4.2 Article

Response of the honey bee (Apis mellifera) proteome to Israeli acute paralysis virus (IAPV) infection

期刊

CANADIAN JOURNAL OF ZOOLOGY
卷 93, 期 9, 页码 711-720

出版社

CANADIAN SCIENCE PUBLISHING
DOI: 10.1139/cjz-2014-0181

关键词

Apis mellifera; Israeli acute paralysis virus; Dicistroviridae; mass spectrometry; proteomics

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资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Genome Canada
  3. Genome British Columbia
  4. British Columbia Honey Producers Association through the Boone-Hodgson-Wilkinson Fund
  5. Canadian Honey Council through the Canadian Bee Research Fund
  6. Canadian Association of Professional Apiculturists through the Canadian Bee Research Fund
  7. British Columbia Blueberry Council
  8. British Columbia Cranberry Marketing Association
  9. University of British Columbia
  10. Agri-Food Canada's Advancing Canadian Agriculture and Agri-Food (ACAAF) program
  11. Canada Foundation for Innovation
  12. British Columbia Knowledge Development Fund
  13. British Columbia Proteomics Network
  14. Canadian Institutes of Health Research Fellowship
  15. National Academy of Sciences
  16. US National Institute of Food and Agriculture AFRI grant [2010-65104-20533]

向作者/读者索取更多资源

Recent declines in honey bee (Apis mellifera L., 1758) populations worldwide have spurred significant research into the impact of pathogens on colony health. The role of the Israeli acute paralysis virus (IAPV) on hive mortality has become of particular concern since being correlated with colony losses. However, the molecular interactions between IAPV and its host remain largely unknown. To investigate changes in host protein expression during IAPV infection, mass-spectrometry-based quantitative proteomics was used to compare IAPV-infected and healthy pupae. Proteins whose expression levels changed significantly during infection were identified and functional analysis was performed to determine host systems and pathways perturbed by IAPV infection. Among the A. mellifera proteins most affected by IAPV, those involving translation and the ubiquitin-proteasome pathway were most highly enriched and future investigation of these pathways will be useful in identifying host proteins required for infection. This analysis represents an important first step towards understanding the honey bee host response to IAPV infection through the systems-level analysis of protein expression.

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