Key result
Ribonucleoprotein transfection of defective influenza A virus RNA resulted in the generation of viable recombinant viruses, indicating that the viral polymerase can mediate RNA recombination.
Ribonucleoprotein transfection can mediate RNA recombination in influenza A viruses, generating novel recombinant strains.
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May inform influenza surveillance by revealing recombination potential; leaves open frequency and relevance in natural infections.
Several mechanisms, including a high mutation rate and reassortment of genes, have been found to be responsible for the variability of influenza A viruses. RNA recombination would be another mechanism leading to genetic variation; however, recombination has only rarely been reported to occur in influenza viruses. During ribonucleoprotein transfection experiments designed to generate viable influenza viruses from in vitro-synthesized RNA, we discovered several viruses which must have originated from recombination events. The ribonucleoprotein transfection system may enhance the formation of viruses which result from jumping of the viral polymerase between RNAs or from ligation of different viral RNAs. Five different recombinant viruses are described. Two of these, REC1 and REC2, contain a neuraminidase (NA) gene whose defective polyadenylation signal has been repaired via intergenic recombination; 124 and 95 nucleotides have been added, respectively. Another virus, REC5, must have originated by multiple recombination events since it contains a mosaic gene with sequences derived from the NA gene of influenza A/WSN/33 virus and the matrix, polymerase protein PB1, and NA genes of influenza A/PR/8/34 virus.
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Bergmann et al. (1992) studied Influenza A virus. Ribonucleoprotein (RNP) transfection was evaluated on Generation of recombinant viruses. Ribonucleoprotein transfection of defective influenza A virus RNA resulted in the generation of viable recombinant viruses, indicating that the viral polymerase can mediate RNA recombination.
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