Small RNAs to probe, decode, and optimise phage-host interactions
Regulatory RNAs have emerged as powerful tools in synthetic biology due to their programmability and ability to modulate gene expression with high specificity. Among these, small RNAs (sRNAs) that act through base-pairing interactions offer a versatile platform for controlling molecular processes in both prokaryotic and eukaryotic systems. Indeed, synthetic regulatory RNAs have already shown potential in metabolic engineering, gene regulation, and diagnostics. However, despite their broad regulatory utility, synthetic regulatory RNAs have not yet been broadly applied to antiviral strategies, especially those targeting RNA-RNA interactions relevant during viral infection. In viruses, RNA structures and RNA-mediated gene regulation are closely linked to replication and host manipulation, making them attractive targets for RNA-based interference. However, rationally designing effective synthetic RNAs remains a major challenge due to the complexity of RNA folding, target recognition, and the dynamic nature of virus host interactions.
All of the WPs are contributing via an integrated approach to the iterative development of our NN to study phage-host interactions
Recent advances in the design of synthetic regulatory RNAs and machine learning, particularly neural networks (NN), now offer a path towards predictive modelling of these interactions. Furthermore, integrating experimental feedback into model training holds promise for accelerating the design-test-learn cycle of the synthetic biology toolbox. In this project, we aim to close this gap by systematically and adaptively optimising antiviral RNAs that target viral and/or host RNAs that are required for virus infection and replication. Specifically, we will develop a neural network- based tool that integrates predictive modelling of RNA-RNA interactions with experimental feedback to optimise synthetic antiviral RNAs. The tool will focus on targeting both coding and non-coding features of viral and host RNAs to disrupt viral entry, replication, and exit. Our initial work will concentrate on bacteriophages, with future expansion to eukaryotic viruses.
The tool will learn from wet-lab data to improve predictions of functional RNA interactions and guide the identification of more potent RNA molecules in iterative cycles. By modelling both interacting and non-interacting RNA pairs, the system will distinguish functional mechanisms from background noise, increasing design accuracy. Through collaborations within the CRC VirusREvolution consortium, the neural network will be enhanced with diverse datasets, improving its generalisability across different phage-host systems following the overall topics G2 and G3.
The resulting platform will provide the foundation for programmable RNA therapeutics with high specificity, adaptability, and reduced likelihood of resistance. It will also establish general principles for RNA-mediated antiviral defence that can be leveraged across different organisms and viral families.
From a broader perspective, this project bridges computational and experimental biology to tackle one of the central challenges in virology and synthetic biology – how to rationally design molecules that can interfere with evolving viral systems. This strategy goes beyond classical design principles and opens avenues for responsive, data-driven synthetic biology. Taken together, the proposed work will (a) advance our understanding of viral adsorption, entry, replication, and escape; (b) support the long-term goal of intelligent, programmable, and adaptive biological interventions; and (c) provide novel intervention strategies targeting viruses at the RNA level. This aligns closely with the overarching research goals of the CRC: understanding of virus evolution (G2), virus-host interactions (G3), and the mechanisms of viral infection (G4).
- WP 1: NN architecture design for optimising synthetic short RNAs (Marz/Papenfort)
- WP 2: Extended neural network (Marz/Papenfort)
- WP 3: Comparing dozens of phage-host systems to identify general principles of resistance (Papenfort)
- WP 4: Improved identification of RNA-RNA interactions (Marz)
- WP 5: Targeting eukaryotic viruses by optimising antiviral RNA-RNA interactions (Marz)
Team Members
N. N.
Doctoral Researcher
Project-Specific Publications
2024
Comprehensive survey of conserved RNA secondary structures in full-genome alignment of hepatitis C virus Journal Article
In: Sci. Rep., vol. 14, iss. 1, pp. 15145, 2024, ISSN: 2045-2322.
Small RNAs direct attack and defense mechanisms in a quorum sensing phage and its host. Journal Article
In: Cell Host Microbe, vol. 32, iss. 5, pp. 727–738.e6, 2024.
2022
An RNA sponge controls quorum sensing dynamics and biofilm formation in emphVibrio cholerae Journal Article
In: Nat Commun, vol. 13, no. 7585, 2022.
Taxonomic classification of DNA sequences beyond sequence similarity using deep neural networks Journal Article
In: Proc Natl Acad Sci, vol. 119, no. 35, 2022.
2021
A dual-function RNA balances carbon uptake and central metabolism in emphVibrio cholerae Journal Article
In: EMBO J, vol. 40, iss. 24, pp. e108542, 2021.
VIDHOP, viral host prediction with deep learning. Journal Article
In: Bioinformatics, vol. 37, iss. 3, pp. 318–325, 2021, ISSN: 1367-4811.
2020
RNA-mediated control of cell shape modulates antibiotic resistance in emphVibrio cholerae Journal Article
In: Nat Commun, vol. 11, iss. 1, pp. 6067, 2020.
2019
A conserved RNA seed-pairing domain directs small RNA-mediated stress resistance in enterobacteria Journal Article
In: EMBO J, vol. 38, iss. 16, pp. e101650, 2019.
In: Genome Res, vol. 29, iss. 9, pp. 1545–1554, 2019, ISSN: 1549-5469.
2016
Prediction of conserved long-range RNA-RNA interactions in full viral genomes Journal Article
In: Bioinformatics, vol. 32, iss. 19, pp. 2928–2935, 2016.