Abstract
The population genetics of Magnaporthe grisea, the rice blast pathogen, were analyzed in a center of rice diversity (the Uttar Pradesh hills of the Indian Himalayas) using multilocus and single-, or low-copy, DNA markers. Based on DNA fingerprinting with the multilocus probe MGR586 and single-locus probes, 157 haplotypes clustered into 56 lineages (at >/=70% MGR586 band similarity, each with unique single-locus profiles) and high diversity indices were detected among 458 isolates collected from 29 sites during 1992-1995. Most valleys sampled had distinct populations (73% of the lineages were site specific) with some containing one or a few lineages, confirming the importance of clonal propagation, and others were very diverse. Widely distributed lineages suggested that migration occurs across the region and into the Indo-Gangetic plains. Repeated sampling at one site, Matli, (170 isolates, 1992-1995) yielded 19 lineages and diversity significantly greater than that reported from similar samples from Colombia and the Philippines. Analysis of allelic associations using pairwise comparisons and multilocus variance analysis failed to reject the hypothesis of gametic phase equilibrium. The Matli population shifted from highly diverse in 1992 to almost complete dominance by one lineage in 1995. Such population dynamics are consistent with recombination followed by differential survival of clonal descendants of recombinant progeny. At another site, Ranichauri, population (n = 84) composition changed from 2 to 11 lineages over 2 yr and yielded additional evidence for equilibrium. Sexually fertile and hermaphrodite isolates of both mating types were recovered from rice in both Matli and Ranichauri. We demonstrate that Himalayan M. grisea populations are diverse and dynamic and conclude that the structure of some populations may be affected to some extent by sexual recombination.
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- Brown A. H., Feldman M. W., Nevo E. Multilocus Structure of Natural Populations of HORDEUM SPONTANEUM. Genetics. 1980 Oct;96(2):523–536. doi: 10.1093/genetics/96.2.523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Burt A., Carter D. A., Koenig G. L., White T. J., Taylor J. W. Molecular markers reveal cryptic sex in the human pathogen Coccidioides immitis. Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):770–773. doi: 10.1073/pnas.93.2.770. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen R. S., McDonald B. A. Sexual reproduction plays a major role in the genetic structure of populations of the fungus Mycosphaerella graminicola. Genetics. 1996 Apr;142(4):1119–1127. doi: 10.1093/genetics/142.4.1119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dobinson K. F., Harris R. E., Hamer J. E. Grasshopper, a long terminal repeat (LTR) retroelement in the phytopathogenic fungus Magnaporthe grisea. Mol Plant Microbe Interact. 1993 Jan-Feb;6(1):114–126. doi: 10.1094/mpmi-6-114. [DOI] [PubMed] [Google Scholar]
- Geiser D. M., Arnold M. L., Timberlake W. E. Sexual origins of British Aspergillus nidulans isolates. Proc Natl Acad Sci U S A. 1994 Mar 15;91(6):2349–2352. doi: 10.1073/pnas.91.6.2349. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hamer J. E., Farrall L., Orbach M. J., Valent B., Chumley F. G. Host species-specific conservation of a family of repeated DNA sequences in the genome of a fungal plant pathogen. Proc Natl Acad Sci U S A. 1989 Dec;86(24):9981–9985. doi: 10.1073/pnas.86.24.9981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hutcheson K. A test for comparing diversities based on the Shannon formula. J Theor Biol. 1970 Oct;29(1):151–154. doi: 10.1016/0022-5193(70)90124-4. [DOI] [PubMed] [Google Scholar]
- Leslie J. F., Klein K. K. Female fertility and mating type effects on effective population size and evolution in filamentous fungi. Genetics. 1996 Oct;144(2):557–567. doi: 10.1093/genetics/144.2.557. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Levy M., Romao J., Marchetti M. A., Hamer J. E. DNA Fingerprinting with a Dispersed Repeated Sequence Resolves Pathotype Diversity in the Rice Blast Fungus. Plant Cell. 1991 Jan;3(1):95–102. doi: 10.1105/tpc.3.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lewontin R. C. The detection of linkage disequilibrium in molecular sequence data. Genetics. 1995 May;140(1):377–388. doi: 10.1093/genetics/140.1.377. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milgroom M. G., Lipari S. E., Powell W. A. DNA fingerprinting and analysis of population structure in the chestnut blight fungus, Cryphonectria parasitica. Genetics. 1992 Jun;131(2):297–306. doi: 10.1093/genetics/131.2.297. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Milgroom M. G. Recombination and the multilocus structure of fungal populations. Annu Rev Phytopathol. 1996;34:457–477. doi: 10.1146/annurev.phyto.34.1.457. [DOI] [PubMed] [Google Scholar]
- Nei M. Analysis of gene diversity in subdivided populations. Proc Natl Acad Sci U S A. 1973 Dec;70(12):3321–3323. doi: 10.1073/pnas.70.12.3321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shull V., Hamer J. E. Genetic differentiation in the rice blast fungus revealed by the distribution of the Fosbury retrotransposon. Fungal Genet Biol. 1996 Mar;20(1):59–69. doi: 10.1006/fgbi.1996.0010. [DOI] [PubMed] [Google Scholar]
- Smith J. M., Smith N. H., O'Rourke M., Spratt B. G. How clonal are bacteria? Proc Natl Acad Sci U S A. 1993 May 15;90(10):4384–4388. doi: 10.1073/pnas.90.10.4384. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Talbot N. J., Salch Y. P., Ma M., Hamer J. E. Karyotypic Variation within Clonal Lineages of the Rice Blast Fungus, Magnaporthe grisea. Appl Environ Microbiol. 1993 Feb;59(2):585–593. doi: 10.1128/aem.59.2.585-593.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tibayrenc M., Kjellberg F., Arnaud J., Oury B., Brenière S. F., Dardé M. L., Ayala F. J. Are eukaryotic microorganisms clonal or sexual? A population genetics vantage. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5129–5133. doi: 10.1073/pnas.88.12.5129. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zeigler R. S. Recombination in Magnaporthe grisea. Annu Rev Phytopathol. 1998;36:249–275. doi: 10.1146/annurev.phyto.36.1.249. [DOI] [PubMed] [Google Scholar]