ANTIGENIC AND MOLECULAR CHARACTERIZATION OF BAT RABIES VIRUS IN EUROPE

被引:132
作者
BOURHY, H [1 ]
KISSI, B [1 ]
LAFON, M [1 ]
SACRAMENTO, D [1 ]
TORDO, N [1 ]
机构
[1] INST PASTEUR MAROC, CASABLANCA, MOROCCO
关键词
D O I
10.1128/JCM.30.9.2419-2426.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The predominant role of Eptesicus serotinus in the epizootic of bat rabies in Europe was further outlined by the first isolation of the rabies virus from this species in France. The distribution of the virus was studied in naturally infected E. serotinus bats at the time of death and suggested that the papillae of the tongue and the respiratory mucosa may play a role in virus production and excretion. The analysis of 501 French rabies virus isolates from various animal species by antinucleocapsid monoclonal antibodies indicated that transmission of the disease from bats to terrestrial animals is unlikely. The antigenic profile of two isolates from French bats corresponded to that of European bat lyssavirus type 1 (EBL1). Comparisons of 12 different isolates from bats with antinucleocapsid and antiglycoprotein monoclonal antibodies and by direct sequencing of the polymerase chain reaction amplification product of the N gene indicated that EBL1, EBL2, Duvenhage virus (serotype 4 of lyssavirus), and the European fox rabies virus (serotype 1) are phylogenetically distant. They formed four tight genetic clusters named genotypes. EBL1 was shown to be antigenically and genetically more closely related to Duvenhage virus than to EBL2. We propose that EBL1 and EBL2 constitute two distinct genotypes which further serologic characterization will probably classify as new serotypes. We also report a simple method for the rapid characterization of EBL based on the digestion of the polymerase chain reaction product of the N gene by three restriction endonucleases.
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页码:2419 / 2426
页数:8
相关论文
共 42 条
[1]  
Abelseth M K, 1964, Can Vet J, V5, P84
[2]  
Baer G.M., 1975, P79
[3]  
BELL JF, 1960, P SOC EXP BIOL MED, V103, P140, DOI 10.3181/00379727-103-25438
[4]   COMPARATIVE FIELD-EVALUATION OF THE FLUORESCENT-ANTIBODY TEST, VIRUS ISOLATION FROM TISSUE-CULTURE, AND ENZYME IMMUNODIAGNOSIS FOR RAPID LABORATORY DIAGNOSIS OF RABIES [J].
BOURHY, H ;
ROLLIN, PE ;
VINCENT, J ;
SUREAU, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1989, 27 (03) :519-523
[5]   MONOCLONAL-ANTIBODIES TO MOKOLA VIRUS FOR IDENTIFICATION OF RABIES AND RABIES-RELATED VIRUSES [J].
BUSSEREAU, F ;
VINCENT, J ;
COUDRIER, D ;
SUREAU, P .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (12) :2489-2494
[6]   RABIES VIRUS IN NASAL MUCOSA OF NATURALLY INFECTED BATS [J].
CONSTANTINE, DG ;
WOODIE, JD ;
EMMONS, RW .
SCIENCE, 1972, 175 (4027) :1255-+
[7]  
CONSTANTINE DG, 1967, RABIES TRANSMISSION, P51
[8]   MOLECULAR-CLONING AND COMPLETE NUCLEOTIDE-SEQUENCE OF THE ATTENUATED RABIES VIRUS SAD-B19 [J].
CONZELMANN, KK ;
COX, JH ;
SCHNEIDER, LG ;
THIEL, HJ .
VIROLOGY, 1990, 175 (02) :485-499
[9]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]  
DIETZSCHOLD B, 1988, REV INFECT DIS, V10, pS785