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1.
J Clin Microbiol ; 41(4): 1617-22, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12682153

ABSTRACT

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.


Subject(s)
Molecular Epidemiology , Salmonella enteritidis/classification , Salmonella enteritidis/genetics , Animals , Bacterial Typing Techniques , Bacteriophage Typing , Chile/epidemiology , Electrophoresis, Gel, Pulsed-Field , Food Microbiology , Genetic Variation , Humans , Phylogeny , Poultry , Poultry Diseases/epidemiology , Poultry Diseases/microbiology , Salmonella Infections/epidemiology , Salmonella Infections/microbiology , Salmonella Infections, Animal/microbiology , Serotyping
2.
Expert Rev Mol Diagn ; 3(1): 105-15, 2003 Jan.
Article in English | MEDLINE | ID: mdl-12528368

ABSTRACT

Shiga toxin-producing Escherichia coli are emerging as a significant source of food-borne infectious disease all over the world. Illness caused by Shiga toxin-producing E. coli can range from self limited, watery diarrhea to life-threatening manifestations such as hemorrhagic colitis, hemolytic uremic syndrome or thrombotic thrombocytopenic purpura and death. Shiga toxin-producing E. coli can potentially enter the human food chain from a number of animal sources, most commonly by contamination of meat with feces or intestinal contents after slaughter or cross-contamination of unpasteurized milk products. Because of the low infectious dose of the O157:H7 Shiga toxin-producing E. coli strain, laboratory diagnosis of Shiga toxin-producing E. coli in food samples has developed a great importance. This review will focus on the microorganism, giving priority to illness prevention and Shiga toxin-producing E. coli detection in food.


Subject(s)
Escherichia coli O157/isolation & purification , Escherichia coli/isolation & purification , Food Microbiology , Genetic Techniques , Shiga Toxin 1/metabolism , Shiga Toxin 2/metabolism , Animals , DNA Probes , Enzyme-Linked Immunosorbent Assay , Escherichia coli/genetics , Escherichia coli/metabolism , Escherichia coli O157/metabolism , Genes, Bacterial , Humans , Nucleic Acid Hybridization , Oligonucleotide Probes , Polymerase Chain Reaction , Reverse Transcriptase Polymerase Chain Reaction , Shiga Toxin 1/isolation & purification , Shiga Toxin 2/isolation & purification
6.
Bol. Cient. Asoc. Chil. Segur ; 2(3): 4-10, jun. 2000. ilus, tab, graf
Article in Spanish | LILACS | ID: lil-318079

ABSTRACT

Chile ha experimentado un cambio epidemiológico en la última década con la desaparición progresiva de la fiebre tifoidea, causada mayoritariamente por Salmonella Typhi y la emergencia epidémica de Salmonella Enteritidis, un agente de diarrea sin tratamiento antibiótico eficaz y ligado estrechamente a productos avícolas contaminados e inadecuadamente preparados. La fiebre tifoidea ha disminuido su importancia debido al desarrollo humano experimentado en Chile con un alto grado de cobertura de agua potable y de manejo de excretas que, en conjunto con un mayor nivel de educación, han limitado la contaminación del ambiente por este agente y la adquisición de él por huéspedes susceptibles. A pesar de este notable avance, un nuevo serotipo de Salmonella ha irrumpido en Chile, denominado Enteritidis, que ha logrado aprovechar el nuevo escenario obtenido con la industrialización avícola donde miles de aves convivenen pequeños espacios, facilitando la infección cruzada entre ellas. La contaminación intermitente de huevos, ya sea por vía transovárica o superficial, ha permitido la llegada de este agente en forma errática, pero persistente al ser humano. Este nuevo panorama obliga a que nuestro país adopte estrategias de prevención que involucran a productores, distribuidores y consumidores de productos avícolas


Subject(s)
Humans , Salmonella Food Poisoning/epidemiology , Salmonella enteritidis , Salmonella Infections , Typhoid Fever , Chile , Salmonella Food Poisoning/prevention & control , Salmonella Infections
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