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Quorum sensing‐disrupting molecules to control virulence of Vibrio vulnificus , a fulminating foodborne pathogen
Author(s) -
Choi Sang Ho,
Kim Byoung Sik,
Choi Garam,
Jang Song Yee,
Kim Myung Hee
Publication year - 2018
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2018.32.1_supplement.lb78
Subject(s) - vibrio vulnificus , virulence , microbiology and biotechnology , quorum sensing , chemistry , virulence factor , bacterial outer membrane , mutant , bacteria , biology , biochemistry , escherichia coli , gene , genetics
Bacterial pathogenicity involves numerous virulence factors required for successful survival in host environments as well as invasion and destruction of host tissues. The pathogenic marine bacterium Vibrio vulnificus is a causative agent of food‐borne diseases such as gastroenteritis and life‐threatening septicemia. It has been reported that expression of V. vulnificus virulence factors is well‐coordinated and regulated by sophisticated mechanisms consisting of many global regulatory proteins. Among them, SmcR, a quorum‐sensing master regulator and homologue of V. harveyi LuxR, has been identified and found to play a critical role in the regulation of the V. vulnificus virulence factors. The crystal structure of SmcR reveals that SmcR belongs to the TetR family protein possessing putative ligand‐binding pockets. To identify the small molecules which bind to and inhibit SmcR, chemical libraries were screened and an SmcR inhibitor exhibiting the most effective SmcR‐inhibition activity was selected and named QStatin. The lack of reduction of intracellular levels of SmcR in QStatin‐treated V. vulnificus suggested direct binding of the chemical to SmcR. Isothermal titration calorimetric (ITC) and crystallization analyses confirmed the chemical binding of QStatin into the pockets of SmcR. Although no big conformational changes were observed in the crystal structure, binding of QStatin reduced the DNA binding affinity of SmcR, and thereby changed the expressions of SmcR regulon similar to those of SmcR mutants. Accordingly, QStatin significantly inhibits expression of V. vulnificus virulence genes, leading to the decreased mortality of a brine shrimp infected with V. vulnificus . Most interestingly, QStatin attenuates pathogenicity of V. vulnificus , but does not inhibit growth itself at all, unlike existing antibiotics. Consequently, the combined results indicate that QStatin could be a novel lead compound to control QS‐mediated pathogenesis of V. vulnificus with the lowest possibility of the appearance of resistant strains. Support or Funding Information This work was supported by the National Research Foundation of the Ministry of Science, ICT, and Future Planning (2015R1A2A1A13001654 to S.H.C.). This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .