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Characterization of quorum regulatory small RNAs in an emerging pathogen and their roles toward type VI secretion system VflT6SS2 modulation. | LitMetric

Characterization of quorum regulatory small RNAs in an emerging pathogen and their roles toward type VI secretion system VflT6SS2 modulation.

Emerg Microbes Infect

National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention (China CDC), Beijing, People's Republic of China.

Published: December 2024

AI Article Synopsis

  • The type VI secretion system (T6SS) is crucial for Gram-negative bacteria, helping them compete and survive against various organisms, with two functional variants (VflT6SS1 and VflT6SS2) identified.
  • The CqsA/LuxS-HapR quorum sensing system regulates VflT6SS2's function through proteins LuxO (which represses) and HapR (which activates), with quorum regulatory small RNAs (Qrr sRNAs) influencing this process.
  • The study discovered four Qrr sRNAs, confirming their role in modulating VflT6SS2 by indirectly affecting HapR and directly repressing key genes, thus shedding light on the interplay between quorum sensing and

Article Abstract

The type VI secretion system (T6SS) is essential for Gram-negative bacteria to antagonize a wide variety of prokaryotic and eukaryotic competitors and thus gain survival advantages. Two sets of T6SS have been found in , namely VflT6SS1 and VflT6SS2, among which VflT6SS2 is functionally expressed. The CqsA/LuxS-HapR quorum sensing (QS) system with CAI-1 and AI-2 as signal molecules can regulate VflT6SS2 by regulators LuxO and HapR, with LuxO repressing while HapR activating VflT6SS2. Quorum regulatory small RNAs (Qrr sRNAs) are Hfq-dependent -encoded sRNAs that control quorum sensing. In , Qrr sRNAs have not been characterized and their regulatory function is unknown. In this study, we first identified four Qrr sRNAs in and demonstrated that these Qrr sRNAs are regulated by LuxO and involved in the modulation of VflT6SS2 function. On the one hand, Qrr sRNAs act on HapR, the activator of both the major and the auxiliary clusters of VflT6SS2, and then indirectly repress VflT6SS2. On the other hand, they directly repress VflT6SS2 by acting on 2 and 2_a, the first gene of the major cluster and the highly transcriptional one among the two units of the first auxiliary cluster, respectively. Our results give insights into the role of Qrr sRNAs in CAI-1/AI-2 based QS and VflT6SS2 modulation in . and further enhance understandings of the network between QS and T6SS regulation in species.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11443567PMC
http://dx.doi.org/10.1080/22221751.2024.2396872DOI Listing

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