Pulsed-field gel electrophoresis subtyping database for foodborne Salmonella enterica serotype discrimination

被引:56
作者
Kerouanton, Annaelle
Marault, Muriel
Lailler, Renaud
Weill, Francois-Xavier
Feurer, Carole
Espie, Emmanuelle
Brisabois, Anne
机构
[1] Agence Francaise Secur Sanitaire Aliments, Lab Etudes Rech Qual Aliments Proc Agro Aliments, Unite Caracterisat Epidemiol Bacterienne, F-94706 Maisons Alfort, France
[2] Inst Pasteur, Ctr Natl Reference Salmonella, Paris, France
[3] Antennes Maisons Alfort, Inst Filiere Porcine, Maisons Alfort, France
[4] Inst Veille Sanitaire, St Maurice, France
关键词
D O I
10.1089/fpd.2007.0090
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Nontyphoid Salmonella is one of the main causes of bacterial gastroenteritis worldwide and is responsible for 65% of reported outbreaks of foodborne diseases in France. Serotyping is widely used for isolate preliminary identification, but it poorly discriminates strains. Rapid, efficient molecular subtyping tools have therefore been developed for the investigation of outbreaks. We evaluated the performance of the pulsed-field gel electrophoresis (PFGE) method for discrimination of 31 Salmonella serotypes frequently isolated in France. We set up a genomic database of Salmonella strains isolated from food, animals, the environment, and humans to improve the management of contamination and reactions to foodborne disease outbreaks. We studied 1128 isolates by PFGE, according to the standardized PulseNet protocol. We identified 452 PFGE patterns, 67.5% of which corresponded to a single isolate. The ability of this method to distinguish between isolates was estimated by calculating the Simpson index and the 95% confidence interval. Values obtained ranged between 0.33 (0.11-0.54) to 0.99 (0.96-1.00), depending on serotype. Epidemiological information about isolates was used for analyses of intra- and interserotype diversity results and for determining whether PFGE patterns were linked to the source of the isolate. Clustering analysis of the PFGE patterns obtained confirmed that serotype and PFGE genotype were closely linked. Some PFGE patterns were identified as major patterns, each of these patterns being found in at least 10 isolates. The database generated has already proved its effectiveness in epidemiological investigations in livestock production and foodborne outbreaks.
引用
收藏
页码:293 / 303
页数:11
相关论文
共 46 条
[1]  
Aarts HJM, 1998, LETT APPL MICROBIOL, V26, P131, DOI 10.1046/j.1472-765X.1998.00302.x
[2]   BACTERIOPHAGE-TYPING DESIGNATIONS OF SALMONELLA-TYPHIMURIUM [J].
ANDERSON, ES ;
WARD, LR ;
DESAXE, MJ ;
DESA, JDH .
JOURNAL OF HYGIENE, 1977, 78 (02) :297-300
[3]   Interpretation of pulsed-field gel electrophoresis patterns in foodborne disease investigations and surveillance [J].
Barrett, TJ ;
Gerner-Smidt, P ;
Swaminathan, B .
FOODBORNE PATHOGENS AND DISEASE, 2006, 3 (01) :20-31
[4]   Epidemiological analysis of Salmonella enterica ssp enterica serovars Hadar, Brancaster and Enteritidis from humans and broiler chickens in Senegal using pulsed-field gel electrophoresis and antibiotic susceptibility [J].
Cardinale, E ;
Gros-Claude, JDP ;
Rivoal, K ;
Rose, V ;
Tall, F ;
Mead, GC ;
Salvat, G .
JOURNAL OF APPLIED MICROBIOLOGY, 2005, 99 (04) :968-977
[5]   An outbreak of multidrug-resistant Salmonella enterica serotype Newport infections linked to the consumption of imported horse meat in France [J].
Espié, E ;
De Valk, H ;
Vaillant, V ;
Quelquejeu, N ;
Le Querrec, F ;
Weill, FX .
EPIDEMIOLOGY AND INFECTION, 2005, 133 (02) :373-376
[6]  
ESPIE E, 2005, EURO SURVEIL, V10
[7]   Suitability of PCR fingerprinting, infrequent-restriction-site PCR, and pulsed-field gel electrophoresis, combined with computerized gel analysis, in library typing of Salmonella enterica serovar enteritidis [J].
Garaizar, J ;
López-Molina, N ;
Laconcha, I ;
Baggesen, DL ;
Rementeria, A ;
Vivanco, A ;
Audicana, A ;
Perales, I .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (12) :5273-5281
[8]   Distribution of molecular subtypes within Salmonella enterica serotype Enteritidis phage type 4 and S. Typhimurium definitive phage type 104 in nine European countries, 2000-2004:: results of an international multi-centre study [J].
Gatto, A. J. ;
Peters, T. M. ;
Green, J. ;
Fisher, I. S. T. ;
Gill, O. N. ;
O'Brien, S. J. ;
Maguire, C. ;
Berghold, C. ;
Lederer, I. ;
Gerner-Smidt, P. ;
Torpdahl, M. ;
Siitonen, A. ;
Lukinmaa, S. ;
Tschaepe, H. ;
Prager, R. ;
Luzzi, I. ;
Dionisi, A. M. ;
van der Zwaluw, W. K. ;
Heck, M. ;
Coia, J. ;
Brown, D. ;
Usera, M. ;
Echeita, A. ;
Threlfall, E. J. .
EPIDEMIOLOGY AND INFECTION, 2006, 134 (04) :729-736
[9]   Determining confidence intervals when measuring genetic diversity and the discriminatory abilities of typing methods for microorganisms [J].
Grundmann, H ;
Hori, S ;
Tanner, G .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (11) :4190-4192
[10]   COMPARISON OF PLASMID PROFILE ANALYSIS, PHAGE TYPING, AND ANTIMICROBIAL SUSCEPTIBILITY TESTING IN CHARACTERIZING SALMONELLA-TYPHIMURIUM ISOLATES FROM OUTBREAKS [J].
HOLMBERG, SD ;
WACHSMUTH, IK ;
HICKMANBRENNER, FW ;
COHEN, ML .
JOURNAL OF CLINICAL MICROBIOLOGY, 1984, 19 (02) :100-104