Literature DB >> 8257115

Genetic manipulation of negative-strand RNA virus genomes.

A García-Sastre1, P Palese.   

Abstract

Negative-strand RNA viruses have been refractory to genetic manipulation using recombinant DNA techniques. Recently, new techniques were developed that allowed the rescue of synthetic RNA molecules into influenza A viruses and, subsequently, into other negative-strand RNA viruses. These techniques are presently being used to study the molecular biology of these viruses. Questions concerning cis- and trans-acting elements that are involved in transcription and replication of negative-sense RNA viral genomes can now be addressed with reverse genetic approaches. Further development of this methodology has enabled the construction--by recombinant DNA techniques--of influenza A viruses that contain altered genomes. The phenotypic characteristics and possible applications of these novel transfectant viruses are also discussed.

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Year:  1993        PMID: 8257115     DOI: 10.1146/annurev.mi.47.100193.004001

Source DB:  PubMed          Journal:  Annu Rev Microbiol        ISSN: 0066-4227            Impact factor:   15.500


  31 in total

1.  NP and L proteins of lymphocytic choriomeningitis virus (LCMV) are sufficient for efficient transcription and replication of LCMV genomic RNA analogs.

Authors:  K J Lee; I S Novella; M N Teng; M B Oldstone; J C de La Torre
Journal:  J Virol       Date:  2000-04       Impact factor: 5.103

2.  Influenza A virus RNA polymerase has the ability to stutter at the polyadenylation site of a viral RNA template during RNA replication.

Authors:  H Zheng; H A Lee; P Palese; A García-Sastre
Journal:  J Virol       Date:  1999-06       Impact factor: 5.103

3.  Given the opportunity, the Sendai virus RNA-dependent RNA polymerase could as well enter its template internally.

Authors:  Diane Vulliémoz; Laurent Roux
Journal:  J Virol       Date:  2002-08       Impact factor: 5.103

4.  Development of a challenge-protective vaccine concept by modification of the viral RNA-dependent RNA polymerase of canine distemper virus.

Authors:  D Silin; O Lyubomska; M Ludlow; W P Duprex; B K Rima
Journal:  J Virol       Date:  2007-09-26       Impact factor: 5.103

5.  Introduction of hepatitis delta virus into animal cell lines via cationic liposomes.

Authors:  V Bichko; H J Netter; J Taylor
Journal:  J Virol       Date:  1994-08       Impact factor: 5.103

6.  Development of a reverse genetic system for infectious salmon anemia virus: rescue of recombinant fluorescent virus by using salmon internal transcribed spacer region 1 as a novel promoter.

Authors:  Daniela Toro-Ascuy; Carolina Tambley; Carolina Beltran; Carolina Mascayano; Nicolas Sandoval; Eduardo Olivares; Rafael A Medina; Eugenio Spencer; Marcelo Cortez-San Martín
Journal:  Appl Environ Microbiol       Date:  2015-02       Impact factor: 4.792

7.  Solid phase synthesis of 5'-diphosphorylated oligoribonucleotides and their conversion to capped m7Gppp-oligoribonucleotides for use as primers for influenza A virus RNA polymerase in vitro.

Authors:  G G Brownlee; E Fodor; D C Pritlove; K G Gould; J J Dalluge
Journal:  Nucleic Acids Res       Date:  1995-07-25       Impact factor: 16.971

8.  Replication and amplification of novel vesicular stomatitis virus minigenomes encoding viral structural proteins.

Authors:  E A Stillman; J K Rose; M A Whitt
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

9.  A plasmid-based reverse genetics system for influenza A virus.

Authors:  S Pleschka; R Jaskunas; O G Engelhardt; T Zürcher; P Palese; A García-Sastre
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

10.  Serine 3 is critical for phosphorylation at the N-terminal end of the nucleoprotein of influenza virus A/Victoria/3/75.

Authors:  M Arrese; A Portela
Journal:  J Virol       Date:  1996-06       Impact factor: 5.103

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