Evolution of T cell receptor beta loci in salmonids

Front Immunol. 2023 Aug 15:14:1238321. doi: 10.3389/fimmu.2023.1238321. eCollection 2023.

Abstract

T-cell mediated immunity relies on a vast array of antigen specific T cell receptors (TR). Characterizing the structure of TR loci is essential to study the diversity and composition of T cell responses in vertebrate species. The lack of good-quality genome assemblies, and the difficulty to perform a reliably mapping of multiple highly similar TR sequences, have hindered the study of these loci in non-model organisms. High-quality genome assemblies are now available for the two main genera of Salmonids, Salmo and Oncorhynchus. We present here a full description and annotation of the TRB loci located on chromosomes 19 and 25 of rainbow trout (Oncorhynchus mykiss). To get insight about variations of the structure and composition of TRB locus across salmonids, we compared rainbow trout TRB loci with other salmonid species and confirmed that the basic structure of salmonid TRB locus is a double set of two TRBV-D-J-C loci in opposite orientation on two different chromosomes. Our data shed light on the evolution of TRB loci in Salmonids after their whole genome duplication (WGD). We established a coherent nomenclature of salmonid TRB loci based on comprehensive annotation. Our work provides a fundamental basis for monitoring salmonid T cell responses by TRB repertoire sequencing.

Keywords: T cell receptor; TRB locus; adaptive immunity; evolution; rainbow trout; repertoire; salmonid fish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomes, Human, Pair 19
  • Humans
  • Immunity, Cellular
  • Oncorhynchus mykiss* / genetics

Grants and funding

SuM was supported by Xunta de Galicia (GRC-ED431C 2020/02). PB was supported by the European Union’s Horizon 2020 research and innovation program under grant agreement No 817923 (AQUAFAANG), by ANR (ANR-21-CE35-0019, LipofishVac), by the Eranet ICRAD-Nucnanofish (ANR_13001498), and by institutional grants from INRAE. UG was supported by the grant #274635 from the Norwegian Research Council.