Identification and DNA fingerprinting of Legionella strains by randomly amplified polymorphic DNA analysis

被引:22
作者
Bansal, NS
McDonell, F
机构
关键词
D O I
10.1128/JCM.35.9.2310-2314.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Thf randomly amplified polymorphic DNA (RAPD) technique mas used in the development of a fingerprinting (typing) and identification protocol for Legionella strains. Twenty decamer random oligonucleotide primers were screened for their discriminatory abilities, Two candidate primers were selected. By using a combination of these primers, RAPD analysis allowed for the differentiation between ail different species, between the serogroups, and further differentiation between subtypes of the same serogroup. The usefulness of RAPD analysis mas also evaluated with outbreak-related clinical and environmental isolates previously typed by the restriction fragment length polymorphism technique, RAPD analysis proved to be as accurate as other genotypic methods, reproducible, and highly discriminatory and is a valuable new-alternative to traditional fingerprinting and identification of Legionella species and strains.
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页码:2310 / 2314
页数:5
相关论文
共 18 条
[1]  
BASSAM BJ, 1992, APPL MICROBIOL BIOT, V38, P70, DOI 10.1007/BF00169422
[2]   MOLECULAR FINGERPRINTING OF LEGIONELLA SPECIES BY REPETITIVE ELEMENT PCR [J].
GEORGHIOU, PR ;
DOGGETT, AM ;
KIELHOFNER, MA ;
STOUT, JE ;
WATSON, DA ;
LUPSKI, JR ;
HAMILL, RJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (12) :2989-2994
[3]   Molecular typing of nosocomial strains of Legionella pneumophila by arbitrarily primed PCR [J].
Grattard, F ;
Berthelot, P ;
Reyrolle, M ;
Ros, A ;
Etienne, J ;
Pozzetto, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (06) :1595-1598
[4]   HYDROXY-FATTY ACID PROFILES OF LEGIONELLA SPECIES - DIAGNOSTIC USEFULNESS ASSESSED BY PRINCIPAL COMPONENT ANALYSIS [J].
JANTZEN, E ;
SONESSON, A ;
TANGEN, T ;
ENG, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (06) :1413-1419
[5]   DISCRIMINATORY GENOMIC FINGERPRINTING OF LEGIONELLA-PNEUMOPHILA BY PULSED-FIELD ELECTROPHORESIS [J].
JOHNSON, WM ;
BERNARD, K ;
MARRIE, TJ ;
TYLER, SD .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (10) :2620-2621
[6]   DEVELOPMENT OF A STANDARDIZED SUBGROUPING SCHEME FOR LEGIONELLA-PNEUMOPHILA SEROGROUP-1 USING MONOCLONAL-ANTIBODIES [J].
JOLY, JR ;
MCKINNEY, RM ;
TOBIN, JO ;
BIBB, WF ;
WATKINS, ID ;
RAMSAY, D .
JOURNAL OF CLINICAL MICROBIOLOGY, 1986, 23 (04) :768-771
[7]   GENETIC-CHARACTERIZATION OF LEGIONELLA-PNEUMOPHILA SEROGROUP-1 ASSOCIATED WITH RESPIRATORY-DISEASE IN AUSTRALIA [J].
LANSER, J ;
ADAMS, M ;
DOYLE, R ;
HEWITT, P ;
SANGSTER, N .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1992, 58 (02) :706-708
[8]   ELECTROPHORETIC CHARACTERIZATION OF SOLUBLE-PROTEIN EXTRACTS OF LEGIONELLA-PNEUMOPHILA AND OTHER MEMBERS OF THE FAMILY LEGIONELLACEAE [J].
LEMA, M ;
BROWN, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1983, 17 (06) :1132-1140
[9]   SUBTYPING OF LEGIONELLA-PNEUMOPHILA SEROGROUP-1 ISOLATES BY MONOCLONAL-ANTIBODY AND PLASMID TECHNIQUES [J].
MAHER, WE ;
PARA, MF ;
PLOUFFE, JF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (12) :2281-2284
[10]  
MATSIOTABERNARD P, 1994, FEMS IMMUNOL MED MIC, V9, P23