Skip to main content
Log in

Components of the gene network associated with genotype-dependent response of wheat to the Fusarium mycotoxin deoxynivalenol

  • Short Communication
  • Published:
Functional & Integrative Genomics Aims and scope Submit manuscript

Abstract

The Fusarium mycotoxin deoxynivalenol (DON) facilitates fungal spread within wheat tissue and the development of Fusarium head blight disease. The ability of wheat spikelets to resist DON-induced bleaching is genotype-dependent. In wheat cultivar (cv.) CM82036 DON resistance is associated with a quantitative trait locus, Fhb1, located on the short arm of chromosome 3B. Gene expression profiling (microarray and real-time RT-PCR analyses) of DON-treated spikelets of progeny derived from a cross between cv. CM82036 and the DON-susceptible cv. Remus discriminated ten toxin-responsive transcripts associated with the inheritance of DON resistance and Fhb1. These genes do not exclusively map to Fhb1. Based on the putative function of the ten Fhb1-associated transcripts, we discuss how cascades involving classical metabolite biotransformation and sequestration processes, alleviation of oxidative stress and promotion of cell survival might contribute to the host response and defence against DON.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1

References

  • Ahlfors R, Lång S, Overmyer K, Jaspers P, Brosché M, Tauriainen A, Kollist H, Tuominen H, Belles-Boix E, Piippo M, Inzé D, Palva ET, Kangasjärvi J (2004) Arabidopsis RADICAL-INDUCED CELL DEATH1 belongs to the WWE protein–protein interaction domain protein family and modulates abscisic acid, ethylene, and methyl jasmonate responses. Plant Cell 16(7):1925–1937

    Article  PubMed  CAS  Google Scholar 

  • Amor Y, Chevion M, Levine A (2000) Anoxia pretreatment protects soybean cells against H2O2-induced cell death: possible involvement of peroxidases and of alternative oxidase. FEBS Lett 477:175–180

    Article  CAS  Google Scholar 

  • Ansari KI, Walter S, Brennan JM, Lemmens M, Kessans S, McGahern A, Egan D, Doohan FM (2007) Retrotransposon and gene activation in wheat in response to mycotoxigenic and non-mycotoxigenic-associated Fusarium stress. Theor Appl Genet 114:927–937

    Article  PubMed  CAS  Google Scholar 

  • Bai G-H, Desjardins AE, Plattner RD (2001) Deoxynivalenol-nonproducing Fusarium graminearum causes initial infection, but does not cause disease spread in wheat spikes. Mycopathologia 153(2):91–98

    Article  Google Scholar 

  • Boddu J, Cho S, Muehlbauer GJ (2007) Transcriptome analysis of trichothecene-induced gene expression in barley. Mol Plant-Microb Interact 20:1364–1375

    Article  CAS  Google Scholar 

  • Buerstmayr H, Steiner B, Hartl L, Griesser M, Angerer N, Lengauer D, Miedaner T, Schneider B, Lemmens M (2003) Molecular mapping of QTLs for Fusarium head blight resistance in spring wheat. II. Resistance to fungal penetration and spread. Theor Appl Genet 107(3):503–508

    Article  PubMed  CAS  Google Scholar 

  • Bushnell WR, Seeland TM (2006) Effects of DON on barley leaf tissues, summary of results. The effects of deoxynivalenol on Barley leaf tissue. In: Canty SM, Clark A, Van Sanford D (eds) Proceedings of the National fusarium head blight forum; 2006 Dec 10–12. Research Triangle Park, North Carolina, USA, pp 35–36

    Google Scholar 

  • Bushnell WR, Seeland TM, Perkins-Veazie P, Krueger DE, Collins J, Russo VM (2004) The effects of deoxynivalenol on Barley leaf tissue. In: Tsuyumu S, Leach JE, Shiraishi T, Wolpert T (eds) Genomic and genetic analysis of plant parasitism and defense. APS and The American Phytopathological Society, St. Paul, Minnesota, pp 270–281

    Google Scholar 

  • Coleman J, Blake-Kalff M, Davies E (1997) Detoxification of xenobiotics by plants: chemical modification and vacuolar compartmentation. Trends Plant Sci 2(4):144–151

    Article  Google Scholar 

  • Desmond OJ, Manners JM, Stephens AE, MacLean DJ, Schenk PM, Gardiner DM, Munn AL, Kazan K (2008) The Fusarium mycotoxin deoxynivalenol elicits hydrogen peroxide production, programmed cell death and defence responses in wheat. Mol Plant Pathol 9(4): doi:10.1111/J.1364-3703.2008.00475.X

  • Doyle JJ, Doyle JL (1987) Isolation of DNA from fresh plant tissue. Focus 12:13–15

    Google Scholar 

  • Golkari S, Gilbert J, Prashar S, Procunier JD (2007) Microarray analysis of Fusarium graminearum-induced wheat genes: identification of organ-specific and differentially expressed genes. Plant Biotechnol J 5(1):38–49

    Article  PubMed  CAS  Google Scholar 

  • Handa H, Namiki N, Xu D, Ban T (2008) Dissecting of the FHB resistance QTL on the short arm of wheat chromosome 2D using a comparative genomic approach: from QTL to candidate gene. Mol Breeding 22:71–84

    Google Scholar 

  • Jones DP (2006) Disruption of mitochondrial redox circuitry in oxidative stress. Chemico-Biol Interact 163:38–53

    Article  CAS  Google Scholar 

  • Kang Z, Buchenauer H (1999) Immunocytochemical localization of Fusarium toxins in infected wheat spikes by Fusarium culmorum. Physiol Mol Plant Pathol 55(5):275–288

    Article  CAS  Google Scholar 

  • Katiyar-Agarwal S, Zhu J, Kim K, Agarwal M, Fu X, Huang A, Zhu J-K (2006) The plasma membrane Na+/H+ antiporter SOS1 interacts with RCD1 and functions in oxidative stress tolerance in Arabidopsis. Proc Natl Acad Sci USA 103(49):18816–18821

    Article  PubMed  CAS  Google Scholar 

  • Lemmens M, Scholz U, Berthiller F, Dall’ Asta C, Koutnik A, Schuhmacher R, Adam G, Buerstmayr H, Mesterházy Á, Krska R, Ruckenbauer P (2005) The ability to detoxify the mycotoxin deoxynivalenol colocalizes with a major quantitative trait locus for Fusarium head blight resistance in wheat. Mol Plant-Microb Interact 18(12):1318–1324

    Article  CAS  Google Scholar 

  • Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative pcr and the 2−ΔΔCT method. Methods 25:402–408

    Article  PubMed  CAS  Google Scholar 

  • Masuda D, Ishida M, Yamaguchi K, Yamaguchi I, Kimura M, Nishiuchi T (2007) Phytotoxic effects of trichothecenes on the growth and morphology of Arabidopsis thaliana. J Exp Bot 58(7):1617–1626

    Article  PubMed  CAS  Google Scholar 

  • Nelson DR (2006) Plant cytochrome P450s from moss to poplar. Phytochem Rev 5:193–204

    Article  CAS  Google Scholar 

  • Noctor G, De Paepe R, Foyer CH (2007) Mitochondrial redox biology and homeostasis in plants. Trends Plant Sci 12(3):125–134

    Article  PubMed  CAS  Google Scholar 

  • Ordog SH, Higgins VJ, Vanlerberghe GC (2002) Mitochondrial alternative oxidase is not a critical component of plant viral resistance but may play a role in the hypersensitive response. Plant Physiol 129:1858–1865

    Article  PubMed  CAS  Google Scholar 

  • Overmyer K (2002) Hormonal regulation of radical-induced programmed cell death in ozone-sensitive mutants of Arabidopsis thaliana. Academic dissertation, University of Helsinki, Finland

  • Parry DW, Jenkinson P, McLeod L (1995) Fusarium ear blight (scab) in small grain cereals—a review. Plant Pathol 44(2):207–238

    Article  Google Scholar 

  • Poppenberger B, Berthiller F, Lucyshyn D, Sieberer T, Schuhmacher R, Krska R, Kuchler K, Glössl J, Luschnig C, Adam G (2003) Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thaliana. J Biol Chem 278(48):47905–47914

    Article  PubMed  CAS  Google Scholar 

  • Poppenberger B, Adam G, Berthiller F, Krska R, Kuchler K, Luschnig C, Glössl J, Lucyshyn D, Schuhmacher R, Sieberer T (2006) Method for the detoxification of mycotoxins. United States Patent Application Publication No. US2006/0183202 A1

  • Robson CA, Vanlerberghe GC (2002) Transgenic plant cells lacking mitochondrial alternative oxidase have increased susceptibility to mitochondria-dependent and -independent pathways of programmed cell death. Plant Physiol 129:1908–1920

    Article  PubMed  CAS  Google Scholar 

  • Sugie A, Naydenov N, Mizuno N, Nakamura C, Takumi S (2006) Overexpression of wheat alternative oxidase gene Waox1a alters respiration capacity and response to reactive oxygen species under low temperature in transgenic Arabidopsis. Genes Genet Syst 81(5):349–354

    Article  PubMed  CAS  Google Scholar 

  • Takabatake R, Hata S, Taniguchi M, Kouchi H, Sugiyama T, Izui K (1999) Isolation and characterization of cDNAs encoding mitochondrial phosphate transporters in soybean, maize, rice, and Arabidopsis. Plant Mol Biol 40:479–486

    Article  PubMed  CAS  Google Scholar 

  • Takamiya K-I, Tsuchiya T, Ohta H (2000) Degradation pathway(s) of chlorophyll: what has gene cloning revealed? Trends Plant Sci 5(10):426–431

    Article  PubMed  CAS  Google Scholar 

  • Zhou W, Kolb FL, Riechers DE (2005) Identification of proteins induced or upregulated by Fusarium head blight infection in the spikes of hexaploid wheat (Triticum aestivum). Genome 48(5):770–780

    PubMed  CAS  Google Scholar 

Download references

Acknowledgements

We thank Fany Doustaly for technical assistance. We thank Dr. Hermann Buerstmayr (IFA-Tulln, Austria) and the Wheat Genetics Resource Center at Kansas State University (Manhattan, Kansas, USA) for providing wheat seed. We also thank Dr. Peader O’ Gaora (Conway Institute, University College Dublin, Ireland) for critical reading of the microarray analyses section.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Stephanie Walter.

Additional information

This research was funded by Science Foundation Ireland (project 03-IN3-B414) and EU FP5 project FUCOMYR (QLRT-2000-02044).

Electronic supplementary material

Below is the link to the electronic supplementary material.

ESM Materials and methods

(DOC 121 KB)

ESM Results

(DOC 53 KB)

ESM Table S1

(XLS 2.80 MB)

ESM Table S2

(DOC 38 KB)

ESM Table S3

(DOC 48.5 KB)

ESM Table S4

(XLS 48.5 KB)

ESM Table S5

(DOC 42.5 KB)

ESM Fig. S1

(PDF 226 KB)

ESM Fig. S2

(PDF 73.3 KB)

ESM Fig. S3

(PDF 77.3.2 KB)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Walter, S., Brennan, J.M., Arunachalam, C. et al. Components of the gene network associated with genotype-dependent response of wheat to the Fusarium mycotoxin deoxynivalenol. Funct Integr Genomics 8, 421–427 (2008). https://doi.org/10.1007/s10142-008-0089-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10142-008-0089-4

Keywords

Navigation