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Global Analysis of the RNA-RNA Interactome in Acinetobacter Baumannii AB5075 Uncovers a Small Regulatory RNA Repressing the Virulence-related Outer Membrane Protein CarO

Overview
Specialty Biochemistry
Date 2024 Aug 16
PMID 39149883
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Abstract

Acinetobacter baumannii is an opportunistic Gram-negative pathogen that infects critically ill patients. The emergence of antimicrobial resistant A. baumannii has exacerbated the need to characterize environmental adaptation, antibiotic resistance and pathogenicity and their genetic regulators to inform intervention strategies. Critical to adaptation to changing environments in bacteria are small regulatory RNAs (sRNAs), however, the role that sRNAs play in the biology of A. baumannii is poorly understood. To assess the regulatory function of sRNAs and to uncover their RNA interaction partners, we employed an RNA proximity ligation and sequencing method (Hi-GRIL-seq) in three different environmental conditions. Forty sRNAs were ligated to sRNA-RNA chimeric sequencing reads, suggesting that sRNA-mediated gene regulation is pervasive in A. baumannii. In-depth characterization uncovered the sRNA Aar to be a post-transcriptional regulator of four mRNA targets including the transcript encoding outer membrane protein CarO. Aar initiates base-pairing with these mRNAs using a conserved seed region of nine nucleotides, sequestering the ribosome binding sites and inhibiting translation. Aar is differentially expressed in multiple stress conditions suggesting a role in fine-tuning translation of the Aar-target molecules. Our study provides mechanistic insights into sRNA-mediated gene regulation in A. baumannii and represents a valuable resource for future RNA-centric research endeavours.

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References
1.
Hamidian M, Nigro S . Emergence, molecular mechanisms and global spread of carbapenem-resistant . Microb Genom. 2019; 5(10). PMC: 6861865. DOI: 10.1099/mgen.0.000306. View

2.
Frohlich K, Gottesman S . Small Regulatory RNAs in the Enterobacterial Response to Envelope Damage and Oxidative Stress. Microbiol Spectr. 2018; 6(4). PMC: 10361636. DOI: 10.1128/microbiolspec.RWR-0022-2018. View

3.
Liao Z, Smirnov A . FinO/ProQ-family proteins: an evolutionary perspective. Biosci Rep. 2023; 43(3). PMC: 9977716. DOI: 10.1042/BSR20220313. View

4.
Corcoran C, Podkaminski D, Papenfort K, Urban J, Hinton J, Vogel J . Superfolder GFP reporters validate diverse new mRNA targets of the classic porin regulator, MicF RNA. Mol Microbiol. 2012; 84(3):428-45. DOI: 10.1111/j.1365-2958.2012.08031.x. View

5.
Shenkutie A, Gebrelibanos D, Yao M, Hundie G, Chow F, Leung P . Impairment of novel non-coding small RNA00203 inhibits biofilm formation and reduces biofilm-specific antibiotic resistance in Acinetobacter baumannii. Int J Antimicrob Agents. 2023; 62(3):106889. DOI: 10.1016/j.ijantimicag.2023.106889. View