Systematic transcriptome analysis allows the identification of new type I and type II Toxin/Antitoxin systems located in the superintegron of Vibrio cholerae.

Res Microbiol

Institut Pasteur, Université Paris Cité, CNRS UMR 3525, Unité de Plasticité du Génome Bactérien, 28 rue du Docteur Roux, F-75015 Paris, France. Electronic address:

Published: January 2023

AI Article Synopsis

  • The study investigates additional Toxin/Antitoxin (TA) systems in the Vibrio cholerae N16961 genome, which already contains 18 known type II TA systems within its chromosomal superintegron.
  • Researchers identified a new functional type II TA system (VCA0497-0498) and found that its antitoxin represses its own gene expression, while also linking it to a newly discovered superfamily of TA systems.
  • Additionally, they uncovered a novel type I TA system (VCA0495) that includes antisense non-coding RNAs; silencing these RNAs caused cell death, indicating the functional role of this TA system, thereby increasing the total number to 19 within the

Article Abstract

Vibrio cholerae N16961 genome encodes 18 type II Toxin/Antitoxin (TA) systems, all but one located inside gene cassettes of its chromosomal superintegron (SI). This study aims to investigate additional TA systems in this genome. We screened for all two-genes operons of uncharacterized function by analyzing previous RNAseq data. Assays on nine candidates, revealed one additional functional type II TA encoded by the VCA0497-0498 operon, carried inside a SI cassette. We showed that VCA0498 antitoxin alone and in complex with VCA0497 represses its own operon promoter. VCA0497-0498 is the second element of the recently identified dhiT/dhiA superfamily uncharacterized type II TA system. RNAseq analysis revealed that another SI cassette encodes a novel type I TA system: VCA0495 gene and its two associated antisense non-coding RNAs, ncRNA495 and ncRNA496. Silencing of both antisense ncRNAs lead to cell death, demonstrating the type I TA function. Both VCA0497 and VCA0495 toxins do not show any homology to functionally characterized toxins, however our preliminary data suggest that their activity may end up in mRNA degradation, directly or indirectly. Our findings increase the TA systems number carried in this SI to 19, preferentially located in its distal end, confirming their importance in this large cassette array.

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http://dx.doi.org/10.1016/j.resmic.2022.103997DOI Listing

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