Abstract

BackgroundBiofilm development, specifically the fundamentally adaptive switch from acute to chronic infection phenotypes, requires global regulators and small non-coding regulatory RNAs (sRNAs). This work utilized RNA-sequencing (RNA-seq) to detect sRNAs differentially expressed in Pseudomonas aeruginosa biofilm versus planktonic state.ResultsA computational algorithm was devised to detect and categorize sRNAs into 5 types: intergenic, intragenic, 5′-UTR, 3′-UTR, and antisense. Here we report a novel RsmY/RsmZ-type sRNA, termed RsmW, in P. aeruginosa up-transcribed in biofilm versus planktonic growth. RNA-Seq, 5’-RACE and Mfold predictions suggest RsmW has a secondary structure with 3 of 7 GGA motifs located on outer stem loops. Northern blot revealed two RsmW binding bands of 400 and 120 bases, suggesting RsmW is derived from the 3’-UTR of the upstream hypothetical gene, PA4570. RsmW expression is elevated in late stationary versus logarithmic growth phase in PB minimal media, at higher temperatures (37 °C versus 28 °C), and in both gacA and rhlR transposon mutants versus wild-type. RsmW specifically binds to RsmA protein in vitro and restores biofilm production and reduces swarming in an rsmY/rsmZ double mutant. PA4570 weakly resembles an RsmA/RsmN homolog having 49 % and 51 % similarity, and 16 % and 17 % identity to RsmA and RsmN amino acid sequences, respectively. PA4570 was unable to restore biofilm and swarming phenotypes in ΔrsmA deficient strains.ConclusionCollectively, our study reveals an interesting theme regarding another sRNA regulator of the Rsm system and further unravels the complexities regulating adaptive responses for Pseudomonas species.Electronic supplementary materialThe online version of this article (doi:10.1186/s12866-016-0771-y) contains supplementary material, which is available to authorized users.

Highlights

  • IntroductionThe fundamentally adaptive switch from acute to chronic infection phenotypes, requires global regulators and small non-coding regulatory RNAs (sRNAs)

  • Biofilm development, the fundamentally adaptive switch from acute to chronic infection phenotypes, requires global regulators and small non-coding regulatory RNAs

  • The ability of P. aeruginosa to adapt to different niches and establish both chronic and acute infections requires differential gene expression and phenotypic alterations coordinated by global regulators [1] and small non-coding regulatory RNAs [2, 3]

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Summary

Introduction

The fundamentally adaptive switch from acute to chronic infection phenotypes, requires global regulators and small non-coding regulatory RNAs (sRNAs). The ability of P. aeruginosa to adapt to different niches and establish both chronic and acute infections requires differential gene expression and phenotypic alterations coordinated by global regulators [1] and small non-coding regulatory RNAs (sRNAs) [2, 3]. Pseudomonas spp. have all been found to encode multiple RsmA homologs, including the redundant RsmE of P. protegens CHA0 and the RsmN paralogue of P. aeruginosa [10,11,12]. These homologs are directly regulated by RsmA, induced under various conditions, differ in sequence, secondary and tertiary structure, and have various RNA-binding affinities and specificities.

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