# N1MΨU-modified mRNA vaccines break the mold in fish by enhancing innate immune activation

**Authors:** Dean Porter, Luc Jouneau, Mathilde Peruzzi, Bertrand Collet, Bernard Verrier, Pierre Boudinot

PMC · DOI: 10.1016/j.omtn.2026.102862 · Molecular Therapy. Nucleic Acids · 2026-02-07

## TL;DR

Modified mRNA vaccines in fish trigger strong immune responses and may work differently than in mammals.

## Contribution

N1MΨU-modified mRNA vaccines in fish do not suppress innate immunity and activate unique immune pathways.

## Key findings

- N1MΨU-modified mRNA vaccines induce robust type I interferon responses in rainbow trout.
- Modified mRNA vaccines trigger autophagy, ubiquitination, and transcription pathways in fish.
- Modified mRNA retains strong immunostimulatory capacity in fish, unlike in mammals.

## Abstract

Messenger RNA (mRNA) vaccines have revolutionized immunization strategies in mammals, with chemical modifications such as N1-methyl-pseudouridine (N1MΨU) enhancing stability, translation, and reducing innate immune activation. However, the immunological implications of such modifications in non-mammalian species, particularly teleost fish, remain unclear. In this study, we evaluated the innate immune responses elicited by four vaccine platforms: a DNA vaccine, a live attenuated viral hemorrhagic septicemia virus (VHSV), an unmodified mRNA, and an N1MΨU-modified mRNA. All four vaccines encode the G protein of VHSV (GVHSV) in rainbow trout. Following intramuscular injection, both mRNA vaccine formats induced robust type I interferon (IFN) responses, comparable to those induced by the DNA and attenuated virus vaccines. Notably, the N1MΨU-modified mRNA vaccine did not suppress IFN induction, as observed in mammalian systems, but instead triggered distinct temporal transcriptional dynamics and stronger enrichment of autophagy, ubiquitination, and transcription-related pathways. These findings suggest that modified mRNA retains a strong immunostimulatory capacity in fish and may activate immune pathways differently than in mammals. Our results emphasize the need to reassess assumptions from mammalian vaccine design when translating mRNA vaccine strategies to non-mammalian vertebrates and highlight the potential for tailored mRNA vaccine development in aquaculture species.

mRNA vaccines in mammals use chemical modifications, such as N1-methyl-pseudouridine, to enhance stability and translation, and to dampen innate immune responses. Here, both modified and unmodified mRNA vaccines against a trout rhabdovirus elicited neutralizing antibodies and comparable type I IFN responses, demonstrating the preserved immunostimulatory capacity of modified mRNA in fish.

## Linked entities

- **Proteins:** LOC100209445 (ras-like protein RAS1)
- **Chemicals:** N1-methyl-pseudouridine (PubChem CID 99543)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** STAT5B (signal transducer and activator of transcription 5B) [NCBI Gene 6777] {aka GHISID2, STAT5}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, PCYT1B (phosphate cytidylyltransferase 1B, choline) [NCBI Gene 9468] {aka CCTB, CTB}, NLRP12 (NLR family pyrin domain containing 12) [NCBI Gene 91662] {aka CLR19.3, FCAS2, NALP12, PAN6, PYPAF7, RNO}, IRF1 (interferon regulatory factor 1) [NCBI Gene 3659] {aka IMD117, IRF-1, MAR}, TLR3 (toll like receptor 3) [NCBI Gene 7098] {aka CD283, IIAE2, IMD83}, SCARB1 (scavenger receptor class B member 1) [NCBI Gene 949] {aka CD36L1, CLA-1, CLA1, HDLCQ6, HDLQTL6, SR-BI}, CMPK2 (cytidine/uridine monophosphate kinase 2) [NCBI Gene 129607] {aka IBGC10, NDK, TMPK2, TYKi, UMP-CMPK2}, HBB (hemoglobin subunit beta) [NCBI Gene 3043] {aka CD113t-C, ECYT6, beta-globin}, ADAR (adenosine deaminase RNA specific) [NCBI Gene 103] {aka ADAR1, AGS6, DRADA, DSH, DSRAD, G1P1}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, P2RX5 (purinergic receptor P2X 5) [NCBI Gene 5026] {aka LRH-1, P2X5, P2X5R}, SAA1 (serum amyloid A1) [NCBI Gene 6288] {aka PIG4, SAA, TP53I4}, DUSP4 (dual specificity phosphatase 4) [NCBI Gene 1846] {aka HVH2, MKP-2, MKP2, TYP}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, IFIT2 (interferon induced protein with tetratricopeptide repeats 2) [NCBI Gene 3433] {aka G10P2, GARG-39, IFI-54, IFI-54K, IFI54, IFIT-2}, NT5E (5'-nucleotidase ecto) [NCBI Gene 4907] {aka CALJA, CD73, E5NT, NT, NT5, NTE}, AGO2 (argonaute RISC catalytic component 2) [NCBI Gene 27161] {aka CASC7, EIF2C2, LESKRES, LINC00980, PPD, Q10}, MDA5 [NCBI Gene 100499612], NCOA4 (nuclear receptor coactivator 4) [NCBI Gene 8031] {aka ARA70, ELE1, PTC3, RFG}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, RIGI (RNA sensor RIG-I) [NCBI Gene 23586] {aka DDX58, RIG-I, RIG1, RLR-1, SGMRT2}, IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}, ASTE1 (asteroid structure-specific endonuclease 1) [NCBI Gene 28990] {aka HT001}, APOL6 (apolipoprotein L6) [NCBI Gene 80830] {aka APOL-VI, APOLVI}, ISG15 (ISG15 ubiquitin like modifier) [NCBI Gene 9636] {aka G1P2, IFI15, IMD38, IP17, UCRP, hUCRP}, ULK1 (unc-51 like autophagy activating kinase 1) [NCBI Gene 8408] {aka ATG1, ATG1A, UNC51, Unc51.1, hATG1}, DICER1 (dicer 1, ribonuclease III) [NCBI Gene 23405] {aka DCR1, Dicer, Dicer1e, GLOW, HERNA, K12H4.8-LIKE}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, UPF3A (UPF3A regulator of nonsense mediated mRNA decay) [NCBI Gene 65110] {aka HUPF3A, RENT3A, UPF3}, STAT5A (signal transducer and activator of transcription 5A) [NCBI Gene 6776] {aka MGF, STAT5}, HERC3 (HECT and RLD domain containing E3 ubiquitin protein ligase 3) [NCBI Gene 8916], EIF2A (eukaryotic translation initiation factor 2A) [NCBI Gene 83939] {aka CDA02, EIF-2A, MST089, MSTP004, MSTP089}, APOC1 (apolipoprotein C1) [NCBI Gene 341] {aka APOC1B, Apo-CI, ApoC-I, apo-CIB, apoC-IB}, PIK3R3 (phosphoinositide-3-kinase regulatory subunit 3) [NCBI Gene 8503] {aka p55, p55-GAMMA, p55PIK}, RPS29 (ribosomal protein S29) [NCBI Gene 6235] {aka DBA13, S29, uS14}, MX1 (MX dynamin like GTPase 1) [NCBI Gene 4599] {aka IFI-78K, IFI78, MX, MxA, lncMX1-215}, SSBP4 (single stranded DNA binding protein 4) [NCBI Gene 170463], SAMHD1 (SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1) [NCBI Gene 25939] {aka CHBL2, DCIP, HDDC1, MOP-5, SBBI88, hSAMHD1}, SQSTM1 (sequestosome 1) [NCBI Gene 8878] {aka A170, DMRV, EBIAP, FTDALS3, NADGP, OSIL}, USP13 (ubiquitin specific peptidase 13) [NCBI Gene 8975] {aka ISOT3, IsoT-3}, TEF (TEF transcription factor, PAR bZIP family member) [NCBI Gene 7008], DAPK3 (death associated protein kinase 3) [NCBI Gene 1613] {aka DLK, ZIP, ZIPK}, EIF2AK2 (eukaryotic translation initiation factor 2 alpha kinase 2) [NCBI Gene 5610] {aka PKR, PPP1R83, PRKR}, DDX17 (DEAD-box helicase 17) [NCBI Gene 10521] {aka P72, RH70}, NUSAP1 (nucleolar and spindle associated protein 1) [NCBI Gene 51203] {aka ANKT, BM037, LNP, NUSAP, PRO0310p1, Q0310}, GAA (alpha glucosidase) [NCBI Gene 2548] {aka IOPD, LOPD, LYAG}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, SAMD9L (sterile alpha motif domain containing 9 like) [NCBI Gene 219285] {aka ATXPC, C7DELq, C7orf6, DEL7q, DRIF2, M7MLS1}, RAVER2 (ribonucleoprotein, PTB binding 2) [NCBI Gene 55225], RSAD2 (radical S-adenosyl methionine domain containing 2) [NCBI Gene 91543] {aka SAND, cig33, cig5, vig1}, TP53INP1 (tumor protein p53 inducible nuclear protein 1) [NCBI Gene 94241] {aka SIP, TP53DINP1, TP53INP1A, TP53INP1B, Teap, p53DINP1}, TLR8 (toll like receptor 8) [NCBI Gene 51311] {aka CD288, IMD98, TLR-8, hTLR8}, CALCOCO2 (calcium binding and coiled-coil domain 2) [NCBI Gene 10241] {aka NDP52}, FFAR2 (free fatty acid receptor 2) [NCBI Gene 2867] {aka FFA2R, GPR43}, ZNF395 (zinc finger protein 395) [NCBI Gene 55893] {aka HDBP-2, HDBP2, HDRF-2, PBF, PRF-1, PRF1}, APEX1 (apurinic/apyrimidinic endodeoxyribonuclease 1) [NCBI Gene 328] {aka APE, APE1, APEN, APEX, APX, HAP1}, CGAS (cyclic GMP-AMP synthase) [NCBI Gene 115004] {aka C6orf150, D4, MB21D1, h-cGAS}
- **Diseases:** VHSV (MESH:D031941), inflammation (MESH:D007249), Hepatitis C. (MESH:D019698), viral infection (MESH:D014777), rhabdovirus infections (MESH:D007239), COVID (MESH:D000086382)
- **Chemicals:** 5-methoxyuridine (MESH:C016562), TRIzol (MESH:C411644), cholesterol (MESH:D002784), GTP (MESH:D006160), adenosine (MESH:D000241), DAP (MESH:C041756), DMG-PEG2000 (MESH:C000626005), DSPC (MESH:C010942), uridine (MESH:D014529), Poly I:C (MESH:D011070), ATP (MESH:D000255), lipid (MESH:D008055), nucleoside (MESH:D009705), UTP (MESH:D014544), sodium acetate (MESH:D019346), cytidine (MESH:D003562), PBS (MESH:D007854), poly(A) (MESH:D011061), DLin (-), CTP (MESH:D003570), pseudo-uridine (MESH:D011560), N1-methyl-pseudouridine (MESH:C013608), phosphatidylcholine (MESH:D010713)
- **Species:** Viral hemorrhagic septicemia virus (no rank) [taxon 11287], Gammacoronavirus (genus) [taxon 694013], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Oncorhynchus tshawytscha (Chinook salmon, species) [taxon 74940], Mus musculus (house mouse, species) [taxon 10090], Infectious hematopoietic necrosis virus (no rank) [taxon 11290], Actinopterygii (fishes, superclass) [taxon 7898], Danio rerio (leopard danio, species) [taxon 7955], Oncorhynchus mykiss (rainbow trout, species) [taxon 8022], Salmo salar (Atlantic salmon, species) [taxon 8030], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** CHSE — Lepomis macrochirus (Bluegill), Spontaneously immortalized cell line (CVCL_G347), CHSE-EC — Oncorhynchus tshawytscha (Chinook salmon), Spontaneously immortalized cell line (CVCL_R822)

## Full text

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## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12934228/full.md

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Source: https://tomesphere.com/paper/PMC12934228