Abstract
Rhynchosporium commune was recently introduced into the Middle East, presumably with the cultivated host barley (Hordeum vulgare). Middle Eastern populations of R. commune on cultivated barley and wild barley (H. spontaneum) were genetically undifferentiated and shared a high proportion of multilocus haplotypes. This suggests that there has been little selection for host specialization on H. spontaneum, a host population often used as a source of resistance genes introduced into its domesticated counterpart, H. vulgare. Low levels of pathogen genetic diversity on H. vulgare as well as on H. spontaneum, indicate that the pathogen was introduced recently into the Middle East, perhaps through immigration on infected cultivated barley seeds, and then invaded the wild barley population. Although it has not been documented, the introduction of the pathogen into the Middle East may have a negative influence on the biodiversity of native Hordeum species.
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References
Abbott DC, Brown AHD, Burdon JJ (1992) Genes for scald resistance from wild barley (Hordeum vulgare ssp. spontaneum) and their linkage to isozyme markers. Euphytica 61:225–231
Agapow PM, Burt A (2001) Indices of multilocus linkage disequilibrium. Mol Ecol Notes 1:101–102
Ali SM, Boyd WJR (1974) Host range and physiologic specialization in Rhynchosporium secalis. Aust J Agric Res 25:21–31
Anagnostakis SL (1987) Chestnut blight: the classical problem of an introduced pathogen. Mycologia 79:23–37
Anderson PK, Cunningham AA, Patel NG, Morales FJ, Epstein PR, Daszak P (2004) Emerging infectious diseases of plants: pathogen pollution, climate change and agrotechnology drivers. Trends Ecol Evol 19:535–544
Arnaud-Haond S, Belkhir K (2007) GENCLONE: a computer program to analyse genotypic data, test for clonality and describe spatial clonal organization. Mol Ecol Notes 7:15–17
Badr A, Sch MKR, El Rabey H, Effgen S, Ibrahim HH, Pozzi C, Rohde W, Salamini F (2000) On the origin and domestication history of barley (Hordeum vulgare). Mol Biol Evol 17:499–510
Borer ET, Hosseini PR, Seabloom EW, Dobson AP (2007) Pathogen-induced reversal of native dominance in a grassland community. Proc Natl Acad Sci USA 104:5473–5478
Brown JS (1990) Pathogenic variation among isolates of Rhynchosporium secalis from barley grass growing in south eastern Australia. Euphytica 50:81–89
Caldwell RM (1937) Rhynchosporium secalis of barley, rye, and other grasses. J Agric Res 55:175–198
Ceccarelli S, Grando S, Amri A, Asaad FA, Benbelkacem A, Harrabi M, Maatougui M, Mekni MS, Himoun H, El-Einen RA, El-Felah M, Sayed AF E-, Shreidi AS, Yahyaoui A (2001) Decentralized and participatory plant breeding from marginal environments CABI Publ. Wallingford, Oxon
Chen RS, Boeger JM, McDonald BA (1994) Genetic stability in a population of a plant pathogenic fungus over time. Mol Ecol 3:209–218
Clarke KR, Warwick RM (2001) Change in marine communities: an approach to statistical analysis and interpretation. PRIMER-E Ltd, Plymouth
Cronin JK, Bundock PC, Henry RJ, Nevo E (2007) Adaptive climatic molecular evolution in wild barley at the Isa defense locus. Proc Natl Acad Sci USA 104:2773–2778
Evanno G, Regnaut S, Goudet J (2005) Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study. Mol Ecol 14:2611–2620
Excoffier L, Smouse PE, Quattro JM (1992) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction sites. Genetics 131:479–491
Genger RK, Brown AHD, Knogge W, Nesbitt K, Burdon JJ (2003) Development of SCAR markers linked to a scald resistance gene derived from wild barley. Euphytica 134:149–159
Goodwin SB, Maroof MAS, Allard RW, Webster RK (1993) Isozyme variation within and among populations of Rhynchosporium secalis in Europe, Australia and the United States. Mycol Res 97:49–58
Grunwald NJ, Goodwin SB, Milgroom MG, Fry WE (2003) Analysis of genotypic diversity data for populations of microorganisms. Phytopathology 93:738–746
Jackson LF, Webster RK (1976) Race differentiation, distribution, and frequency of Rhynchosporium secalis in California. Phytopathology 66:719–725
Kimura M, Crow J (1964) The number of alleles that can be maintained in a finite population. Genetics 49:725–738
Lessa EP (1990) Multidimensional analysis of geographic genetic structure. Syst Zool 39:242–252
Lewontin RC (1972) The appointment of human diversity. Evol Biol 6:381–391
Linde CC, Zala M, McDonald BA (2005) Isolation and characterization of microsatellite loci from the barley scald pathogen, Rhynchosporium secalis. Mol Ecol Notes 5:546–548
Linde CC, Zala M, McDonald BA (2009) Molecular evidence for recent founder populations and human-mediated migration in the barley scald pathogen Rhynchosporium secalis. Mol Phylogenet Evol 51:454–464
McDonald BA, Zhan J, Burdon JJ (1999) Genetic structure of Rhynchosporium secalis in Australia. Phytopathology 89:639–645
Nei M (1973) Analysis of gene diversity in subdivided populations. Proc Natl Acad Sci USA 70:3321–3323
Nei M (1978) Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics 89:583–590
Peakall R, Smouse PE (2006) GENALEX 6: genetic analysis in Excel. Population genetic software for teaching and research. Mol Ecol Notes 6:288–295
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959
Salamini F, Özkan H, Brandolini A, Schäfer-Pregl R, Martin W (2002) Genetics and geography of wild cereal domestication in the Near East. Genetics 3:429–441
Schwartz MW, Hermann SM, Vogel CS (1995) The catastrophic loss of Torreya taxifolia: assessing environmental induction of disease hypotheses. Ecol Appl 5:501–516
Shannon CE, Weaver W (1949) The mathematical theory of communication Urbana. University of Illinois Press, IL
Stoddart JA, Taylor JF (1988) Genotype diversity: estimation and prediction in samples. Genetics 118:705–711
von Bothmer R, Jacobsen N, Baden C, Jørgensen RB, Linde-Laursen I (1995) An ecogeographical study of the genus Hordeum, systematic and ecogeographic studies on crop genepools, 2nd edn. International Plant Genetic Resources Institute, Rome
von Bothmer R, Sato K, Komatsuda T, Yasuda S, Fischbeck G (2003) The domestication of cultivated barley. In: von Bothmer R, van Hintum T, Knüpffer H, Sato K (eds) Diversity in barley (Hordeum vulgare). Elsevier, Amsterdam, pp 9–27
von Korff M, Udupa SM, Yahyaoui A, Baum M (2004) Genetic variation among Rhynchosporium secalis populations of West Asia and North Africa as revealed by RAPD and AFLP analysis. J Phytopathol 152:106–113
Wright S (1969) Evolution and the genetics of populations. University of Chicago Press, Chicago
Zaffarano PL, McDonald BA, Zala M, Linde CC (2006) Global hierarchical gene diversity analysis suggests the Fertile Crescent is not the center of origin of the barley scald pathogen Rhynchosporium secalis. Phytopathology 96:941–950
Zaffarano PL, McDonald BA, Linde CC (2008) Rapid speciation followed host specialization in Rhynchosporium. Evolution 62:1418–1436
Zaffarano PL, McDonald BA, Linde CC (2009) Phylogeographical analyses reveal global migration patterns of the barley scald pathogen Rhynchosporium secalis. Mol Ecol 18:279–293
Zaffarano PL, McDonald BA, Linde CC (2010) Two new species of Rhynchosporium. Mycologia (in press)
Zhu Y, Chen H, Fan J, Wang Y, Li Y, Chen J, Fan J, Yang S, Hu L, Leung H, Mew TW, Teng PS, Wang Z, Mundt CC (2000) Genetic diversity and disease control in rice. Nature 406:718–722
Zohary D, Hopf M (2000) Domestication of Plants in the Old World. Oxford University Press/Clarendon Press, Oxford
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Kiros-Meles, A., Gomez, D., McDonald, B.A. et al. Invasion of Rhynchosporium commune onto wild barley in the Middle East. Biol Invasions 13, 321–330 (2011). https://doi.org/10.1007/s10530-010-9808-6
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DOI: https://doi.org/10.1007/s10530-010-9808-6