4.8 Article

Alterations in the human oral and gut microbiomes and lipidomics in COVID-19

期刊

GUT
卷 70, 期 7, 页码 1253-1265

出版社

BMJ PUBLISHING GROUP
DOI: 10.1136/gutjnl-2020-323826

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资金

  1. National S&T Major Project of China [2018ZX10301201]
  2. China Postdoctoral Science Foundation [2020T130609, 2020T130109ZX]
  3. National Key Research and Development Program of China [2018YFC2000500]
  4. National Natural Science Foundation of China [U2004121, 82070643, U1904164]
  5. Henan Province Science and Technology Project [202102310055]
  6. COVID-19 Prevention and Control Program of International Peace Maternity and Child Health Hospital, School of Medicine, Shanghai Jiao Tong University [2020-COVID-19-01]
  7. State Key Laboratory for Diagnosis and Treatment of Infectious Diseases and Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases
  8. First Affiliated Hospital, College of Medicine, Zhejiang University [SKLID2019KF03]

向作者/读者索取更多资源

This study characterized the oral microbiome in patients with COVID-19, showing decreased microbial diversity and changes in specific bacteria. The study also identified potential biomarkers for diagnosing COVID-19 with high accuracy across different regions and successfully distinguished recovered patients from active patients based on lipid profiles.
Objective To characterise the oral microbiome, gut microbiome and serum lipid profiles in patients with active COVID-19 and recovered patients; evaluate the potential of the microbiome as a non-invasive biomarker for COVID-19; and explore correlations between the microbiome and lipid profile. Design We collected and sequenced 392 tongue-coating samples, 172 faecal samples and 155 serum samples from Central China and East China. We characterised microbiome and lipid molecules, constructed microbial classifiers in discovery cohort and verified their diagnostic potential in 74 confirmed patients (CPs) from East China and 37 suspected patients (SPs) with IgG positivity. Results Oral and faecal microbial diversity was significantly decreased in CPs versus healthy controls (HCs). Compared with HCs, butyric acid-producing bacteria were decreased and lipopolysaccharide-producing bacteria were increased in CPs in oral cavity. The classifiers based on 8 optimal oral microbial markers (7 faecal microbial markers) achieved good diagnostic efficiency in different cohorts. Importantly, diagnostic efficacy reached 87.24% in the cross-regional cohort. Moreover, the classifiers successfully diagnosed SPs with IgG antibody positivity as CPs, and diagnostic efficacy reached 92.11% (98.01% of faecal microbiome). Compared with CPs, 47 lipid molecules, including sphingomyelin (SM)(d40:4), SM(d38:5) and monoglyceride(33:5), were depleted, and 122 lipid molecules, including phosphatidylcholine(36:4p), phosphatidylethanolamine (PE)(16:0p/20:5) and diglyceride(20:1/18:2), were enriched in confirmed patients recovery. Conclusion This study is the first to characterise the oral microbiome in COVID-19, and oral microbiomes and lipid alterations in recovered patients, to explore their correlations and to report the successful establishment and validation of a diagnostic model for COVID-19.

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