Evidence map›Paper›PMID 41039191›Full record

ArticleBMC microbiology2025

Salivary mycobiome diversity at different stages of human immunodeficiency virus infection.

Lu Lin, Wenshan Duan, Yixi Yu, Yan Wang, Jie Cao, Yuchen Li, Xintong Sun, Shuo Wen, Xin Wang, Zhen Fang and 2 more

Abstract read
In one paragraph

Article in BMC microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Lu LinDepartment of Prosthodontics, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing, 100070, China.
Wenshan DuanClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Yixi YuDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Yan WangDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Jie CaoDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Yuchen LiDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Xintong SunDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Shuo WenDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Xin WangDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Zhen FangClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China.
Ying GuoDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, 100069, China. crystalsean@126.com.
Qingsong JiangDepartment of Prosthodontics, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing, 100070, China. qsjiang@ccmu.edu.cn.

Funding

the Beijing Institute of Hepatology Reform and Development Project-Beijing Municipal Health Commission 2025Y-KF-Q07the Beijing Municipal Administration of Hospitals Incubation Programme PX2022069
6 · The paper itself

Abstract

backgroundThe oral cavity is a common site for fungal infections in people living with HIV/AIDS (PLWHA), yet reports on oral mycobiome alterations remain limited. This study aimed to analyze differences in mycobiome diversity and community composition in the saliva of PLWHA at different infection stages.

methodsNon-stimulated whole saliva samples were collected from 63 HIV-infected/AIDS patients, who were divided into four groups based on the CDC staging criteria (stage 0, n = 10; stage 1, n = 13; stage 2, n = 24; stage 3, n = 16), as well as from 24 HIV-negative individuals. Internal Transcribed Spacer (ITS) sequencing was employed to analyze species diversity and community composition differences, and correlations at the genus level with CD4⁺ T cell counts and HIV blood viral load (BVL) were evaluated.

resultsAt the operational taxonomic unit (OTU) level, the alpha diversity of the mycobiome community in the HIV-positive groups exhibited a gradual decline as the disease progressed, with the lowest Shannon index in HIV stage 3 (p < 0.05 vs. other groups). At the phylum level, all groups were predominantly composed of Ascomycota, followed by Basidiomycota. At the genus level, Candida was the predominant genus in all groups, with its abundance increasing to varying degrees in HIV stages 1, 2, and 3 compared to the HIV-negative control group (HIV_neg), showing significant differences in stage 1 (p = 0.006 vs. HIV_neg), stage 2 (p < 0.05 vs. HIV_neg), and stage 3 (p < 0.001 vs. HIV_neg). The most pronounced increase was observed in stage 3, while non-dominant species were relatively reduced. Correlation analysis showed that Debaryomyces and Talaromyces were positively associated with CD4⁺ T cell counts. These genera may play a role in immune regulation during HIV progression and warrant further functional analysis. Whereas Penicillium showed a significant negative correlation with BVL, indicating its abundance may decrease with higher viral loads.

conclusionThe oral fungal microecology undergoes dynamic changes with HIV progression. In stage 3, there appears to be a noticeable increase in Candida, accompanied by a relative decrease in other normally present non-dominant fungal species, potentially resulting in opportunistic fungal infections.

Indexed as

FungiHIV InfectionsMycobiomeSalivaAdultBiodiversityCD4 Lymphocyte CountDNA, FungalDNA, Ribosomal SpacerFemaleHumansMaleMiddle AgedSequence Analysis, DNAViral LoadDNA, FungalDNA, Ribosomal SpacerCD4⁺ T cell countDiversityMycobiomePLWHASaliva

Identifiers

PMID41039191
PMCPMC12492769

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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.