Biodiversity of apidaecin-type peptide antibiotics: Prospects of manipulating the antibacterial spectrum and combating acquired resistance Journal Article


Authors: Casteels, P.; Romagnolo, J.; Castle, M.; Casteels-Josson, K.; Erdjument-Bromage, H.; Tempst, P.
Article Title: Biodiversity of apidaecin-type peptide antibiotics: Prospects of manipulating the antibacterial spectrum and combating acquired resistance
Abstract: Insects have a unique repertoire of peptide antibiotics but, to date, prospects of clinical applications are not clear. Apidaecin, a small peptide isolated from honeybees, inhibits viability of Gram-negative bacteria; lethal activity is near immediate, independent of a conventional 'lytic' mechanism, and involves stereoselective recognition of target molecules. Here we report structural analysis of 14 naturally occurring apidaecin-type peptides and the existence of evolutionarily conserved ('constant') regions. By detailed analysis of activities against clinically relevant bacteria, we demonstrate that the diversity of the intervening ('variable') regions confers specificity to the antibacterial spectrum of each homolog. As a result, apidaecin-homolog-based antibiograms (using 16 peptides) differ markedly between bacterial strains, contrasting the most between Yersinia enterocolitica and Campylobacter jejuni. Furthermore, in at least one instance, acquired resistance to apidaecin could be negated by minor substitutions in the variable regions. The delineation in a short peptide of constant and variable regions, responsible for, respectively, general antibacterial capacity and specificity of the antibacterial spectrum, is unprecedented. Taken together, we provide evidence that antibacterial spectra of apidaecin-type peptides can be manipulated, and that, in some cases, resistance can be countered and perhaps prevented. The current findings will guide rational design of second generation peptide antibiotics for clinical trials.
Keywords: unclassified drug; nonhuman; amino acid substitution; drug structure; drug specificity; drug synthesis; structure-activity relationship; bacteria (microorganisms); antibiotic resistance; amino acid sequence; molecular sequence data; peptides; hexapoda; endopeptidases; antibacterial activity; insect; bacteria; biodiversity; anti-infective agents; campylobacter jejuni; minimum inhibitory concentration; drug resistance, microbial; gram negative bacterium; negibacteria; polypeptide antibiotic agent; priority journal; article; support, non-u.s. gov't; yersinia enterocolitica; apidaecin
Journal Title: Journal of Biological Chemistry
Volume: 269
Issue: 42
ISSN: 0021-9258
Publisher: American Society for Biochemistry and Molecular Biology  
Date Published: 1994-10-21
Start Page: 26107
End Page: 26115
Language: English
PROVIDER: scopus
PUBMED: 7929322
DOI/URL:
Notes: Export Date: 14 January 2019 -- Article -- Source: Scopus
Citation Impact
MSK Authors
  1. Paul J Tempst
    324 Tempst
  2. Madalyn   Castle
    2 Castle