SARS-CoV-2 infection and viral load are associated with the upper respiratory tract microbiome.
SARS-CoV-2 infection and viral load are associated with the upper respiratory tract microbiome.
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DOI:
10.1016/j.jaci.2021.02.001
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发表时间:
2021-04
期刊:
影响因子:
--
通讯作者:
Das SR
中科院分区:
文献类型:
--
作者:
Rosas-Salazar C;Kimura KS;Shilts MH;Strickland BA;Freeman MH;Wessinger BC;Gupta V;Brown HM;Rajagopala SV;Turner JH;Das SR
Little is known about the relationships between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the respiratory virus responsible for the ongoing coronavirus disease 2019 (COVID-19) pandemic, and the upper respiratory tract (URT) microbiome. We sought to compare the URT microbiome between SARS-CoV-2–infected and –uninfected adults and to examine the association of SARS-CoV-2 viral load with the URT microbiome during COVID-19. We characterized the URT microbiome using 16S ribosomal RNA sequencing in 59 adults (38 with confirmed, symptomatic, mild to moderate COVID-19 and 21 asymptomatic, uninfected controls). In those with COVID-19, we measured SARS-CoV-2 viral load using quantitative reverse transcription PCR. We then examined the association of SARS-CoV-2 infection status and its viral load with the ⍺-diversity, β-diversity, and abundance of bacterial taxa of the URT microbiome. Our main models were all adjusted for age and sex. The observed species index was significantly higher in SARS-CoV-2–infected than in –uninfected adults (β linear regression coefficient = 7.53; 95% CI, 0.17-14.89; P = .045). In differential abundance testing, 9 amplicon sequence variants were significantly different in both of our comparisons, with Peptoniphilus lacrimalis, Campylobacter hominis, Prevotella 9 copri, and an Anaerococcus unclassified amplicon sequence variant being more abundant in those with SARS-CoV-2 infection and in those with high viral load during COVID-19, whereas Corynebacterium unclassified, Staphylococcus haemolyticus, Prevotella disiens, and 2 Corynebacterium_1 unclassified amplicon sequence variants were more abundant in those without SARS-CoV-2 infection and in those with low viral load during COVID-19. Our findings suggest complex associations between SARS-CoV-2 and the URT microbiome in adults. Future studies are needed to examine how these viral-bacterial interactions can impact the clinical progression, severity, and recovery of COVID-19.
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DOI:
10.1016/j.jaci.2017.10.049
发表时间:
2018-11
期刊:
The Journal of allergy and clinical immunology
影响因子:
--
作者:
Rosas-Salazar C;Shilts MH;Tovchigrechko A;Schobel S;Chappell JD;Larkin EK;Gebretsadik T;Halpin RA;Nelson KE;Moore ML;Anderson LJ;Peebles RS Jr;Das SR;Hartert TV
通讯作者:
Hartert TV
影响因子:
14.9
作者:
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通讯作者:
Glöckner FO
影响因子:
48
作者:
Callahan BJ;McMurdie PJ;Rosen MJ;Han AW;Johnson AJ;Holmes SP
通讯作者:
Holmes SP
影响因子:
15.5
作者:
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通讯作者:
Callahan, Benjamin J
DOI:
10.1111/j.2517-6161.1995.tb02031.x
发表时间:
1995-01-01
影响因子:
5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者:
HOCHBERG, Y