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High levels of genetic diversity and cryptic recombination is widespread in introduced Diplodia pinea populations

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Abstract

Introduced populations of organisms typically have reduced diversity compared to those that are native. It is, therefore, unusual that introduced populations of the fungal tree pathogen Diplodia pinea have been shown to have high levels of genetic diversity, even surpassing diversity in some native regions. This is thought to be due to multiple introductions over time or the existence of a cryptic and yet undiscovered sexual cycle. In this study, we consider whether populations of D. pinea in Southern Hemisphere countries have similar patterns of diversity, share some level of genetic identity and how they might be influenced by sexual recombination. A total of 173 isolates from Argentina, Australia, Ethiopia and South Africa were characterized using 12 microsatellite markers. The results show that all these populations have high gene and genotype diversities, with the Australian population having the lowest diversity. Very few private alleles were found, suggesting that isolates from different countries might share a source of introduction. However, based on allele distribution and frequency, each of the populations appeared to be evolving independently. The results showed that in all but the Australian population, alleles are randomly associated, suggesting that widespread sexual recombination has influenced population structure.

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References

  • Agapow PM, Burt A (2000) ‘Multilocus 1.2’. Department of Biology, Imperial College, Ascot

    Google Scholar 

  • Arie T, Kaneko I, Yoshida T, Noguchi M, Nomura Y, Yamaguchi I (2000) Mating-type genes from asexual phytopathogenic ascomycets Fusarium oxysprum and Alternaria alternata. Mol Plant Microbe Interact 13:1330–1339

    Article  PubMed  CAS  Google Scholar 

  • Bihon W, Burgess T, Slippers B, Wingfield MJ, Wingfield BD (2011a) Distribution of D. pinea and its genotypic diversity within asymptomatic P. patula trees. Australas Plant Pathol 40:540–548. doi:10.1007/s13313-011-0060-z

    Article  Google Scholar 

  • Bihon W, Slippers B, Burgess T, Wingfield MJ, Wingfield BD (2011b) Diverse sources of infection and cryptic recombination revealed in South African Diplodia pinea populations. Fungal Biol (submitted)

  • Bihon W, Slippers B, Burgess T, Wingfield MJ, Wingfield BD (2010) Sources of Diplodia pinea endophytic infections in Pinus patula and P. radiata seedlings in South Africa. Forest Pathol. doi:10.1111/j.1439-0329.2010.00691.x

  • Burgess T, Wingfield BD, Wingfield MJ (2001a) Comparison of genotypic diversity in native and introduced populations of Sphaeropsis sapinea isolated from Pinus radiata. Mycol Res 105:1331–1339

    Article  Google Scholar 

  • Burgess T, Wingfield MJ, Wingfield BD (2001b) Simple sequence repeat markers distinguished among morphotypes of Sphaeropsis sapinea. Appl Environ Microbiol 67:354–362

    Article  PubMed  CAS  Google Scholar 

  • Burgess TI, Wingfield MJ (2002) Quarantine is important in restricting the spread of exotic seed-borne tree pathogens in the southern hemisphere. Int Forest Rev 4:56–65

    Google Scholar 

  • Burgess T, Wingfield MJ, Wingfield BD (2004) Global distribution of Diplodia pinea genotypes revealed using simple sequence repeat (SSR) markers. Australas Plant Pathol 33:513–519

    Article  CAS  Google Scholar 

  • Feci E, Smith D, Stanosz DR (2003) Association of Sphaeropsis sapinea with insect-damaged red pine shoots and cones. Forest Pathol 33:7–13

    Article  Google Scholar 

  • Geiser DM, Arnold ML, Timberlake WE (1994) Sexual origins of British Aspergillus nidulans isolates. Proc Natl Acad Sci USA 91:2349–2352

    Article  PubMed  CAS  Google Scholar 

  • Goss EM, Larsen M, Chastagner GA, Givens DR, Grunwald NJ (2009) Population genetic analysis infers migration pathways of Phytophthora ramorum in US nurseries. PLoS Pathog 5:e1000583. doi:10.1371/journal.ppat.1000583

    Article  PubMed  Google Scholar 

  • Groenewald M, Linde CC, Groenewald JZ, Crous PW (2008) Indirect evidence for sexual reproduction in Cercospora beticola populations from sugar beet. Plant Pathol 57:25–32

    CAS  Google Scholar 

  • Halliburton R (2004) Introduction to population genetics. Pearson Education, Inc., USA

    Google Scholar 

  • Hunter GC, van der Merwe NA, Burgess TI, Carnegie AJ, Wingfield BD, Crous PW, Wingfield MJ (2008) Global movement and population biology of Mycosphaerella nubilosa infecting leaves of cold-tolerant Eucalyptus globulus and E. nitens. Plant Pathol 57:235–242

    Article  Google Scholar 

  • Kohli Y, Kohn LM (1998) Random association among alleles in clonal populations of Sclerotinia sclerotiorum. Fungal Genet Biol 23:139–149

    Article  PubMed  CAS  Google Scholar 

  • Kuck U, Poggeler S (2009) Cryptic sex in fungi. Fungal Biol Rev 23:86–90

    Article  Google Scholar 

  • Linde CC (2010) Population genetic analyses of plant pathogens: new challenges and opportunities. Australas Plant Pathol 39:23–28, Blackwell

    Article  Google Scholar 

  • McDonald BA (1997) The population genetics of fungi: tools and techniques. Phytopathology 87:448–453

    Article  PubMed  CAS  Google Scholar 

  • McDonald BA, Linde C (2002) Pathogen population genetics, evolutionary potential and durable resistance. Annu Rev Phytopathol 40:349–379

    Article  PubMed  CAS  Google Scholar 

  • McDonald BA, McDermott JM (1993) Population genetics of plant pathogenic fungi: electrophoretic markers give unprecedented precision to analyses of genetic structure of populations. Bioscience 43:311–319

    Article  Google Scholar 

  • Milgroom MG, Fry WE (1997) Contributions of population genetics to plant disease epidemiology and management. Adv Bot Res 24:1–30

    Article  Google Scholar 

  • Milgroom MG, Sotirovski K, Spica D, Davis JE, Brewer MT, Milev M, Cortesi P (2008) Clonal population structure of the chestnut blight fungus in expanding ranges in South Eastern Europe. Mol Ecol 17:4446–4458

    Article  PubMed  Google Scholar 

  • Morgan JAT, Vredenburg VT, Rachowicz LJ, Knapp RA, Stice MJ, Tunstall REB, Parker JM, Longcore JE, Moitz C, Briggs CJ, Taylor JW (2007) Population genetics of the from-killing fungus Batrachochytrium dendrobatidis. Proc Natl Acad Sci USA 104:13845–13850

    Article  PubMed  CAS  Google Scholar 

  • Nevo E (1978) Genetic variation in natural populations: patterns and theory. Theor Popul Biol 13:121–177

    Article  PubMed  CAS  Google Scholar 

  • Palmer MA, Stewart EL, Wingfield MJ (1987) Variation among isolates of Sphaeropsis sapinea in the north central United States. Phytopathology 77:944–948

    Article  Google Scholar 

  • Peakall R, Smouse PE (2006) GENALEX 6: genetic analysis in excel. Population genetic software for teaching and research. Mol Ecol Notes 6:288–295

    Article  Google Scholar 

  • Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155:945–959

    PubMed  CAS  Google Scholar 

  • Smith H, Wingfield MJ, de Wet J, Coutinho TA (2000) Genotypic diversity of Sphaeropsis sapinea from South Africa and Northern Sumatra. Plant Dis 84:139–142

    Article  Google Scholar 

  • Stanosz GR, Swart WJ, Smith DR (1999) RAPD marker and isozyme characterization of Sphaeropsis sapinea from diverse coniferous hosts and locations. Mycol Res 103:1193–1202

    Article  CAS  Google Scholar 

  • Stoddart JA, Taylor JF (1988) Genotype diversity: estimation and prediction in samples. Genetics 118:705–711

    PubMed  CAS  Google Scholar 

  • Sutton BC (1980) The Coelomycetes. Commonwealth Mycological Institute, Kew

    Google Scholar 

  • Swart WJ, Knox-Davis PS, Wingfield MJ (1985) Sphaeiopsis sapinea, with special reference to its occurrence on Pinus spp. in South Africa. S Afr For J 35:1–8

    Google Scholar 

  • Swart WJ, Wingfield MJ (1991) Biology and control of Sphaeropsis sapinea on Pinus species in South Africa. Plant Dis 75:761–766

    Article  Google Scholar 

  • Taylor JW, Jacobson DJ, Fisher MC (1999) The evolution of asexual fungi: reproduction, speciation and classification. Annu Rev Phytopathol 37:197–246

    Article  PubMed  CAS  Google Scholar 

  • Weir BS (1997) Genetic data analysis II. Sinauer Associates Inc, Sunderland

    Google Scholar 

  • Wingfield MJ, Knox-Davies PS (1980) Association of Diplodia pinea with a root disease of pines in South Africa. Plant Dis 64:22–223

    Google Scholar 

  • Wingfield MJ, Slippers B, Roux J, Wingfield BD (2001) Worldwide movement of exotic forest fungi, especially in the tropics and the southern hemisphere. Bioscience 51:134–140

    Article  Google Scholar 

  • Wingfield MJ, Slippers B, Hurley BP, Coutinho TA, Wingfield BD, Roux J (2008) Eucalypt pests and diseases: growing threats to plantation productivity. Southern Forests 70:139–144

    Article  Google Scholar 

  • Yeh FC, Yang RC, Boyle T (1999) POPEGENE version 1.31 Microsoft windows based freeware for population genetic analysis. Alberta

  • Zhan J, McDonald BA (2004) The interaction among evolutionary forces in the pathogenic fungus Mycosphaerella graminicola. Fungal Genet Biol 41:590–599

    Article  PubMed  CAS  Google Scholar 

  • Zwolinski JB, Swart WJ, Wingfield MJ (1990) Economic impact of a post-hail outbreak of dieback induced by Sphaeropsis sapinea. Eur J Forest Pathol 20:405–411

    Article  Google Scholar 

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Acknowledgements

This research was financially supported by the DST/NRF Centre of Excellence in Tree Health Biotechnology (CTHB), members of the Tree Protection Co-operative Program (TPCP) and the International Foundation for Sciences, Stockholm, Sweden, through a grant to Wubetu Bihon.

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Correspondence to Wubetu Bihon.

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Bihon, W., Burgess, T., Slippers, B. et al. High levels of genetic diversity and cryptic recombination is widespread in introduced Diplodia pinea populations. Australasian Plant Pathol. 41, 41–46 (2012). https://doi.org/10.1007/s13313-011-0086-2

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