Three species of Borrelia burgdorferi sensu late (B-burgdorferi sensu stricto, B-afzelii, and B-garinii) identified from cerebrospinal fluid isolates by pulsed-field gel electrophoresis and PCR

被引:86
作者
Busch, U
HizoTeufel, C
Boehmer, R
Fingerle, V
Nitschko, H
Wilske, B
PreacMursic, V
机构
关键词
D O I
10.1128/JCM.34.5.1072-1078.1996
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A total of 36 European Borrelia burgdorferi sensu lato cerebrospinal fluid isolates (mainly from southern Germany) were analyzed by pulsed-field gel electrophoresis (PFGE) for large restriction fragment pattern (LRFP) and linear plasmid profiles. Analyzing this large panel of isolates, me detected all three species of B. burgdorferi sensu late pathogenic for humans in cerebrospinal fluid from patients with Lyme neuroborreliosis by PFGE typing after MluI digestion: 21 B. garinii (58%), 10 B. afzelii (28%), and 4 B. burgdorferi sensu stricto (11%) strains as well as 1 isolate with bands characteristic of both B. afzelii and B. garinii. Species classification by PFGE typing was confirmed by 16S rRNA-specific PCR. Eighteen isolates (11 B. garinii, 6 a B, afzelii, and 1 B. burgdorferi sensu stricto isolate) were further characterized by LRFP with four different restriction enzymes (ApaI, KspI, SmaI, and KhoI). All B. afzelii isolates showed identical patterns for each restriction enzyme group. Considerable heterogeneity was demonstrated within the B. garinii group. Subsequent analysis of plasmid profiles revealed only marginal differences for B. afzelii strains but different patterns for B. garinii isolates. In one B. afzelii strain we found a linear plasmid of about 110 kbp not described before. LRFP analysis by PFGE is a suitable tool for the molecular characterization of B. borgdorferi sensu late strains and allows determination not only of the species but also of the subtypes within B. garinii.
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页码:1072 / 1078
页数:7
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共 65 条
[1]   CHRONIC NEUROLOGIC MANIFESTATIONS OF ERYTHEMA MIGRANS BORRELIOSIS [J].
ACKERMANN, R ;
REHSEKUPPER, B ;
GOLLMER, E ;
SCHMIDT, R .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1988, 539 :16-23
[2]   EVIDENCE FOR THE INVOLVEMENT OF DIFFERENT GENOSPECIES OF BORRELIA IN THE CLINICAL OUTCOME OF LYME-DISEASE IN BELGIUM [J].
ANTHONISSEN, FM ;
DEKESEL, M ;
HOET, PP ;
BIGAIGNON, GH .
RESEARCH IN MICROBIOLOGY, 1994, 145 (04) :327-331
[3]   WESTERN-BLOT-ANALYSIS OF SERA FROM LYME BORRELIOSIS PATIENTS ACCORDING TO THE GENOMIC SPECIES OF THE BORRELIA STRAINS USED AS ANTIGENS [J].
ASSOUS, MV ;
POSTIC, D ;
PAUL, G ;
NEVOT, P ;
BARANTON, G .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1993, 12 (04) :261-268
[4]   BORRELIA-BURGDORFERI SHOWS SPECIFICITY OF BINDING TO GLYCOSPHINGOLIPIDS [J].
BACKENSON, PB ;
COLEMAN, JL ;
BENACH, JL .
INFECTION AND IMMUNITY, 1995, 63 (08) :2811-2817
[5]   ASSOCIATION BETWEEN DIFFERENT CLINICAL MANIFESTATIONS OF LYME-DISEASE AND DIFFERENT SPECIES OF BORRELIA-BURGDORFERI SENSU LATO [J].
BALMELLI, T ;
PIFFARETTI, JC .
RESEARCH IN MICROBIOLOGY, 1995, 146 (04) :329-340
[6]   DELINEATION OF BORRELIA-BURGDORFERI SENSU-STRICTO, BORRELIA-GARINII SP-NOV, AND GROUP VS461 ASSOCIATED WITH LYME BORRELIOSIS [J].
BARANTON, G ;
POSTIC, D ;
SAINTGIRONS, I ;
BOERLIN, P ;
PIFFARETTI, JC ;
ASSOUS, M ;
GRIMONT, PAD .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1992, 42 (03) :378-383
[7]   PLASMID ANALYSIS OF BORRELIA-BURGDORFERI, THE LYME-DISEASE AGENT [J].
BARBOUR, AG .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (03) :475-478
[8]   GENOMIC FINGERPRINTING OF BORRELIA-BURGDORFERI SENSU-LATO BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
BELFAIZA, J ;
POSTIC, D ;
BELLENGER, E ;
BARANTON, G ;
STGIRONS, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (11) :2873-2877
[9]   MOLECULAR ANALYSIS OF LINEAR PLASMID-ENCODED MAJOR SURFACE-PROTEINS, OSPA AND OSPB, OF THE LYME-DISEASE SPIROCHETE BORRELIA-BURGDORFERI [J].
BERGSTROM, S ;
BUNDOC, VG ;
BARBOUR, AG .
MOLECULAR MICROBIOLOGY, 1989, 3 (04) :479-486
[10]   EXTRACHROMOSOMAL ELEMENTS OF SPIROCHETES [J].
BERGSTROM, S ;
GARON, CF ;
BARBOUR, AG ;
MACDOUGALL, J .
RESEARCH IN MICROBIOLOGY, 1992, 143 (06) :623-628