Nucleotide sequence analysis shows that Rhopalosiphum padi virus is a member of a novel group of insect-infecting RNA viruses

被引:76
作者
Moon, JS
Domier, LL [1 ]
McCoppin, NK
D'Arcy, CJ
Jin, H
机构
[1] Univ Illinois, Dept Crop Sci, Urbana, IL 61801 USA
[2] Agr Res Serv, USDA, Crop Protect Res Unit, Urbana, IL 61801 USA
关键词
D O I
10.1006/viro.1998.9043
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Rhopalosiphum padi virus (RhPV) is an aphid virus that has been considered a member of the Picornaviridae based on physicochemical properties. The 10,011-nt polyadenylated RNA genome of RhPV was completely sequenced, Analysis of the sequence revealed the presence of two open reading frames (ORFs). The predicted amino acid sequence of ORF1, representing the first 6600 ne of the RhPV genome, showed significant similarity to the nonstructural proteins of several plant and animal RNA viruses. Direct sequence analysis of the RhPV capsid proteins showed that ORF2, which represents the last 2900 nt, encodes the three structural proteins (28, 29, and 30 kDa). The predicted amino acid sequence of ORF2 is Very similar to the corresponding regions of Drosophila C virus, Plautia stali intestine virus, and to a partial sequence from the 3' end of the cricket paralysis virus genome. The sire Of initiation of protein synthesis for ORF2 could not be determined from the amino acid and nucleotide sequences. ORF1 is preceded by 579 nt of noncoding RNA and the two ORFs are separated by more than 500 nt of noncoding RNA. Like picornaviruses, these regions may function to facilitate the cap-independent initiation of translation of the two ORFs. These data suggest that RhPV, Drosophila C virus, Plautia stali intestine virus, and probably cricket paralysis virus are members of a unique group of small RNA viruses that infect primarily insects. (C) 1998 Academic Press.
引用
收藏
页码:54 / 65
页数:12
相关论文
共 55 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Development of recombinant baculoviruses for insect control [J].
Bonning, BC ;
Hammock, BD .
ANNUAL REVIEW OF ENTOMOLOGY, 1996, 41 :191-210
[3]   Comparison of picornaviral IRES-driven internal initiation of translation in cultured cells of different origins [J].
Borman, AM ;
LeMercier, P ;
Girard, M ;
Kean, KM .
NUCLEIC ACIDS RESEARCH, 1997, 25 (05) :925-932
[4]   MUTATIONAL ANALYSIS OF THE SLIPPERY-SEQUENCE COMPONENT OF A CORONAVIRUS RIBOSOMAL FRAMESHIFTING SIGNAL [J].
BRIERLEY, I ;
JENNER, AJ ;
INGLIS, SC .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 227 (02) :463-479
[5]   ONE-HOUR DOWNWARD ALKALINE CAPILLARY TRANSFER FOR BLOTTING OF DNA AND RNA [J].
CHOMCZYNSKI, P .
ANALYTICAL BIOCHEMISTRY, 1992, 201 (01) :134-139
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   PURIFICATION AND CHARACTERIZATION OF A VIRUS FROM THE APHID RHOPALOSIPHUM-PADI [J].
DARCY, CJ ;
BURNETT, PA ;
HEWINGS, AD ;
GOODMAN, RM .
VIROLOGY, 1981, 112 (01) :346-349
[8]   DETECTION, BIOLOGICAL EFFECTS, AND TRANSMISSION OF A VIRUS OF THE APHID RHOPALOSIPHUM-PADI [J].
DARCY, CJ ;
BURNETT, PA ;
HEWINGS, AD .
VIROLOGY, 1981, 114 (01) :268-272
[9]   ANALYSIS OF THE INVITRO CLEAVAGE PRODUCTS OF THE TOMATO BLACK RING VIRUS RNA-1-ENCODED 250K POLYPROTEIN [J].
DEMANGEAT, G ;
GREIF, C ;
HEMMER, O ;
FRITSCH, C .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1649-1654
[10]   IDENTIFICATION OF PROTEOLYTIC PROCESSING SITES WITHIN THE GAG AND POL POLYPROTEINS OF FELINE IMMUNODEFICIENCY VIRUS [J].
ELDER, JH ;
SCHNOLZER, M ;
HASSELKUSLIGHT, CS ;
HENSON, M ;
LERNER, DA ;
PHILLIPS, TR ;
WAGAMAN, PC ;
KENT, SBH .
JOURNAL OF VIROLOGY, 1993, 67 (04) :1869-1876