Understanding range-wide immune gene variation in an endangered big cat ( Panthera tigris )

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ID: 338718
2026
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Abstract
Abstract Assessing genetic diversity at loci putatively involved in fitness, such as immune genes, could provide important insights into the survival and vulnerability of endangered species. Research on immune genes in wild species has traditionally focused on the Major Histocompatibility Complex (MHC) genes, which represent only a small proportion of the immune gene repertoire, thereby limiting our understanding of immunity in non-model species. Here, we investigate five families of non-MHC immune genes - Tumor Necrosis Factors, interleukins, Toll-like Receptors, Leukocyte Immunoglobulin-Like Receptors, and chemokines - involved in adaptive and innate immunity in tiger Panthera tigris, an endangered carnivore known to have experienced historical bottlenecks and inbreeding. By leveraging 107 publicly available whole genomes, this study provides a comparative, multi-subspecific assessment of non-MHC immunogenetic diversity in tigers and identifies populations of conservation concern. We found higher genetic variation in immune receptor genes than in neutral regions and immune signalling genes. Site frequency spectra suggest balancing selection on Toll-like receptor genes. Further, tiger populations with histories of bottlenecks and inbreeding, such as South China tigers and North-western Indian tigers, exhibit reduced genetic diversity and higher mutation load in immune genes compared to large, connected tiger populations. Overall, we find that genetic drift is likely the predominant evolutionary force shaping genetic variation in tigers at both neutral and immune loci. However, some immune polymorphisms persist despite drift, thereby maintaining elevated variation, indicating that tigers have not been entirely stripped of their immunogenetic resilience. Such immunogenetic resilience may prove vital as spillover threats intensify.
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Authors B.V. Aditi, Uma Ramakrishnan
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Journal genome biology and evolution
Year 2026
DOI
10.1093/gbe/evag276
URL
https://academic.oup.com/gbe/advance-article-pdf/doi/10.1093/gbe/evag276/72943550/evag276.pdf
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