Evidence map›Paper›PMID 42658330›Full record

ArticleMolecular biology reports2026

Identification and differential expression analysis of Hfq-bound novel small RNAs in Serratia marcescens by nitrocellulose-based partitioning.

Kunasegaran Vickineshwari, Selva Raju Kishan Raj, Suresh V Chinni, Marimuthu Citartan, Nazahiyah Ahmad Rodzli

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kunasegaran VickineshwariSchool of Biotechnology, MILA University, No 1, MIU Boulevard, Putra Nilai, Nilai, 71800, Negeri Sembilan, Malaysia.
Selva Raju Kishan RajSchool of Biotechnology, MILA University, No 1, MIU Boulevard, Putra Nilai, Nilai, 71800, Negeri Sembilan, Malaysia. kishan.selvaraju@mila.edu.my.
Suresh V ChinniDepartment of Biochemistry, Faculty of Medicine, Bioscience, and Nursing, MAHSA University, Jenjarom, 42610, Selangor, Malaysia.
Marimuthu CitartanSchool of Biotechnology, MILA University, No 1, MIU Boulevard, Putra Nilai, Nilai, 71800, Negeri Sembilan, Malaysia.
Nazahiyah Ahmad RodzliMalaysia Genome and Vaccine Institute (MGVI), National Institute of Biotechnology Malaysia (NIBM), Jalan Bangi, Kajang, 43000, Selangor, Malaysia.

Funding

Ministry of Higher Education (KPT) Malaysia FRGS/1/2022/STG01/MIU/02/1
6 · The paper itself

Abstract

backgroundThe rising prevalence of multidrug-resistant bacteria poses a looming threat to healthcare and necessitates novel therapeutic strategies beyond conventional antibiotics. One such organism is Serratia marcescens, which possesses a broad range of virulence factors and has been listed as a high-priority pathogen by the WHO due to its increasing antibiotic resistance. Small RNAs are promising targets against antibiotic-resistant bacteria, as they are key regulators of bacterial gene expression. This study aimed to identify novel sRNA and elucidate their roles in regulating virulence-associated genes in S. marcescens. METHODS AND

resultsHfq-associated sRNA were isolated using nitrocellulose membrane-based partitioning following Hfq overexpression and purification, and identified through high-throughput sequencing. A total of 159 novel sRNA candidates were identified. Two candidates, SM_Hfq_npc119 and SM_Hfq_npc07, exhibited growth phase-dependent differential expression in Northern blot analysis. SM_Hfq_npc119 was highly expressed during the lag phase and under biofilm conditions but downregulated under oxidative stress, suggesting a role in early adaptation and virulence. An inverse correlation between SM_Hfq_npc119 and its predicted target, Type IV pilus PilW mRNA, suggests negative post-transcriptional regulation. SM_Hfq_npc07 expression peaked during log phase and was predicted to target the tssB gene of the Type VI secretion system, implicating a role in virulence regulation.

conclusionsThis study expands the current understanding of sRNA-mediated post-transcriptional regulation in S. marcescens by identifying novel Hfq-associated sRNA with potential roles in virulence. This findings provides a foundation for future functional investigations and highlight sRNAs as promising targets for the development of novel diagnostics and therapeutic strategies.

Indexed as

Host Factor 1 ProteinRNA, Small UntranslatedSerratia marcescensBacterial ProteinsBiofilmsGene Expression ProfilingGene Expression Regulation, BacterialRNA, BacterialVirulenceVirulence FactorsBacterial ProteinsHost Factor 1 ProteinRNA, BacterialRNA, Small UntranslatedVirulence FactorsDifferential expressionHfq proteinMultidrug resistanceSerratia marcescensSmall RNA

Identifiers

PMID42658330

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