SEMLIKI FOREST VIRUS EXPRESSION SYSTEM - PRODUCTION OF CONDITIONALLY INFECTIOUS RECOMBINANT PARTICLES

被引:233
作者
BERGLUND, P
SJOBERG, M
GAROFF, H
ATKINS, GJ
SHEAHAN, BJ
LILJESTROM, P
机构
[1] KAROLINSKA INST, NOVUM, DEPT MOLEC BIOL, S-14157 HUDDINGE, SWEDEN
[2] NATL UNIV IRELAND UNIV COLL DUBLIN, FAC VET MED, DEPT VET PATHOL, DUBLIN 4, IRELAND
[3] UNIV DUBLIN TRINITY COLL, MOYNE INST, DEPT MICROBIOL, DUBLIN 2, IRELAND
来源
BIO-TECHNOLOGY | 1993年 / 11卷 / 08期
基金
英国惠康基金;
关键词
D O I
10.1038/nbt0893-916
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the recently developed Semliki Forest virus (SFV) DNA expression system, recombinant RNA encoding the viral replicase, and helper RNA molecules encoding the structural proteins needed for virus assembly are cotransfected into cells. Since the helper RNA lacks the sequence needed for its packaging into nucleocapsids, only recombinant RNAs should be packaged. We have found, however, that small amounts of replication-proficient SFV particles can still be produced. Here we describe the construction of a helper variant with a mutation in the gene encoding the viral spike protein such that its product cannot undergo normal proteolytic processing to activate viral entry functions. Hence, the recombinant stock is noninfectious, but may be activated by cleavage with chymotrypsin. When recombinant virus produced with the new helper was examined in a variety of assays, including sensitive animal tests, we were unable to detect any replication-competent SFV particles. We therefore conclude that this conditional expression system meets extremely stringent biosafety requirements.
引用
收藏
页码:916 / 920
页数:5
相关论文
共 33 条
[1]   MAMMALIAN SUBTILISINS - THE LONG-SOUGHT DIBASIC PROCESSING ENDOPROTEASES [J].
BARR, PJ .
CELL, 1991, 66 (01) :1-3
[2]   VIRULENCE OF ORIGINAL AND DERIVED STRAINS OF SEMLIKI FOREST VIRUS FOR MICE, GUINEA-PIGS AND RABBITS [J].
BRADISH, CJ ;
ALLNER, K ;
MABER, HB .
JOURNAL OF GENERAL VIROLOGY, 1971, 12 (AUG) :114-&
[3]  
BREDENBEEK PJ, 1992, SEMIN VIROL, V3, P297
[4]   MEMBRANE-FUSION OF SEMLIKI FOREST VIRUS IN A MODEL SYSTEM - CORRELATION BETWEEN FUSION KINETICS AND STRUCTURAL-CHANGES IN THE ENVELOPE GLYCOPROTEIN [J].
BRON, R ;
WAHLBERG, JM ;
GAROFF, H ;
WILSCHUT, J .
EMBO JOURNAL, 1993, 12 (02) :693-701
[5]   DISSECTION OF SEMLIKI FOREST VIRUS GLYCOPROTEIN DELIVERY FROM THE TRANS-GOLGI NETWORK TO THE CELL-SURFACE IN PERMEABILIZED BHK CELLS [J].
DECURTIS, I ;
SIMONS, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :8052-8056
[6]   THE SIGNAL SEQUENCE OF THE P62-PROTEIN OF SEMLIKI FOREST VIRUS IS INVOLVED IN INITIATION BUT NOT IN COMPLETING CHAIN TRANSLOCATION [J].
GAROFF, H ;
HUYLEBROECK, D ;
ROBINSON, A ;
TILLMAN, U ;
LILJESTROM, P .
JOURNAL OF CELL BIOLOGY, 1990, 111 (03) :867-876
[7]   COMPLEMENTATION BETWEEN SINDBIS VIRAL RNAS PRODUCES INFECTIOUS PARTICLES WITH A BIPARTITE GENOME [J].
GEIGENMULLERGNIRKE, U ;
WEISS, B ;
WRIGHT, R ;
SCHLESINGER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) :3253-3257
[8]   2 MUTATIONS IN THE ENVELOPE GLYCOPROTEIN-E2 OF SEMLIKI FOREST VIRUS AFFECTING THE MATURATION AND ENTRY PATTERNS OF THE VIRUS ALTER PATHOGENICITY FOR MICE [J].
GLASGOW, GM ;
SHEAHAN, BJ ;
ATKINS, GJ ;
WAHLBERG, JM ;
SALMINEN, A ;
LILJESTROM, P .
VIROLOGY, 1991, 185 (02) :741-748
[9]  
Griffin D. E., 1986, TOGAVIRIDAE FLAVIVIR, P209
[10]  
KUNKEL TA, 1987, METHOD ENZYMOL, V154, P367