17 research outputs found

    Typical and atypical enteropathogenic Escherichia coli bacterial translocation associated with tissue hypoperfusion in rats

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    Although enteropathogenic Escherichia coli (EPEC) are well-recognized diarrheal agents, their ability to translocate and cause extraintestinal alterations is not known. We investigated whether a typical EPEC (tEPEC) and an atypical EPEC (aEPEC) strain translocate and cause microcirculation injury under conditions of intestinal bacterial overgrowth. Bacterial translocation (BT) was induced in female Wistar-EPM rats (200-250 g) by oroduodenal catheterization and inoculation of 10 mL 10(10) colony forming unit (CFU)/mL, with the bacteria being confined between the duodenum and ileum with ligatures. After 2 h, mesenteric lymph nodes (MLN), liver and spleen were cultured for translocated bacteria and BT-related microcirculation changes were monitored in mesenteric and abdominal organs by intravital microscopy and laser Doppler flow, respectively. tEPEC (N = 11) and aEPEC (N = 11) were recovered from MLN (100%), spleen (36.4 and 45.5%), and liver (45.5 and 72.7%) of the animals, respectively. Recovery of the positive control E. coli R-6 (N = 6) was 100% for all compartments. Bacteria were not recovered from extraintestinal sites of controls inoculated with non-pathogenic E. coli strains HB101 (N = 6) and HS (N = 10), or saline. Mesenteric microcirculation injuries were detected with both EPEC strains, but only aEPEC was similar to E. coli R-6 with regard to systemic tissue hypoperfusion. In conclusion, overgrowth of certain aEPEC strains may lead to BT and impairment of the microcirculation in systemic organs

    Prevalence Of Virulence Factors In Escherichia Coli Isolated From Healthy Animals And Water Sources In Brazil

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    The aim of this work was to verify the presence of seven virulence factors (ST, LT, eae, stx 1, stx 2, INV and EAEC) among Escherichia coli strains isolated from healthy humans, bovines, chickens, sheep, pigs and goats, from two sewage treatment plants and from the TietêRiver. We have found a high prevalence of eae, stx 1 and stx 2 in ruminants. The EAEC gene was only found in humans and sewage. No strains presented ST, LT or INV. BOX-PCR fingerprints revealed a high diversity among the strains analysed and a non-clonal origin of strains that presented the same virulence factors. Therefore, we concluded that ruminants may constitute an important reservoir of most diarrheagenic E. coli in Brazil, except for EAEC strains. These results emphasize the importance of the identification of the animal source of fecal contamination for the correct water risk assessment. © IWA Publishing 2011.91138142Beutin, L., Stroeher, U.H., Manning, P., Isolation of enterohemolysin (Ehly2)-associated sequences encoded on temperate phages of Escherichia coli (1993) Gene, 132, pp. 95-99Brett, K.N., Ramachandran, V., Hornitzky, M.A., Bettelheim, K.A., Walker, M.J., Djordjevic, S.P., stx1 c is the most common Shiga-toxin 1 subtype among Shiga toxin producing Escherichia coli isolates from sheep but not among isolates from cattle (2003) J. Clin. Microbiol., 41, pp. 926-936Carlos, C., Pires, M.M., Stoppe, N.C., Hachich, E.M., Sato, M.I.Z., Gomes, T.A.T., Amaral, L.A., Ottoboni, L.M.M., Escherichia coli phylogenetic group determination and its application in the identification of the major animal source of fecal contamination (2010) BMC Microbiol., 10, p. 161Cebula, T.A., Payne, W.L., Feng, P., Simultaneous identification of strains of Escherichia coli serotype O157:H7 and their Shigalike toxin by mismatch amplification mutation assay-multiplex PCR (1995) J. Clin. Microbiol., 33, pp. 248-250Cerqueira, A.M.F., Guth, B.E.C., Joaquim, R.M., Andrade, J.R.C., High occurrence of Shiga toxin-producing Escherichia coli (STEC) in healthy cattle in Rio de Janeiro State, Brazil (1999) Veterinary Microbiology, 70 (1-2), pp. 111-121. , DOI 10.1016/S0378-1135(99)00123-6, PII S0378113599001236Clermont, O., Bonacorsi, S., Bingen, E., Rapid and simple determination of the Escherichia coli phylogenetic group (2000) Appl. Environ. Microbiol., 66, pp. 4555-4558Escobar-Páramo, P., Blanc-Potard, A.B., Bui, H., Le Bouguenec, C., Denamur, E., A specific genetic background is required for acquisition and expression of virulence factors in Escherichia coli (2004) Mol. Biol. Evol., 2, pp. 1085-1094Gannon, V.P.J., Rashed, M., King, K.R., Golsteyn, T.E.J., Detection and characterization of the eae gene of shiga-like toxinproducing Escherichia coli using polymerase chain reaction (1993) J. Clin. Microbiol., 31, pp. 1268-1274Hassan, W.M., Ellender, R.D., Wang, S.Y., Fidelity of bacterial source tracking: Escherichia coli vs. Enterococcus spp and minimizing assignment of isolates from nonlibrary sources (2007) J. Appl. 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    Serogroups And Virulence Genes Of Escherichia Coli Isolated From Psittacine Birds

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    Escherichia coli isolates from 24 sick psittacine birds were serogrouped and investigated for the presence of genes encoding the following virulence factors: attaching and effacing (eae), enteropathogenic E. coli EAF plasmid (EAF), pili associated with pyelonephritis (pap), S fimbriae (sfa), afimbrial adhesin (afa), capsule K1 (neu), curli (crl, csgA), temperature--sensitive hemagglutinin (tsh), enteroaggregative heat-stable enterotoxin-1 (astA), heat--stable enterotoxin -1 heat labile (LT) and heat stable (STa and STb) enterotoxins, Shiga-like toxins (stx1 and stx2), cytotoxic necrotizing factor 1 (cnf1), haemolysin (hly), aerobactin production (iuc) and serum resistance (iss). The results showed that the isolates belonged to 12 serogroups: O7; O15; O21; O23; O54; O64; O76; O84; O88; O128; O152 and O166. The virulence genes found were: crl in all isolates, pap in 10 isolates, iss in seven isolates, csgA in five isolates, iuc and tsh in three isolates and eae in two isolates. The combination of virulence genes revealed 11 different genotypic patterns. All strains were negative for genes encoding for EAF, EAEC, K1, sfa, afa, hly, cnf, LT, STa, STb, stx1 and stx2. Our findings showed that some E. coli isolated from psittacine birds present the same virulence factors as avian pathogenic E. coli (APEC), uropathogenic E. coli (UPEC) and Enteropathogenic E. coli (EPEC) pathotypes.3110916921Baldini, M.M., Kaper, J.B., Levine, M.M., Candy, D.C.A., Moon, H.W., Plasmid-mediated adhesion of enteropathogenic Escherichia coli (1983) J. Pediatr. Gastroenterol. Nutr., 2, pp. 534-538Bangert, R.L., Cho, B.R., Widders, P.R., Strauber, E.H., Ward, A.C.S., A survey of aerobic bacteria and fungi in the healthy psittacine birds (1988) Avian Dis, 32, pp. 46-52Baudry, B., Savarino, S.J., Vial, P., Kaper, J.P., Levine, M.M.A., A sensitive and specific DNMA probe to identify enteroaggregative E. coli, a recently discovered diarrheal pathogen (1990) J. Infect. 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    Genes Coding For Shiga-like Toxins In Bovine Verotoxin-producing Escherichia Coli (vtec) Strains Belonging To Different O:k:h Serotypes

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    Forty-six verotoxin-producing Escherichia coli (VTEC) strains isolated from diarrhoeic and healthy calves in Spain were examined for DNA sequences homologous to genes for verotoxins (VT1 and VT2) and enterotoxins (LT-I, LT-II, STaH, STaP and STb). Hybridisation showed that 26 (57%) of VTEC strains carried VT1 genes, 13 (28%) possessed VT2 genes, and 7 (15%) carried both VT1 and VT2 genes. No VTEC strains hybridised with DNA probes for enterotoxins. A correlation was found between the serotype and type of VT produced. Thus, all strains of serotypes O26:K-:H11 (13 strains), O103:K-:H2 (3 strains) and O128:K?:H- (4 strains) hybridised with the VT1 probe only, whereas all strains of serotypes O4:K-:H4 (3 strains) and O113:K-:H21 (4 strains) were positive with the VT2 probe only. By contrast, O81:K?:H28 (2 strains) and O157:K-:H- (2 strains) strains hybridised with both VT1 and VT2 probes. 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