Key result
Transfection of exogenous rotavirus rearranged RNA segment 5 or 11 into cells infected with a WT helper rotavirus resulted in subsequent gene rearrangements in the viral progeny.
The study demonstrates that transfection of exogenous rearranged RNA segments into rotavirus-infected cells leads to spontaneous secondary rearrangements, complicating the use of this reverse genetics system.
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May complicate rotavirus reverse genetics reliability; leaves open protocol refinements for consistent reassortants.
Group A rotaviruses, members of the family Reoviridae, are a major cause of infantile acute gastroenteritis. The rotavirus genome consists of 11 dsRNA segments. In some cases, an RNA segment is replaced by a rearranged RNA segment, which is derived from its standard counterpart by partial sequence duplication. It has been shown that some rearranged segments are preferentially encapsidated into viral progenies after serial passages in cell culture. Based on this characteristic, a reverse genetics system was used previously to introduce exogenous segment 7 rearrangements into an infectious rotavirus. This study extends this reverse genetics system to RNA segments 5 and 11. Transfection of exogenous rotavirus rearranged RNA segment 5 or 11 into cells infected with a WT helper rotavirus (bovine strain RF) resulted in subsequent gene rearrangements in the viral progeny. Whilst recombinant viruses were rescued with an exogenous rearranged segment 11, the exogenous segment was modified by a secondary rearrangement. The occurrence of spontaneous rearrangements of WT or exogenous segments is a major hindrance to the use of this reverse genetics approach.
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Duponchel et al. (2014) studied Rotavirus infection. Transfection of exogenous rotavirus rearranged RNA segment 5 or 11 was evaluated on Gene rearrangements in the viral progeny. Transfection of exogenous rotavirus rearranged RNA segment 5 or 11 into cells infected with a WT helper rotavirus resulted in subsequent gene rearrangements in the viral progeny.
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