Cargando…
Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection
The human organism is inhabited by trillions of microorganisms, known as microbiota, which are considered to exploit a pivotal role in the regulation of host health and immunity. Recent investigations have suggested a relationship between the composition of the human microbiota and COVID-19 infectio...
Autores principales: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581039/ https://www.ncbi.nlm.nih.gov/pubmed/37728335 http://dx.doi.org/10.1128/spectrum.02194-23 |
_version_ | 1785122065036083200 |
---|---|
author | Mancabelli, Leonardo Taurino, Giuseppe Ticinesi, Andrea Ciociola, Tecla Vacondio, Federica Milani, Christian Fontana, Federico Lugli, Gabriele Andrea Tarracchini, Chiara Alessandri, Giulia Viappiani, Alice Bianchi, Massimiliano Nouvenne, Antonio Chetta, Alfredo Antonio Turroni, Francesca Meschi, Tiziana Mor, Marco Bussolati, Ovidio Ventura, Marco |
author_facet | Mancabelli, Leonardo Taurino, Giuseppe Ticinesi, Andrea Ciociola, Tecla Vacondio, Federica Milani, Christian Fontana, Federico Lugli, Gabriele Andrea Tarracchini, Chiara Alessandri, Giulia Viappiani, Alice Bianchi, Massimiliano Nouvenne, Antonio Chetta, Alfredo Antonio Turroni, Francesca Meschi, Tiziana Mor, Marco Bussolati, Ovidio Ventura, Marco |
author_sort | Mancabelli, Leonardo |
collection | PubMed |
description | The human organism is inhabited by trillions of microorganisms, known as microbiota, which are considered to exploit a pivotal role in the regulation of host health and immunity. Recent investigations have suggested a relationship between the composition of the human microbiota and COVID-19 infection, highlighting a possible role of bacterial communities in the modulation of the disease severity. In this study, we performed a shotgun metagenomics analysis to explore and compare the nasopharyngeal microbiota of 38 hospitalized Italian patients with and without COVID-19 infection during the third and fourth pandemic waves. In detail, the metagenomic analysis combined with specific correlation analyses suggested a positive association of several microbial species, such as S. parasanguinis and P. melaninogenica, with the severity of COVID-19 infection. Furthermore, the comparison of the microbiota composition between the nasopharyngeal and their respective fecal samples highlighted an association between these different compartments represented by a sharing of several bacterial species. Additionally, lipidomic and deep-shotgun functional analyses of the fecal samples suggested a metabolic impact of the microbiome on the host’s immune response, indicating the presence of key metabolic compounds in COVID-19 patients, such as lipid oxidation end products, potentially related to the inflammatory state. Conversely, the patients without COVID-19 displayed enzymatic patterns associated with the biosynthesis and degradation of specific compounds like lysine (synthesis) and phenylalanine (degradation) that could positively impact disease severity and contribute to modulating COVID-19 infection. IMPORTANCE: The human microbiota is reported to play a major role in the regulation of host health and immunity, suggesting a possible impact on the severity of COVID-19 disease. This preliminary study investigated the possible correlation between nasopharyngeal microbiota and COVID-19 infection. In detail, the analysis of the nasopharyngeal microbiota of hospitalized Italian patients with and without COVID-19 infection suggested a positive association of several microbial species with the severity of the disease and highlighted a sharing of several bacteria species with the respective fecal samples. Moreover, the metabolic analyses suggested a possible impact of the microbiome on the host's immune response and the disease severity. |
format | Online Article Text |
id | pubmed-10581039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-105810392023-10-18 Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection Mancabelli, Leonardo Taurino, Giuseppe Ticinesi, Andrea Ciociola, Tecla Vacondio, Federica Milani, Christian Fontana, Federico Lugli, Gabriele Andrea Tarracchini, Chiara Alessandri, Giulia Viappiani, Alice Bianchi, Massimiliano Nouvenne, Antonio Chetta, Alfredo Antonio Turroni, Francesca Meschi, Tiziana Mor, Marco Bussolati, Ovidio Ventura, Marco Microbiol Spectr Research Article The human organism is inhabited by trillions of microorganisms, known as microbiota, which are considered to exploit a pivotal role in the regulation of host health and immunity. Recent investigations have suggested a relationship between the composition of the human microbiota and COVID-19 infection, highlighting a possible role of bacterial communities in the modulation of the disease severity. In this study, we performed a shotgun metagenomics analysis to explore and compare the nasopharyngeal microbiota of 38 hospitalized Italian patients with and without COVID-19 infection during the third and fourth pandemic waves. In detail, the metagenomic analysis combined with specific correlation analyses suggested a positive association of several microbial species, such as S. parasanguinis and P. melaninogenica, with the severity of COVID-19 infection. Furthermore, the comparison of the microbiota composition between the nasopharyngeal and their respective fecal samples highlighted an association between these different compartments represented by a sharing of several bacterial species. Additionally, lipidomic and deep-shotgun functional analyses of the fecal samples suggested a metabolic impact of the microbiome on the host’s immune response, indicating the presence of key metabolic compounds in COVID-19 patients, such as lipid oxidation end products, potentially related to the inflammatory state. Conversely, the patients without COVID-19 displayed enzymatic patterns associated with the biosynthesis and degradation of specific compounds like lysine (synthesis) and phenylalanine (degradation) that could positively impact disease severity and contribute to modulating COVID-19 infection. IMPORTANCE: The human microbiota is reported to play a major role in the regulation of host health and immunity, suggesting a possible impact on the severity of COVID-19 disease. This preliminary study investigated the possible correlation between nasopharyngeal microbiota and COVID-19 infection. In detail, the analysis of the nasopharyngeal microbiota of hospitalized Italian patients with and without COVID-19 infection suggested a positive association of several microbial species with the severity of the disease and highlighted a sharing of several bacteria species with the respective fecal samples. Moreover, the metabolic analyses suggested a possible impact of the microbiome on the host's immune response and the disease severity. American Society for Microbiology 2023-09-20 /pmc/articles/PMC10581039/ /pubmed/37728335 http://dx.doi.org/10.1128/spectrum.02194-23 Text en Copyright © 2023 Mancabelli et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Mancabelli, Leonardo Taurino, Giuseppe Ticinesi, Andrea Ciociola, Tecla Vacondio, Federica Milani, Christian Fontana, Federico Lugli, Gabriele Andrea Tarracchini, Chiara Alessandri, Giulia Viappiani, Alice Bianchi, Massimiliano Nouvenne, Antonio Chetta, Alfredo Antonio Turroni, Francesca Meschi, Tiziana Mor, Marco Bussolati, Ovidio Ventura, Marco Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title | Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title_full | Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title_fullStr | Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title_full_unstemmed | Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title_short | Disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of COVID-19 infection |
title_sort | disentangling the interactions between nasopharyngeal and gut microbiome and their involvement in the modulation of covid-19 infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581039/ https://www.ncbi.nlm.nih.gov/pubmed/37728335 http://dx.doi.org/10.1128/spectrum.02194-23 |
work_keys_str_mv | AT mancabellileonardo disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT taurinogiuseppe disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT ticinesiandrea disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT ciociolatecla disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT vacondiofederica disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT milanichristian disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT fontanafederico disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT lugligabrieleandrea disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT tarracchinichiara disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT alessandrigiulia disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT viappianialice disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT bianchimassimiliano disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT nouvenneantonio disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT chettaalfredoantonio disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT turronifrancesca disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT meschitiziana disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT mormarco disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT bussolatiovidio disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection AT venturamarco disentanglingtheinteractionsbetweennasopharyngealandgutmicrobiomeandtheirinvolvementinthemodulationofcovid19infection |