Antimicrobial peptides extend lifespan in Drosophila

PLoS One. 2017 May 17;12(5):e0176689. doi: 10.1371/journal.pone.0176689. eCollection 2017.

Abstract

Antimicrobial peptides (AMPs) are important defense molecules of the innate immune system. High levels of AMPs are induced in response to infections to fight pathogens, whereas moderate levels induced by metabolic stress are thought to shape commensal microbial communities at barrier tissues. We expressed single AMPs in adult flies either ubiquitously or in the gut by using the inducible GeneSwitch system to tightly regulate AMP expression. We found that activation of single AMPs, including Drosocin, resulted in a significant extension of Drosophila lifespan. These animals showed reduced activity of immune pathways over lifetime, less intestinal regenerative processes, reduced stress response and a delayed loss of gut barrier integrity. Furthermore, intestinal Drosocin induction protected the animals against infections with the natural Drosophila pathogen Pseudomonas entomophila, whereas a germ-reduced environment prevented the lifespan extending effect of Drosocin. Our study provides new insights into the crosstalk of innate immunity, intestinal homeostasis and ageing.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Antimicrobial Cationic Peptides / genetics*
  • Antimicrobial Cationic Peptides / metabolism*
  • Drosophila / physiology*
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism*
  • Glycopeptides / genetics
  • Glycopeptides / metabolism
  • Immunity
  • Intestinal Mucosa / metabolism
  • Intestines / immunology
  • Longevity* / genetics
  • Longevity* / immunology
  • Reactive Oxygen Species / metabolism
  • Regeneration / drug effects
  • Regeneration / immunology
  • Stress, Physiological / drug effects
  • Stress, Physiological / immunology

Substances

  • Antimicrobial Cationic Peptides
  • Drosophila Proteins
  • Glycopeptides
  • Reactive Oxygen Species
  • drosocin
  • cecropin A
  • Adenosine Triphosphate

Grants and funding

This work was supported by grants from the DFG to M.H. (SFBs 645, 704 and cluster of excellence ImmunoSensation) (www.dfg.de) and the Young Researcher Overseas Visits Program for Vitalizing Brain Circulation by Oversees Training Program Division, International Program Department, Japan Society for the Promotion of Science to T.M. and H.T. (www.jsps.go.jp/english/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.