Evidence map›Paper›PMID 34252627›Full record

ArticleGenomics, proteomics & bioinformatics2022

Metagenomic Analysis Reveals A Possible Association Between Respiratory Infection and Periodontitis.

Zhenwei Liu, Tao Zhang, Keke Wu, Zhongshan Li, Xiaomin Chen, Shan Jiang, Lifeng Du, Saisai Lu, Chongxiang Lin, Jinyu Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Current Status of Next-Generation Sequencing in Bone Genetic Diseases.International journal of molecular sciences · 2023
    Review
  4. 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

11 authors at 1 institution in 1 country.

Zhenwei LiuInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Tao ZhangInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Keke WuWenzhou Center for Disease Control and Prevention, Wenzhou 325000, China.
Zhongshan LiInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Xiaomin ChenInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Shan JiangInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Lifeng DuInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China.
Saisai LuRheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 352000, China.
Chongxiang LinDepartment of Stomatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Jinyu WuInstitute of Genomic Medicine, Wenzhou Medical University, Wenzhou 325000, China. Electronic address: iamwujy@wmu.edu.cn.
Xiaobing WangRheumatology Department, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 352000, China. Electronic address: wangxiaobing@wzhospital.cn.
Wenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis is an inflammatory disease that is characterized by progressive destruction of the periodontium and causes tooth loss in adults. Periodontitis is known to be associated with dysbiosis of the oral microflora, which is often linked to various diseases. However, the complexity of plaque microbial communities of periodontitis, antibiotic resistance, and enhanced virulence make this disease difficult to treat. In this study, using metagenomic shotgun sequencing, we investigated the etiology, antibiotic resistance genes (ARGs), and virulence genes (VirGs) of periodontitis. We revealed a significant shift in the composition of oral microbiota as well as several functional pathways that were represented significantly more abundantly in periodontitis patients than in controls. In addition, we observed several positively selected ARGs and VirGs with the Ka/Ks ratio > 1 by analyzing our data and a previous periodontitis dataset, indicating that ARGs and VirGs in oral microbiota may be subjected to positive selection. Moreover, 5 of 12 positively selected ARGs and VirGs in periodontitis patients were found in the genomes of respiratory tract pathogens. Of note, 91.8% of the background VirGs with at least one non-synonymous single-nucleotide polymorphism for natural selection were also from respiratory tract pathogens. These observations suggest a potential association between periodontitis and respiratory infection at the gene level. Our study enriches the knowledge of pathogens and functional pathways as well as the positive selection of antibiotic resistance and pathogen virulence in periodontitis patients, and provides evidence at the gene level for an association between periodontitis and respiratory infection.

Indexed as

MicrobiotaPeriodontitisAdultAnti-Bacterial AgentsDysbiosisHumansMetagenomeMetagenomicsAnti-Bacterial AgentsAntibiotic resistance geneMetagenomic sequencingPeriodontitisRespiratory infectionVirulence gene

Identifiers

PMID34252627
PMCPMC9684085
OpenAlexW3178956121

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.