Functional RNAs in Virology

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "General Virology".

Deadline for manuscript submissions: 15 December 2026 | Viewed by 876

Special Issue Editor


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Guest Editor
1. Department of Theoretical Chemistry, University of Vienna, 1090 Vienna, Austria
2. RNA Forecast, 1140 Vienna, Austria
Interests: computational virology; virus bioinformatics; RNA design; synthetic RNA devices; RNA structure prediction
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Special Issue Information

Dear Colleagues,

Functional RNAs are central to the biology of viruses. Far beyond serving as passive carriers of genetic information, viral RNAs actively shape every stage of the infection cycle, from regulating translation and replication to evading host immunity and coordinating genome packaging. Structured elements like IRESs, frame-shifting pseudoknots, and exoribonuclease-resistant RNAs, as well as unstructured sequence motifs, form an intricate regulatory network that enables viruses to thrive in diverse cellular environments. Recent discoveries, including computationally predicted highly conserved RNA elements across viral families, highlight the depth and evolutionary significance of RNA-based regulation. Understanding how viruses exploit RNA structure and sequence is essential not only for understanding viral strategies but also for identifying novel targets for antiviral intervention. This Special Issue aims to collate the latest knowledge on the functional roles played by viral RNAs, demonstrating that RNA is not merely a medium but rather a molecular toolkit that viruses rely on for survival and success.

Viral RNAs are no longer viewed as passive carriers of genetic information; they are now recognized as active players in nearly every aspect of the viral lifecycle. From translation and replication to genome packaging, immune evasion, and host adaptation, functional RNAs have emerged as essential regulatory elements in viruses. These include a wide range of cis-acting RNA structures, long-range interactions, and non-coding RNAs, all of which orchestrate key steps in infection and pathogenesis.

In recent years, both experimental advances and large-scale sequencing efforts have dramatically expanded our ability to detect and characterize functional RNA elements in viral genomes. This growing body of research is reshaping our understanding of viral strategies and opening up new opportunities for antiviral intervention.

This Special Issue aims to provide a comprehensive overview of functional RNAs in virology, highlighting both well-characterized elements and emerging discoveries. Topics of interest include experimentally validated RNA structures and regulatory motifs, as well as computational predictions with functional or evolutionary significance. This Special Issue lies at the core of Viruses’ mission to advance knowledge on virus biology, pathogenesis, and antiviral strategies. By focusing on RNA-mediated regulation across viral families, this Special Issue bridges molecular virology, RNA biology, and computational genomics.

This Special Issue will serve as a timely and interdisciplinary resource for researchers interested in RNA-based mechanisms in viruses, and we aim to showcase the central role played by RNA as a regulatory molecule in infection biology.

For this Special Issue, original research articles and reviews are welcome to be submitted.

Research areas may include, but are not limited to, the following:

  • Functional RNA structures involved in translation, replication, and genome packaging;
  • Long-range RNA–RNA interactions and RNA conformational switches;
  • Viral non-coding RNAs;
  • Exoribonuclease-resistant RNAs (xrRNAs) and RNA-based immune evasion mechanisms;
  • RNA structural conservation and covariation across virus species or lineages;
  • Computational predictions of structured RNAs and their functional validation;
  • RNA–protein interactions involving viral RNAs and host factors;
  • RNA structure probing and high-throughput functional RNA screening in viruses.

We look forward to receiving your contributions.

Dr. Michael T. Wolfinger
Guest Editor

Manuscript Submission Information

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Keywords

  • functional RNA elements
  • viral RNA structure
  • cis-acting RNA motifs
  • non-coding RNAs
  • RNA–protein interactions
  • RNA-based regulation
  • RNA virus biology
  • structured RNA
  • computational RNA analysis
  • virus bioinformatics

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Published Papers (1 paper)

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Research

16 pages, 3342 KB  
Article
Comprehensive Transcriptomic Profiling Reveals Rotavirus-Induced Alterations in Both Coding and Long Non-Coding RNA Expression in MA104 Cells
by Xiaopeng Song, Yanwei Wu, Xiaocai Yin, Xiaoqing Hu, Jinyuan Wu, Xiangjing Kuang, Rong Chen, Xiaochen Lin, Jun Ye, Guangming Zhang, Maosheng Sun, Yan Zhou and Hongjun Li
Viruses 2026, 18(1), 129; https://doi.org/10.3390/v18010129 - 20 Jan 2026
Viewed by 527
Abstract
Rotavirus (RV) is the primary cause of severe gastroenteritis in young children, yet the long noncoding RNA (lncRNA) regulatory landscape governing the host response remains largely unmapped. To address this gap, the present study performed an integrated transcriptomic analysis of mRNA and lncRNA [...] Read more.
Rotavirus (RV) is the primary cause of severe gastroenteritis in young children, yet the long noncoding RNA (lncRNA) regulatory landscape governing the host response remains largely unmapped. To address this gap, the present study performed an integrated transcriptomic analysis of mRNA and lncRNA expression profiles in RV-infected MA104 cells at 24 h post-infection. Deep sequencing identified 11,919 high-confidence lncRNAs, revealing a massive transcriptional shift: 3651 mRNAs and 4655 lncRNAs were differentially expressed, with both populations predominantly upregulated. Functional enrichment analysis confirmed the strong activation of key innate immunity pathways, including the RIG-I-like receptor, Toll-like receptor, and TNF signaling pathways. Conversely, fundamental metabolic pathways were found to be suppressed. Crucially, the analysis of lncRNA targets highlighted their involvement in coordinating the host antiviral defense, particularly through transregulation. Experimental validation confirmed the significant upregulation of key immune-related mRNAs (OASL and C3) as well as two novel lncRNAs (lncRNA-6479 and lncRNA-4290) by qRT-PCR. The significant upregulation of OASL and C3 was validated at the protein level, confirming the biological relevance of the transcriptomic data. This study provides a foundational, genome-wide resource, identifying novel lncRNA targets for future mechanistic investigation into host–RV interactions. Full article
(This article belongs to the Special Issue Functional RNAs in Virology)
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