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10.1002/jmv.27738

http://scihub22266oqcxt.onion/10.1002/jmv.27738
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35324008!9088479!35324008
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suck abstract from ncbi

pmid35324008      J+Med+Virol 2022 ; 94 (7): 3017-3031
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  • Reverse genetics systems for SARS-CoV-2 #MMPMID35324008
  • Wang W; Peng X; Jin Y; Pan JA; Guo D
  • J Med Virol 2022[Jul]; 94 (7): 3017-3031 PMID35324008show ga
  • The ongoing pandemic of coronavirus disease 2019 (COVID-19) has caused severe public health crises and heavy economic losses. Limited knowledge about this deadly virus impairs our capacity to set up a toolkit against it. Thus, more studies on severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) biology are urgently needed. Reverse genetics systems, including viral infectious clones and replicons, are powerful platforms for viral research projects, spanning many aspects such as the rescues of wild-type or mutant viral particles, the investigation of viral replication mechanism, the characterization of viral protein functions, and the studies on viral pathogenesis and antiviral drug development. The operations on viral infectious clones are strictly limited in the Biosafety Level 3 (BSL3) facilities, which are insufficient, especially during the pandemic. In contrast, the operation on the noninfectious replicon can be performed in Biosafety Level 2 (BSL2) facilities, which are widely available. After the outbreak of COVID-19, many reverse genetics systems for SARS-CoV-2, including infectious clones and replicons are developed and given plenty of options for researchers to pick up according to the requirement of their research works. In this review, we summarize the available reverse genetics systems for SARS-CoV-2, by highlighting the features of these systems, and provide a quick guide for researchers, especially those without ample experience in operating viral reverse genetics systems.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2/genetics[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]
  • |Replicon[MESH]


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