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10.1016/j.jaci.2021.02.001

http://scihub22266oqcxt.onion/10.1016/j.jaci.2021.02.001
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33577896!7871823!33577896
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suck abstract from ncbi


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pmid33577896      J+Allergy+Clin+Immunol 2021 ; 147 (4): 1226-1233.e2
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  • SARS-CoV-2 infection and viral load are associated with the upper respiratory tract microbiome #MMPMID33577896
  • Rosas-Salazar C; Kimura KS; Shilts MH; Strickland BA; Freeman MH; Wessinger BC; Gupta V; Brown HM; Rajagopala SV; Turner JH; Das SR
  • J Allergy Clin Immunol 2021[Apr]; 147 (4): 1226-1233.e2 PMID33577896show ga
  • BACKGROUND: 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. OBJECTIVE: 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. METHODS: 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, beta-diversity, and abundance of bacterial taxa of the URT microbiome. Our main models were all adjusted for age and sex. RESULTS: The observed species index was significantly higher in SARS-CoV-2-infected than in -uninfected adults (beta 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. CONCLUSIONS: 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.
  • |*Microbiota/genetics[MESH]
  • |*SARS-CoV-2[MESH]
  • |*Viral Load[MESH]
  • |Adult[MESH]
  • |Biodiversity[MESH]
  • |COVID-19/*microbiology/*virology[MESH]
  • |Case-Control Studies[MESH]
  • |Female[MESH]
  • |Host Microbial Interactions[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |RNA, Ribosomal, 16S/genetics[MESH]
  • |Respiratory System/*microbiology[MESH]


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