Sockeye salmon immunoglobulin VH usage and pathogen loads differ between spawning sites.
Maxwell E Chappell1, Lidia Epp1, Patty Zwollo1
1Department of Biology, The College of William and Mary, Williamsburg, VA, 23185, United States.
Juvenile salmon develop long-lived plasma cells (LLPCs) for pathogen protection at their natal sites. This study confirms site-specific antibody gene usage in sockeye salmon, supporting natural immunization against local fish pathogens.
Area of Science:
- Immunology
- Ichthyology
- Genetics
Background:
- The Immunological Imprinting Hypothesis suggests juvenile fish develop pathogen-specific immunity at natal sites.
- Long-lived plasma cells (LLPCs) produce antibodies, conferring protection upon return to native waters.
Purpose of the Study:
- To test the Immunological Imprinting Hypothesis in Alaskan sockeye salmon populations.
- To investigate the relationship between antibody gene usage, pathogen exposure, and site-specific immunity.
Main Methods:
- Analysis of Immunoglobulin VH gene family usage via RT-qPCR in spleen and anterior kidney samples.
- Quantification of pathogen loads and infection prevalence for Renibacterium salmoninarum, Flavobacterium psychrophilum, and Infectious Hematopoietic Necrosis Virus.
- Comparison of immunological and pathological data across six distinct spawning sites.
Main Results:
- Significant differences in VH gene usage, pathogen prevalence, and loads were observed between spawning sites.
- Infection probability varied by location for each pathogen.
- Negative correlations were found between specific VH gene usage patterns and pathogen loads.
Conclusions:
- Findings support the Immunological Imprinting Hypothesis, demonstrating site-dependent VH gene usage in sockeye salmon.
- This suggests a mechanism for natural immunization, potentially protecting wild and farmed fish populations from endemic pathogens.
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