Cited by 207Dental Research and COVID-19Oral microbiology and periodontitis researchCOVID-19 Clinical Research Studies

The DOI matches its Crossref record; 158 of the 158 references it cites were found in a registry or an index; none of the 173 sources its claims cite is checked for support yet.

Oral Microbiome and SARS-CoV-2: Beware of Lung Co-infection

Open access
Bao, Lirong, Zhang, Cheng, Dong, Jiajia, Zhao, Lei, Li, Yan, Sun, Jianxun·2020·Frontiers in Microbiology

Abstract

The new coronavirus SARS-CoV-2, the cause of COVID-19, has become a public health emergency of global concern. Like the SARS and influenza pandemics, there have been a large number of cases coinfected with other viruses, fungi, and bacteria, some of which originate from the oral cavity. Capnocytophaga, Veillonella, and other oral opportunistic pathogens were found in the BALF of the COVID-19 patients by mNGS. Risk factors such as poor oral hygiene, cough, increased inhalation under normal or abnormal conditions, and mechanical ventilation provide a pathway for oral microorganisms to enter the lower respiratory tract and thus cause respiratory disease. Lung hypoxia, typical symptoms of COVID-19, would favor the growth of anaerobes and facultative anaerobes originating from the oral microbiota. SARS-CoV-2 may aggravate lung disease by interacting with the lung or oral microbiota via mechanisms involving changes in cytokines, T cell responses, and the effects of host conditions such as aging and the oral microbiome changes due to systemic diseases. Because the oral microbiome is closely associated with SARS-CoV-2 co-infections in the lungs, effective oral health care measures are necessary to reduce these infections, especially in severe COVID-19 patients. We hope this review will draw attention from both the scientific and clinical communities on the role of the oral microbiome in the current global pandemic.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

This review argues that the oral microbiome can serve as a reservoir for lung co-infections in COVID-19, with aspiration, mechanical ventilation, poor oral hygiene, and lung hypoxia as key pathways. It recommends oral hygiene measures for COVID-19 patients and outlines research approaches including better diagnostics, lung organoids, and co-infection animal models.

Key findings

  • Oral opportunistic pathogens such as *Capnocytophaga*, *Veillonella*, *Leptotrichia buccalis*, *Veillonella parvula*, *Capnocytophaga gingivalis*, and *Prevotella melaninogenica* were found in COVID-19 patient BALF by mNGS; in an Eastern China multicenter study, 11 of 20 co-infections were identified in laboratory-confirmed COVID-19 cases, with common pathogens including *Acinetobacter baumannii*, *Klebsiella pneumoniae*, *Aspergillus flavus*, *Candida glabrata*, and *Candida albicans*, and 5 cases coinfected with a virus.
  • Risk factors including poor oral hygiene, cough, increased inhalation, and mechanical ventilation provide a route for oral microorganisms to enter the lower respiratory tract; lung hypoxia favors growth of anaerobes and facultative anaerobes from the oral microbiota, and ventilator-associated pneumonia incidence is reported as 5% to 67%.
  • SARS-CoV-2 receptor ACE2 is expressed in 0.52% of oral cells, with 95.86% expressed in tongue epithelial cells; SARS-CoV-2 was detected in initial saliva of 91.7% (11/12) of patients, and viral load in throat swabs and sputum peaked at 5–6 days after onset at 10^4 to 10^7 copies/ml.
  • Oral care agents including povidone iodine (0.23–1%), cetylpyridinium chloride (0.05–0.10%), and hydrogen peroxide (0.5–1.5%) reduce oral microbiota; 0.02% chlorhexidine is ineffective against coronaviruses while 0.05% is SARS-CoV-2 sensitive, and improved oral hygiene care can reduce aspiration pneumonia risk and mortality risk by as much as 60%.

Methods

  • Narrative review; no primary experiments or systematic search strategy are reported. The authors synthesize published literature on SARS-CoV-2/COVID-19, SARS, influenza, oral microbiome, co-infections, host immunity, oral care, diagnostics, lung organoids, and animal models.
  • Evidence cited includes clinical studies, mNGS/metagenomic sequencing, BALF and saliva sample studies, prior reviews, and preclinical models; the paper includes a table of mouth rinse components and a schematic figure of the oral-lung axis.
  • Formal inclusion criteria, search terms, and risk-of-bias assessment are not stated in the paper.

Limitations

  • The authors state that little work has been done on coronaviruses and oral microbiomes, that the mechanism of interaction between oral bacteria and respiratory viruses to promote lung infection has not been studied in depth, and that more mechanism studies are needed.
  • The authors note limited data available to date, that one cited saliva study had a small sample size, and that the frequency of asymptomatic or RT-PCR-negative patients with CT pneumonia-like lesions is unknown.
  • Evident from the text: this is a narrative review relying partly on preprints and indirect evidence from influenza and SARS; it does not directly test whether oral care improves COVID-19 outcomes or establish causality between oral microbiota and SARS-CoV-2 lung co-infection.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.3389/fmicb.2020.01840

Cites

158 of 158 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Figures

FIGURE 1 Schematic representation outlining the oral-lung-axis mechanism of viral-bacterial lung co-infection during respiratory viral infections and effect of the oral care interventions for patients. Risk factors such as poor oral hygiene, cough, increased inhalation and mechanical ventilation provide a pathway for oral microorganisms to enter the lower respiratory tract and thus cause co-infection to aggravate respiratory disease via mechanisms involving changes in cytokines, T cell responses, and the effects of host conditions such as aging and the oral microbiome changes due to systemic diseases. Improving oral hygiene care by either mechanical or chemical control of dental plaque biofilm formation would reduce the number of potential respiratory pathogens and inhibit droplet-borne virus route through oral cavity, and hence consequently reduce the risk and mortality risk of aspiration pneumonia.
FIGURE 1 Schematic representation outlining the oral-lung-axis mechanism of viral-bacterial lung co-infection during respiratory viral infections and effect of the oral care interventions for patients. Risk factors such as poor oral hygiene, cough, increased inhalation and mechanical ventilation provide a pathway for oral microorganisms to enter the lower respiratory tract and thus cause co-infection to aggravate respiratory disease via mechanisms involving changes in cytokines, T cell responses, and the effects of host conditions such as aging and the oral microbiome changes due to systemic diseases. Improving oral hygiene care by either mechanical or chemical control of dental plaque biofilm formation would reduce the number of potential respiratory pathogens and inhibit droplet-borne virus route through oral cavity, and hence consequently reduce the risk and mortality risk of aspiration pneumonia.CC BY · PubMed Central

Verification

Claims the paper makes

133 Not checked yet · 23 Own interpretation · 6 No basis given · 2 Sources not found

Verify all 170 references — free account

Show all 88 claims

  • Probably not a substantial claim. 35
  • It may state two separate claims as one. 51
76 of 76
  • The paper relies on this without support.

    Lung hypoxia favors the growth of anaerobes and facultative anaerobes originating from the oral microbiota.

    “Additionally, lung hypoxia would stimulate the growth of anaerobes and facultative anaerobes derived from oral microbiota.”
  • The paper relies on this without support.

    Compared with healthy individuals, those with chronic diseases have a certain degree of microecological disorder.

    “Compared with healthy individuals, those with chronic diseases have a certain degree of microecological disorder.”
  • The paper relies on this without support.

    Oral microbiota is prone to entering the lower respiratory tract due to increased aspiration and the presence of mechanical ventilation.

    “Given the fact that oral microbiota is prone to entering the lower respiratory tract due to increased aspiration and the presence of mechanical ventilation, the prevalence of fatal VAP may increase.”
  • The paper relies on this without support.

    Current guidelines for the management of COVID-19 scarcely emphasize oral care.

    “However, current guidelines for the management of COVID-19 scarcely emphasize oral care.”
  • The paper relies on this without support.

    SARS-CoV-2 is vulnerable to oxidation.

    “Since SARS-CoV-2 is vulnerable to oxidation, antiseptic mouthwash or gel containing broad spectrum oxidative agents, such as hydrogen peroxide or PV-I, is recommended to reduce the oral microbiota and potentially SARS-CoV-2 as well.”
  • The paper relies on this without support.

    Little work has been done on the coronaviruses and oral microbiomes.

    “Until now, little work had been done on the coronaviruses and oral microbiomes, and much remains for future study.”
6 of 6

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Citations

Cites

Research works printed but not linked: 3

  1. 2020, Guideline for the Diagnosis and Treatment of Novel Coronavirus Pneumonia
  2. 2020, Coronavirus Disease (COVID-2019) Situation Report – 151.
  3. Zheng, 2003, The clinical characteristics of secondary infections of lower respiratory tract in severe acute respiratory syndrome., Chin. J. Respir. Crit. Care Med., 2, 270

Cited by

Sorted by citations

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Metadata

Authors
Bao, L., Zhang, C., Dong, J., Zhao, L., Li, Y., & Sun, J.
Affiliations
Sichuan University (CN)
Corresponding author
  • Li, Yan
  • Sun, Jianxun
Venue
Frontiers in Microbiology
Published
2020-07-31
Volume
11
Pages
1840-1840
ISSN
1664-302X (ISSN-L)
OpenAlex
W3046848575
Cited by
207
References
158
Citations by year
2026: 7 · 2025: 11 · 2024: 26 · 2023: 47 · 2022: 57 · 2021: 53 · 2020: 6
FWCI
1.95
Type
journal article
Language
en
Open access
Locations
  • Frontiers in Microbiology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
National Natural Science Foundation of China (81771085, 81700036, 81991502, 81970944)
Topics
  • Health Sciences › Dentistry › General Dentistry › Dental Research and COVID-19
  • Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
  • Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
Keywords
SARS-CoV-2, COVID-19 pandemic, oral microbiota, Capnocytophaga, Veillonella, lower respiratory tract infection, mechanical ventilation, poor oral hygiene, anaerobic bacteria, cytokines, T cell response, aging, oral care

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