Evidence map›Paper›PMID 42271189›Full record

ArticleMicrobiologyOpen2026

Phylogenetic Profiling of the Diabetic Foot Ulcer Microbiome of an Afro-Caribbean Population.

Nkemcho Ojeh, Bidyut R Mohapatra, Margaret O'Shea, Dale Springer, Judy Ward, Mohmmed Sallu, Natacha Paquette, Keith Gooding, Anna Springer, O Peter Adams

Abstract read
In one paragraph

Article in MicrobiologyOpen, 2026. 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

10 authors.

Nkemcho OjehDepartment of Preclinical and Health Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.ORCID https://orcid.org/0000-0002-2507-2209
Bidyut R MohapatraDepartment of Biological and Chemical Sciences, The University of the West Indies, Bridgetown, Barbados.
Margaret O'SheaDepartment of Clinical Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Dale SpringerDepartment of Clinical Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Judy WardDepartment of Clinical Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Mohmmed SalluDepartment of Clinical Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Natacha PaquetteDepartment of Clinical Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Keith GoodingDepartment of Preclinical and Health Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
Anna SpringerDepartment of Preclinical and Health Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.
O Peter AdamsDepartment of Preclinical and Health Sciences, Faculty of Medical Sciences, The University of the West Indies, Bridgetown, Barbados.

Funding

University of the West indies
6 · The paper itself

Abstract

Diabetic foot ulcers (DFUs) are associated with high morbidity, amputation rates, and healthcare costs in Barbados. This pilot study compares the microbiome diversity of chronic DFUs and paired normal skin (controls) from biopsies in Afro-Caribbean patients with type 2 diabetes using Illumina amplicon sequencing targeting the 16S ribosomal RNA (rRNA) gene and the internal transcribed spacer 2 (ITS2) region. Both DFUs and controls harbored diverse bacterial and fungal communities, with differences in taxonomic composition and relative abundance profiles. The dominant bacterial genera were Corynebacterium (18.3% in DFUs, 24.3% in controls) and Staphylococcus (14.9% in DFUs, 14.1% in controls). The dominant bacterial species was Corynebacterium striatum (17.3% in DFUs, 23.8% in controls) followed by Pseudomonas aeruginosa in DFUs (8.9%) and Staphylococcus aureus in controls (13.3%). The dominant fungal genera was Densospora (12% in DFUs, 12.6% in controls). The dominant fungal species was Rhodotorula graminis in DFUs (6.18%) and Paracamarosporium leucadendri in controls (3.85%). Candida duobushaemulonii, with intrinsic resistance to antifungal agents, was detected with higher relative abundance in DFUs than in controls (4.44% vs. 2.36%). Fungal Shannon alpha diversity was significantly reduced in DFUs (p = 0.039), while beta diversity did not differ between groups for bacteria (p = 0.982) or fungi (p = 0.975). The differences in taxonomic composition and relative abundance profiles, and co-occurrence of clinically relevant bacterial and fungal taxa, highlight the potential role of polymicrobial communities in DFU chronicity in the Afro-Caribbean cohort studied, and supports future studies to evaluate implications for antimicrobial stewardship.

Indexed as

BacteriaDiabetic FootFungiMicrobiotaPhylogenyAgedBarbadosCaribbean PeopleDiabetes Mellitus, Type 2DNA, BacterialDNA, Ribosomal SpacerFemaleHumansMaleMiddle AgedPilot ProjectsDNA, BacterialDNA, Ribosomal SpacerRNA, Ribosomal, 16Sdiabetic foot ulcerfungimicrobial communitiesmicrobiomenext‐generation sequencingwound healing

Identifiers

PMID42271189
PMCPMC13253613

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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.