Differentiation of Leptospira interrogans isolates by IS1500 hybridization and PCR assays

被引:49
作者
Zuerner, RL
Bolin, CA
机构
关键词
D O I
10.1128/JCM.35.10.2612-2617.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Genetic variability among Leptospira interrogans (sensu stricto) serovars was assessed by Southern blot hybridization and PCR analyses. The experiments used probes directed to sequences in a recently described insertion element, IS1500. Hybridization analysis showed that IS1500 was present on polymorphic fragments and that differences in these patterns could be used to identify serovars. Hybridization analysis was also useful in discriminating between serovar pomona type kennewicki isolates, making possible the identification of 15 previously unrecognized genetic groups. A PCR assay was developed in which the primers are positioned near the terminal inverted repeats of the element and directed outward. This assay yielded characteristic amplification patterns from isolates, allowing them to be identified. We applied these assays to several new animal isolates of L. interrogans from Nicaragna, which recently had an outbreak of human leptospirosis. Three groups of isolates were identified: one strain of serovar pomona type kennewicki and two genetically distinct groups of isolates which may be genetic intermediates between serovars canicola and portlandvere. The IS-based typing assays described should be useful for epidemiological analysis of leptospirosis.
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页码:2612 / 2617
页数:6
相关论文
共 34 条
[1]   Correlation between DNA restriction fragment length polymorphisms in Leptospira interrogans serovar pomona type kennewicki and host animal source [J].
Bolin, CA ;
Zuerner, RL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (02) :424-425
[2]  
BOLIN CA, 1994, P 8 M EUR LEPT WORK, P41
[3]   IS1500, AN IS3-LIKE ELEMENT FROM LEPTOSPIRA-INTERROGANS [J].
BOURSAUXEUDE, C ;
SAINTGIRONS, I ;
ZUERNER, R .
MICROBIOLOGY-UK, 1995, 141 :2165-2173
[4]   PREVALENCE AND SEROVARS OF LEPTOSPIRA INVOLVED IN EQUINE ABORTIONS IN CENTRAL KENTUCKY DURING THE 1991-1993 FOALING SEASONS [J].
DONAHUE, JM ;
SMITH, BJ ;
POONACHA, KB ;
DONAHOE, JK ;
RIGSBY, CL .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 1995, 7 (01) :87-91
[5]  
DWYER AE, 1995, J AM VET MED ASSOC, V207, P1327
[6]  
ELLINGHAUSEN HC, 1965, AM J VET RES, V26, P45
[7]   DETECTION OF 7 SPECIES OF PATHOGENIC LEPTOSPIRES BY PCR USING 2 SETS OF PRIMERS [J].
GRAVEKAMP, C ;
VANDEKEMP, H ;
FRANZEN, M ;
CARRINGTON, D ;
SCHOONE, GJ ;
VANEYS, GJJM ;
EVERARD, COR ;
HARTSKEERL, RA ;
TERPSTRA, WJ .
JOURNAL OF GENERAL MICROBIOLOGY, 1993, 139 :1691-1700
[8]   PULSED-FIELD GEL-ELECTROPHORESIS OF NOTI DIGESTS OF LEPTOSPIRAL DNA - A NEW RAPID METHOD OF SEROVAR IDENTIFICATION [J].
HERRMANN, JL ;
BELLENGER, E ;
PEROLAT, P ;
BARANTON, G ;
SAINTGIRONS, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (07) :1696-1702
[9]   GENOME CONSERVATION IN ISOLATES OF LEPTOSPIRA-INTERROGANS [J].
HERRMANN, JL ;
BARIL, C ;
BELLENGER, E ;
PEROLAT, P ;
BARANTON, G ;
SAINTGIRONS, I .
JOURNAL OF BACTERIOLOGY, 1991, 173 (23) :7582-7588
[10]   DIFFERENTIATION OF PATHOGENIC AND SAPROPHYTIC LEPTOSPIRES .I. GROWTH AT LOW TEMPERATURES [J].
JOHNSON, RC ;
HARRIS, VG .
JOURNAL OF BACTERIOLOGY, 1967, 94 (01) :27-&