Reverse transcriptase activity in chicken embryo fibroblast culture supernatants is associated with particles containing endogenous avian retrovirus EAV-0 RNA

被引:50
作者
Weissmahr, RN [1 ]
Schupbach, J [1 ]
Boni, J [1 ]
机构
[1] UNIV ZURICH,SWISS NATL CTR RETROVIRUSES,CH-8028 ZURICH,SWITZERLAND
关键词
D O I
10.1128/JVI.71.4.3005-3012.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have recently shown that live attenuated virus vaccines produced on chicken-derived cells contain low levels of particle-associated reverse transcriptase (RT). In both virus and corresponding control harvests produced on chicken embryo fibroblasts, these activities were present at significantly higher concentrations than in the vaccines. In order to identify the putative retrovirus sequence responsible for this activity, a novel method for the selective PCR amplification of particle-associated retrovirus RNA that uses DNA primers complementary to the primer binding sites of the known exogenous retroviruses in combination with an anchor primer was applied. A product of the endogenous avian retrovirus family EAV-0, termed EAV-0(B1), was reproducibly generated with a tRNA(Trp)-derived primer from the RT peak fraction of a sucrose density gradient run with a harvest of a live attenuated measles vaccine. In contrast, no products were detected with primers derived from tRNA(Pro), tRNA(1,2)(Lys) or tRNA(3)(Lys). In the same fraction, genomic RNA of EAV-0(B1) was demonstrated by long PCR. Analysis of several sucrose density gradients from different harvests of various manufacturers demonstrated accumulation of and colocalization with, RT activity for the EAV-0(B1) RNA but not for a chicken cellular mRNA. Synthesis of cDNA from EAV-0(B1) RNA with RT were demonstrated. Taken together, these datas strongly suggest that EAV-0 is able to produce virus-like particles with an active RT.
引用
收藏
页码:3005 / 3012
页数:8
相关论文
共 29 条
[1]   VIRAL RNA-DEPENDENT DNA POLYMERASE - RNA-DEPENDENT DNA POLYMERASE IN VIRIONS OF RNA TUMOUR VIRUSES [J].
BALTIMORE, D .
NATURE, 1970, 226 (5252) :1209-+
[2]   PCR AMPLIFICATION OF UP TO 35-KB DNA WITH HIGH-FIDELITY AND HIGH-YIELD FROM LAMBDA-BACTERIOPHAGE TEMPLATES [J].
BARNES, WM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2216-2220
[3]   PURIFICATION AND CHARACTERIZATION OF PARTICLES CONTAINING RNA-DEPENDENT DNA-POLYMERASE, IN ALLANTOIC FLUID OF UNINFECTED LEUKOSIS VIRUS-FREE CHICKEN EGGS [J].
BAUER, G ;
FRIIS, RR ;
JILEK, G ;
HOFSCHNEIDER, PH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 518 (01) :125-137
[4]   RNA-DEPENDENT DNA-POLYMERASE, DIFFERENT FROM KNOWN VIRAL REVERSE TRANSCRIPTASES, IN CHICKEN SYSTEM [J].
BAUER, G ;
HOFSCHNEIDER, PH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (09) :3025-3029
[5]   CONTROLLED RELEASE OF PARTICLE-ASSOCIATED RNA-DEPENDENT DNA-POLYMERASE BY PRIMARY CHICK-EMBRYO CELL-CULTURES [J].
BAUER, G ;
FRIIS, RR ;
MATTERSBERGER, H ;
HOFSCHNEIDER, PH .
EXPERIMENTAL CELL RESEARCH, 1978, 117 (02) :383-392
[6]  
Boni J, 1996, J MED VIROL, V49, P23, DOI 10.1002/(SICI)1096-9071(199605)49:1&lt
[7]  
23::AID-JMV4&gt
[8]  
3.0.CO
[9]  
2-M
[10]   Detection of reverse transcriptase activity in live attenuated virus vaccines [J].
Boni, J ;
Stalder, J ;
Reigel, F ;
Schupbach, J .
CLINICAL AND DIAGNOSTIC VIROLOGY, 1996, 5 (01) :43-53