PMID- 37995964 OWN - NLM STAT- MEDLINE DCOM- 20231216 LR - 20240213 IS - 1872-7492 (Electronic) IS - 0168-1702 (Print) IS - 0168-1702 (Linking) VI - 339 DP - 2024 Jan 2 TI - DUSP1 mRNA modulation during porcine circovirus type 2 and porcine reproductive and respiratory syndrome virus co-infection regulates viruses replication. PG - 199282 LID - S0168-1702(23)00244-7 [pii] LID - 10.1016/j.virusres.2023.199282 [doi] LID - 199282 AB - The effects of porcine circovirus type 2b (PCV2b) and porcine reproductive and respiratory syndrome virus (PRRSV) co-infection in epithelial cells of the swine respiratory tract is unknown. In the present study, the newborn pig trachea cell line NPTr-CD163, which is permissive to both viruses, was persistently infected with PCV2b and then with PRRSV. Viral replication, cell viability, cytokines' mRNA expression, and modulation of cellular genes expression were evaluated in infected cells. In NPTr-CD163 co-infection model, PCV2b replication was enhanced while PRRSV replication was suppressed. Cell viability was significantly decreased during PCV2b single infection and co-infection compared to mock-infected and PRRSV single infected cells. However, no difference was observed in cell viability between PCV2b and PCV2b/PRRSV infected cells. The IL6, IL8 and IL10 mRNA expression was significantly higher in co-infected cells compared to PCV2b and PRRSV single infected cells. Moreover, the IFN-alpha/beta expression was significantly reduced in co-infected cells compared to PCV2b infected cells whereas it remained higher compared to PRRSV infected cells. The differential gene expression analysis revealed that the mRNA expression level of the cellular gene DUSP1 was significantly higher in all PRRSV infection models compared to PCV2b single infected cells. Knockdown of DUSP1 expression in co-infected cells significantly reduced PCV2b replication, suggesting a role for DUSP1 in PCV2b/PRRSV pathogenesis. CI - Copyright (c) 2023. Published by Elsevier B.V. FAU - Burgher-Pulgaron, Yaima AU - Burgher-Pulgaron Y AD - The Swine and Poultry Infectious Diseases Research Centre (CRIPA-FRQNT), Faculte de Medecine Veterinaire (FMV), Universite de Montreal, 3200 rue Sicotte, St-Hyacinthe, Quebec, Canada, J2S 2M2. FAU - Provost, Chantale AU - Provost C AD - Molecular Diagnostic Laboratory, Centre de Diagnostic Veterinaire de l'Universite de Montreal (CDVUM), FMV, Canada. FAU - Alvarez, Fernando AU - Alvarez F AD - Infectious Diseases and Immunity in Global Health (IDIGH), McGill University, 1001 Decarie, Montreal, Quebec, Canada, H4A 3J1. FAU - Meza-Serrano, Europa AU - Meza-Serrano E AD - Centre de Recherche en Reproduction Animale, FMV, Universite de Montreal, Canada. FAU - Pesant, Marie-Jeanne AU - Pesant MJ AD - The Swine and Poultry Infectious Diseases Research Centre (CRIPA-FRQNT), Faculte de Medecine Veterinaire (FMV), Universite de Montreal, 3200 rue Sicotte, St-Hyacinthe, Quebec, Canada, J2S 2M2. FAU - Price, Christopher A AU - Price CA AD - Centre de Recherche en Reproduction Animale, FMV, Universite de Montreal, Canada. FAU - Gagnon, Carl A AU - Gagnon CA AD - The Swine and Poultry Infectious Diseases Research Centre (CRIPA-FRQNT), Faculte de Medecine Veterinaire (FMV), Universite de Montreal, 3200 rue Sicotte, St-Hyacinthe, Quebec, Canada, J2S 2M2; Molecular Diagnostic Laboratory, Centre de Diagnostic Veterinaire de l'Universite de Montreal (CDVUM), FMV, Canada. Electronic address: carl.a.gagnon@umontreal.ca. LA - eng PT - Journal Article DEP - 20231201 PL - Netherlands TA - Virus Res JT - Virus research JID - 8410979 SB - IM MH - Swine MH - Animals MH - *Porcine respiratory and reproductive syndrome virus MH - *Circovirus/genetics MH - *Coinfection MH - *Swine Diseases MH - Virus Replication MH - *Porcine Reproductive and Respiratory Syndrome PMC - PMC10711501 OTO - NOTNLM OT - Co-infection OT - DUSP1 OT - NPTr-CD163 cells OT - PCV2b OT - PRRSV COIS- Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. EDAT- 2023/11/24 00:42 MHDA- 2023/12/17 13:19 PMCR- 2023/12/01 CRDT- 2023/11/23 19:31 PHST- 2023/08/02 00:00 [received] PHST- 2023/11/18 00:00 [revised] PHST- 2023/11/20 00:00 [accepted] PHST- 2023/12/17 13:19 [medline] PHST- 2023/11/24 00:42 [pubmed] PHST- 2023/11/23 19:31 [entrez] PHST- 2023/12/01 00:00 [pmc-release] AID - S0168-1702(23)00244-7 [pii] AID - 199282 [pii] AID - 10.1016/j.virusres.2023.199282 [doi] PST - ppublish SO - Virus Res. 2024 Jan 2;339:199282. doi: 10.1016/j.virusres.2023.199282. Epub 2023 Dec 1.