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1.
Virol J ; 19(1): 134, 2022 08 19.
Artículo en Inglés | MEDLINE | ID: mdl-35986298

RESUMEN

BACKGROUND: Bovine viral diarrhea virus 1 (BVDV-1) of the pestivirus genus is an economically crippling virus in the cattle industry; this positive RNA virus causes mucosal disease resulting in reproductive losses and other disease syndromes. The pathogenesis mechanism of the disease caused by BVDV infection is not well understood; for a better understanding of in vivo host BVDV-1 interactions, we conducted a transcriptomic study of infected cells at different times post-infection. METHODS: We compared the permissiveness and cellular response of a BVDV-1 cytopathogenic strain on Madin-Darby Bovine Kidney cells (MDBK) and bovine lung primary cells, a model closer to in vivo infection. Then a RNAseq analysis was realized on the infected bovine lung primary cells, at 10 hpi and 30 hpi (hours post-infection), to identify transcriptomic signatures. RESULTS: RNAseq analysis on BVDV-1 infected bovine primary cells showed 2,759 and 5,376 differentially expressed genes at respectively 10 hpi and 30 hpi with an absolute Fold Change ≥ 2. Among the different pathways deregulated, data analysis revealed a deregulation of Wnt signaling pathway, a conserved process that play a critical role in embryogenesis, cellular proliferation, and differentiation as well as in viral responses against viruses such as Influenza or Hepatitis C. We demonstrated here that the deregulation of the Wnt/ßcatenin signaling pathway plays a role in viral replication of BVDV cp strain. Interestingly, we showed that the inhibition of this Wnt pathway using two inhibitors, FZM1 and iCRT14, induced a delay in onset of the establishment of a cytopathic effect of primary cells. CONCLUSIONS: Thereby, this study highlighted a role of the Wnt signaling pathway in the BVDV-1 viral replication in bovine cells, suggesting an interesting option to explore as a new therapeutic target.


Asunto(s)
Diarrea Mucosa Bovina Viral , Virus de la Diarrea Viral Bovina , Animales , Diarrea Mucosa Bovina Viral/genética , Bovinos , Línea Celular , Efecto Citopatogénico Viral , Virus de la Diarrea Viral Bovina/genética , Replicación Viral/genética , Vía de Señalización Wnt
2.
Virology ; 567: 34-46, 2022 02.
Artículo en Inglés | MEDLINE | ID: mdl-34953294

RESUMEN

The bovine viral diarrhea virus 1 (BVDV-1), belonging to the Pestivirus genus, is characterized by the presence of two biotypes, cytopathogenic (cp) or non-cytopathogenic (ncp). For a better understanding of the host pathogen interactions, we set out to identify transcriptomic signatures of bovine lung primary cells (BPCs) infected with a cp or a ncp strain. For this, we used both a targeted approach by reverse transcription droplet digital PCR and whole genome approach using RNAseq. Data analysis showed 3571 differentially expressed transcripts over time (Fold Change >2) and revealed that the most deregulated pathways for cp strain are signaling pathways involved in responses to viral infection such as inflammatory response or apoptosis pathways. Interestingly, our data analysis revealed a deregulation of Wnt signaling pathway, a pathway described in embryogenesis, that was specifically seen with the BVDV-1 cp but not the ncp suggesting a role of this pathway in viral replication.


Asunto(s)
Proteínas Reguladoras de la Apoptosis/genética , Diarrea Mucosa Bovina Viral/genética , Efecto Citopatogénico Viral/genética , Virus de la Diarrea Viral Bovina Tipo 1/genética , Transcriptoma , Vía de Señalización Wnt/genética , Animales , Apoptosis/genética , Proteínas Reguladoras de la Apoptosis/metabolismo , Diarrea Mucosa Bovina Viral/metabolismo , Diarrea Mucosa Bovina Viral/patología , Diarrea Mucosa Bovina Viral/virología , Bovinos , Virus de la Diarrea Viral Bovina Tipo 1/metabolismo , Virus de la Diarrea Viral Bovina Tipo 1/patogenicidad , Células Epiteliales/metabolismo , Células Epiteliales/virología , Perfilación de la Expresión Génica , Regulación de la Expresión Génica , Interacciones Huésped-Patógeno/genética , Interleucinas/genética , Interleucinas/metabolismo , Pulmón/metabolismo , Pulmón/virología , Potencial de la Membrana Mitocondrial , Mitocondrias/genética , Mitocondrias/metabolismo , Mitocondrias/virología , FN-kappa B/genética , FN-kappa B/metabolismo , Cultivo Primario de Células , Mucosa Respiratoria/metabolismo , Mucosa Respiratoria/virología , Receptores Toll-Like/genética , Receptores Toll-Like/metabolismo , Replicación Viral
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