Skip to main content
Log in

Cold acclimation of forage grasses in relation to pink snow mould (Microdochium nivale) resistance

  • Original Paper
  • Published:
Acta Physiologiae Plantarum Aims and scope Submit manuscript

Abstract

The aim of our work is to investigate the changes in phenolic level, PAL activity and heat production rate induced during pre-hardening at 12°C and cold acclimation at 2°C of the forage grasses Festulolium, meadow fescue, tall fescue and Italian ryegrass in relation to their resistance to snow mould caused by Microdochium nivale. Meadow fescue and tall fescue were most resistant to M. nivale infection, while Italian ryegrass demonstrated the least resistance to this fungus inoculation. Festulolium, meadow fescue and tall fescue responded similarly to low temperature, while Italian ryegrass demonstrated considerable disturbance of energy balance and lower phenolic concentration, which could explain a higher susceptibility of the latter species to infection by M. nivale. The enhanced level of phenolic compounds, probably utilised for cell wall lignification as well as equilibrium of the metabolic activity observed in meadow fescue and tall fescue, is very important for both cold and pathogen-resistance mechanisms. The studied Festulolium cultivar ‘Felopa’, a hybrid of the Lolium multiflorum and Festuca pratensis genomes, was characterised by changes in biochemical parameters similar to the resistant meadow fescue and tall fescue.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

Abbreviations

ASI:

Average Severity Index

DW:

Dry weight

FW:

Fresh weight

MEC:

Metabolic efficiency coefficient

PAL:

Phenylalanine ammonia-lyase

PPFD:

Photosynthetic photon flux density (μmol m−2 s−1)

TAL:

Tyrosine ammonia-lyase

References

  • Anekonda TS, Criddle RS, Libby WJ, Breidenbach RW, Hansen LD (1994) Respiration rates predict differences in growth of coast redwood. Plant Cell Environ 17:1793–1798

    Article  Google Scholar 

  • Bowler C, Fluhr R (2000) The role of calcium and activated oxygens as signals for controlling cross-tolerance. Trends Plant Sci 5:241–246

    Article  CAS  PubMed  Google Scholar 

  • Bradford M (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Christie PJ, Alfenito MR, Walbot V (1994) Impact of low temperature stress on general phenylpropanoid and anthocyanin pathways: Enhancement of transcript abundance and anthocyanin pigmentation in maize seedlings. Planta 194:541–549

    Article  CAS  Google Scholar 

  • Criddle RS, Breidenbach RW, Rank DR, Hopkin MS, Hansen LD (1990) Simultaneous calorimetric and respirometric measurements on plant tissues. Thermochimica Acta 172:213–221

    Article  CAS  Google Scholar 

  • Criddle RS, Fontana AJ, Rank DR, Paige D, Hansen LD, Breidenbach RW (1991) Simultaneous measurement of metabolic heat rate, CO2 production, and O2 consumption by microcalorimetry. Anal Biochem 194:413–417

    Article  CAS  PubMed  Google Scholar 

  • Dixon RA, Paiva NL (1995) Stress-induced phenylpropanoid metabolism. Plant Cell 7:1085–1097

    Article  CAS  PubMed  Google Scholar 

  • Gaudet DA, Laroche A, Yoshida M (1999) Low temperature-wheat-fungal interaction: a carbohydrate connection. Physiol Plant 106:437–444

    Article  CAS  Google Scholar 

  • Gaudet DA, Laroche A, Trick M, Huel R, Puchalski B (2003) Cold induced expression of plant defensin and lipid transfer protein transcripts in winter wheat. Physiol Plant 117:195–205

    Article  CAS  Google Scholar 

  • Hahlbrock K, Scheel D (1989) Physiology and molecular biology of phenylpropanoid metabolism. Annu Rev Plant Physiol Plant Mol Biol 40:347–369

    Article  CAS  Google Scholar 

  • Hartman CL, McCoy TJ, Knous TR (1984) Selection of alfalfa (Medicago sativa) cell lines and regeneration of plant resistant to the toxin(s) produced by Fusarium oxysporum f.sp. medicaginis. Plant Sci Lett 34:183–194

    Article  Google Scholar 

  • Itai C, Richmond A, Vaadia Y (1968) The role of root cytokinine during water and salinity stress. Israel J Bot 17:187–195

    CAS  Google Scholar 

  • Kang Z, Huang L, Buchenauer H (2004) Ultrastructural and cytochemical studies on infection of wheat spikes by Microdochium nivale. J Plant Dis Prot 111:351–361

    Google Scholar 

  • Kefu Z, Munns R, King RW (1991) Abscisic acid levels in NaCl-treated barley, cotton and salt-bush. Austr J Plant Physiol 18:17–24

    Article  CAS  Google Scholar 

  • Laroche A, Gaudet DA, Audy P, Frick MM, Mullin J (1997) Induction of freezing tolerance and snow mould resistance in winter wheat: biochemical and molecular perspectives. In: Proceedings of the international symposium on cereal adaptation to low temperature stress, Martonvásár, Hungary, June 2–4, 1997

  • Peltonen S, Karjalainen R (1995) Phenylalanine ammonia-lyase activity in barley after infection with Bipolaris sorokiniana or treatment with purified xylanase. J Phytopathol 143:239–245

    Article  CAS  Google Scholar 

  • Płażek A, Żur I (2003) Cold-induced plant resistance to necrotrophic pathogens and antioxidant enzyme activities and cell membrane permeability. Plant Sci 164:1019–1028

    Article  CAS  Google Scholar 

  • Prończuk M, Prończuk S (1987) Przydatność “metody chłodniowej” w ocenie odporności życicy trwałej na Fusarium nivale (Fr) Ces. Biuletyn IHAR 162:27–32

    Google Scholar 

  • Sanchez-Ballesta M, Lafuente MT, Zacarias L, Granell A (2000) Involvement of phenylalanine ammonia-lyase in the response of Fortune mandarin fruits to cold temperature. Physiol Plant 108:382–389

    Article  CAS  Google Scholar 

  • Singleton VS, Rossi JA Jr (1965) Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagent. Am J Enol Viticult 16:144–157

    CAS  Google Scholar 

  • Solecka D, Kacperska A (1993) Activity of l-phenylalanine ammonia-lyase in winter rape leaves treated with cold. Acta Biochim Pol 40:113–115

    CAS  PubMed  Google Scholar 

  • Streuter N, Moerschbacher BM, Fischer Y, Noll U, Reisener HJ (1989) Fructose-2,6-bisphosphate in wheat leaves infected with steam rust. J Plant Physiol 134:254–257

    CAS  Google Scholar 

  • Tronsmo AM (1984) Resistance to the rust fungus Puccinia poae-nemoralis in Poa pratensis induced by low-temperature hardening. Can J Bot 62:2891–2892

    Article  Google Scholar 

  • Tronsmo AM (1985) Effects of dehardening on resistance to freezing and to infection by Typhula ishicariensis in Phleum Pratense. Acta Agric Scand 35:113–116

    Article  Google Scholar 

  • Tronsmo AM (1986) Host water potentials may restrict development of snow mould fungi in low temperature-hardened grasses. Physiol Plant 68:175–179

    Article  Google Scholar 

  • Wiśniewski K, Zagdańska B, Prończuk M (1997) Interrelationship between frost tolerance, drought and resistance to snow mould (Microdochium nivale). (W:). In: Proceedings of the international symposium on cereal adaptation to low temperature stress. Agricultural Research Institute of the Hungarian Academy of Sciences, Martonvásár, Hungary, pp 221–226

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Ewa Pociecha.

Additional information

Communicated by B. Barna.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Pociecha, E., Płażek, A. Cold acclimation of forage grasses in relation to pink snow mould (Microdochium nivale) resistance. Acta Physiol Plant 32, 37–43 (2010). https://doi.org/10.1007/s11738-009-0373-5

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11738-009-0373-5

Keywords

Navigation