SEQUENCES OF WILD PUUMALA VIRUS GENES SHOW A CORRELATION OF GENETIC-VARIATION WITH GEOGRAPHIC ORIGIN OF THE STRAINS

被引:83
作者
PLYUSNIN, A
VAPALAHTI, O
ULFVES, K
LEHVASLAIHO, H
APEKINA, N
GAVRILOVSKAYA, I
BLINOV, V
VAHERI, A
机构
[1] MOSCOW POLIOMYELITIS & VIRAL ENCEPHALITIS RES INS, MOSCOW, RUSSIA
[2] KOLTSOVO MOLEC BIOL RES INST, KOLTSOV, RUSSIA
关键词
D O I
10.1099/0022-1317-75-2-405
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
An experimental scheme was developed for direct sequence analysis of Puumala virus-containing specimens from wild rodents (Clethrionomys glareolus). Total RNA isolated from rodent lung tissues was reverse-transcribed in the presence of a universal 11 nucleotide primer complementary to all three viral RNA segments followed by amplification in a PCR with gene-specific primers. A full-length PCR product of approximately 1800 bp from the S segment encoding the viral nucleoprotein and a product of approximately 900 bp from the M segment (encoding the C-terminal two-thirds of the G2 protein and including the 3' non-coding region) of Puumala virus (from C. glareolus trapped in Udmurtia) were prepared and sequenced. No pronounced differences to Vero cell-grown viruses were seen. The Udmurtia/894Cg/91 strain was more closely related to the Bashkiria/CG18-20/84 strain than to the Finnish prototype strain of Puumala virus, Sotkamo/V-2969/81. Thus there is a correlation with the geographic origin of the three strains. The results indicate the occurrence of genetic drift and different selection pressures leading to (i) clustering of mutations, (ii) a lower frequency of nucleotide substitutions in the coding than in the 3' noncoding regions and (iii) a higher frequency of amino acid substitutions in G2 than in the N protein.
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页码:405 / 409
页数:5
相关论文
共 15 条
[1]   COMPARISON OF THE DEDUCED GENE-PRODUCTS OF THE L-GENOME, M-GENOME AND S-GENOME SEGMENTS OF HANTAVIRUSES [J].
ANTIC, D ;
KANG, CY ;
SPIK, K ;
SCHMALJOHN, C ;
VAPALAHTI, O ;
VAHERI, A .
VIRUS RESEARCH, 1992, 24 (01) :35-46
[2]  
BECKER Y, 1992, DIAGNOSIS HUMAN VIRU, V1
[3]   NEPHROPATHIA EPIDEMICA - DETECTION OF ANTIGEN IN BANK VOLES AND SEROLOGIC DIAGNOSIS OF HUMAN INFECTION [J].
BRUMMERKORVENKONTIO, M ;
VAHERI, A ;
HOVI, T ;
VONBONSDORFF, CH ;
VUORIMIES, J ;
MANNI, T ;
PENTTINEN, K ;
OKERBLOM, N ;
LAHDEVIRTA, J .
JOURNAL OF INFECTIOUS DISEASES, 1980, 141 (02) :131-134
[4]  
BRUMMERKORVENKONTIO M, 1982, SCAND J INFECT DIS, P88
[5]   DETECTION OF HEMORRHAGIC-FEVER WITH RENAL SYNDROME (HFRS) VIRUS IN THE LUNGS OF BANK VOLES CLETHRIONOMYS-GLAREOLUS AND REDBACKED VOLES CLETHRIONOMYS-RUTILUS TRAPPED IN HFRS FOCI IN THE EUROPEAN PART OF USSR AND SERODIAGNOSIS OF THIS INFECTION IN MAN [J].
CHUMAKOV, MP ;
GAVRILOVSKAYA, IN ;
BOIKO, VA ;
ZAKHAROVA, MA ;
MYASNIKOV, YA ;
BASHKIREV, TA ;
APEKINA, NS ;
SAFIULLIN, RS ;
POTAPOV, VS .
ARCHIVES OF VIROLOGY, 1981, 69 (3-4) :295-300
[6]   A LEAST-SQUARES ALGORITHM FOR FITTING ADDITIVE TREES TO PROXIMITY DATA [J].
DESOETE, G .
PSYCHOMETRIKA, 1983, 48 (04) :621-626
[7]  
ELLIOTT RM, 1991, CURR TOP MICROBIOL, V169, P91
[8]   DETERMINATION OF THE CODING CAPACITY OF THE M-GENOME SEGMENT OF NEPHROPATHIA EPIDEMICA VIRUS-STRAIN HALLNAS B1 BY MOLECULAR-CLONING AND NUCLEOTIDE-SEQUENCE ANALYSIS [J].
GIEBEL, LB ;
STOHWASSER, R ;
ZOLLER, L ;
BAUTZ, EKF ;
DARAI, G .
VIROLOGY, 1989, 172 (02) :498-505
[9]   RAPID DIAGNOSIS OF HANTAVIRUS DISEASE WITH AN IGG-AVIDITY ASSAY [J].
HEDMAN, K ;
VAHERI, A ;
BRUMMERKORVENKONTIO, M .
LANCET, 1991, 338 (8779) :1353-1356
[10]  
LEE HW, 1990, ARCH VIROL S, V1, P5