GENOMIC FINGERPRINTING OF CLOSTRIDIUM-DIFFICILE ISOLATES BY USING A RANDOM AMPLIFIED POLYMORPHIC DNA (RAPD) ASSAY

被引:40
作者
BARBUT, F
MARIO, N
DELMEE, M
GOZIAN, J
PETIT, JC
机构
[1] UNIV CATHOLIQUE LOUVAIN,UNITE MICROBIOL,B-1200 BRUSSELS,BELGIUM
[2] HOP ST ANTOINE,COMMUN BIOL MOLEC LAB,F-75571 PARIS 12,FRANCE
关键词
CLOSTRIDIUM-DIFFICILE; RAPD ASSAY; GENETIC MARKER;
D O I
10.1016/0378-1097(93)90513-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
This study describes the use of a new and easy method called random amplified polymorphic DNA (RAPD) assay to distinguish strains of C. difficile. We used two single short primers (AP4 and AP5) with arbitrary nucleotide sequences in a polymerase chain reaction to amplify genomic DNA. The profiles observed after electrophoretic separation were able to distinguish 20 reference C difficile strains previously serotyped by Delmee's method. The fingerprints of 11 epidemiologically unrelated C. difficile strains clearly yielded a DNA polymorphism between all the strains. Latterly, RAPD profiles of 11 C difficile strains isolated from 2 independant suspected outbreaks showed, in each case, a predominant banding pattern correponding to an epidemic strain. These results suggest that RAPD assay could be a valuable tool for epidemiological studies.
引用
收藏
页码:161 / 166
页数:6
相关论文
共 15 条
[1]   CLINICAL AND LABORATORY OBSERVATIONS IN CLOSTRIDIUM DIFFICILE COLITIS [J].
BARTLETT, JG ;
TAYLOR, NS ;
CHANG, TW ;
DZINK, JA .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1980, 33 (11) :2521-2526
[2]   PRESENCE OF CLOSTRIDIUM-DIFFICILE AND ANTIBIOTIC AND BETA-LACTAMASE ACTIVITIES IN FECES OF VOLUNTEERS TREATED WITH ORAL CEFIXIME, ORAL CEFPODOXIME PROXETIL, OR PLACEBO [J].
CHACHATY, E ;
DEPITRE, C ;
MARIO, N ;
BOURNEIX, C ;
SAULNIER, P ;
CORTHIER, G ;
ANDREMONT, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (09) :2009-2013
[3]  
DELMEE M, 1986, J CLIN MICROBIOL, V24, P991
[4]   SEROGROUPING OF CLOSTRIDIUM-DIFFICILE STRAINS BY SLIDE AGGLUTINATION [J].
DELMEE, M ;
HOMEL, M ;
WAUTERS, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 1985, 21 (03) :323-327
[5]   APPLICATION OF WHOLE-CELL DNA RESTRICTION ENDONUCLEASE PROFILES TO THE EPIDEMIOLOGY OF CLOSTRIDIUM-DIFFICILE-INDUCED DIARRHEA [J].
KUIJPER, EJ ;
OUDBIER, JH ;
STUIFBERGEN, WNHM ;
JANSZ, A ;
ZANEN, HC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1987, 25 (04) :751-753
[6]  
LUS PG, 1993, J CLIN MICROBIOL, V31, P1940
[7]   DEVELOPMENT AND APPLICATION OF A MULTIPLE TYPING SYSTEM FOR CLOSTRIDIUM-DIFFICILE [J].
MAHONY, DE ;
CLOW, J ;
ATKINSON, L ;
VAKHARIA, N ;
SCHLECH, WF .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (07) :1873-1879
[8]   DNA sequence of the insertional hot spot of Tn916 in the Clostridium difficile genome and discovery of a Tn916-like element in an environmental isolate integrated in the same hot spot [J].
Wang, HM ;
Roberts, AP ;
Mullany, P .
FEMS MICROBIOLOGY LETTERS, 2000, 192 (01) :15-20
[9]   DNA FRAGMENT LENGTH POLYMORPHISM ANALYSIS OF MYCOBACTERIUM-TUBERCULOSIS ISOLATES BY ARBITRARILY PRIMED POLYMERASE CHAIN-REACTION [J].
PALITTAPONGARNPIM, P ;
CHOMYC, S ;
FANNING, A ;
KUNIMOTO, D .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (04) :975-978
[10]   RANDOM AMPLIFIED POLYMORPHIC DNA ASSAY IS LESS DISCRIMINANT THAN PULSED-FIELD GEL-ELECTROPHORESIS FOR TYPING STRAINS OF METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
SAULNIER, P ;
BOURNEIX, C ;
PREVOST, G ;
ANDREMONT, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (04) :982-985