The mouse Pol I terminator is more efficient than the hepatitis delta virus ribozyme in generating influenza-virus-like RNAs with precise 3' ends in a plasmid-only-based virus rescue system

被引:11
作者
Feng, Liqiang [1 ,2 ]
Li, Feng [1 ]
Zheng, Xuehua [1 ]
Pan, Weiqi [1 ]
Zhou, Kai [2 ,3 ]
Liu, Yichu [1 ]
He, Hongxuan [3 ]
Chen, Ling [1 ]
机构
[1] Chinese Acad Sci, Ctr Vaccines & Biotherapeut, Guangzhou Inst Biomed & Hlth, Guangzhou 510663, Guangdong, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Key Lab Anim Ecol & Conservat Biol, Natl Res Ctr Wildlife Born Dis, Inst Zool, Beijing 100101, Peoples R China
关键词
REVERSE GENETICS SYSTEM; A VIRUS; PACKAGING SIGNALS; SEGMENTS; VIRIONS; REGIONS; GENES; VRNA; DNA;
D O I
10.1007/s00705-009-0422-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Reverse genetics systems for generating recombinant influenza viruses are based on two different mechanisms for obtaining the 3' end of the viral RNA: one uses the self-cleaving hepatitis delta virus ribozyme (HDVR), and the other uses the murine RNA polymerase I (Pol I) terminator. In this study, we employed EGFP and Renilla luciferase reporter constructs to compare the efficiency of both methods. Our results indicate that the murine Pol I terminator was more efficient than the HDVR, which will be helpful in choosing an influenza virus rescue system, as well as in establishing other RNA virus rescue systems.
引用
收藏
页码:1151 / 1156
页数:6
相关论文
共 19 条
[11]   Virus-inducible reporter genes as a tool for detecting and quantifying influenza A virus replication [J].
Lutz, A ;
Dyall, J ;
Olivo, PD ;
Pekosz, A .
JOURNAL OF VIROLOGICAL METHODS, 2005, 126 (1-2) :13-20
[12]   Highly conserved regions of influenza A virus polymerase gene segments are critical for efficient viral RNA packaging [J].
Marsh, Glenn A. ;
Rabadan, Raul ;
Levine, Arnold J. ;
Palese, Peter .
JOURNAL OF VIROLOGY, 2008, 82 (05) :2295-2304
[13]   Hierarchy among viral RNA (vRNA) segments in their role in vRNA incorporation into influenza A virions [J].
Muramoto, Y ;
Takada, A ;
Fujii, K ;
Noda, T ;
Iwatsuki-Horimoto, K ;
Watanabe, S ;
Horimoto, T ;
Kida, H ;
Kawaoka, Y .
JOURNAL OF VIROLOGY, 2006, 80 (05) :2318-2325
[14]   An improved reverse genetics system for influenza A virus generation and its implications for vaccine production [J].
Neumann, G ;
Fujii, K ;
Kino, Y ;
Kawaoka, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (46) :16825-16829
[15]   Generation of influenza A viruses entirely from cloned cDNAs [J].
Neumann, G ;
Watanabe, T ;
Ito, H ;
Watanabe, S ;
Goto, H ;
Gao, P ;
Hughes, M ;
Perez, DR ;
Donis, R ;
Hoffmann, E ;
Hobom, G ;
Kawaoka, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9345-9350
[16]   An adenovirus vector-mediated reverse genetics system for influenza A virus generation [J].
Ozawa, Makoto ;
Goto, Hideo ;
Horimoto, Taisuke ;
Kawaoka, Yoshihiro .
JOURNAL OF VIROLOGY, 2007, 81 (17) :9556-9559
[17]   Ribozyme cleavage of a 2′,5′-phosphodiester linkage:: Mechanism and a restricted divalent metal-ion requirement [J].
Shih, IH ;
Been, MD .
RNA, 1999, 5 (09) :1140-1148
[18]   Characterization of the reconstructed 1918 Spanish influenza pandemic virus [J].
Tumpey, TM ;
Basler, CF ;
Aguilar, PV ;
Zeng, H ;
Solórzano, A ;
Swayne, DE ;
Cox, NJ ;
Katz, JM ;
Taubenberger, JK ;
Palese, P ;
García-Sastre, A .
SCIENCE, 2005, 310 (5745) :77-80
[19]   Exploitation of nucleic acid packaging signals to generate a novel influenza virus-based vector stably expressing two foreign genes [J].
Watanabe, T ;
Watanabe, S ;
Noda, T ;
Fujii, Y ;
Kawaoka, Y .
JOURNAL OF VIROLOGY, 2003, 77 (19) :10575-10583