AI Article Synopsis

  • Vibrio vulnificus is a harmful organism linked to increasing food-borne and wound infections, fueled by climate change, leading to higher rates of sickness and death.
  • A variant known as biotype 3 emerged during a tilapia-related outbreak in Israel in the late '90s, indicating it may possess unique virulence traits that differ from other strains.
  • Research revealed that the MARTX toxin from biotype 3 is crucial for causing severe skin infections, and its structure includes a new active enzyme similar to one found in another pathogen, highlighting its role in virulence.

Article Abstract

Vibrio vulnificus is an environmental organism that causes both food-borne and wound infections with high morbidity and mortality in humans. The annual incidence and global distribution of infections associated with this pathogen are increasing with climate change. In the late 1990s, an outbreak of tilapia-associated wound infections in Israel was linked to a previously unrecognized variant of V. vulnificus designated biotype 3. The sudden emergence and clonality of the outbreak suggest that this strain may be a true newly emergent pathogen with novel virulence properties compared to those of other V. vulnificus strains. In a subcutaneous infection model to mimic wound infection, the multifunctional autoprocessing RTX (MARTX) toxin of biotype 3 strains was shown to be an essential virulence factor contributing to highly inflammatory skin wounds with severe damage affecting every tissue layer. We conducted a sequencing-based analysis of the MARTX toxin and found that biotype 3 MARTX toxin has an effector domain structure distinct from that of either biotype 1 or biotype 2. Of the two new domains identified, a domain similar to Pseudomonas aeruginosa ExoY was shown to confer adenylate cyclase activity on the MARTX toxin. This is the first demonstration that the biotype 3 MARTX toxin is essential for virulence and that the ExoY-like MARTX effector domain is a catalytically active adenylate cyclase.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993422PMC
http://dx.doi.org/10.1128/IAI.00017-14DOI Listing

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