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1.
Rev Argent Microbiol ; 42(4): 284-7, 2010.
Article in Spanish | MEDLINE | ID: mdl-21229199

ABSTRACT

Shiga toxin-producing Escherichia coli is an emerging foodborne pathogen. There are many STEC serotypes associated with human diseases, being the O157:H7 serotype the most prevalent. Ground beef is the main transmission vehicle. In Concepción city, Tucumán Province, between September and December 2004, two hemolytic uremic syndrome (HUS) cases were diagnosed. The main objective of this work was to detect, isolate and characterize STEC O157 and non-O157 strains in fresh ground beef. Between September and December 2004, 53 fresh ground beef samples were collected from butcher shops in Concepción city. The USDA-FSIS (2002) methodology was used for detection, isolation and characterization of STEC O157:H7. Two PCR techniques for E. coli non-O157 detection and a previous intra-laboratory validated methodology for the isolation and characterization of these strains were used. The stx2 gen was identified in seven samples and the rfbO157 gene also in four of them. However, only one E. coli O157:H7 strain, biotype C, carrying the eae, stx2 and ehxA genes, was isolated. The present study shows the importance of implementing techniques for the detection of this emerging pathogen in meat samples.


Subject(s)
Escherichia coli O157/isolation & purification , Food Contamination , Food Microbiology , Meat/microbiology , Shiga-Toxigenic Escherichia coli/isolation & purification , Adhesins, Bacterial/genetics , Animals , Argentina/epidemiology , Cattle , Endemic Diseases , Escherichia coli Proteins/genetics , Hemolysin Proteins/genetics , Hemolytic-Uremic Syndrome/epidemiology , Hemolytic-Uremic Syndrome/microbiology , Humans , Serotyping , Shiga Toxin 2/genetics , Shiga-Toxigenic Escherichia coli/genetics
2.
J Appl Microbiol ; 103(6): 2448-56, 2007 Dec.
Article in English | MEDLINE | ID: mdl-18045430

ABSTRACT

AIMS: To determine the presence of Vibrio cholerae in different areas of Argentina in three sample types, to determine the composition of planktonic communities in areas at which this pathogen was detected and to characterize the virulence properties and antimicrobial resistance of the recovered environmental isolates. METHODS AND RESULTS: Water and plankton samples were collected in marine, brackish and freshwater environments. Vibrio cholerae non-O1, non-O139 was isolated in 36.1% of the samples analysed. The micro-organism was detected in freshwater but not in marine or brackish samples. No relationship was found between isolation of V. cholerae and presence of any species of plankton. All the isolates presented very similar virulence profiles by PCR, lacking ctxA and tcpA El Tor and containing hlyA (98.7%), rtxA (99.0%), toxR (98.7%) and stn-sto (1.9%). Resistance to ampicillin was found in both Tucumán (21%) and Buenos Aires isolates (45%). CONCLUSIONS: We identified two geographic areas in Argentina where V. cholerae was present: freshwaters of the rivers from Tucumán and the Río de la Plata. SIGNIFICANCE AND IMPACT OF THE STUDY: The identification of V. cholerae strains in the environment, carrying both virulence factors and resistance to antimicrobial agents, highlight the need for a continuous and active surveillance of this pathogen.


Subject(s)
Vibrio cholerae/isolation & purification , Water Microbiology , Argentina , Drug Resistance, Bacterial , Environmental Monitoring/methods , Fresh Water , Microbial Sensitivity Tests , Plankton/microbiology , Seawater , Vibrio cholerae/genetics , Vibrio cholerae/physiology , Virulence
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