Evidence map›Paper›PMID 35493727›Full record

ArticleFrontiers in cellular and infection microbiology2022

More Positive or More Negative? Metagenomic Analysis Reveals Roles of Virome in Human Disease-Related Gut Microbiome.

Mo Li, Chunhui Wang, Qian Guo, Congmin Xu, Zhongjie Xie, Jie Tan, Shufang Wu, Peihong Wang, Jinyuan Guo, Zhencheng Fang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% of its field
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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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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

14 authors at 3 institutions in 1 country.

Mo LiPeking University-Tsinghua University-National Institute of Biological Sciences (PTN) Joint Ph.D. Program, School of Life Sciences, Peking University, Beijing, China.
Chunhui WangPeking University-Tsinghua University-National Institute of Biological Sciences (PTN) Joint Ph.D. Program, School of Life Sciences, Peking University, Beijing, China.
Qian GuoDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Congmin XuDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Zhongjie XieDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Jie TanDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Shufang WuDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Peihong WangDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Jinyuan GuoDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Zhencheng FangDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Shiwei ZhuDepartment of Gastroenterology, Peking University Third Hospital, Beijing, China.
Liping DuanDepartment of Gastroenterology, Peking University Third Hospital, Beijing, China.
Xiaoqing JiangDepartment of Biomedical Engineering, College of Future Technology, Peking University, Beijing, China.
Huaiqiu ZhuPeking University-Tsinghua University-National Institute of Biological Sciences (PTN) Joint Ph.D. Program, School of Life Sciences, Peking University, Beijing, China.
Peking University · CNPeking University Third Hospital · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses are increasingly viewed as vital components of the human gut microbiota, while their roles in health and diseases remain incompletely understood. Here, we first sequenced and analyzed the 37 metagenomic and 18 host metabolomic samples related to irritable bowel syndrome (IBS) and found that some shifted viruses between IBS and controls covaried with shifted bacteria and metabolites. Especially, phages that infect beneficial lactic acid bacteria depleted in IBS covaried with their hosts. We also retrieved public whole-genome metagenomic datasets of another four diseases (type 2 diabetes, Crohn's disease, colorectal cancer, and liver cirrhosis), totaling 438 samples including IBS, and performed uniform analysis of the gut viruses in diseases. By constructing disease-specific co-occurrence networks, we found viruses actively interacting with bacteria, negatively correlated with possible dysbiosis-related and inflammation-mediating bacteria, increasing the connectivity between bacteria modules, and contributing to the robustness of the networks. Functional enrichment analysis showed that phages interact with bacteria through predation or expressing genes involved in the transporter and secretion system, metabolic enzymes,

Indexed as

BacteriophagesDiabetes Mellitus, Type 2Gastrointestinal MicrobiomeIrritable Bowel SyndromeMicrobiotaVirusesBacteriaHumansViromegut microbiomehealth and diseasemicrobial communityviral databasevirus

Identifiers

PMID35493727
PMCPMC9040671
OpenAlexW4223444461

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.