4.7 Article

Modified horseshoe crab peptides target and kill bacteria inside host cells

期刊

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-021-04041-z

关键词

Antimicrobial peptide; Selective membrane-active mechanism; Host defence; Macrophages; Intracellular niche; Uropathogenic Escherichia coli

资金

  1. Australian Government scholarships (ASA. Research Training Program Scholarship)
  2. Australian Research Council (Centre of Excellence for Innovations in Peptide and Protein Science) [CE200100012]
  3. Australian Research Council [FL150100146, FT150100398]
  4. National Health and Medical Research Council [1183927, 1098337]
  5. Chan Zuckerberg Initiative DAF, an advised fund of Silicon Valley Community Foundation [2020-225648]
  6. National Health and Medical Research Council of Australia [1183927, 1098337] Funding Source: NHMRC
  7. Australian Research Council [FT150100398] Funding Source: Australian Research Council

向作者/读者索取更多资源

Bacteria that inhabit intracellular niches can evade host immune responses and antimicrobial molecules. Cell-penetrating antimicrobial peptides from horseshoe crabs show broad antimicrobial activity and can effectively target UPEC bacteria.
Bacteria that occupy an intracellular niche can evade extracellular host immune responses and antimicrobial molecules. In addition to classic intracellular pathogens, other bacteria including uropathogenic Escherichia coli (UPEC) can adopt both extracellular and intracellular lifestyles. UPEC intracellular survival and replication complicates treatment, as many therapeutic molecules do not effectively reach all components of the infection cycle. In this study, we explored cell-penetrating antimicrobial peptides from distinct structural classes as alternative molecules for targeting bacteria. We identified two beta-hairpin peptides from the horseshoe crab, tachyplesin I and polyphemusin I, with broad antimicrobial activity toward a panel of pathogenic and non-pathogenic bacteria in planktonic form. Peptide analogs [I11A]tachyplesin I and [I11S]tachyplesin I maintained activity toward bacteria, but were less toxic to mammalian cells than native tachyplesin I. This important increase in therapeutic window allowed treatment with higher concentrations of [I11A]tachyplesin I and [I11S]tachyplesin I, to significantly reduce intramacrophage survival of UPEC in an in vitro infection model. Mechanistic studies using bacterial cells, model membranes and cell membrane extracts, suggest that tachyplesin I and polyphemusin I peptides kill UPEC by selectively binding and disrupting bacterial cell membranes. Moreover, treatment of UPEC with sublethal peptide concentrations increased zinc toxicity and enhanced innate macrophage antimicrobial pathways. In summary, our combined data show that cell-penetrating peptides are attractive alternatives to traditional small molecule antibiotics for treating UPEC infection, and that optimization of native peptide sequences can deliver effective antimicrobials for targeting bacteria in extracellular and intracellular environments.

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