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REVIEW article

Front. Immunol.

Sec. Viral Immunology

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1632283

Catch Me if You Can: Viral Nucleic Acids to Host Sensors

Provisionally accepted
Yohan  JungYohan JungHarmony  GraingerHarmony GraingerShizhuo  YangShizhuo YangSohaumn  MondalSohaumn MondalKiven  Erique LukongKiven Erique LukongKristen  ConnKristen ConnYuliang  WuYuliang Wu*
  • University of Saskatchewan, Saskatoon, Canada

The final, formatted version of the article will be published soon.

The 2002 movie Catch Me If You Can is a cat-and-mouse story in which Frank Abagnale Jr.successfully conned his way into several high-profile jobs while evading capture by FBI agent Carl Hanratty. Similarly, after entering host cells, viruses interact with or hijack host cellular machinery to replicate their genetical materials and assemble themselves for the next round of infection. Analogous to an FBI agent, host cells have numerous molecular "detectives" that recognize viral nucleic acids (NAs). These include RIG-I, MDA5, LGP2, TLR3, TLR7, TLR8, DHX36, DICER1, PKR, OAS1, ZAP, and NLRP1/6 for viral RNA, as well as cGAS, TLR9, AIM2, IFI16, IFIX, Ku70, MRE11, RNA polymerase III, hnRNPA2B1, LRRFIP1, DAI, DHX9 and DDX41 for viral DNA. However, much like the brilliant Frank Abagnale Jr., viruses have developed various strategies to evade host cellular surveillance-for example, by sequestering or modifying viral NAs and inhibiting or degrading host sensors. In this review, we will summarize the host sensors identified so far, discuss the latest understandings of the various strategies employed by viruses, and highlight the challenges associated with drug development to target virus or host factors. Considering recent global health challenges such as the COVID-19 pandemic and undergoing measles outbreak, understanding virus-host interactions at the molecular and cellular levels remains essential for the development of novel therapeutic strategies.

Keywords: Sensor, DNA virus, RNA virus, innate immunity, Adaptive Immunity

Received: 20 May 2025; Accepted: 07 Jul 2025.

Copyright: © 2025 Jung, Grainger, Yang, Mondal, Lukong, Conn and Wu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Yuliang Wu, University of Saskatchewan, Saskatoon, Canada

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