AHL-Lactonase Producing Psychrobacter sp. From Palk Bay Sediment Mitigates Quorum Sensing-Mediated Virulence Production in Gram Negative Bacterial Pathogens

• Published in: Frontiers in microbiology 2021-04, Vol.12, p.634593-634593
• Main Authors: Packiavathy, Issac Abraham Sybiya Vasantha, Kannappan, Arunachalam, Thiyagarajan, Sivaprakasam, Srinivasan, Ramanathan, Jeyapragash, Danaraj, Paul, John Bosco John, Velmurugan, Pazhanivel, Ravi, Arumugam Veera
• Format: Article
• Language: English
• Subjects: AHL-lactonase; marine Palk Bay sediment; Microbiology; Pseudomonas aeruginosa; Psychrobacter sp; quorum quenching
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2021.634593

Quorum sensing (QS) is a signaling mechanism governed by bacteria used to converse at inter- and intra-species levels through small self-produced chemicals called N-acylhomoserine lactones (AHLs). Through QS, bacteria regulate and organize the virulence factors' production, including biofilm formation. AHLs can be degraded by an action called quorum quenching (QQ) and hence QQ strategy can effectively be employed to combat biofilm-associated bacterial pathogenesis. The present study aimed to identify novel bacterial species with QQ potential. Screening of Palk Bay marine sediment bacteria for QQ activity ended up with the identification of marine bacterial isolate 28 (MSB-28), which exhibited a profound QQ activity against QS biomarker strain ATCC 12472. The isolate MSB-28 was identified as sp. through 16S-rRNA sequencing. sp. also demonstrated a pronounced activity in controlling the biofilm formation in different bacteria and biofilm-associated virulence factors' production in PAO1. Solvent extraction, heat inactivation, and proteinase K treatment assays clearly evidence the enzymatic nature of the bioactive lead. Furthermore, AHL's lactone ring cleavage was confirmed with experiments including ring closure assay and chromatographic analysis, and thus the AHL-lactonase enzyme production in sp. To conclude, this is the first report stating the AHL-lactonase mediated QQ activity from marine sediment bacteria sp. Future work deals with the characterization, purification, and mass cultivation of the purified protein and should pave the way to assessing the feasibility of the identified protein in controlling QS and biofilm-mediated multidrug resistant bacterial infections in mono or multi-species conditions.