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1996 | 37 | 3 |

Tytuł artykułu

Use of random amplified polymorphic DNA [RAPD] assay for differentiation among isolates of Stagonospora spp. and Septoria tritici

Treść / Zawartość

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The genetic similarity of three species: Septoria tritici, Stagonospora nodorum and Stagonospora avenae f. sp. triticea - important pathogens in many cereal production areas worldwide was assessed by random amplified polymorphic DNA (RAPD) assay. In preliminary research DNA of 14, 9, and 7 monopyenidios- pore isolates of S. nodorum, S. tritici, and S. a. tritícea, respectively, were amplified by PCR with four primers. Afterwards the research was focused on three mono- pyenidiospore isolates from each species studied. The isolates of each species selected for the study varied in pathogenicity and were diverse geographically. PCR with the set of 14 selected primers resulted in 99 different bands, ranged from 180 to 2500 base pairs in length. Most primers in PCR (especially RAD11, RAD31, RAD32, RAD33) revealed uniform bands for isolates of S. a. tritícea, that allow to identify this species among the others. The cluster analysis using Unweighed Pair-Group Method with Averaging (UPGMA) revealed interspecies disagreement among the isolates ranging from 32 to 53%. The intraspecies disagreement ranges were 17-20%, 38-43%, 42-44% for S. avenae f. sp. triticea, S. nodorum and S. tritici, respectively. Cluster analysis classified isolates into three homogeneous clusters. Each cluster grouped isolates of one species according to their current taxonomie ranks based on spore size, colony morphology and host ranges. In addition, two of the clusters represented by isolates of S. nodorum and S. a. tritícea were distinctly separated at a lower linkage distance from the third one comprising isolates of S. tritici. A slight inconsistency found in grouping some isolates indicates that such groupings should be done with caution. The present study indicates that the PCR- RAPD assay is of a potential use in taxonomy of Stagonospora spp. and Septoria tritici as well as in molecular identification of casual disease agents.

Wydawca

-

Rocznik

Tom

37

Numer

3

Opis fizyczny

p.239-251,fig.

Twórcy

autor
  • Department of Plant Pathology, Plant Breeding and Acclimatization Institute, Radzikow, 05-870 Blonie, Poland
autor
  • Department of Plant Pathology, Plant Breeding and Acclimatization Institute, Radzikow, 05-870 Blonie, Poland

Bibliografia

  • ARSENIUK F., CZEMBOR H.J, SOWA W., KRYSIAK H. (1989). Preliminary studies of Septoria spp. on triticale in Poland. In: Proc. 3rd International Workshop on Septoria Diseases of Cereals. Zurich, Switzerland, July 4-7, pp. 16-18.
  • BECK J.J., LIGON J.M. (1995). Polymerase chain reaction assays for the detection of Stagonospora nodorum and Septoria tritici in wheat. Phytopathology 85: 319-324.
  • CAETANO-ANOLLÉS G., BASSAM B.J., GRESSHOFF P.M. (1991). DNA amplification fingerprinting using very short arbitrary oligonucleotide primers. Bio/Technology 9: 553-557.
  • COOLEY N.R., CATEN CH.E. (1991). Variation in eleclrophoretic karyotype between strains of Seploria nodorum. Mol. Gen. Genet. 228: 17-23.
  • CUNFER M.B. (1994). Taxonomy and nomenclature of Seploria and Stagonospora species on cereals. Hodowla Rośl. Aklim. Nasienn. (Special Edition) 38: 15-19.
  • CUNFER M.B., YOUMANS J. (1983). Seploria nodorum on barley and relationships among isolates from several hosts. Phytopathology 73: 911-914.
  • DAVIS L.G., DIBNER M.D., BATTEY J.F. (1986). Basic methods in molecular biology, Elsevier Science Publishing Co., Inc., New York: 42-43.
  • DOUDRIC R.L., NANCE W.L., NELSON C.D., SNOW G.A., HAMELIN R.C. (1993). Detection of DNA polymorphisms in a single uredinoiospore-derived culture of Cronartium quercuum f.sp. fusiforme. Phytopathology 83: 388-392.
  • EYAL Z., SCHAREN A.L., PRESCOTT M.J., VAN GINKEL M. (1987). The Septoria Diseases of Wheat: Concepts and methods of disease management. Mexico, D.F.: CIMMYT.
  • GÓRAL T., ARSENIUK E., SCHAREN A.L. (1994). Spore dispersal studies of Phaeosphaeria nodorum. Hodowla Rośl. Aklim. Nasienn. (Special Edition) 38: 235-240.
  • GUTHRIE P.A.I., MAGILL C.W., FREDERIKSEN R.A., ODVODY G.N. (1992). Random amplified polymorphic DNA markers: a system for identifying and differentiating isolates of Colletotrichum graminicola. Phytopathology 82: 832-835.
  • JEFFREYS A.J., WILSON V., NEUMANN R., KEYTE J. (1988). Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells. Nucleic Acids Research 16: 10053-10071.
  • MANIATIS T., FRITSCH E.F., SAMBROOK J. (1982). Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory: Cold Spring Harbor, New York.
  • McDONALD B.A., MARTINEZ J.P. (1990a). Restriction fragment length polymorphisms in Septoria tritici occur at a high frequency. Current Genetics 17: 133-138.
  • McDONALD B.A., MARTINEZ J.P. (1990b). DNA restriction fragment length polymorphisms among Mycosphaerella graminicola (anamorph Seploria tritici) isolates collected from a single wheat field. Phytopathology 80: 1368-1373.
  • McDONALD B.A., MARTINEZ J.P. (1991a). DNA fingerprinting of the plant pathogenic fungus Mycosphaerella graminicola (anamorph Septoria tritici). Experimental Mycology 15: 146-158.
  • McDONALD B.A., MARTINEZ J.P. (1991b). Chromosome length polymorphisms in a Seploria tritici population. Current Genetics 19: 265-271.
  • McDONALD B.A., McDERMOTT J.M. (1993). Population genetics of plant pathogenic fungi. Electrophoretic markers give unprecedented precision to analyses of genetic structure of populations. BioScience 43: 311 -319.
  • McDONALD B.A., MILES J., NELSON L.R., PETTWAY R.E. (1994). Genetic variability in neclear DNA in field populations of Stagonospora nodorum. Phytopathology 84: 250-255.
  • NEWTON A.C. (1991). Isozyme variability in isolates of some facultative phytopathogenic fungi. J. Phytopathol. 131: 199-204.
  • NEWTON A.C., CATEN C.E. (1991). Characteristics of strains of Septoria nodorum adapted to wheat or to barley. Plant Pathol. 40: 546-553.
  • OUELLET T., SEIFERT K. (1993). Genetic characterization of Fusarium graminearum strains using RAPD and PCR amplification. Phytopathology 83: 1003-1007.
  • SCHÄFER O., WÖSTEMEYER J. (1992). Random primer dependent PCR differentiates aggressive from non-aggressive isolates of the oilseed rape pathogen Phoma Ungarn (Leptosphaeria maculans). J. Phytopathol. 136: 24-136.
  • TISSERATN.A., HULBERT S.H., NUS A. (1991). Identification of Leptosphaeria korrae by cloned DNA probes. Phytopathology 81: 917-921.
  • UENG P.P., BERGSTROM G.C., SLAY R.M., GEIGER E.A., SHANER G., SCHAREN A.L. (1992). Restriction Fragment Length Polymorphisms in the wheat glume blotch fungus, Phaeosphaeria nodorum. Phytopathology 82: 1302-1305.
  • UENG P.P., CHEN W. (1994). Genetic differentiation between Phaeosphaeria nodorum and P. avenaria using restriction fragment lenght polymorphisms. Phytopathology 84: 800-806.
  • UENG P. P., CUNFER B. M., ALANO A. S., YOUMANS J. D., CHEN W. (1995). Correlation between molecular and biological characters in identifying the wheat and barley biotypes of Stagonospora nodorum. Phytopathology 85: 44-52.
  • WEBER J.L., MAY P.E. (1989). Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. Hum. Genet. 44: 388-396.
  • WEISING K., NYBOM H., WOLFF K., MEYER W. (1995). DNA fingerprinting in plants and fungi. CRC Press Inc., 2000 Corporate Blvd., N.W., Boca Raton, Florida 33431.
  • WELSH J., McCLELLAND M. (1990). Fingerprinting genomes using PCR with arbitrary primers. Nucleic Acids Research 18: 7213-7218.
  • WILLIAMS J.G.K., KUBELIK A.R., LIVAK K.J., RAFALSKI J.A., TINGEY S.V. (1990). DNA polymorphisms amplified by arbitrary primers are useful as genetic markers. Nucleic Acids Research 18: 6531-6535.
  • ZILBERSTEIN A., PLNI-COHEN S., EYAL Z., SHUSTER S., HILLEL J., LAVI U. (1993). Application of DNA fingerprinting for detecting genetical variation among isolates of the wheat pathogen Mycosphaerella graminicola. In: Biotechnology in Plant Disease Control (Chet ed.), Wiley-Liss. Inc.: 341-353.

Typ dokumentu

Bibliografia

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