A total of 45 strains of Escherichia coli isolates from chickens with colisepticemia were examined for virulence factors commonly found in pathogenic groups of E. coli. These strains were studied for the following: pathogenicity in 1-day-old chicks; toxin, hemolysin, and colicin production; cell invasiveness and adherence; hemagglutination for fimbriae detection; serum resistance; aerobactin production in iron-limited conditions; and plasmid content. The characteristics exhibited by virulent strains were invasion for HeLa and chicken fibroblast cells, serum resistance, colicin V, and aerobactin production. None of the isolates were toxigenic or positive in hemagglutination tests. The molecular genetic studies of the virulence factors by agarose electrophoresis showed that the plasmids of these strains are of high molecular weight.

Cooccidiosis is one of the most important causes of economic losses within the poultry industry. The objective of this study was to evaluate the pathogenicity of E. tenella, E. acervulina, and E. maxima strains in commercial broilers chicks. Thirty nine commercial one day old broiler chicks, unvaccinated against coccidiosis, were used during this experiment. At day 14, chickens of G1 (n=10), G2 (n=10) and G3 (n=10) were infected with 2 x 10 4 sporulated oocysts of E. tenella, E. acervulina, and E. maxima respectively; G4 (n=9) served as the uninfected control group. All birds were sacrificed with 21 day old (seven days after infection). The prepatent period (PPP) for G1 and G3 was seven days, however, E. acervulina (G2) had a PPP of five days. No statistical differences were observed when the average weight gain (G1=182.7±63.4; G2=145.2±51.0; G3=183.3±56.8; and G4=211.5±89.0, p>0.10) of the evaluated groups was compared. Average of lesion scores were determined G1 (1.3±0.48, scores 1(n=7) and 2(n=3)), G2 (0.4±0.52, scores 0(n=6), 1(n=4)), and G3 (1.1±0.99, scores 0(n=4), 1(n=1) and 2(n=5)). Chickens from the infected groups (G1, G2 and G4) did not demonstrate a lesion score above 2. The histopathological lesions induced by these strains were consistent with those described for infection by Eimeria spp.

Using monoclonal anti-fumonisin B1 antibody (anti-FB1) and avidin-biotin-peroxidase system, liver and kidneys of broiler chicks were evaluated for the detection and distribution of fumonisins (FBs). One hundred and fifty micrograms of FB1 or culture extract of Fusarium moniliforme str. 113F containing 150 microg of FB1 and 4 microg of FB2 were administered into the vitelline sac of 1-day old, specific pathogen-free chicks. The animals were killed 24 h after injection, and renal and hepatic tissues submitted for immunohistochemical analysis. FBs were detected in the epithelial cells of convoluted distal and proximal tubules of the kidneys, as well as in the cytoplasm of hepatocytes. This novel immunohistochemical method developed is expected to be an efficient way for monitoring the target of the FB toxins in tissues.

Neste trabalho, relata-se o isolamento de Escherichia coli em frangos de corte apresentando lesão de celulite na região cervical. Foi realizado o isolamento de E. coli da lesão de celulite e realizado exames histopatológicos que caracterizaram a lesão. Na epiderme foram verificadas lesões ulcerativas, presença de fibrina na derme e infiltração difusa de linfócitos e heterófilos no tecido subcutâneo.

Using monoclonal anti-fumonisin B1 antibody (anti-FB1) and avidin-biotin-peroxidase system, liver and kidneys of broiler chicks were evaluated for the detection and distribution of fumonisins (FBs). One hundred and fifty micrograms of FB1 or culture extract of Fusarium moniliforme str. 113F containing 150 microg of FB1 and 4 microg of FB2 were administered into the vitelline sac of 1-day old, specific pathogen-free chicks. The animals were killed 24 h after injection, and renal and hepatic tissues submitted for immunohistochemical analysis. FBs were detected in the epithelial cells of convoluted distal and proximal tubules of the kidneys, as well as in the cytoplasm of hepatocytes. This novel immunohistochemical method developed is expected to be an efficient way for monitoring the target of the FB toxins in tissues.