Salmonid Alphavirus Subtype 3 Induces Prolonged Local B Cell Responses in Atlantic Salmon (Salmo salar) After Intraperitoneal Infection

• Published in: Frontiers in Immunology
• Main Authors: Shiferaw Jenberie, Ma. Michelle D. Peñaranda, Hanna L. Thim, Morten Bay Styrvold, Guro Strandskog, Jorunn B. Jørgensen, Ingvill Jensen
• Format: Article in Journal/Newspaper
• Language: English
• Published: Frontiers Media S.A. 2020
• Subjects: antibody secreting cells; Atlantic salmon; B cells; peritoneal cavity; Salmonid alphavirus; teleost; Immunologic diseases. Allergy; RC581-607; Salmo salar
• Online Access: https://doi.org/10.3389/fimmu.2020.01682; https://doaj.org/article/266fb818f2554ee5b8d0875bae420b76

B cell responses are a crucial part of the adaptive immune response to viral infection. Infection by salmonid alphavirus subtype 3 (SAV3) causes pancreas disease (PD) in Atlantic salmon (Salmo salar) and is a serious concern to the aquaculture industry. In this study, we have used intraperitoneal (IP) infection with SAV3 as a model to characterize local B cell responses in the peritoneal cavity (PerC) and systemic immune tissues (head kidney/spleen). Intraperitoneal administration of vaccines is common in Atlantic salmon and understanding more about the local PerC B cell response is fundamental. Intraperitoneal SAV3 infection clearly induced PerC B cell responses as assessed by increased frequency of IgM+ B cells and total IgM secreting cells (ASC). These PerC responses were prolonged up to nine weeks post-infection and positively correlated to the anti-SAV3 E2 and to neutralizing antibody responses in serum. For the systemic immune sites, virus-induced changes in B cell responses were more modest or decreased compared to controls in the same period. Collectively, data reported herein indicated that PerC could serve as a peripheral immunological site by providing a niche for prolonged maintenance of the ASC response in Atlantic salmon.