A clone of Leptospira interroganssensu stricto is the major cause of leptospirosis in the archipelago of Andaman and Nicobar Islands, India

被引:10
作者
Roy, S [1 ]
Biswas, D [1 ]
Vijayachari, P [1 ]
Sugunan, AP [1 ]
Sehgal, SC [1 ]
机构
[1] Indian Council Med Res, Reg Med Res Ctr, WHO Collaborating Ctr Diag Res Training & Referen, Port Blair 744101, Andaman Nicobar, India
关键词
arbitrarily primed PCR; characterization; clone; epidemiology; identification; isolate; sequencing;
D O I
10.1111/j.1472-765X.2005.01740.x
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
Aims: Andaman and Nicobar Islands in India has a century long history of human leptospirosis. Several isolates have been recovered over the years from different locations. The present study was undertaken to understand the clonal relationship between all these pathogenic leptospires recovered from these islands. Methods and Results: Arbitrarily primed polymerase chain reaction (AP-PCR) was employed to genetically characterize 40 isolates recovered during 1995-2001 and their fingerprints were compared with those of 26 reference strains of known genetic and serological affinities. Sequences of PCR-amplified products from representative isolates were compared with those of different strains belonging to seven genospecies. AP-PCR fingerprints revealed that 32 of the 40 isolates were clonal in nature and fingerprints of all the isolates matched with known reference strains of pathogenic Leptospira interrogans sensu stricto. Comparison of sequence data of PCR amplified products of reference strains and isolates also corroborated these findings. Conclusions: The study revealed that 80% of the isolates recovered from these islands were clonal in nature and all the isolates taken in the study belonged to Leptospira interrogans sensu stricto. Significance and Impact of the Study: An extension of the study in animal population would help in understanding the transmission dynamics of this commonly circulating clone in these islands, which in turn might help in effective control of this public health problem.
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收藏
页码:179 / 185
页数:7
相关论文
共 18 条
[1]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[2]   Further determination of DNA relatedness between serogroups and serovars in the family Leptospiraceae with a proposal for Leptospira alexanderi sp. nov. and four new Leptospira genomospecies [J].
Brenner, DJ ;
Kaufmann, AF ;
Sulzer, KR ;
Steigerwalt, AG ;
Rogers, FC ;
Weyant, RS .
INTERNATIONAL JOURNAL OF SYSTEMATIC BACTERIOLOGY, 1999, 49 :839-858
[3]   Differentiation of Leptospira species and serovars by PCR-restriction endonuclease analysis, arbitrarily primed PCR and low-stringency PCR [J].
Brown, PD ;
Levett, PN .
JOURNAL OF MEDICAL MICROBIOLOGY, 1997, 46 (02) :173-181
[4]  
ELLINGHAUSEN HC, 1965, AM J VET RES, V26, P45
[5]   RANDOM AMPLIFIED POLYMORPHIC DNA-FINGERPRINTING FOR RAPID IDENTIFICATION OF LEPTOSPIRAS OF SEROGROUP SEJROE [J].
GERRITSEN, MA ;
SMITS, MA ;
OLYHOEK, T .
JOURNAL OF MEDICAL MICROBIOLOGY, 1995, 42 (05) :336-339
[6]   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
[7]   DIFFERENTIATION OF PATHOGENIC AND SAPROPHYTIC LEPTOSPIRES .I. GROWTH AT LOW TEMPERATURES [J].
JOHNSON, RC ;
HARRIS, VG .
JOURNAL OF BACTERIOLOGY, 1967, 94 (01) :27-&
[8]  
KMETY E, 1978, METHOD MICROBIOL, P260
[9]  
Pereira MM, 2000, J CLIN MICROBIOL, V38, P450
[10]   A 22-mer primer enhances discriminatory power of AP-PCR fingerprinting technique in characterization of leptospires [J].
Roy, S ;
Biswas, D ;
Vijayachari, P ;
Sugunan, AP ;
Sehgal, SC .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 2004, 9 (11) :1203-1209