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Journal of Virology, May 2000, p. 4831-4838, Vol. 74, No. 10
Wyeth-Lederle Vaccines, Pearl River, New York
10965
Received 13 December 1999/Accepted 23 February 2000
A complete DNA copy of the genome of a Jeryl Lynn strain of mumps
virus (15,384 nucleotides) was assembled from cDNA fragments such that
an exact antigenome RNA could be generated following transcription by
T7 RNA polymerase and cleavage by hepatitis delta virus ribozyme. The
plasmid containing the genome sequence, together with support plasmids
which express mumps virus NP, P, and L proteins under control of the T7
RNA polymerase promoter, were transfected into A549 cells previously
infected with recombinant vaccinia virus (MVA-T7) that expressed T7 RNA
polymerase. Rescue of infectious virus from the genome cDNA was
demonstrated by amplification of mumps virus from transfected-cell
cultures and by subsequent consensus sequencing of reverse
transcription-PCR products generated from infected-cell RNA to verify
the presence of specific nucleotide tags introduced into the genome
cDNA clone. The only coding change (position 8502, A to G) in the cDNA
clone relative to the consensus sequence of the Jeryl Lynn plaque
isolate from which it was derived, resulting in a lysine-to-arginine
substitution at amino acid 22 of the L protein, did not prevent rescue
of mumps virus, even though an amino acid alignment for the L proteins
of paramyxoviruses indicates that lysine is highly conserved at that
position. This system may provide the basis of a safe and effective
virus vector for the in vivo expression of immunologically and
biologically active proteins, peptides, and RNAs.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Rescue of Mumps Virus from cDNA
*
Corresponding author. Mailing address: 401 N. Middletown Rd., Bldg. 180, Pearl River, NY 10965. Phone: (914)
732-3465. Fax: (914) 732-4941. E-mail:
clarked3{at}war.wyeth.com.
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