A Broad Survey and Functional Analysis of Immunoglobulin Loci Variation in Rhesus Macaques

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Abstract

Rhesus macaques (RMs) are vital models for studying human disease, and are invaluable to pre-clinical pipelines for vaccine discovery and testing. Particularly in this regard, they are often used to study infection and vaccine-associated broadly neutralizing antibody responses. This has resulted in an increasing demand for improved genetic resources for the immunoglobulin (IG) loci, which harbor antibody-encoding genes. However, the highly polymorphic and structurally variable nature of these loci have them historically challenging to sequence and characterize at the level of both the genome and expressed repertoire. To address these challenges, we have developed a novel integrated analysis workflow for conducting the combined processing of B cell receptor repertoire sequencing data with matched whole-genome and targeted long-read genomic sequencing data. Using this novel approach, we have assembled the largest collection of IG germline alleles reported to date, amassed from 106 Indian origin RMs. Using a conservative annotation approach, requiring sample-level internal validation from both genomic and expressed datasets, we created a comprehensive resource that captures extensive diversity of IG heavy and light chain variable (V), diversity (D), and joining (J) alleles, as well as leader, intronic, and recombination signal sequences (RSSs). This publicly available, continually updated database will advance vaccine research for infectious disease, and provide a robust foundation for immunogenomics and future translational research.

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