Gene expression and biochemical changes of carbohydrate metabolism in in vitro micro-propagated apple plantlets infected by 'Candidatus Phytoplasma mali'

Plant Physiol Biochem. 2013 Sep:70:311-7. doi: 10.1016/j.plaphy.2013.05.040. Epub 2013 Jun 13.

Abstract

'Candidatus Phytoplasma mali' (Ca. P. mali) is the disease agent causing apple proliferation (AP), which has detrimental effects on production in many apple growing areas of Central and Southern Europe. The present study investigated transcriptional and biochemical changes related to the sugar metabolism as well as expression of pathogenesis-related (PR) protein genes in in vitro micro-propagated AP-infected and healthy control plantlets with the aim of shedding light on host plant response to 'Ca. P. mali' infection. Expression changes between infected and control plantlets were detected by quantitative real-time PCR analysis. The most significant transcriptional changes were observed for genes coding for pathogenesis-related proteins and for heat shock protein 70, as well as for some genes related to the sugar metabolism, such as a sorbitol transporter (SOT5), hexokinase, sucrose-phosphate synthase or granule bound starch synthase. Furthermore, biochemical analyses revealed that infected plantlets were characterized by a significant accumulation of starch and sucrose, while hexoses, such as glucose and fructose, and sorbitol were present at lower concentrations. In summary, the present analysis provides an overview of a gene set that is involved in response to phytoplasma infection and, therefore, it may help for a better understanding of the molecular mechanisms involved in phytoplasma-host plant interaction in apple.

Keywords: APP; Apple proliferation; Carbohydrate metabolism; Gene expression; Hsp70; Malus x domestica; PR; PS II; Stress response; apple proliferation phytoplasma; heat shock protein 70; pathogenesis related; photosystem II; qRT-PCR; quantitative reverse transcriptase real-time PCR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Metabolism / genetics*
  • Gene Expression Regulation, Plant
  • Gene Expression*
  • Genes, Plant*
  • HSP70 Heat-Shock Proteins / genetics
  • HSP70 Heat-Shock Proteins / metabolism
  • Hexoses / genetics
  • Hexoses / metabolism
  • Host-Pathogen Interactions / genetics
  • Malus / genetics*
  • Malus / metabolism
  • Malus / microbiology
  • Phytoplasma*
  • Plant Diseases / genetics*
  • Plant Diseases / microbiology
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Real-Time Polymerase Chain Reaction
  • Starch / genetics
  • Starch / metabolism
  • Stress, Physiological / genetics
  • Sucrose / metabolism

Substances

  • HSP70 Heat-Shock Proteins
  • Hexoses
  • Plant Proteins
  • Sucrose
  • Starch