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Sequence diversity of mating-type genes in Phaeosphaeria avenaria

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Abstract.

Phaeosphaeria avenaria, one of the causal agents of stagonospora leaf blotch diseases in cereals, is composed of two subspecies, P. avenaria f. sp. triticea (Pat) and P. avenaria f. sp. avenaria (Paa). The Pat subspecies was grouped into Pat1–Pat3, based on restriction fragment length polymorphism (RFLP) and ribosomal DNA (rDNA) internal transcribed spacer (ITS) sequences in previous studies. Mating-type genes and their potential use in phylogeny and molecular classification were studied by DNA hybridization and PCR amplification. The majority of Pat1 isolates reported to be homothallic and producing sexual reproduction structures on cultural media had only the MAT1-1 gene. Minor sequence variations were found in the conserved region of MAT1-1 gene in Pat1 isolates. However, both mating-type genes, MAT1-1 and MAT1-2, were identified in P. avenaria isolates represented by ATCC12277 from oats (Paa) and the Pat2 isolates from foxtail barley (Hordeum jubatum L.). Cluster analyses based on mating-type gene conserved regions revealed that cereal Phaeosphaeria is not phylogenetically closely related to other ascomycetes, including Mycosphaerella graminicola (anamorph Septoria tritici). The sequence diversity of mating-type genes in Pat and Paa supports our previous phylogenetic relationship and molecular classification based on RFLP fingerprinting and rDNA ITS sequences.

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References

  • Arseniuk E, Czembor HJ, Sowa W, Krysiak H (1989) Preliminary studies of Septoria spp on triticale in Poland. In: Fried PM (ed) Septoria of cereals: proceedings. Swiss Federal Research Station for Agronomy, Zurich, pp 16–18

    Google Scholar 

  • Beck JJ, Ligon JM (1995) Polymerase chain reaction assays for the detection of Stagonospora nodorum and Septoria tritici in wheat. Phytopathology 85:319–324

    CAS  Google Scholar 

  • Beck JJ, Ligon JM, Etienne L, Binder A (1996) Detection of crop fungal pathogens by polymerase chain reaction technology. In: Marshall G (ed) Diagnostics in crop production. The British Crop Protection Council, Farnham, pp 111–118

  • Bennett RS, Yun SH, Lee TY, Turgeon BG, Cunfer B, Arseniuk E, Bergstrom GC (1999) Mating type-specific PCR primers for Stagonospora nodorum field studies. In: Ginkel M van, McNab MA, Krupinsky J (eds) Septoria and Stagonospora diseases of cereals: a compilation of global research. CIMMYT, Mexico, D.F., pp 90–92

    Google Scholar 

  • Câmara MPS, Palm ME, Berkum P van, O'Neill NR (2002) Molecular phylogeny of Leptosphaeria and Phaeosphaeria. Mycologia 94:630–640

    Google Scholar 

  • Caten CE, Newton AC (2000) Variation in cultural characteristics, pathogenicity, vegetative compatibility and electrophoretic karyotype within field populations of Stagonospora nodorum. Plant Pathol 49:219–226

    Article  Google Scholar 

  • Clark RV, Gourley CO, Johnston HW, Piening LJ, Pelletier G, Santerre J, Genereux H (1975) Oat yield losses from Septoria leaf blotch at four locations in eastern Canada. Can Plant Dis Surv 55:36–43

    Google Scholar 

  • Coppin E, Debuchy R, Arnaise S, Picard M (1997) Mating-types and sexual development in filamentous ascomycetes. Microbiol Mol Biol Rev 61:411–428

    CAS  PubMed  Google Scholar 

  • Cunfer BM, Ueng PP (1999) Taxonomy and identification of Septoria and Stagonospora species on small-grain cereals. Annu Rev Phytopathol 37:267–284

    Article  CAS  PubMed  Google Scholar 

  • Czembor PC, Arseniuk E (2000) Segregation and recombination of PCR based markers in sexual progeny of Phaeosphaeria species. Mycol Res 104:919–926

    Article  CAS  Google Scholar 

  • Dai Q, Arseniuk E, Cunfer BM, Cui K, Ueng PP (2001) Segregation, aggressiveness and sexuality in Phaeosphaeria nodorum. Phytopathology 91:S20

    Google Scholar 

  • Glass NL, Kuldau GA (1992) Mating type and vegetative incompatibility in filamentous ascomycetes. Annu Rev Phytopathol 30:201–224

    Article  Google Scholar 

  • Glass NL, Smith ML (1994) Structure and function of a mating-type gene from the homothallic species Neurospora africana. Mol Gen Genet 244:401–409

    CAS  PubMed  Google Scholar 

  • Glass NL, Metzenberg RL, Raju NB (1990) Homothallic Sordariaceae from nature: the absence of strains containing only the α mating type sequence. Exp Mycol 14:273–289

    Google Scholar 

  • Goodwin SB, Zismann VL (2001) Phylogenetic analyses of the ITS region of ribosomal DNA reveal that Septoria passerinii from barley is closely related to the wheat pathogen Mycosphaerella graminicola. Mycologia 93:934–946

    CAS  Google Scholar 

  • Goodwin SB, Dunkle LD, Zismann VL (2001) Phylogenetic analysis of Cercospora and Mycosphaerella based on the internal transcribed spacer region of ribosomal DNA. Phytopathology 91:648–658

    CAS  Google Scholar 

  • Halama P (2002) Mating relationships between isolates of Phaeosphaeria nodorum, (anamorph Stagonospora nodorum) from geographical locations. Eur J Plant Pathol 108:593–596

    Google Scholar 

  • Halama P, Lacoste L (1991) Déterminisme de la reproduction sexuée de Phaeosphaeria (Leptosphaeria) nodorum, agent de la septoriose du blé. I. Hétérothallisme et rôle des microspores. Can J Bot 69:95–99

    Google Scholar 

  • Halama P, Skajennikoff M, Dehorter B (1999) Tetra analysis of mating type, mutations, esterase and aggressiveness in Phaeosphaeria nodorum. Mycol Res 103:43–49

    Article  Google Scholar 

  • Hosford RM Jr, Hogenson RO, Huguelet JE, Kiesling RL (1969) Studies of Leptosphaeria avenaria f. sp. triticea on wheat in North Dakota. Plant Dis Rep 53:378–381

    Google Scholar 

  • Johnson T (1947) A form of Leptosphaeria avenaria on wheat in Canada. Can J Res Sect C 25:259–270

    Google Scholar 

  • Keller SM, McDermott JM, Pettway RE, Wolfe MS, McDonald BA (1997) Gene flow and sexual reproduction in the wheat glume blotch pathogen Phaeosphaeria nodorum (anamorph Stagonospora nodorum). Phytopathology 87:353–358

    Google Scholar 

  • Krüger J, Hoffmann GM (1978) Differenzierung von Septoria nodorum Berk. und Septoria avenae Frank f. sp. triticea T. Johnson. Z Pflanzenkr Pflanzenschutz 85:645–650

    Google Scholar 

  • Luz WC da, Bergstrom GC (1985) Septoria avenae spot as an additional component of the fungal leaf spot syndrome of spring wheat in New York. Plant Dis 69:724–725

    Google Scholar 

  • Mäkelä K (1977) Septoria and Selenophoma species on Gramineae in Finland. Ann Agric Fenn 16:256–276

    Google Scholar 

  • McDonald BA, Zhan J, Yarden O, Hogan K, Garton J, Pettway RE (1999) The population genetics of Mycosphaerella graminiola and Phaeosphaeria nodorum. In: Lucas JA, Bowyer P, Anderson HM (eds) Septoria on cereals: a study of pathosystems. CAB, Wallingford, pp 44–69

    Google Scholar 

  • Metzenberg RL, Glass NL (1990) Mating type and mating strategies in Neurospora. BioEssays 12:53–59

    CAS  PubMed  Google Scholar 

  • Mielke H (1975) Über die Blattfleckenkrankheit (Septoria avenae Frank) des Hafers. Mitt Biol Bundesanst Land Forstwirtsch Berlin-Dahlem 163:41–47

    Google Scholar 

  • Pöggeler S (1999) Phylogenetic relationships between mating-type sequences from homothallic and heterothallic ascomycetes. Curr Genet 36:222–231

    Article  PubMed  Google Scholar 

  • Pöggeler S, Risch S, Kück U, Osiewacz HD (1997) Mating-type genes from the homothallic fungus Sordaria macrospora are functionally expressed in a heterothallic ascomycete. Genetics 147:567–580

    PubMed  Google Scholar 

  • Richardson MJ, Noble M (1970) Septoria species on cereals—a note to aid their identification. Plant Pathol 19:159–163

    Google Scholar 

  • Shaw DE (1957) Studies on Leptosphaeria avenaria f. sp. triticea on cereals and grasses. Can J Bot 35:113–118

    Google Scholar 

  • Shearer BL, Skovmand B, Wilcoxson RD (1977) Hordeum jubatum as a source of inoculum of Septoria avenae f. sp. triticea and S. passerinii. Phytopathology 67:1338–1341

    Google Scholar 

  • Shipton WA, Boyd WJR, Rosielle AA, Shearer BL (1971) The common Septoria diseases of wheat. Bot Rev 37:231–262

    Google Scholar 

  • Southern EM (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol 98:503–517

    CAS  PubMed  Google Scholar 

  • Sprague R (1950) Disease of cereals and grasses in North America. Ronald Press: New York

    Google Scholar 

  • Staben C, Yanofsky C (1990) Neurospora crassa a mating-type region. Proc Natl Acad Sci USA 87:4917–4921

    CAS  PubMed  Google Scholar 

  • Turgeon BG (1998) Application of mating type gene technology to problems in fungal biology. Annu Rev Phytopathol 36:115–137

    Article  CAS  Google Scholar 

  • Turgeon BG, Yoder OC (2000) Proposed nomenclature for mating type genes of filamentous Ascomycetes. Fungal Genet Biol 31:1–5

    Article  CAS  PubMed  Google Scholar 

  • Ueng PP, Chen W (1994) Genetic differentiation between Phaeosphaeria nodorum and P. avenaria using restriction fragment length polymorphisms. Phytopathology 84:800–806

    Google Scholar 

  • Ueng PP, Bergstrom GC, Slay RM, Geiger EA, Shaner G, Scharen AL (1992) Restriction fragment length polymorphisms in the wheat glume blotch fungus, Phaeosphaeria nodorum. Phytopathology 82:1302–1305

    Google Scholar 

  • Ueng PP, Cunfer BM, Alano AS, Youmans JD, Chen W (1995) Correlation between molecular and biological characters in identifying the wheat and barley biotypes of Stagonospora nodorum. Phytopathology 85:44–52

    Google Scholar 

  • Ueng PP, Subramaniam K, Chen W, Arseniuk E, Wang L, Cheung AM, Hoffmann GM, Bergstrom GC (1998) Intraspecific genetic variation of Stagonospora avenae and its differentiation from S. nodorum. Mycol Res 102:607–614

    Article  CAS  Google Scholar 

  • Waalwijk C, Mendes O, Verstappen ECP, Waard MA de, Kema GHJ (2002) Isolation and characterization of the mating-type idiomorphs from the wheat septoria leaf blotch fungus Mycosphaerella graminicola. Fungal Genet Biol 35:277–286

    Article  CAS  PubMed  Google Scholar 

  • Weber GF (1922) Septoria diseases of cereals. I. Speckled blotch of oats caused by Leptosphaeria. Phytopathology 12:449–470

    Google Scholar 

  • Yun S, Berbee ML, Yoder OC, Turgeon BG (1999) Evolution of the fungal self-fertile reproductive life style from self-sterile ancestors. Proc Natl Acad Sci USA 96:5592–5597

    CAS  PubMed  Google Scholar 

  • Yun S, Arie T, Kaneko I, Yoder OC, Turgeon BG (2000) Molecular organization of mating type loci in heterothallic, homothallic, and asexual Gibberella/Fusarium species. Fungal Genet Biol 31:7–20

    Article  CAS  PubMed  Google Scholar 

  • Zeiders KE, Berg CC, Sherwood RT (1984) Effect of recurrent phenotypic selection on resistance to purple leaf spot in orchardgrass. Crop Sci 24:182–185

    Google Scholar 

  • Zhan J, Kema GHJ, Waalwijk C, McDonald BA (2002) Distribution of mating type alleles in the wheat pathogen Mycosphaerella graminicola over spatial scales from lesions to continents. Fungal Genet Biol 36:128–136

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements.

We thank Rosemarie Hammond of the USDA–ARS for reviewing the manuscript and Z. Ye of the University of Maryland for technical support. This research is partially supported by the USDA–ARS CRIS and the US–Poland Maria Sklodowska–Curie Joint Fund Projects.

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Correspondence to Peter P. Ueng.

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Communicated by U. Kück

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Ueng, P.P., Dai, Q., Cui, Kr. et al. Sequence diversity of mating-type genes in Phaeosphaeria avenaria . Curr Genet 43, 121–130 (2003). https://doi.org/10.1007/s00294-003-0377-4

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