Mucosal immune responses of gut IgM in common carp (Cyprinus carpio) following infection with spring viremia of carp virus (SVCV).

Fish Shellfish Immunol

Key Laboratory of Breeding Biotechnology and Sustainable Aquaculture, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China. Electronic address:

Published: February 2024

AI Article Synopsis

  • IgM is a vital antibody that helps the immune system by recognizing pathogens, activating complement, and promoting phagocytosis, but its response in common carp after viral infection hasn't been well studied.
  • Researchers created a model to examine IgM responses in common carp, revealing significant increases in immune markers (IL1-β and Igs) after viral infection, indicating a robust immune reaction.
  • The study found that IgM responses were notably stronger in the hindgut compared to other gut parts, and responses to secondary infections were quicker, with increased IgM B cells detected by 14 days post-infection.

Article Abstract

Immunoglobulin M (IgM) specifically recognizes various antigens and can activate complement, mediate cytotoxicity, opsonize and agglutinate pathogens to induce phagocytosis, all of which play an important role in immunity. However, the IgM response of common carp (Cyprinus carpio) in the intestinal mucosa after viral infection has not been thoroughly. Therefore, we successfully produced an anti-carp IgM monoclonal antibody and developed a model of viral infection to study the kinetics of immune responses after viral infection. Our results showed that the expression of IL1-β and Igs were dramatically increased, implying that common carp exhibited a significant innate and adaptive immune response to viral infection. Furthermore, we found that the IgM responses varied between the two infection strategies. At 14 days post-infection (DPI), a significant population of IgM B cells were observed in the gut, accompanied by a sharp rise in IgM levels. The immune response to secondary infection started at 7 DPI, suggesting that the IgM response is faster in the gut after re-infection. Importantly, we also explored the variability of different gut compartments to viral infection, and result revealed a stronger immune response in the hindgut than in the foregut and midgut. Overall, our findings indicate that IgM plays an important role in the intestinal immune response following primary and secondary viral infection, in which the hindgut plays a major immune function.

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Source
http://dx.doi.org/10.1016/j.fsi.2023.109326DOI Listing

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