Evidence map›Paper›PMID 40164980›Full record

ArticleGut microbes2025

Genomic and functional co-diversification imprint African Hominidae microbiomes to signal dietary and lifestyle adaptations.

Saria Otani, Marie Louise Jespersen, Christian Brinch, Frederik Duus Møller, Bo Pilgaard, Emilie Egholm Bruun Jensen, Pimlapas Leekitcharoenphon, Christina Aaby Svendsen, Amalie H Aarestrup, Tolbert Sonda and 8 more

Abstract read
In one paragraph

Article in Gut microbes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Interactions at theMicrobiology (Reading, England) · 2026
    Review
  4. A Hadza-enrichedGut microbes reports · 2026
    Article
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

18 authors.

Saria OtaniResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.ORCID 0000-0002-2538-8086
Marie Louise JespersenResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Christian BrinchResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Frederik Duus MøllerResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Bo PilgaardDepartment of Biotechnology and Biomedicine, Section for Protein Chemistry and Enzyme Technology, Technical University of Denmark, Lyngby, Denmark.
Emilie Egholm Bruun JensenResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Pimlapas LeekitcharoenphonResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Christina Aaby SvendsenResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Amalie H AarestrupResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.
Tolbert SondaBiotechnology Research Laboratory, Kilimanjaro Clinical Research Institute (KCRI), Moshi, Tanzania.
Teresa J SylvinaNational Academies of Sciences, Engineering and Medicine, Washington, DC, USA.
Jeff LeachMicrobiome Network and Department of Agricultural Biology, Colorado State University, Fort Collins, CO, USA.
Alexander PielDepartment of Human Origins, Max Planck Institute of Evolutionary Anthropology, Leipzig, Germany.
Fiona StewartDepartment of Human Origins, Max Planck Institute of Evolutionary Anthropology, Leipzig, Germany.
Panagiotis SapountzisUniversité Clermont Auvergne, INRAE, UMR 0454 MEDIS, Clermont-Ferrand, France.
Paul E KazyobaNational Institute for Medical Research, Dar-Es-Salaam, Tanzania.
Happiness KumburuBiotechnology Research Laboratory, Kilimanjaro Clinical Research Institute (KCRI), Moshi, Tanzania.
Frank M AarestrupResearch group for Genomic Epidemiology, National Food Institute, Technical University of Denmark, Lyngby, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the diverse landscape of African hominids, the obligate relationship between the host and its microbiome narrates signals of adaptation and co-evolution. Sequencing 546 African hominid metagenomes, including those from indigenous Hadza and wild chimpanzees, identified similar bacterial richness and diversity surpassing those of westernized populations. While hominids share core bacterial communities, they also harbor distinct, population-specific bacterial taxa tailored to specific diets, ecology and lifestyles, differentiating non-indigenous and indigenous humans and chimpanzees. Even amongst shared bacterial communities, several core bacteria have co-diversified to fulfil unique dietary degradation functions within their host populations. These co-evolutionary trends extend to non-bacterial elements, such as mitochondrial DNA, antimicrobial resistance, and parasites. Our findings indicate that microbiome-host co-adaptations have led to both taxonomic and within taxa functional displacements to meet host physiological demands. The microbiome, in turn, transcends its taxonomic interchangeable role, reflecting the lifestyle, ecology and dietary history of its host.

Indexed as

BacteriaDietGastrointestinal MicrobiomeHominidaeAdaptation, PhysiologicalAfricaAnimalsHumansLife StyleMetagenomePan troglodytesPhylogenyAfrican hominidaeevolutionhost adaptationMicrobiome

Identifiers

PMID40164980
PMCPMC11959905

What OpenQuestion holds

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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.