4.7 Article

Unity in defence: honeybee workers exhibit conserved molecular responses to diverse pathogens

期刊

BMC GENOMICS
卷 18, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12864-017-3597-6

关键词

Apis mellifera; Nosema; Varroa destructor; DWV; IAPV; RNA virus; Meta-analysis; Transcriptomics; Co-expression network; Immunity

资金

  1. sDiv, the Synthesis Centre for Biodiversity Sciences within the German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig - German Science Foundation [FZT 118]
  2. Insect Pollinators Initiative (IPI) [BB/I000100/1, BB/I000151/1]
  3. BBSRC [BB/I025220/1]
  4. Biotechnology and Biological Sciences Research Council
  5. Department for Environment, Food and Rural Affairs
  6. Natural Environment Research Council
  7. Scottish Government
  8. Wellcome Trust
  9. Office Of The Director
  10. Office of Integrative Activities [1443108] Funding Source: National Science Foundation
  11. Biotechnology and Biological Sciences Research Council [BB/I025220/1] Funding Source: researchfish
  12. BBSRC [BB/I000151/1, BB/I025220/1, BB/I000100/1] Funding Source: UKRI

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Background: Organisms typically face infection by diverse pathogens, and hosts are thought to have developed specific responses to each type of pathogen they encounter. The advent of transcriptomics now makes it possible to test this hypothesis and compare host gene expression responses to multiple pathogens at a genome-wide scale. Here, we performed a meta-analysis of multiple published and new transcriptomes using a newly developed bioinformatics approach that filters genes based on their expression profile across datasets. Thereby, we identified common and unique molecular responses of a model host species, the honey bee (Apis mellifera), to its major pathogens and parasites: the Microsporidia Nosema apis and Nosema ceranae, RNA viruses, and the ectoparasitic mite Varroa destructor, which transmits viruses. Results: We identified a common suite of genes and conserved molecular pathways that respond to all investigated pathogens, a result that suggests a commonality in response mechanisms to diverse pathogens. We found that genes differentially expressed after infection exhibit a higher evolutionary rate than non-differentially expressed genes. Using our new bioinformatics approach, we unveiled additional pathogen-specific responses of honey bees; we found that apoptosis appeared to be an important response following microsporidian infection, while genes from the immune signalling pathways, Toll and Imd, were differentially expressed after Varroa/virus infection. Finally, we applied our bioinformatics approach and generated a gene co-expression network to identify highly connected (hub) genes that may represent important mediators and regulators of anti-pathogen responses. Conclusions: Our meta-analysis generated a comprehensive overview of the host metabolic and other biological processes that mediate interactions between insects and their pathogens. We identified key host genes and pathways that respond to phylogenetically diverse pathogens, representing an important source for future functional studies as well as offering new routes to identify or generate pathogen resilient honey bee stocks. The statistical and bioinformatics approaches that were developed for this study are broadly applicable to synthesize information across transcriptomic datasets. These approaches will likely have utility in addressing a variety of biological questions.

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