Evidence map›Paper›PMID 40501981›Full record

ArticlebioRxiv : the preprint server for biology2025

The genomic legacy of selectively breeding rhesus macaques for HIV/AIDS-related research.

M 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 readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

M M LykeSouthwest National Primate Research Center, San Antonio, TX.
A BagwellSouthwest National Primate Research Center, San Antonio, TX.
D NewmanSouthwest National Primate Research Center, San Antonio, TX.
S GalindoSouthwest National Primate Research Center, San Antonio, TX.
T ChurchSouthwest National Primate Research Center, San Antonio, TX.
C ChristensenSouthwest National Primate Research Center, San Antonio, TX.
S B GraySouthwest National Primate Research Center, San Antonio, TX.
L A CoxCenter for Precision Medicine, Wake Forest University School of Medicine, Winston-Salem, NC.ORCID 0000-0002-8836-3783
C N RossSouthwest National Primate Research Center, San Antonio, TX.
D KaushalSouthwest National Primate Research Center, San Antonio, TX.
I H CheesemanSouthwest National Primate Research Center, San Antonio, TX.
S A ColeSouthwest National Primate Research Center, San Antonio, TX.

Funding

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 HHS U42 OD010442
6 · The paper itself

Abstract

Background: Rhesus macaques are the preferred non-human primate model for HIV/AIDS-related research. Specific major histocompatibility complex (MHC) haplotypes and genetic ancestry are linked to slow disease progression of Simian Immunodeficiency Virus (SIV) infections in macaques. To maximize their utility for HIV/AIDS research, the Southwest National Primate Research Center (SNPRC) has introduced targeted breeding strategies to reduce the prevalence of SIV-refractory MHC haplotypes and levels of admixture between Indian- and Chinese-origin macaques. Results: We characterized the MHC region in SNPRC macaques by targeted deep sequencing of 1,458 animals born over a ten-year period. Following the implementation of MHC management strategies, the prevalence of SIV-refractory MHC haplotypes reduced significantly while overall haplotype diversity was maintained. We 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 some Chinese ancestry, though population substructure more closely reflected primate research center source than geographical origin. The levels of Chinese ancestry declined significantly over time, though genetic diversity remains high. 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 within the colony. Conclusions: We 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

captive breeding managementgenetic admixtureHIV/AIDSmajor histocompatibility complexRhesus macaquewhole exome sequencing

Identifiers

PMID40501981
PMCPMC12154786

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.