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10.1016/j.crmeth.2021.100091

http://scihub22266oqcxt.onion/10.1016/j.crmeth.2021.100091
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suck abstract from ncbi


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pmid34790908      Cell+Rep+Methods 2021 ; 1 (6): ä
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  • Metatranscriptomics to characterize respiratory virome, microbiome, and host response directly from clinical samples #MMPMID34790908
  • Rajagopala SV; Bakhoum NG; Pakala SB; Shilts MH; Rosas-Salazar C; Mai A; Boone HH; McHenry R; Yooseph S; Halasa N; Das SR
  • Cell Rep Methods 2021[Oct]; 1 (6): ä PMID34790908show ga
  • We developed a metatranscriptomics method that can simultaneously capture the respiratory virome, microbiome, and host response directly from low biomass samples. Using nasal swab samples, we capture RNA virome with sufficient sequencing depth required to assemble complete genomes. We find a surprisingly high frequency of respiratory syncytial virus (RSV) and coronavirus (CoV) in healthy children, and a high frequency of RSV-A and RSV-B co-detections in children with symptomatic RSV. In addition, we have identified commensal and pathogenic bacteria and fungi at the species level. Functional analysis revealed that H. influenzae was highly active in symptomatic RSV subjects. The host nasal transcriptome reveled upregulation of the innate immune system, anti-viral response and inflammasome pathway, and downregulation of fatty acid pathways in children with symptomatic RSV. Overall, we demonstrate that our method is broadly applicable to infer the transcriptome landscape of an infected system, surveil respiratory infections, and to sequence RNA viruses directly from clinical samples.
  • |*Microbiota/genetics[MESH]
  • |*Respiratory Syncytial Virus Infections/genetics[MESH]
  • |*Respiratory Syncytial Virus, Human/genetics[MESH]
  • |Child[MESH]
  • |Humans[MESH]
  • |Transcriptome/genetics[MESH]


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