Analysis of molecular epidemiology of Chilean Salmonella enterica serotype enteritidis isolates by pulsed-field gel electrophoresis and bacteriophage typing

被引:35
作者
Fernandez, J
Fica, A
Ebensperger, G
Calfullan, H
Prat, S
Fernandez, A
Alexandre, M
Heitmann, I
机构
[1] Univ Chile, Hosp Clin, Secc Infectol, Santiago, Chile
[2] Inst Salud Publ Chile, Subdept Microbiol, Santiago, Chile
[3] Inst Salud Publ Chile, Unidad Desarrollo, Santiago, Chile
[4] Serv Salud Metropolitano Ambiente, Santiago, Chile
关键词
D O I
10.1128/JCM.41.4.1617-1622.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Human Salmonella enterica serotype Enteritidis infections emerged in Chile in 1994. S. enterica serotype Enteritidis phage type 1 isolates predominated in the north, and phage type 4 isolates predominated in the central and southern regions. A study was planned to characterize this epidemic using the best discriminatory typing technique. Research involved 441 S. enterica serotype Enteritidis isolates, including clinical preepidemic samples (n=74; 1975 to 1993) and epidemic (n=199), food (n=72), poultry (n=57), and some Latin American (n=39) isolates. The best method was selected based on a sample of preepidemic isolates, analyzing the discriminatory power (DP) obtained by phage typing and randomly amplified polymorphic DNA and pulsed-field gel electophoresis (PFGE) analysis. The highest DP was associated with BlnI PFGE-bacteriophage typing analysis (0.993). A total of 38 BlnI patterns (B patterns) were identified before the epidemic period, 19 since 1994, and only 4 in both periods. Two major clusters were identified by phylogenetic analysis, and the predominant B patterns clustered in the same branch. Combined analysis revealed that specific B pattern-phage type combinations (subtypes) disappeared before 1994, that different genotypes associated with S. enterica serotype Enteritidis phage type 4 had been observed since 1988, and that strain diversity increased before the expansion of S. enterica serotype Enteritidis in 1994. Predominant subtype B3-phage type 4 was associated with the central and southern regions, and subtype B38-phage type 1 was associated with the north (P<0.0001). Food and poultry isolates matched the predominant S. enterica serotype Enteritidis subtypes, but isolates identified in neighboring countries (Peru and Bolivia) did not match S. enterica serotype Enteritidis subtypes identified in the north of Chile. The results of this work demonstrate that genetic diversity, replacement, and expansion of specific S. enterica serotype Enteritidis subtypes were associated with epidemic changes.
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页码:1617 / 1622
页数:6
相关论文
共 30 条
[1]  
Alexandre M, 2000, REV MED CHILE, V128, P1075
[2]   Emerging foodborne diseases [J].
Altekruse, SF ;
Cohen, ML ;
Swerdlow, DL .
EMERGING INFECTIOUS DISEASES, 1997, 3 (03) :285-293
[3]   Epidemiological analysis of Salmonella enteritidis isolates from humans and broiler chickens in Thailand by phage typing and pulsed-field gel electrophoresis [J].
Boonmar, S ;
Bangtrakulnonth, A ;
Pornrunangwong, S ;
Terajima, J ;
Watanabe, H ;
Kaneko, KI ;
Ogawa, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :971-974
[4]   CONSTRUCTION AND FINE MAPPING OF RECOMBINANT PLASMIDS CONTAINING THE RRNB RIBOSOMAL-RNA OPERON OF ESCHERICHIA-COLI [J].
BROSIUS, J ;
ULLRICH, A ;
RAKER, MA ;
GRAY, A ;
DULL, TJ ;
GUTELL, RR ;
NOLLER, HF .
PLASMID, 1981, 6 (01) :112-118
[5]   Pathogenicity of Salmonella enteritidis phage types 4, 8, and 23 in broiler chicks [J].
Dhillon, AS ;
Alisantosa, B ;
Shivaprasad, HL ;
Jack, O ;
Schaberg, D ;
Bandli, D .
AVIAN DISEASES, 1999, 43 (03) :506-515
[6]  
Edwards P. R., 1972, IDENTIFICATION ENTER, p[146, 208]
[7]   ANALYSIS OF SALMONELLA-ENTERITIDIS ISOLATES BY ARBITRARILY PRIMED PCR [J].
FADL, AA ;
NGUYEN, AV ;
KHAN, MI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (04) :987-989
[8]  
Fica A, 1997, REV MED CHILE, V125, P544
[9]   Epidemic typhoid in Chile: Analysis by molecular and conventional methods of Salmonella typhi strain diversity in epidemic (1977 and 1981) and nonepidemic (1990) years [J].
Fica, AE ;
PratMiranda, S ;
FernandezRicci, A ;
DOttone, K ;
Cabello, FC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (07) :1701-1707
[10]  
Fica C.A., 2001, REV CHIL INFECTOLOG, V18, P85, DOI [10.4067/S0716-10182012000200014, DOI 10.4067/S0716-10182012000200014]