Genetic Diversity of Blumeria graminis f. sp. hordei in Central Europe and Its Comparison with Australian Population

. 2016 ; 11 (11) : e0167099. [epub] 20161122

Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection

Typ dokumentu srovnávací studie, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid27875588

Population surveys of Blumeria graminis f. sp. hordei (Bgh), a causal agent of more than 50% of barley fungal infections in the Czech Republic, have been traditionally based on virulence tests, at times supplemented with non-specific Restriction fragment length polymorphism or Random amplified polymorphic DNA markers. A genomic sequence of Bgh, which has become available recently, enables identification of potential markers suitable for population genetics studies. Two major strategies relying on transposable elements and microsatellites were employed in this work to develop a set of Repeat junction markers, Single sequence repeat and Single nucleotide polymorphism markers. A resolution power of the new panel of markers comprising 33 polymorphisms was demonstrated by a phylogenetic analysis of 158 Bgh isolates. A core set of 97 Czech isolates was compared to a set 50 Australian isolates on the background of 11 diverse isolates collected throughout the world. 73.2% of Czech isolates were found to be genetically unique. An extreme diversity of this collection was in strong contrast with the uniformity of the Australian one. This work paves the way for studies of population structure and dynamics based on genetic variability among different Bgh isolates originating from geographically limited regions.

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United Nations Department of Economic and Social Affairs/Population Division World Population Prospects: The 2015 Revision, Key Findings and Advance Tables. 2015; Available: https://www.un.org/. Accessed 22 October 2015

FAOSTAT—Food and Agriculture Organization of the United Nations, FAO Statistical Databases Agricultural production data. 2015; Available: http://faostat3.fao.org/. Accessed 22 October 2015

Czech Statistical Office Agriculture data: Time series 2015. Available: https://www.czso.cz/. Accessed 22 October 2015

Dean R, van Kan JAL, Pretorius ZA, Hammond-Kosack KE, di Pietro A, Spanu PD, Rudd JJ, et al. The Top 10 fungal pathogens in molecular plant pathology. Mol Plant Pathol. 2012; 13:414–430. 10.1111/j.1364-3703.2011.00783.x PubMed DOI PMC

Dreiseitl A, Jurečka D. Disease occurrence on spring barley in the Czech Republic in 1989–1995. Ochrana Rostlin. 1996; 32:221–229.

Dreiseitl A, Jurečka D. Disease occurrence on winter barley in the Czech Republic in 1989–1996. Ochrana Rostlin. 1997; 33:177–186.

Andrivon D, de Vallavieille-Pope C. Racial diversity and complexity in regional populations of

Brown JKM, Slater SE, See KA. Sensitivity of

Bousset L, Hovmøller MS, Caffier V, de Vallavieille-Pope C, Østergård H. Observed and predicted changes over eight years in frequency of barley powdery mildew avirulent to spring barely in France and Denmark. Plant Pathol. 2002; 51:33–44.

Caffier V, Hoffstadt T, Leconte M, de Vallavieille-Pope C. Seasonal changes in pathotype complexity in French populations of barley powdery mildew. Plant Pathol. 1996;45:454–468

Dreiseitl A, Pickering RA. Pathogenicity of

Dreiseitl A, Wang J. Virulence and diversity of

Hossain MA, Rahman MS. Pathogenic variability of

Hovmøller MS, Caffier V, Jalli M, Andersen O, Besenhofer G, Czembor JH, Dreiseitl A, et al. The European barley powdery mildew virulence survey and disease nursery 1993–1999. Agronomie. 2000; 20:729–743.

Hovmøller MS, Munk L, Østergård H. Observed and predicted changes in virulence gene frequencies at 11 loci in a local barley powdery mildew population. Phytopathology. 1993; 83:253–260.

Limpert E. Frequencies of virulence and fungicide resistance in the European barley mildew population in 1985. J Phytopathol. 1987; 119:298–311.

Limpert E, Andrivon D, Fischbeck G. Virulence patterns in population of

Müller K, McDermott JM, Wolfe MS, Limpert E. Analysis of diversity in populations of plant pathogens: The barley powdery mildew pathogen across Europe. Eur J Plant Pathol. 1996; 102:385–395.

Yahyaoui AH, Reinhold M, Scharen AL. Virulence spectrum in populations of the barley powdery mildew pathogen,

Koch G, Köhler W. Isozyme variation and genetic distances of

Koch G, Köhler W. Isozyme variation and genetic diversity of the European barley powdery mildew population. J Phytopathol. 1991; 131:333–344.

Brown JKM, O’Dell M, Simpson CG, Wolfe MS. The use of DNA polymorphisms to test hypotheses about a population of

Damgaard C, Giese H. Genetic variation in Danish populations of

O’Dell M, Wolfe MS, Flavell RB, Simpson CG, Summers RW. Molecular variation in populations of

Whisson DL. Molecular characterization and pathogenicity of

Caffier V, Brändle UE, Wolfe MS. Genotypic diversity in barley powdery mildew populations in northern France. Plant Pathol; 1999. 48:582–587.

McDermott JM, Brändle U, Dutly F, Haemmerli UA, Keller S, Müller KE, et al. Genetic variation in powdery mildew of barley: Development of RAPD, SCAR and VNTR markers. Phytopathology. 1994; 84:1316–1321.

Newton AC, Hackett CA, Guy DC. Diversity and complexity of

Wyand RA, Brown JKM. Genetic and PubMed DOI

Inuma T, Khodaparast SA, Takamatsu S. Multilocus phylogenetic analysis within PubMed DOI

Oberhaensli S, Parlange F, Buchmann JP, Jenny FH, Abbott JC, Burgis TA. Comparative sequence analysis of wheat and barley powdery mildew fungi reveals collinearity, dates divergence and indicates host-pathogen co-evolution. Fungal Genet Biol. 2011; 48: 327–334. 10.1016/j.fgb.2010.10.003 PubMed DOI

Wang M, Xue F, Yang P, Duan XY, Zhou YL, Shen CY, et al. Development of SSR markers for a phytopathogenic fungus,

Spanu PD, Abbott JC, Amselem J, Burgis TA, Soanes DM, Stüber K, et al. Genome expansion and gene loss in powdery mildew fungi reveal tradeoffs in extreme parasitism. Science. 2010; 330:1543–1546. 10.1126/science.1194573 PubMed DOI

Hacquard S, Kracher B, Maekawa T, Vernaldi S, Schulze-Lefert P, van Themaat EVL. Mosaic genome structure of the barley powdery mildew pathogen and conservation of transcriptional programs in divergent hosts. P Natl Acad Sci USA. 2013; 110: E2219–E2228. PubMed PMC

Tucker MA, Moffat CS, Ellwood SR, Tan KC, Jayasena K, Oliver RP. Development of genetic SSR markers in

Dreiseitl A. Pathogenic divergence of Central European and Australian populations of

Chen H, Xie W, He H, Yu H, Chen W, Li J, et al. A high-density SNP genotyping array for rice biology and molecular breeding. Mol Plant. 2014; 7:541–553. 10.1093/mp/sst135 PubMed DOI

Close T, Bhat PR, Lonardi S, Wu Y, Rostoks N, Ramsay L, Druka A. Development and implementation of high-throughput SNP genotyping in barley. BMC Genomics. 2009; 10:582 10.1186/1471-2164-10-582 PubMed DOI PMC

Sim S, Durstewitz G, Plieske J, Wieseke R, Gana MW, Van Deynze A. Development of a large SNP genotyping array and generation of high-density genetic maps in tomato. Plos One. 2012; 7:e40563 10.1371/journal.pone.0040563 PubMed DOI PMC

Excoffier L, Smouse PE, Quattro JM. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics. 1992; 131:479–491. PubMed PMC

Peakall R, Smouse PE. GenAlEx 6: genetic analysis in Excel. Population genetic software for teaching and research. Mol Ecol Notes. 2006; 6:288–295. PubMed PMC

Narasimhamoorthy B, Saha MC, Swaller T, Bouton JH. Genetic diversity in switchgrass collections assessed by EST-SSR markers. Bioenerg Res. 2008; 1:136–146.

Ferrucho RL, Ceresini PC, Ramirez-Escobar UM, McDonald BA, Cubeta MA, García-Domínguez C. The population genetic structure of Rhizoctonia solani AG-3PT from potato in the Colombian Andes. Phytopathology. 2013; 103:862–869. 10.1094/PHYTO-11-12-0278-R PubMed DOI

Dreiseitl A. Changes in virulence frequencies and higher fitness of simple pathotypes in the Czech population of

McDermott JM, McDonald BA. Gene flow in plant pathosystems. Annu Rev Phytopathol. 1993; 31:353–373.

Dreiseitl A, Fowler RA, Platz GJ. Pathogenicity of

Dreiseitl A. Changes in the population of

Dreiseitl A, Kosman E. Virulence phenotypes of

Dreiseitl A, Dinoor A, Kosman E. Virulence and diversity of PubMed

Jurka J, Kohany O. LTR retrotransposons from barley powdery mildew. Repbase Reports. 2011; 11:2333–2333.

Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990; 215:403–410. 10.1016/S0022-2836(05)80360-2 PubMed DOI

Rozen S, Skaletsky HJ. Primer3 on the www for general users and for biologist programmers In: Krawetz S, Misener S (eds) Bioinformatics Methods and Protocols: Methods in Molecular Biology. Humana Press, Totowa, NJ, USA, 2000; pp 365–386 PubMed

Martins WS, Lucas DCS, Neves KFS, Bertioli DJ. WebSat—a web software for microsatellite marker development. Bioinformation. 2009; 3:282–283. PubMed PMC

Tamura K, Peterson D, Peterson N, Stecher G, Nei M, and Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011; 28:2731–2739. 10.1093/molbev/msr121 PubMed DOI PMC

Felsenstein J. PHYLIP (Phylogeny Inference Package) version 3.6. Distributed by the author. Department of Genome Sciences, University of Washington, Seattle: 2005. Available: http://evolution.genetics.washington.edu/phylip.html.

Saitou N, Nei M. The neighbor-joining method: A new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987; 4:406–425. PubMed

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