Evidence map›Paper›PMID 42292458›Full record

ArticleFrontiers in immunology2026

High-throughput profiling of the T cell receptor delta CDR3 repertoire reveals species-specific patterns in cattle (Bos taurus) and water buffalo (Bubalus bubalis).

Yueheng Zhang, Fengli Wu, Long Ma, Xinsheng Yao, Jun Li

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yueheng Zhang *Department of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.
Fengli Wu *Department of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.
Long MaDepartment of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.
Xinsheng YaoDepartment of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.
Jun LiDepartment of Immunology, Center of Immunomolecular Engineering, Innovation & Practice Base for Graduate Students Education, Zunyi Medical University, Zunyi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: γδ T cells constitute a substantial proportion of lymphocytes in ruminants, and the diversity of their immune receptors is critical for understanding species-specific immune functions. The complementarity-determining region 3 (CDR3) of the T cell receptor delta chain (TRD) is a key structural determinant of γδ T cell antigen recognition; however, systematic comparative analyses of TRD immune repertoire characteristics across different bovine species remain limited. In this study, high-throughput sequencing and comprehensive analysis of the TRD CDR3 immune repertoire were performed in 7 cattle (Bos taurus) and 5 water buffalo (Bubalus bubalis). Results: The results demonstrated good consistency in sequencing depth and data quality between the two groups. Diversity analysis revealed that the cattle TRD CDR3 repertoire exhibited higher clonal evenness and overall diversity than that of buffalo. Clonotype composition analysis showed that both species were dominated by medium- to high-frequency clonotypes, whereas buffalo relied more heavily on a limited number of highly expanded clonotypes. V(D)J gene usage analysis identified pronounced species-specific preferences in TRDV gene usage, with high intra-group consistency but low inter-species correlation; in contrast, TRDJ gene usage was highly conserved between the two species. The CDR3 length distributions in both groups displayed similar bell-shaped patterns, suggesting structural constraints during evolution, while K-mer and motif analyses revealed differences in CDR3 microstructural features between species. Furthermore, shared clonotype analysis indicated a limited number of public CDR3 amino acid sequences between cattle and buffalo, with highly abundant shared clonotypes enriched only in a small subset of individuals. Conclusions: Collectively, this study provides a systematic characterization of the similarities and differences in the TRD CDR3 immune repertoires of cattle and water buffalo, offering fundamental data and a comparative perspective for understanding the mechanisms shaping γδ TCR diversity and their potential immunological functions in high γδ T cell species.

Indexed as

BuffaloesComplementarity Determining RegionsReceptors, Antigen, T-Cell, gamma-deltaAnimalsCattleHigh-Throughput Nucleotide SequencingSpecies SpecificityComplementarity Determining RegionsReceptors, Antigen, T-Cell, gamma-deltacattleTCR CDR3 repertoireV(D)J recombinationwater buffaloγδ T cells

Identifiers

PMID42292458
PMCPMC13253796

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.