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Journal of Virology, June 2008, p. 6073-6077, Vol. 82, No. 12
0022-538X/08/$08.00+0 doi:10.1128/JVI.00121-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

and
Yasutaka Hoshino*
Epidemiology Section, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892
Received 17 January 2008/ Accepted 4 April 2008
Serial undiluted passage of a porcine rotavirus in MA104 cells yielded three distinct virus populations, each of which bore different rearranged genes. Sequencing revealed that each of two populations bore a distinct intragenic recombinant NSP3 gene consisting of a partial duplication in a head-to-tail orientation without altering the NSP3 open reading frame and the third population carried both an intragenic recombinant NSP3 gene and an intergenic recombinant gene (1,647 nucleotides in length) which contained a truncated NSP2 gene inserted into the NSP5 gene at residue 332. The former two populations were viable, whereas the latter population was defective and interfering.
Published ahead of print on 16 April 2008.
Present address: Global Vaccines, Inc., Research Triangle Park, NC.
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