2021
DOI: 10.1016/j.virusres.2021.198576
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Rotavirus reverse genetics: A tool for understanding virus biology

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Cited by 7 publications
(4 citation statements)
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“…59 Subsequently, Himetobi P virus (Hipve) 59,61 and Nilla-parvata lugens symbiont X virus (NLCXV) 62 were found in planthopper populations. With the rapid development of HTS [64][65][66] In sustainable agricultural pest management, it offers significant potential for modifying and controlling insect viruses. Despite the development of many reverse genetics systems for arthropod-borne viruses, their widespread agricultural application has been limited by the lack of suitable insect cell lines.…”
Section: Planthoppermentioning
confidence: 99%
See 1 more Smart Citation
“…59 Subsequently, Himetobi P virus (Hipve) 59,61 and Nilla-parvata lugens symbiont X virus (NLCXV) 62 were found in planthopper populations. With the rapid development of HTS [64][65][66] In sustainable agricultural pest management, it offers significant potential for modifying and controlling insect viruses. Despite the development of many reverse genetics systems for arthropod-borne viruses, their widespread agricultural application has been limited by the lack of suitable insect cell lines.…”
Section: Planthoppermentioning
confidence: 99%
“…Reverse genetics technology, a rapidly growing field in virology, deciphers complex viral genome structures and functions. It allows viral genome manipulation in vitro , analysis of recombinant viruses, and virus vector modification for purposes like foreign protein expression, gene silencing, and vaccine development 64–66 . In sustainable agricultural pest management, it offers significant potential for modifying and controlling insect viruses.…”
Section: Reverse Genetics Technology For Agricultural Insect Virusesmentioning
confidence: 99%
“…The RG system developed by Sánchez-Tacuba et al, which capitalizes on a plasmid encoding a fusion protein consisting of T7 polymerase and the African swine fever virus NP868R capping enzyme, as well as an IFN-insensitive MA104 cell line, has been used to recover hard-to-culture RV strains, including simian RRV and human CDC-9; a recombinant RRV expressing EGFP; a murine RV reassortment D6/2-like virus ( 104 ); a murine RV lacking NSP1 expression ( 112 ); and a murine RV encoding a Nano-Luciferase bioluminescent reporter ( 113 ). Extensive reviews of the current plasmid-only RG systems are available elsewhere ( 7 , 114 116 ).…”
Section: Rv Studies In the Era Of Reverse Geneticsmentioning
confidence: 99%
“…(a) RNA sensing and antagonism of type I and III IFN signaling. Upon entry into the cell, RLR-sensing of RV dsRNA activates MAVS ( 116 , 117 ). Previous studies have demonstrated that RIG-I and MDA5 are independently essential for antiviral responses to RV in vitro , suggesting that RV generates RNA species recognized by both receptors, which are degraded by NSP1 ( 12 , 118 , 119 ).…”
Section: Rv Studies In the Era Of Reverse Geneticsmentioning
confidence: 99%