Evidence map›Paper›PMID 42078528›Full record

ArticleFrontiers in microbiology2026

Identification of novel CRESS-DNA viruses in the human vaginal microbiome.

Ziyuan Dai, Qiang Lu, Mingzhong Sun, Hongmei Chen, Yuchen Jiang, Taotao Yu, Zhipeng Wang, Yungang Wang, Rong Zhu, Yuqing Han

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

10 authors.

Ziyuan DaiDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Qiang LuDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Mingzhong SunDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Hongmei ChenDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Yuchen JiangDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Taotao YuDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Zhipeng WangDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Yungang WangDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Rong ZhuDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.
Yuqing HanDepartment of Clinical Laboratory, Yancheng Third People's Hospital, The Affiliated Hospital of Jiangsu Medical College, Affiliated Hospital 6 of Nantong University, Yancheng, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Circular replication-associated protein (Rep)-encoding single-stranded DNA (CRESS-DNA) viruses are widely distributed across diverse hosts and environments, yet their diversity within the human vaginal virome remains poorly characterized. This study aimed to investigate the presence, diversity, and evolutionary relationships of CRESS-DNA viruses in the human vaginal niche. Methods: Viral metagenomic sequencing was performed on 24 pooled vaginal swab libraries derived from women with and without vaginitis. After host sequence removal and quality control, de novo assembly and viral identification were conducted. Candidate viral genomes were curated based on genomic features, followed by functional annotation, phylogenetic analysis using Rep protein sequences, and genome-wide pairwise nucleotide identity comparisons. Results: A total of five CRESS-DNA viral genomes were identified, including four complete and one nearly complete circular genomes. All genomes exhibited canonical architectures, encoding Rep and Cap proteins and containing conserved HUH endonuclease and superfamily 3 helicase motifs. Phylogenetic analysis placed these viruses within the orders Rohanvirales, Ringavirales, Cirlivirales, and Cremevirales, representing multiple distinct evolutionary lineages. Genome-wide pairwise identity analysis showed that all identified viruses fell below established species- and genus-level thresholds, indicating that they represent novel taxa. Comparative analyses further revealed substantial divergence from known environmental and vertebrate-associated viruses. Discussion: These findings expand the known diversity of CRESS-DNA viruses in the human vaginal virome and highlight their broad evolutionary diversity. The detected viruses likely represent diverse ecological origins rather than stable host-specific infections, and no clear association with vaginitis was observed. This study provides new insights into the evolutionary landscape of CRESS-DNA viruses in the human reproductive tract and underscores the need for further investigation into their biological roles and potential health implications.

Indexed as

Cressdnaviricotahumanmetagenomicsphylogenetic analysisvaginal virome

Identifiers

PMID42078528
PMCPMC13133057

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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.