2021
DOI: 10.3389/fcimb.2021.625581
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Nasopharyngeal Microbiome Signature in COVID-19 Positive Patients: Can We Definitively Get a Role to Fusobacterium periodonticum?

Abstract: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) caused the pandemic Coronavirus Disease 2019 (COVID-19). This virus is highly transmissible among individuals through both droplets and aerosol leading to determine severe pneumonia. Among the various factors that can influence both the onset of disease and the severity of its complications, the microbiome composition has also been investigated. Recent evidence showed the possible relationship between gut, lung, nasopharyngeal, or oral microbiome and… Show more

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Cited by 71 publications
(117 citation statements)
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“…Recently, a Chinese team from Wuhan institute of virology published a metagenomic sequencing study that reveals the potential linkages between pharyngeal microbiota and COVID-19 [ 15 ]. Our study is a novel metagenomic study to reveal the nasopharyngeal microbiome features of COVID-19 patients in China, which also have been reported by other studies in USA [ 14 ] and Italy [ 27 ].…”
Section: Discussionsupporting
confidence: 71%
“…Recently, a Chinese team from Wuhan institute of virology published a metagenomic sequencing study that reveals the potential linkages between pharyngeal microbiota and COVID-19 [ 15 ]. Our study is a novel metagenomic study to reveal the nasopharyngeal microbiome features of COVID-19 patients in China, which also have been reported by other studies in USA [ 14 ] and Italy [ 27 ].…”
Section: Discussionsupporting
confidence: 71%
“…Recent cross-sectional studies have attempted to distinguish nasal microbial profiles collected from COVID-19-positive and negative subjects using nasopharyngeal swab [ 5 8 ]. Of the four prior studies using nasopharyngeal swabs, our results are most similar to those of Mostafa et al [ 7 ].…”
Section: Discussionmentioning
confidence: 99%
“…, Meisel et al [ 26 ]), Propionibacterium were not well represented and no direct comparison with the results of Mostafa et al could be made. Elsewhere, Nardelli and colleagues targeted the V1-V3 variable regions of 16S rRNA genes using amplicon sequencing [ 8 ], while De Maio et al targeted the V5-V6 variable regions [ 5 ]. Differences in PCR conditions can make direct comparison of results generated with different primer sets challenging, as PCR conditions can introduce substantial bias into observed microbial communities.…”
Section: Discussionmentioning
confidence: 99%
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