,et al.  How clonal are bacteria? , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[26]  F. Ayala,et al.  Are eukaryotic microorganisms clonal or sexual? A population genetics vantage. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[27]  M. Farman,et al.  Analysis of the structure of the AVR1-CO39 avirulence locus in virulent rice-infecting isolates of Magnaporthe grisea. , 2002, Molecular plant-microbe interactions : MPMI.

[28]  Ignazio Carbone,et al.  A method for designing primer sets for speciation studies in filamentous ascomycetes , 1999 .

[29]  J. Nottéghem,et al.  Evidence of a gene-for-gene relationship in the Oryza sativa-Magnaporthe grisea pathosystem , 1992 .

[30]  P. Pukkila,et al.  Inheritance of DNA methylation in Coprinus cinereus , 1986, Molecular and cellular biology.

[31]  H. U. Böhnert,et al.  A Putative Polyketide Synthase/Peptide Synthetase from Magnaporthe grisea Signals Pathogen Attack to Resistant Ricew⃞ , 2004, The Plant Cell Online.

[32]  F. Chumley,et al.  Ultrastructural interactions of one strain of Magnaporthe grisea with goosegrass and weeping lovegrass , 1992 .

[33]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[34]  V. Grant,et al.  Origin of Cultivated Rice , 1988 .

[35]  David Posada,et al.  MODELTEST: testing the model of DNA substitution , 1998, Bioinform..

[36]  Curtis H. Flather,et al.  Patchy Reaction‐Diffusion and Population Abundance: The Relative Importance of Habitat Amount and Arrangement , 2002, The American Naturalist.

[37]  F. Chumley,et al.  Genetic studies of fertility and pathogenicity in Magnaporthe grisea (Pyricularia oryzae) , 1984 .

[38]  C. Higham,et al.  The origins and dispersal of rice cultivation , 1998, Antiquity.

[39]  K. Crandall,et al.  TCS: a computer program to estimate gene genealogies , 2000, Molecular ecology.

[40]  H. Leung,et al.  Genetic differentiation among isolates of Pyricularia infecting rice and weed hosts. , 1993 .

[41]  M. Farman,et al.  Chromosome walking to the AVR1-CO39 avirulence gene of Magnaporthe grisea: discrepancy between the physical and genetic maps. , 1998, Genetics.

[42]  H. Nakayashiki,et al.  Pathogenicity, Mating Ability and DNA Restriction Fragment Length Polymorphisms of Pyricularia Populations Isolated from Gramineae, Bambusideae and Zingiberaceae Plants , 2000, Journal of General Plant Pathology.

[43]  N. Talbot On the trail of a cereal killer: Exploring the biology of Magnaporthe grisea. , 2003, Annual review of microbiology.

[44]  Daniel H. Huson,et al.  Analyzing and Visualizing Sequence and Distance Data Using SplitsTree , 1996, Discret. Appl. Math..

[45]  H. Nakayashiki,et al.  Comparative analyses of the distribution of various transposable elements in Pyricularia and their activity during and after the sexual cycle , 2001, Molecular and General Genetics MGG.

[46]  F. Chumley,et al.  Host species-specific conservation of a family of repeated DNA sequences in the genome of a fungal plant pathogen. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[47]  B. Valent,et al.  Direct interaction of resistance gene and avirulence gene products confers rice blast resistance , 2000, The EMBO journal.

[48]  R. Nelson,et al.  RFLP mapping of genes conferring complete and partial resistance to blast in a durably resistant rice cultivar. , 1994, Genetics.

[49]  L. Kohn,et al.  A multilocus gene genealogy concordant with host preference indicates segregation of a new species, Magnaporthe oryzae, from M. grisea , 2002 .

[50]  M. Marchetti Dilatory Resistance to Rice Blast in USA Rice , 1983 .

[51]  R DeSalle,et al.  Multiple sources of character information and the phylogeny of Hawaiian drosophilids. , 1997, Systematic biology.

[52]  F. Chumley,et al.  A Telomeric Avirulence Gene Determines Efficacy for the Rice Blast Resistance Gene Pi-ta , 2000, Plant Cell.

[53]  張 光直 The archaeology of ancient China , 1964, The Journal of Asian Studies.

[54]  H. Kishino,et al.  Estimating the rate of evolution of the rate of molecular evolution. , 1998, Molecular biology and evolution.

[55]  B. Valent Rice blast as a model system for plant pathology. , 1990 .

[56]  R. Zeigler,et al.  Sexually Fertile Magnaporthe grisea Rice Pathogens in Thailand. , 1999, Plant disease.

[57]  K. Zheng,et al.  Genetic differentiation of wild relatives of rice as assessed by RFLP analysis , 2002, Theoretical and Applied Genetics.

[58]  F. Chumley,et al.  Isolation of the mating-type genes of the phytopathogenic fungus Magnaporthe grisea using genomic subtraction. , 1994, Genetics.

[59]  T. Chang The origin, evolution, cultivation, dissemination, and diversification of Asian and African rices , 2004, Euphytica.

[60]  F. Gao,et al.  Origins and diversity of human immunodeficiency viruses , 1994 .

[61]  Mark P. Simmons,et al.  Gaps as characters in sequence-based phylogenetic analyses. , 2000, Systematic biology.

[62]  John P. Huelsenbeck,et al.  MRBAYES: Bayesian inference of phylogenetic trees , 2001, Bioinform..

[63]  N. L. Glass,et al.  Development of primer sets designed for use with the PCR to amplify conserved genes from filamentous ascomycetes , 1995, Applied and environmental microbiology.

[64]  You-Liang Peng,et al.  Temporal sequence of cytological events in rice leaves infected with Pyricularia oryzae , 1988 .

[65]  R. DeSalle,et al.  Assessing the relative contribution of molecular and morphological characters in simultaneous analysis trees. , 1998, Molecular phylogenetics and evolution.

[66]  D. Mackill,et al.  Inheritance of Partial Resistance to Blast in Indica Rice Cultivars , 1989 .

[67]  S. Kang,et al.  Gain of virulence caused by insertion of a Pot3 transposon in a Magnaporthe grisea avirulence gene. , 2001, Molecular plant-microbe interactions : MPMI.

[68]  J. Thompson,et al.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. , 1994, Nucleic acids research.

[69]  M. Farman Pyricularia grisea Isolates Causing Gray Leaf Spot on Perennial Ryegrass (Lolium perenne) in the United States: Relationship to P. grisea Isolates from Other Host Plants. , 2002, Phytopathology.

[70]  C. Brasier,et al.  Rapid Evolutionary Changes in a Globally Invading Fungal Pathogen (Dutch Elm Disease) , 2004, Biological Invasions.

[71]  F. Chumley,et al.  Magnaporthe grisea genes for pathogenicity and virulence identified through a series of backcrosses. , 1991, Genetics.

[72]  M. Lorieux,et al.  Identification of five new blast resistance genes in the highly blast-resistant rice variety IR64 using a QTL mapping strategy , 2003, Theoretical and Applied Genetics.

[73]  J. Hutchinson The Biology and Evolution of HIV , 2001 .

[74]  L. Kohn,et al.  A microbial population–species interface: nested cladistic and coalescent inference with multilocus data , 2001, Molecular ecology.

[75]  H. Nakayashiki,et al.  Molecular Analysis of the Wheat Blast Population in Brazil with a Homolog of Retrotransposon MGR583 , 1999 .

[76]  Michael P. Cummings,et al.  PAUP* [Phylogenetic Analysis Using Parsimony (and Other Methods)] , 2004 .

[77]  W. Crepet,et al.  THE EARLIEST REMAINS OF GRASSES IN THE FOSSIL RECORD , 1991 .

[78]  A. Dress,et al.  Split decomposition: a new and useful approach to phylogenetic analysis of distance data. , 1992, Molecular phylogenetics and evolution.

[79]  J. Nottéghem,et al.  Production of perithecia of Magnaporthe grisea on rice plants , 1990 .

[80]  G. Pontecorvo The parasexual cycle in fungi. , 1956, Annual review of microbiology.

[81]  M. Sanderson Estimating absolute rates of molecular evolution and divergence times: a penalized likelihood approach. , 2002, Molecular biology and evolution.

[82]  Jerrold I. Davis,et al.  Phylogeny and subfamilial classification of the grasses (Poaceae) , 2001 .

[83]  J. Dekker The foxtail (Setaria) species-group , 2003, Weed Science.

[84]  Simon Easteal,et al.  A program for calculating and displaying compatibility matrices as an aid in determining reticulate evolution in molecular sequences , 1996, Comput. Appl. Biosci..

[85]  K. Bremer GONDWANAN EVOLUTION OF THE GRASS ALLIANCE OF FAMILIES (POALES) , 2002, Evolution; international journal of organic evolution.

[86]  David L. Dilcher,et al.  The fossil record , 1992 .

[87]  C. Sing,et al.  A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation. , 1992, Genetics.

[88]  J. Hamer,et al.  Genetic diversity of the rice blast fungus in a disease nursery in Colombia , 1993 .

[89]  M. Milgroom,et al.  Diversity of Pathotypes and DNA Fingerprint Haplotypes in Populations of Magnaporthe grisea in Korea over Two Decades. , 2003, Phytopathology.

[90]  H. Leung,et al.  Evidence of parasexual exchange of DNA in the rice blast fungus challenges its exclusive clonality. , 1997, Phytopathology.

[91]  M. Whitlock The Red Queen Beats the Jack-Of-All-Trades: The Limitations on the Evolution of Phenotypic Plasticity and Niche Breadth , 1996, The American Naturalist.

[92]  M. Kimura The number of heterozygous nucleotide sites maintained in a finite population due to steady flux of mutations. , 1969, Genetics.

[93]  N. Mori,et al.  Genetic Constitution and Pathogenicity of Lolium Isolates of Magnaporthe oryzae in Comparison with Host Species-Specific Pathotypes of the Blast Fungus. , 2004, Phytopathology.

[94]  D. Ho,et al.  Human immunodeficiency virus type 2 (HIV-2) seroprevalence and characterization of a distinct HIV-2 genetic subtype from the natural range of simian immunodeficiency virus-infected sooty mangabeys , 1997, Journal of virology.

[95]  R. Hudson,et al.  Statistical properties of the number of recombination events in the history of a sample of DNA sequences. , 1985, Genetics.

[96]  G. Khush Green revolution: the way forward , 2001, Nature Reviews Genetics.

[97]  R. Zeigler Recombination in Magnaporthe grisea. , 1998, Annual review of phytopathology.

[98]  T. T. Hebert The perfect stage of Pyricularia grísea. , 1971 .