Evidence map›Paper›PMID 42316366›Full record

ArticleBMC genomics2026

Mergers and migrations: drivers of population genetic structure in a captive rhesus macaque colony.

Martha M Lyke, A Bagwell, D Newman, S Galindo, T Church, C Christensen, S B Gray, L A Cox, C N Ross, D Kaushal and 2 more

Abstract read
In one paragraph

Article in BMC genomics, 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Martha M LykeSouthwest National Primate Research Center, San Antonio, Texas, USA. mlyke@txbiomed.org.
A BagwellSouthwest National Primate Research Center, San Antonio, Texas, USA.
D NewmanSouthwest National Primate Research Center, San Antonio, Texas, USA.
S GalindoSouthwest National Primate Research Center, San Antonio, Texas, USA.
T ChurchSouthwest National Primate Research Center, San Antonio, Texas, USA.
C ChristensenSouthwest National Primate Research Center, San Antonio, Texas, USA.
S B GraySouthwest National Primate Research Center, San Antonio, Texas, USA.
L A CoxCenter for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
C N RossSouthwest National Primate Research Center, San Antonio, Texas, USA.
D KaushalSouthwest National Primate Research Center, San Antonio, Texas, USA.
I H Cheeseman *Southwest National Primate Research Center, San Antonio, Texas, USA.
S A Cole *Southwest National Primate Research Center, San Antonio, Texas, USA.

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
WNV REPLIVAX VACCINE IN NON-HUMAN PRIMATESP51RR013986 · NCRR · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI GOLDBERG, ERWIN · 1999 to 2011
$79.1M
Viral Testing CoreU42OD010442 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Deepak Kaushal · 2012 to 2026
$35.6M
NCRR NIH HHS P51 RR013986NIH grant U42 OD010442NIH HHS P51 OD011133NIH HHS U42 OD010442NIH NCRR grant P51 RR013986
6 · The paper itself

Abstract

backgroundRhesus macaques play a valuable role in biomedical research, and their genetic characterization is critical for effective colony management. Levels of genetic diversity, genomic admixture, and genetic substructure can all impact the suitability of macaques for biomedical research. The Southwest National Primate Research Center (SNPRC) houses one of the largest rhesus macaque colonies in the United States. Their genetic management includes the ongoing assessment of genetic diversity, ancestral origin (India or China), and deep sequencing of the major histocompatibility complex (MHC). A goal of the SNPRC has been the reduction of levels of admixture between Indian- and Chinese-origin macaques and the prevalence of simian immunodeficiency virus (SIV) refractory MHC haplotypes while maintaining overall genetic and MHC haplotype diversity. This has been achieved by targeted sequencing of the MHC and removing animals with haplotypes more prevalent in Chinese-origin macaques from breeding.

resultsWe investigated the impact of management strategies on admixture, population genetic structure, genetic diversity, and inbreeding using whole exome sequencing of founding and colony-born animals (n = 488). Admixture analysis of founders showed one animal to be of Chinese origin and an additional 37 considered admixed (> 15% Chinese ancestry; range 16.3-84.5%) with population substructure closely reflecting primate research center source. The levels of Chinese ancestry in the colony declined over time, though genetic diversity remains high (heterozygosity = 0.320). We characterized the MHC through targeted sequencing of 1,069 SNPRC macaques born over a twelve-year period. MHC management strategies reduced the prevalence of SIV-refractory MHC haplotypes, with Mamu-B*008 reaching significance (p = 0.027), while overall haplotype diversity was maintained (Mamu-A, h = 0.907; Mamu-B, h = 0.952). Finally, we performed genome-wide scans for genetic selection over time. We identify numerous genomic regions where allele frequencies have shifted significantly, supporting the presence of short-term adaptation under colony management.

conclusionsWe show that colony management strategies have been successful without reducing genetic diversity of the MHC or exonic regions. We also show that colony genetic substructure is related to animal colony source and that mergers and migrations have reduced inbreeding and increased overall genetic diversity.

Indexed as

Genetic VariationMacaca mulattaAnimal HusbandryAnimalsBreedingExome SequencingFemaleGenetics, PopulationInbreedingMajor Histocompatibility ComplexMaleSimian Immunodeficiency VirusSpecific Pathogen-Free OrganismsCaptive breeding managementGenetic admixtureMajor histocompatibility complexRhesus macaqueWhole exome sequencing

Identifiers

PMID42316366
PMCPMC13523324

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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.