Transcriptome Analysis of Kiwifruit (Actinidia chinensis) Bark in Response to Armoured Scale Insect (Hemiberlesia lataniae) Feeding

PLoS One. 2015 Nov 16;10(11):e0141664. doi: 10.1371/journal.pone.0141664. eCollection 2015.

Abstract

The kiwifruit cultivar Actinidia chinensis 'Hort16A' is resistant to the polyphagous armoured scale insect pest Hemiberlesia lataniae (Hemiptera: Diaspididae). A cDNA microarray consisting of 17,512 unigenes selected from over 132,000 expressed sequence tags (ESTs) was used to measure the transcriptomic profile of the A. chinensis 'Hort16A' canes in response to a controlled infestation of H. lataniae. After 2 days, 272 transcripts were differentially expressed. After 7 days, 5,284 (30%) transcripts were differentially expressed. The transcripts were grouped into 22 major functional categories using MapMan software. After 7 days, transcripts associated with photosynthesis (photosystem II) were significantly down-regulated, while those associated with secondary metabolism were significantly up-regulated. A total of 643 transcripts associated with response to stress were differentially expressed. This included biotic stress-related transcripts orthologous with pathogenesis related proteins, the phenylpropanoid pathway, NBS-LRR (R) genes, and receptor-like kinase-leucine rich repeat signalling proteins. While transcriptional studies are not conclusive in their own right, results were suggestive of a defence response involving both ETI and PTI, with predominance of the SA signalling pathway. Exogenous application of an SA-mimic decreased H. lataniae growth on A. chinensis 'Hort16A' plants in two laboratory experiments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actinidia / immunology
  • Actinidia / metabolism*
  • Animals
  • DNA, Complementary / metabolism
  • Data Mining
  • Expressed Sequence Tags
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Plant
  • Hemiptera / pathogenicity*
  • Herbivory*
  • Oligonucleotide Array Sequence Analysis
  • Photosynthesis
  • Plant Bark*
  • Plant Immunity*
  • Polymerase Chain Reaction
  • Signal Transduction
  • Software
  • Transcriptome*

Substances

  • DNA, Complementary

Grants and funding

The work was funded by the New Zealand Foundation for Research Science and Technology (latterly Ministry for Business, Innovation and Employment) grant CO6X0301 and New Zealand Institute for Plant & Food Research core funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.