Abstract

BackgroundDespite increasing interest in γδ T cells and their non-classical behaviour, most studies focus on animals with low numbers of circulating γδ T cells, such as mice and humans. Arguably, γδ T cell functions might be more prominent in chickens where these cells form a higher proportion of the circulatory T cell compartment. The TCR repertoire defines different subsets of γδ T cells, and such analysis is facilitated by well-annotated TCR loci. γδ T cells are considered at the cusp of innate and adaptive immunity but most functions have been identified in γδ low species. A deeper understanding of TCR repertoire biology in γδ high and γδ low animals is critical for defining the evolution of the function of γδ T cells. Repertoire dynamics will reveal populations that can be classified as innate-like or adaptive-like as well as those that straddle this definition.ResultsHere, a recent discrepancy in the structure of the chicken TCR gamma locus is resolved, demonstrating that tandem duplication events have shaped the evolution of this locus. Importantly, repertoire sequencing revealed large differences in the usage of individual TRGV genes, a pattern conserved across multiple tissues, including thymus, spleen and the gut. A single TRGV gene, TRGV3.3, with a highly diverse private CDR3 repertoire dominated every tissue in all birds. TRGV usage patterns were partly explained by the TRGV-associated recombination signal sequences. Public CDR3 clonotypes represented varying proportions of the repertoire of TCRs utilising different TRGVs, with one TRGV dominated by super-public clones present in all birds.ConclusionsThe application of repertoire analysis enabled functional annotation of the TCRG locus in a species with a high circulating γδ phenotype. This revealed variable usage of TCRGV genes across multiple tissues, a pattern quite different to that found in γδ low species (human and mouse). Defining the repertoire biology of avian γδ T cells will be key to understanding the evolution and functional diversity of these enigmatic lymphocytes in an animal that is numerically more reliant on them. Practically, this will reveal novel ways in which these cells can be exploited to improve health in medical and veterinary contexts.

Highlights

  • The adaptive immune system of jawed vertebrates functions through the production of antibodies by B lymphocytes, combined with the cytotoxic, helper and regulatory functions of T lymphocytes

  • Defining the repertoire biology of avian γδ T cells will be key to understanding the evolution and functional diversity of these enigmatic lymphocytes in an animal that is numerically more reliant on them

  • The T cell receptor (TCR) gamma locus of this assembly was recently contradicted by Liu et al 2020 [30] in a paper that used a BAC resequencing approach to correct an older genome assembly, galGal4. galGal6a features a 15 kb region not present in the BAC derived gamma locus [30]

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Summary

Introduction

The adaptive immune system of jawed vertebrates functions through the production of antibodies by B lymphocytes, combined with the cytotoxic, helper and regulatory functions of T lymphocytes. At least some populations of γδ T cells are considered part of the innate immune system, operating in the early phases of the host’s response. These γδ T cell subsets have very restricted TCR diversity, which is characteristic of an innate-like response [5, 6]. Other γδ T cell populations have diverse CDR3 repertoires, as are seen in classical αβ T cells, more characteristic of the adaptive immune system. Γδ T cells are considered at the cusp of innate and adaptive immunity but most functions have been identified in γδ low species. Repertoire dynamics will reveal populations that can be classified as innate-like or adaptive-like as well as those that straddle this definition

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