A 22-mer primer enhances discriminatory power of AP-PCR fingerprinting technique in characterization of leptospires

被引:8
作者
Roy, S [1 ]
Biswas, D [1 ]
Vijayachari, P [1 ]
Sugunan, AP [1 ]
Sehgal, SC [1 ]
机构
[1] Reg Med Res Ctr, Indian Council Med Res, WHO Collaborating Ctr Diag Res Training & Referen, Port Blair, India
关键词
Leptospira; arbitrarily primed-polymerase chain reaction; characterization; discrimination;
D O I
10.1111/j.1365-3156.2004.01322.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
OBJECTIVES To evaluate the discriminatory power and usefulness of arbitrarily primed-polymerase chain reaction (AP-PCR) characterization of leptospires with M16 primer. METHODS AP-PCR fingerprints of 20 reference strains of Leptospira representing 20 different serovars belonging to seven genospecies (Leptospira interrogans, 11; L. noguchii, 2; L. borgpetersenii, 1; L. santarosai, 2; L. biflexa, 2; L. kirschneri, 1; L. weilii, 1) were generated by employing M16 primer. Fingerprints generated with this primer were compared with those generated with two other commonly used primers PB1, and L10. An attempt was also made to type 20 leptospiral isolates with the M16 primer. RESULTS AND CONCLUSION Fingerprints with M16 primer could not only differentiate between strains of different genospecies, but also between strains of the same genospecies belonging to different serovars. While two commonly used primers (PB1 and L10) failed to discriminate between some of the different serovars belonging to the same genospecies, this primer was able to generate discriminatory fingerprints for all strains tested. All 20 Leptospira isolates, recovered from patients in Andaman Islands, could also be typed by fingerprints generated with the M16 primer. The discriminatory power of M16 primer adds more specificity to the rapidity of this system of characterization and can be used as an excellent tool in epidemiological studies on Leptospira.
引用
收藏
页码:1203 / 1209
页数:7
相关论文
共 20 条
[1]   THE INFERENCE OF EVOLUTIONARY TREES FROM MOLECULAR-DATA [J].
BEANLAND, TJ ;
HOWE, CJ .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1992, 102 (04) :643-659
[2]   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
[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]   IMPROVED MICROTECHNIQUE FOR LEPTOSPIRAL MICROSCOPIC AGGLUTINATION TEST [J].
COLE, JR ;
SULZER, CR ;
PURSELL, AR .
APPLIED MICROBIOLOGY, 1973, 25 (06) :976-980
[5]   RAPID IDENTIFICATION OF SOME LEPTOSPIRA ISOLATES FROM CATTLE BY RANDOM AMPLIFIED POLYMORPHIC DNA-FINGERPRINTING [J].
CORNEY, BG ;
COLLEY, J ;
DJORDJEVIC, SP ;
WHITTINGTON, R ;
GRAHAM, GC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (11) :2927-2932
[6]   Simplified analysis of pathogenic leptospiral serovars by random amplified polymorphic DNA fingerprinting [J].
Corney, BG ;
Colley, J ;
Graham, GC .
JOURNAL OF MEDICAL MICROBIOLOGY, 1997, 46 (11) :927-932
[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]   Leptospirosis [J].
Levett, PN .
CLINICAL MICROBIOLOGY REVIEWS, 2001, 14 (02) :296-+
[9]   Reemerging leptospirosis, California [J].
Meites, E ;
Jay, MT ;
Deresinski, S ;
Shieh, WJ ;
Zaki, SR ;
Tompkins, L ;
Smith, DS .
EMERGING INFECTIOUS DISEASES, 2004, 10 (03) :406-412
[10]  
Natarajaseenivasan K, 2000, INDIAN J ANIM SCI, V70, P551