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Tytuł artykułu

Analyses of air samples for ascospores of Leptosphaeria maculans and L. biglobosa by light microscopy and molecular techniques

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Spores of many fungal pathogens are dispersed by wind. Detection of these airborne inocula is important in forecasting both the onset and the risk of epiphytotics. Species-specific primers targeted at the internal transcribed spacer (ITS) region of Leptosphaeria maculans and L. biglobosa - the causal organisms of phoma stem canker and stem lesions of Brassica spp., including oilseed rape - were used to detect DNA extracted from particles deposited on tapes obtained from a spore trap operated in Rarwino (northwest Poland) from September to November in 2004 and 2006. The quantities of DNA assessed by traditional end-point PCR and quantitative real-time PCR were compared to microscopic counts of airborne ascospores. Results of this study showed that fluctuations in timing of ascospore release corresponded to the dynamics of combined concentrations of DNA from L. maculans and L. biglobosa, with significant positive correlations between ascospore number and DNA yield. Thus the utilization of PCR-based molecular diagnostic techniques enabled the detection, identification, and accurate quantification of airborne inoculum at the species level. Moreover, real-time PCR was more sensitive than traditional PCR, especially in years with low ascospore numbers.

Wydawca

-

Rocznik

Tom

50

Numer

4

Opis fizyczny

p.411-419,fig.,ref.

Twórcy

autor
  • Institute of Plant Genetics, Polish Academy of Sciences, Strzeszynska 34, 60-479 Poznan, Poland
autor
  • Institute of Plant Genetics, Polish Academy of Sciences, Strzeszynska 34, 60-479 Poznan, Poland
autor
  • Rothamsted Research, Harpenden, United Kingdom
autor
  • Rothamsted Research, Harpenden, United Kingdom
  • Rothamsted Research, Harpenden, United Kingdom

Bibliografia

  • Fitt BDL, Brun H, Barbetti MJ, Rimmer RS, 2006. World-wide importance of phoma stem canker (Leptosphaeria maculans and L. biglobosa) on oilseed rape (Brassica napus). Eur J Plant Pathol 114: 3-15.
  • Fountaine JA, Shaw MW, Napier B, Ward E, Fraaije BA, 2007. Application of real-time and multiplex polymerase chain reaction assays to study leaf blotch epidemics in barley. Phytopathology 97: 297-303.
  • Gladders P, Symonds BV, Hardwick NV, Sansford CE, 1998. Opportunities to control canker (L. maculans) in winter oilseed rape by improving spray timing. Int Org Biol Integr Cont (IOBC) Bull. 21: 111-120.
  • Graham GC, Mayers P, Henry RJ, 1994. A simplified method for the preparation of fungal genomic DNA for PCR and RAPD analysis. Biotechniques 16: 48-50.
  • Guo XW, Fernando WGD, 2005. Seasonal and diurnal patterns of spore dispersal by Leptosphaeria maculans from canola stubble in relation to environmental conditions. Plant Dis 89: 97-104.
  • Hammond KE, Lewis BG, Musa TM, 1985. A systemic pathway for the infection of oilseed rape plants by Leptosphaeria maculans. Plant Pathol 34: 57-65.
  • Huang YJ, Liu Z, West JS, Todd AD, Hall AM, Fitt BDL, 2007. Effects of temperature and rainfall on date of release of ascospores of Leptosphaeria maculans (phoma stem canker) from winter oilseed rape (Brassica napus) debris in the UK. Annals Appl Biol 151:99-111.
  • Jędryczka M, Kaczmarek J, Dawidziuk A, Brachaczek A, 2008. System for Forecasting Disease Epidemics - aerobiological methods in Polish agriculture. Aspects Appl Biol 89: 65-70.
  • Kaczmarek J, Fitt BDL, Jędryczka M, Latunde-Dada AO, 2008. Detection by Real-Time PCR and quantification of Leptosphaeria maculans and L. biglobosa in air samples from north Poland. Aspects Appl Biol 89: 71-76.
  • Kaczmarek J, Jędryczka M, Irzykowski W, Fitt BDL, Lucas JA, Latunde-Dada AO, 2009. Comparative analyses of ratio between ascospores of Leptosphaeria maculans and L. biglobosa in air samples, using traditional PCR and Real-time PCR. Dissertations and Monographs, IPG PAS, Poznan, vol. 18 (in press).
  • Lacey M, West JS, 2006. The air spora: a manual for catching and identifying airborne biological particles. Springer-Verlag GmbH: 156.
  • Li H, Sivasithamparam K, Barbetti MJ, 2003. Breakdown of a Brassica rapa subsp. sylvestris single dominant blackleg resistance gene in B. napus rapeseed by Leptosphaeria maculans field isolates in Australia. Plant Dis 87: 752.
  • Luo Y, Ma Z, Reyes HC, Morgan D, Michailides TJ, 2007. Quantification of airborne spores of Monilinia fructicola in stone fruit orchards of California using real-time PCR. Eur J Plant Pathol 118: 145-154.
  • Mahuku GS, Hall R, Goodwin PH, 1996. Co-infection and induction of systemic acquired resistance by weakly and highly virulent isolates of Leptosphaeria maculans in oilseed rape. Physiol Mol Plant Pathol 49: 61-72.
  • McDevitt JJ, Lees PSJ, Merz WG, Schwab KJ, 2007. Inhibition of quantitative PCR analysis of fungal conidia associated with indoor air particulate matter. Aerobiologia 23: 35-45.
  • Payne RW, Harding SA, Murray DA, Soutar DM, Baird DB, Welham SJ, et al. 2007. The guide to GenStat release 10, Part 2: Statistics, Oxford: VSN International, UK: 1096.
  • Paul VH, Rawlinson CJ, 1992. Diseases and pests of oilseed rape. Gelsenkirchen-Buer: Verlag Theodore Mann, Germany.
  • Rouxel T, Penaud A, Pinochet X, Brun H, Gout L, Delourme R, et al. 2003. A 10-year survey of populations of Leptosphaeria maculans in France indicates a rapid adaptation towards the Rlm1 resistance gene of oilseed rape. Eur J Plant Pathol 109: 871-881.
  • Shoemaker RA, Brun H, 2001. The teleomorph of the weakly aggressive segregate of Leptosphaeria maculans. Can J Bot 79: 412-419.
  • Toscano-Underwood C, Huang YJ, Fitt BDL, Hall AM, 2003. Effects of temperature on maturation of pseudothecia of Leptosphaeria maculans and L. biglobosa on oilseed rape stem debris. Plant Pathol 52: 726-736.
  • Walsh K, Korimbocus N, Boonham P, Jennings P, Hims M, 2005. Using real-time PCR to discriminate and quantify the closely related wheat pathogens Oculimacula yallundae and Oculimacula acuformis. J Phytopathol 153: 715-721.
  • West JS, Balesdent MH, Rouxel T, Narcy JP, Huang YJ, Roux J, et al. 2002. Colonization of winter oilseed rape tissues by A/Tox(+) and B/Tox(0) Leptosphaeria maculans (phoma stem canker) in France and England. Plant Pathol 51: 311-321.
  • West JS, Biddulph JE, Fitt BDL, Gladders P, 1999. Epidemiology of Leptosphaeria maculans in relation to forecasting stem canker severity on winter oilseed rape in the UK. Ann Appl Biol 135: 535-546.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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