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Characterization of Escherichia coli producing toxins Shiga (STEC) isolated in the production of beef cattle and in the carcasses of their animals slaughtered

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Author(s):
Ana Eucares von Laer
Total Authors: 1
Document type: Doctoral Thesis
Press: São Paulo.
Institution: Universidade de São Paulo (USP). Conjunto das Químicas (IQ e FCF) (CQ/DBDCQ)
Defense date:
Examining board members:
Maria Teresa Destro; Kinue Irino; Mariza Landgraf; Marina Baquerizo Martinez; José Paes de Almeida Nogueira Pinto
Advisor: Maria Teresa Destro
Abstract

Shiga toxin (Stx)-producing Escherichia coli (STEC) are considered important foodborne pathogens that have the intestinal tract of ruminants, in particular cattle, as reservoir. These microorganisms are associated with severe human diseases as hemorrhagic colitis (HC) and hemolytic-uremic syndrome (HUS). The aims of this research were to evaluate the occurrence of STEC from different sources during the feedlot cattle breeding and slaughtering; detecting the presence of stx1, stx2, ehxA and eaeA genes; identifying O157:H7 strains through uidA; evidencing Stx and Eh production capacity; identifying stx and eaeA variants and determining STEC strains serotypes and genetic diversity. The potentially pathogenic strains were screened by detection of stx1, stx2, ehxA, eaeA and uidA, and Eh production, amongst 628 isolates studied. Fifty isolates were identified as STEC and 12 others as atypical EPEC. Among the STEC isolates, 76% were from feces, 18% from carcasses and 6% from water samples. Six strains isolated from feces and one from carcass were serotyped as O157:H7, ali being positive for the uidA. No other serogroup linked to outbreaks or sporadic cases of HC and HUS were found. From the 30 strains that showed cytotoxic effect on Vero cells, the great majority (96.7%) was positive for stx. Using an immunochromatographic assay, it was possible to identify the type of Stx produced by 17 out of the 50 STEC strains. All but one of these strains harbored the gene correspondent to the identified toxin. The other strain, even though producing both toxins, presented only stx2. It was possible to determine by PFGE the dissemination and persistence of STEC strains among the animals. 14/50 (28%) STEC strains were positive for the variant Stx2d activatable. Amongst 21 eaeA-positive strains, the variants of this gene were detected only in eight, being seven positive for eae-γ and the other eae-β. The results showed that uidA gene can be considered an excellent tool for screening O157:H7 strains. On the other hand, ehxA and Eh production, could not be considered as good markers for Stx-positive strains detection. A great diversity of serotypes/serogroups was observed among typical STEC strains. It is important to notice that this is the first report of O157:H7 strains in carcasses trom feedlot cattle in Brazil. The detection of STEC strain in fecal samples and in carcasses trom feedlot cattle evidences the potential public health risk, once these strains can contaminate the final product. (AU)