Evidence map›Paper›PMID 38779561›Full record

ArticleFrontiers in cellular and infection microbiology2024

Crosstalk between human immunodeficiency virus infection and salivary bacterial function in men who have sex with men.

Ying Guo, Wenjing Wang, Yixi Yu, Xintong Sun, Baojin Zhang, Yan Wang, Jie Cao, Shuo Wen, Xin Wang, Yuchen Li and 11 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2024. 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

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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

21 authors.

Ying Guo *Department of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Wenjing Wang *Clinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Yixi YuDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Xintong SunDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Baojin ZhangDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Yan WangDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Jie CaoDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Shuo WenDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Xin WangDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Yuchen LiDepartment of Stomatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Siyu CaiCenter for Clinical Epidemiology and Evidence-Based Medicine, Beijing Children's Hospital, Capital Medical University, Beijing, China.
Ruojun WuHarvard School of Dental Medicine, Boston, MA, United States.
Wenshan DuanClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Wei XiaClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Feili WeiBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Junyi DuanClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Haozhi DongDepartment of Stomatology, Beijing Daxing District Hospital of Integrated Chinese and Western Medicine, Beijing, China.
Shan GuoBeijing Institute of Hepatology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
Fengqiu ZhangDepartment of Periodontology, Beijing Stomatological Hospital, Capital Medical University, Beijing, China.
Zheng SunDepartment of Oral Medicine, Beijing Stomatological Hospital, Capital Medical University, Beijing, China.
Xiaojie HuangClinical and Research Center for Infectious Diseases, Beijing Youan Hospital, Capital Medical University, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Engaging in anal sexual intercourse markedly increases the risk of developing HIV among men who have sex with men (MSM); oral sexual activities tend to uniquely introduce gut-derived microbes to salivary microbiota, which, combined with an individual's positive HIV status, may greatly perturb oral microecology. However, till date, only a few published studies have addressed this aspect. Methods: Based on 16S rRNA sequencing data of bacterial taxa, MicroPITA picks representative samples for metagenomic analysis, effectively revealing how the development and progression of the HIV disease influences oral microbiota in MSM. Therefore, we collected samples from 11 HIV-negative and 44 HIV-positive MSM subjects (stage 0 was defined by HIV RNA positivity, but negative or indeterminate antibody status; stages 1, 2, and 3 were defined by CD4 Results: The core functions of oral microbiota were maintained across each of the five groups, including metabolism, genetic and environmental information processing. All HIV-positive groups displayed KEGG functions of abnormal proliferation, most prominently at stage 0, and others related to metabolism. Clustering relationship analysis tentatively identified functional relationships between groups, with bacterial function being more similar between stage 0-control groups and stage 1-2 groups, whereas the stage 3 group exhibited large functional changes. Although we identified most metabolic pathways as being common to all five groups, several unique pathways formed clusters for certain groups; the stage 0 group had several, while the stage 2 and 3 groups had few, such clusters. The abundance of K03046 was positively correlated with CD4 counts. Conclusion: As HIV progresses, salivary bacterial function and metabolic pathways in MSM progressively changes, which may be related to HIV promoting abnormal energy metabolism and exacerbate pathogen virulence. Further, infection and drug resistance of acute stage and immune cell destruction of AIDS stage were abnormally increased, predicting an increased risk for MSM individuals to develop systemic and oral diseases.

Indexed as

HIV InfectionsHomosexuality, MaleRNA, Ribosomal, 16SSalivaAdultBacteriaCD4 Lymphocyte CountHumansMaleMetagenomicsMicrobiotaMiddle AgedSexual and Gender MinoritiesYoung AdultRNA, Ribosomal, 16SbacteriaHIVmen who have sex with menmetagenomic analysissaliva

Identifiers

PMID38779561
PMCPMC11109444

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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.