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10.1016/j.ijid.2021.03.036

http://scihub22266oqcxt.onion/10.1016/j.ijid.2021.03.036
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33737129!7959680!33737129
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suck abstract from ncbi


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pmid33737129      Int+J+Infect+Dis 2021 ; 105 (ä): 735-738
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  • Genomic surveillance of SARS-CoV-2 in the Republic of Congo #MMPMID33737129
  • Ntoumi F; Mfoutou Mapanguy CC; Tomazatos A; Pallerla SR; Linh LTK; Casadei N; Angelov A; Sonnabend M; Peter S; Kremsner PG; Velavan TP
  • Int J Infect Dis 2021[Apr]; 105 (ä): 735-738 PMID33737129show ga
  • OBJECTIVE: The aim of this study was to carry out whole-genome sequencing (WGS) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), using samples collected from Congolese individuals between April and July 2020. METHODS: Ninety-six samples were screened for SARS-CoV-2 using RT-PCR, and 19 samples with Ct values <30 were sequenced using Illumina Next-Generation Sequencing (NGS). The genomes were annotated and screened for mutations using the web tool 'coronapp'. Subsequently, different SARS-CoV-2 lineages were assigned using PANGOLIN and Nextclade. RESULTS: Eleven SARS-CoV-2 genomes were successfully sequenced and submitted to the GSAID database. All genomes carried the spike mutation D614G and were classified as part of the GH clade. The Congolese SARS-CoV-2 sequences were shown to belong to lineage B1 and Nextclade 20A and 20C, which split them into distinct clusters, indicating two separate introductions of the virus into the Republic of Congo. CONCLUSION: This first study provides valuable information on SARS CoV-2 transmission in the central African region, contributing to SARS CoV-2 surveillance on a temporal and spatial scale.
  • |*Genome, Viral[MESH]
  • |COVID-19/*virology[MESH]
  • |Congo[MESH]
  • |High-Throughput Nucleotide Sequencing[MESH]
  • |Humans[MESH]
  • |Mutation[MESH]
  • |SARS-CoV-2/*genetics[MESH]


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