Association of Acinetobacter baumannii EF-Tu with cell surface, outer membrane vesicles, and fibronectin.

A conundrum has long lingered over association of cytosol elongation factor Tu (EF-Tu) with bacterial surface. Here we investigated it with Acinetobacter baumannii, an emerging opportunistic pathogen associated with a wide spectrum of infectious diseases. The gene for A.

Adhesion of acinetobacter baumannii to extracellular proteins detected by a live cell-protein binding assay.

Introduction: Acinetobacter baumannii is involved in various infectious diseases ranging from nosocomial community-acquired infections to those acquired following war or natural disasters. The treatment has become exceedingly difficult partly because the bacterium can form biofilms. Therefore, it is imperative to elucidate mechanisms of the biofilm formation that may be exploited to develop therapeutic strategies.

Pseudomonas aeruginosa, under DNA replication inhibition, tends to form biofilms via Arr.

Bacteria infecting eukaryotic hosts often encounter therapeutic antimicrobial and DNA damaging agents and respond by forming biofilms. While mechanisms of biofilm response are incompletely understood, they seem to involve bacterial second messenger bis-(3'-5')-cyclic dimeric guanosine monophosphate (c-di-GMP) signaling. We hypothesized that DNA replication inhibition induces bacterial biofilm formation via c-di-GMP signaling.