A novel plasmid-encoded transposon-derived small RNA reveals the mechanism of sRNA-regulated bacterial persistence

Shu-Ling Lin, Qi-Chang Nie, Carmen Oi-Kwan Law, Hoa-Quynh Pham, Ho-Fai Chau, Terrence Chi-Kong Lau*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

1 Citation (Scopus)
26 Downloads (CityUHK Scholars)

Abstract

Small regulatory RNAs (sRNAs) in bacteria are crucial for controlling various cellular functions and provide immediate response to the environmental stresses. Antibiotic persistence is a phenomenon that a small subpopulation of bacteria survives under the exposure of a lethal concentration of antibiotics, potentially leading to the development of drug resistance in bacteria. Here, we reported a novel transposon-derived sRNA called stnpA, which can modulate fosfomycin persistence of the bacteria. The stnpA sRNA located in the transposon with its own promoter is highly conserved among the prevalent multidrug resistance (MDR) plasmids in various pathogenic bacteria and expressed in response to the fosfomycin stress. It can directly bind to the ABC transporter, YadG, whereas this protein–RNA interaction modulated the export of fosfomycin and led to the enhancement of bacterial persistence. According to our knowledge, stnpA is the first identified transposon-derived sRNA, which controlled antibiotic persistence of bacteria, and our work demonstrated that nonresistance genes on MDR plasmids such as plasmid-encoded sRNA can provide additional survival advantages to the bacterial host against the antibiotics. In addition, the stnpA sRNA can be potentially utilized as the druggable target for the development of novel therapeutic strategies to overcome bacterial persistence. Copyright © 2025 Lin et al.
Original languageEnglish
Article numbere03814-24
JournalmBio
Volume16
Issue number4
Online published25 Feb 2025
DOIs
Publication statusPublished - 9 Apr 2025

Funding

We would like to thank Michael Wai Lun Chiang for providing expertise and reagents for TEM, Antony Ho Fai Chau for assisting with the LC-MS/MS for protein identification, Biomedical Technology Support Center for assisting with the LC-MS/MS for accumulation assay, and Kun Zhang and Haizhou Zhao for the technical advice on EMSA. Author contributions: T.C.K.L. conceived and supervised the work. S.L. performed the experiments, analyzed the data, and wrote the manuscript. O.L. performed northern Blot. H.P. provided technical support in B3H assay and EMSA. Q.N. conducted the TEM experiments. C.H. conducted the RNA-seq analysis. Research Grants Council, University Grants Committee (CityU 11101518 and 11102122). Health and Medical Research Fund (20190932 and 22211142), Food and Health Bureau, Hong Kong. Tung Biomedical Sciences Centre, City University of Hong Kong, Hong Kong. Open Access made possible with partial support from the Open Access Publishing Fund of the City University of Hong Kong.

Research Keywords

  • fosfomycin persistence
  • fosfomycin transporter YadG
  • plasmid-encoded sRNA
  • sRNA–transporter interaction

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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