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10.1371/journal.pbio.3001158

http://scihub22266oqcxt.onion/10.1371/journal.pbio.3001158
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33780434!8032198!33780434
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suck abstract from ncbi


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pmid33780434      PLoS+Biol 2021 ; 19 (3): e3001158
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  • Disparate temperature-dependent virus-host dynamics for SARS-CoV-2 and SARS-CoV in the human respiratory epithelium #MMPMID33780434
  • V'kovski P; Gultom M; Kelly JN; Steiner S; Russeil J; Mangeat B; Cora E; Pezoldt J; Holwerda M; Kratzel A; Laloli L; Wider M; Portmann J; Tran T; Ebert N; Stalder H; Hartmann R; Gardeux V; Alpern D; Deplancke B; Thiel V; Dijkman R
  • PLoS Biol 2021[Mar]; 19 (3): e3001158 PMID33780434show ga
  • Since its emergence in December 2019, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has spread globally and become a major public health burden. Despite its close phylogenetic relationship to SARS-CoV, SARS-CoV-2 exhibits increased human-to-human transmission dynamics, likely due to efficient early replication in the upper respiratory epithelium of infected individuals. Since different temperatures encountered in the human upper and lower respiratory tract (33 degrees C and 37 degrees C, respectively) have been shown to affect the replication kinetics of several respiratory viruses, as well as host innate immune response dynamics, we investigated the impact of temperature on SARS-CoV-2 and SARS-CoV infection using the primary human airway epithelial cell culture model. SARS-CoV-2, in contrast to SARS-CoV, replicated to higher titers when infections were performed at 33 degrees C rather than 37 degrees C. Although both viruses were highly sensitive to type I and type III interferon pretreatment, a detailed time-resolved transcriptome analysis revealed temperature-dependent interferon and pro-inflammatory responses induced by SARS-CoV-2 that were inversely proportional to its replication efficiency at 33 degrees C or 37 degrees C. These data provide crucial insight on pivotal virus-host interaction dynamics and are in line with characteristic clinical features of SARS-CoV-2 and SARS-CoV, as well as their respective transmission efficiencies.
  • |Animals[MESH]
  • |Antiviral Agents/pharmacology[MESH]
  • |Cells, Cultured[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Epithelial Cells/drug effects/metabolism/virology[MESH]
  • |Gene Expression Profiling/*methods[MESH]
  • |Gene Expression Regulation, Viral/drug effects/*genetics[MESH]
  • |Host-Pathogen Interactions/drug effects/genetics[MESH]
  • |Humans[MESH]
  • |Interferons/pharmacology[MESH]
  • |SARS-CoV-2/drug effects/*genetics/physiology[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/drug effects/*genetics/physiology[MESH]
  • |Species Specificity[MESH]
  • |Temperature[MESH]
  • |Vero Cells[MESH]


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