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10.1016/j.jinf.2020.03.058

http://scihub22266oqcxt.onion/10.1016/j.jinf.2020.03.058
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C7195303!7195303!32283146
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suck abstract from ncbi


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pmid32283146      J+Infect 2020 ; 81 (1): e24-7
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  • Evolutionary analysis of SARS-CoV-2: how mutation of Non-Structural Protein 6 (NSP6) could affect viral autophagy #MMPMID32283146
  • Benvenuto D; Angeletti S; Giovanetti M; Bianchi M; Pascarella S; Cauda R; Ciccozzi M; Cassone A
  • J Infect 2020[Jul]; 81 (1): e24-7 PMID32283146show ga
  • Background: SARS-CoV-2 is a new coronavirus that has spread globally, infecting more than 150000 people, and being declared pandemic by the WHO. We provide here bio-informatic, evolutionary analysis of 351 available sequences of its genome with the aim of mapping genome structural variations and the patterns of selection. Methods: A Maximum likelihood tree has been built and selective pressure has been investigated in order to find any mutation developed during the SARS-CoV-2 epidemic that could potentially affect clinical evolution of the infection. Finding: We have found in more recent isolates the presence of two mutations affecting the Non-Structural Protein 6 (NSP6) and the Open Reding Frame10 (ORF 10) adjacent regions. Amino acidic change stability analysis suggests both mutations could confer lower stability of the protein structures. Interpretation: One of the two mutations, likely developed within the genome during virus spread, could affect virus intracellular survival. Genome follow-up of SARS-CoV-2 spread is urgently needed in order to identify mutations that could significantly modify virus pathogenicity.
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