COMPARATIVE-STUDY OF 5 DIFFERENT DNA FINGERPRINT TECHNIQUES FOR MOLECULAR TYPING OF STREPTOCOCCUS-PNEUMONIAE STRAINS

被引:122
作者
HERMANS, PWM
SLUIJTER, M
HOOGENBOEZEM, T
HEERSMA, H
VANBELKUM, A
DEGROOT, R
机构
[1] ERASME UNIV HOSP,DEPT CLIN MICROBIOL,3000 DR ROTTERDAM,NETHERLANDS
[2] NATL INST PUBL HLTH & ENVIRONM PROTECT,MOLEC MICROBIOL UNIT,3720 BA BILTHOVEN,NETHERLANDS
关键词
D O I
10.1128/JCM.33.6.1606-1612.1995
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The aim of this study was to identify the strengths and weaknesses of five DNA fingerprint methods for epidemiological typing of Streptococcus pneumoniae, We investigated the usefulness of (i) ribotyping, (ii) BOX fingerprinting with the BOX repetitive sequence of S, pneumoniae as a DNA probe, (iii) PCR fingerprinting with a primer homologous to the enterobacterial repetitive intergenic consensus sequence, (iv) pulsed-field gel electrophoresis of large DNA fragments, and (v) restriction fragment end labeling to detect restriction fragment length polymorphism of small DNA fragments, Twenty-eight S. pneumoniae strains isolated from the blood and/or cerebrospinal fluid of 21 patients were analyzed, Genetic clustering among the 28 strains was independent of the DNA fingerprint technique used, However, the discriminatory power and the similarity values differed significantly among the individual techniques. BOX fingerprinting, pulsed-field gel electrophoresis, and restriction fragment end labeling provided the highest degree of discriminatory power, Furthermore, the ease with which computerized fingerprint analysis could be conducted also varied significantly among the techniques. Ribotyping, BOX fingerprinting, and restriction fragment end labeling were very suitable techniques for accurate computerized data analysis. Because of their high discriminatory potential and ease of accurate analysis, we conclude that BOX fingerprinting and restriction fragment end labeling are the most suitable techniques to type pneumococcal strains.
引用
收藏
页码:1606 / 1612
页数:7
相关论文
共 26 条
[1]   A CLUSTER OF INVASIVE PNEUMOCOCCAL DISEASE IN YOUNG-CHILDREN IN CHILD-CARE [J].
CHERIAN, T ;
STEINHOFF, MC ;
HARRISON, LH ;
ROHN, D ;
MCDOUGAL, LK ;
DICK, J .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (09) :695-697
[2]   HORIZONTAL TRANSFER OF PENICILLIN-BINDING PROTEIN GENES IN PENICILLIN-RESISTANT CLINICAL ISOLATES OF STREPTOCOCCUS-PNEUMONIAE [J].
DOWSON, CG ;
HUTCHISON, A ;
BRANNIGAN, JA ;
GEORGE, RC ;
HANSMAN, D ;
LINARES, J ;
TOMASZ, A ;
SMITH, JM ;
SPRATT, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8842-8846
[3]  
FENOLL A, 1991, REV INFECT DIS, V13, P56
[4]  
FINLAND M, 1982, BACTERIAL INFECTIONS, P417
[5]  
HERMANS PE, UNPUB
[6]   INSERTION ELEMENT IS987 FROM MYCOBACTERIUM-BOVIS BCG IS LOCATED IN A HOT-SPOT INTEGRATION REGION FOR INSERTION ELEMENTS IN MYCOBACTERIUM-TUBERCULOSIS COMPLEX STRAINS [J].
HERMANS, PWM ;
VANSOOLINGEN, D ;
BIK, EM ;
DEHAAS, PEW ;
DALE, JW ;
VANEMBDEN, JDA .
INFECTION AND IMMUNITY, 1991, 59 (08) :2695-2705
[7]   MOLECULAR EPIDEMIOLOGY OF PENICILLIN-RESISTANT PNEUMOCOCCI ISOLATED IN NAIROBI, KENYA [J].
KELL, CM ;
JORDENS, JZ ;
DANIELS, M ;
COFFEY, TJ ;
BATES, J ;
PAUL, J ;
GILKS, C ;
SPRATT, BG .
INFECTION AND IMMUNITY, 1993, 61 (10) :4382-4391
[8]   INCREASING PENICILLIN RESISTANCE IN PNEUMOCOCCI IN ICELAND [J].
KRISTINSSON, KG ;
HJALMARSDOTTIR, MA ;
STEINGRIMSSON, O .
LANCET, 1992, 339 (8809) :1606-1607
[9]   DNA-FINGERPRINTING OF STREPTOCOCCUS-PNEUMONIAE STRAINS BY PULSED-FIELD GEL-ELECTROPHORESIS [J].
LEFEVRE, JC ;
FAUCON, G ;
SICARD, AM ;
GASC, AM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (10) :2724-2728
[10]  
Lund E., 1978, METHOD MICROBIOL, P1241