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The core and accessory Hfq interactomes across Pseudomonas aeruginosa lineages

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  • Julian Trouillon

    (Université Grenoble Alpes, CNRS, CEA, IBS UMR 5075
    Institute of Molecular Systems Biology, ETH Zurich)

  • Kook Han

    (Harvard Medical School)

  • Ina Attrée

    (Université Grenoble Alpes, CNRS, CEA, IBS UMR 5075)

  • Stephen Lory

    (Harvard Medical School)

Abstract

The major RNA-binding protein Hfq interacts with mRNAs, either alone or together with regulatory small noncoding RNAs (sRNAs), affecting mRNA translation and degradation in bacteria. However, studies tend to focus on single reference strains and assume that the findings may apply to the entire species, despite the important intra-species genetic diversity known to exist. Here, we use RIP-seq to identify Hfq-interacting RNAs in three strains representing the major phylogenetic lineages of Pseudomonas aeruginosa. We find that most interactions are in fact not conserved among the different strains. We identify growth phase-specific and strain-specific Hfq targets, including previously undescribed sRNAs. Strain-specific interactions are due to different accessory gene sets, RNA abundances, or potential context- or sequence- dependent regulatory mechanisms. The accessory Hfq interactome includes most mRNAs encoding Type III Secretion System (T3SS) components and secreted toxins in two strains, as well as a cluster of CRISPR guide RNAs in one strain. Conserved Hfq targets include the global virulence regulator Vfr and metabolic pathways involved in the transition from fast to slow growth. Furthermore, we use rGRIL-seq to show that RhlS, a quorum sensing sRNA, activates Vfr translation, thus revealing a link between quorum sensing and virulence regulation. Overall, our work highlights the important intra-species diversity in post-transcriptional regulatory networks in Pseudomonas aeruginosa.

Suggested Citation

  • Julian Trouillon & Kook Han & Ina Attrée & Stephen Lory, 2022. "The core and accessory Hfq interactomes across Pseudomonas aeruginosa lineages," Nature Communications, Nature, vol. 13(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28849-w
    DOI: 10.1038/s41467-022-28849-w
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    1. C. K. Stover & X. Q. Pham & A. L. Erwin & S. D. Mizoguchi & P. Warrener & M. J. Hickey & F.S. L. Brinkman & W. O. Hufnagle & D. J. Kowalik & M. Lagrou & R. L. Garber & L. Goltry & E. Tolentino & S. We, 2000. "Complete genome sequence of Pseudomonas aeruginosa PAO1, an opportunistic pathogen," Nature, Nature, vol. 406(6799), pages 959-964, August.
    2. Ping Lin & Qinqin Pu & Qun Wu & Chuanmin Zhou & Biao Wang & Jacob Schettler & Zhihan Wang & Shugang Qin & Pan Gao & Rongpeng Li & Guoping Li & Zhenyu Cheng & Lefu Lan & Jianxin Jiang & Min Wu, 2019. "High-throughput screen reveals sRNAs regulating crRNA biogenesis by targeting CRISPR leader to repress Rho termination," Nature Communications, Nature, vol. 10(1), pages 1-12, December.
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