Interaction of human defensins with Escherichia coli. Mechanism of bactericidal activity.

TLDR

Defensins are small, cysteine‑rich antimicrobial peptides that constitute 30–50 % of azurophil granule protein in human neutrophils. The study examined the mechanism of HNP‑mediated bactericidal activity against Escherichia coli ML‑35 and its plasmid‑transformed derivative. The authors assessed HNP‑1 effects by monitoring sequential permeabilization of the outer and inner membranes, cessation of nucleic acid and protein synthesis, and periplasmic electron‑dense deposits via electron microscopy. HNP‑1 sequentially permeabilized the outer and inner membranes, with inner‑membrane permeabilization being the lethal event; OM permeabilization could be partially dissociated under plasmolysis, and electron‑dense periplasmic deposits were observed.

Abstract

Defensins are small, cysteine-rich antimicrobial peptides that are abundant in human, rabbit, and guinea pig neutrophils (PMN). Three defensins (human neutrophil peptide defensin [HNP]-1, HNP-2, and HNP-3) constitute between 30 and 50% of the total protein in azurophil granules of human PMN. We examined the mechanism of HNP-mediated bactericidal activity against Escherichia coli ML-35 (i-, y-, z+) and its pBR322-transformed derivative, E. coli ML-35p. Under conditions that supported bactericidal activity, HNP-1 sequentially permeabilized the outer membrane (OM) and inner membrane (IM) of E. coli. Coincident with these events, bacterial synthesis of DNA, RNA, and protein ceased and the colony count fell. Although these events were closely coupled under standard assay conditions, OM permeabilization was partially dissociated from IM permeabilization when experiments were performed with E. coli that had been plasmolyzed by mannitol. Under such conditions, the rate and extent of bacterial death more closely paralled loss of IM integrity than OM permeabilization. Electron microscopy of E. coli that had been killed by defensins revealed the presence of striking electron-dense deposits in the periplasmic space and affixed to the OM. Overall, these studies show that HNP-mediated bactericidal activity against E. coli ML-35 is associated with sequential permeabilization of the OM and IM, and that inner membrane permeabilization appears to be the lethal event.