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ACE2 expression in saliva of patients with COVID-19 and its association with Candida albicans and Aggregatibacter actinomycetemcomitans
Background: A relationship between oral microbiota and susceptibility to SARS-CoV-2 infection has been extensively studied. However, the relationship between oral commensal flora and expression of angiotensin-converting enzyme 2 ( ACE2) remains to be established. In this observational study, we coll...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000 Research Limited
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445561/ https://www.ncbi.nlm.nih.gov/pubmed/36112976 http://dx.doi.org/10.12688/f1000research.111965.2 |
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author | Bachtiar, Endang W Bachtiar, Boy M Kusumaningrum, Ardiana Sunarto, Hari Soeroso, Yuniarti Sulijaya, Benso Apriyanti, Efa Theodorea, Citra Fragrantia Pratomo, Irandi Putra ., Yudhistira Efendi, Defi Razak, Fathilah Abdul |
author_facet | Bachtiar, Endang W Bachtiar, Boy M Kusumaningrum, Ardiana Sunarto, Hari Soeroso, Yuniarti Sulijaya, Benso Apriyanti, Efa Theodorea, Citra Fragrantia Pratomo, Irandi Putra ., Yudhistira Efendi, Defi Razak, Fathilah Abdul |
author_sort | Bachtiar, Endang W |
collection | PubMed |
description | Background: A relationship between oral microbiota and susceptibility to SARS-CoV-2 infection has been extensively studied. However, the relationship between oral commensal flora and expression of angiotensin-converting enzyme 2 ( ACE2) remains to be established. In this observational study, we collected saliva from patients with COVID-19 and evaluated the relationship between ACE2 expression and Candida albicans as well as with selected gram-negative bacteria ( Aggregatibacter actin o mycetemcomitans, Fusobacterium nucleatum, and Veillonella parvula). We investigated how this may be directly or indirectly involved in oral dysbiosis in patients with COVID-19. Methods: We included 23 hospitalized patients admitted to Universitas Indonesia Hospital with PCR-confirmed COVID-19, with six healthy participants serving as controls. Saliva and tongue surface swabs were collected from patients with diabetes (DG) and without diabetes (NDG) and subject controls. Using quantitative PCR (qPCR) we assessed the mRNA expression of ACE2, the abundance of C. albicans, and the transcription levels of its biofilm-associated genes, agglutinin-like protein 3 ( ALS3), hyphal wall protein 1 ( HWP1), and yeast-form wall protein 1 ( YWP1). We also counted the relative proportion of the three selected gram-negative oral bacteria in saliva. All analyses were performed to determine the relationship between ACE2 expression and C. albicans and gram-negative bacteria. Results: ACE2 mRNA expression was significantly higher in tongue swab samples than in saliva. However, no significant difference was observed between the patient groups. Conversely, DG patients had a significantly higher abundance of C. albicans in saliva compared to NDG patients and control group patients. The correlation and sensitivity/specificity relationship between ACE2 expression and C. albicans or the selected oral bacteria were also observed. Conclusions: The data show that ACE2 expression can be detected in saliva of patients with COVID-19 and its association with C. albicans and gram-negative oral bacteria might contribute toward developing an oral dysbiosis based predictor for prognosis of COVID-19 severity. |
format | Online Article Text |
id | pubmed-9445561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-94455612022-09-14 ACE2 expression in saliva of patients with COVID-19 and its association with Candida albicans and Aggregatibacter actinomycetemcomitans Bachtiar, Endang W Bachtiar, Boy M Kusumaningrum, Ardiana Sunarto, Hari Soeroso, Yuniarti Sulijaya, Benso Apriyanti, Efa Theodorea, Citra Fragrantia Pratomo, Irandi Putra ., Yudhistira Efendi, Defi Razak, Fathilah Abdul F1000Res Research Article Background: A relationship between oral microbiota and susceptibility to SARS-CoV-2 infection has been extensively studied. However, the relationship between oral commensal flora and expression of angiotensin-converting enzyme 2 ( ACE2) remains to be established. In this observational study, we collected saliva from patients with COVID-19 and evaluated the relationship between ACE2 expression and Candida albicans as well as with selected gram-negative bacteria ( Aggregatibacter actin o mycetemcomitans, Fusobacterium nucleatum, and Veillonella parvula). We investigated how this may be directly or indirectly involved in oral dysbiosis in patients with COVID-19. Methods: We included 23 hospitalized patients admitted to Universitas Indonesia Hospital with PCR-confirmed COVID-19, with six healthy participants serving as controls. Saliva and tongue surface swabs were collected from patients with diabetes (DG) and without diabetes (NDG) and subject controls. Using quantitative PCR (qPCR) we assessed the mRNA expression of ACE2, the abundance of C. albicans, and the transcription levels of its biofilm-associated genes, agglutinin-like protein 3 ( ALS3), hyphal wall protein 1 ( HWP1), and yeast-form wall protein 1 ( YWP1). We also counted the relative proportion of the three selected gram-negative oral bacteria in saliva. All analyses were performed to determine the relationship between ACE2 expression and C. albicans and gram-negative bacteria. Results: ACE2 mRNA expression was significantly higher in tongue swab samples than in saliva. However, no significant difference was observed between the patient groups. Conversely, DG patients had a significantly higher abundance of C. albicans in saliva compared to NDG patients and control group patients. The correlation and sensitivity/specificity relationship between ACE2 expression and C. albicans or the selected oral bacteria were also observed. Conclusions: The data show that ACE2 expression can be detected in saliva of patients with COVID-19 and its association with C. albicans and gram-negative oral bacteria might contribute toward developing an oral dysbiosis based predictor for prognosis of COVID-19 severity. F1000 Research Limited 2022-09-12 /pmc/articles/PMC9445561/ /pubmed/36112976 http://dx.doi.org/10.12688/f1000research.111965.2 Text en Copyright: © 2022 Bachtiar EW et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bachtiar, Endang W Bachtiar, Boy M Kusumaningrum, Ardiana Sunarto, Hari Soeroso, Yuniarti Sulijaya, Benso Apriyanti, Efa Theodorea, Citra Fragrantia Pratomo, Irandi Putra ., Yudhistira Efendi, Defi Razak, Fathilah Abdul ACE2 expression in saliva of patients with COVID-19 and its association with Candida albicans and Aggregatibacter actinomycetemcomitans |
title |
ACE2 expression in saliva of patients with COVID-19 and its association with
Candida albicans and
Aggregatibacter actinomycetemcomitans
|
title_full |
ACE2 expression in saliva of patients with COVID-19 and its association with
Candida albicans and
Aggregatibacter actinomycetemcomitans
|
title_fullStr |
ACE2 expression in saliva of patients with COVID-19 and its association with
Candida albicans and
Aggregatibacter actinomycetemcomitans
|
title_full_unstemmed |
ACE2 expression in saliva of patients with COVID-19 and its association with
Candida albicans and
Aggregatibacter actinomycetemcomitans
|
title_short |
ACE2 expression in saliva of patients with COVID-19 and its association with
Candida albicans and
Aggregatibacter actinomycetemcomitans
|
title_sort | ace2 expression in saliva of patients with covid-19 and its association with
candida albicans and
aggregatibacter actinomycetemcomitans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9445561/ https://www.ncbi.nlm.nih.gov/pubmed/36112976 http://dx.doi.org/10.12688/f1000research.111965.2 |
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