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Significance and Impact of the Study: This study provides relevant data about the high phylogenetic and antimicrobial susceptibility diversity observed in Escherichia coli colony-forming units (CFUs) from a bacteriological culture of faeces from healthy calves, foals and lambs. The selection pressure exerted by the herd treatment may directly impact the intestinal microflora of animals that have never been treated. Finally, we emphasize the importance of Clinical Laboratory Standards Institute guidelines and we recommended to analyse at least four E. coli CFUs to determine, in particular, the antimicrobial susceptibility profile of faecal isolates, independent of the animal's health status. AbstractData about phylogenetic classification of Escherichia coli colonizing calves, lambs and foals are routinely neglected and restricted to outdated methodologies, even in the context of antimicrobial susceptibility (AS) testing. Thus, the aim of this study was to determine the phylogenetic diversity and the AS profile of E. coli colony-forming units (CFUs) from faecal samples of healthy animals. Five CFUs of E. coli were randomly selected from each faecal culture of calves (n = 13), foals (n = 13) and lambs (n = 13), totalizing 195 CFUs phylo-typed by quadruplex PCR. The AS profile of five CFUs from 15 samples (five from each animal species; n = 75 isolates) against nine drugs was determined by agar diffusion test. We found E. coli belonging to all phylogroups already described, except D group, with the predominance of B1 (65% CFUs; 126/195) in the three-animal species sampled. Most faecal samples of calves (77%; 10/13) and foals (69%; 9/13) harboured both pathogenic and nonpathogenic E. coli. All faecal samples showed CFUs with diverse AS profile, highlighting the ineffectiveness of tetracycline, sulphonamide and ampicillin. As a key point, our data reinforce the importance to select at least four E. coli CFUs for AS testing.

Toxoplasma gondii and Neospora caninum are two intracellular apicomplexan protozoa with worldwide distribution, and are responsible for reproductive disorders in sheep and cattle. These protozoa may infect a wide variety of domestic and wild animals, including birds, and backyard chickens can be used as sentinels of their infection. Parasites investigation in backyard chickens may be useful for the evaluation of environmental contamination with oocysts, of the disease cycle, and of risk factors associated with public health. The aim of this study was establish the importance of backyard chickens as T. gondii and N. caninum hosts. A number of 137 serum samples were collected from chickens in 23 farms in Rio Grande do Sul State, Brazil, and tested for toxoplasmosis and neosporosis by indirect fluorescence antibody test (IFAT). Anti-Toxoplasma and anti-Neospora antibodies were detected in 20 (87%) farms. Total prevalence of T. gondii was 74.4% (102/137) and 36.5% (50/137) for N. caninum, while 12.4% (17/137) of the chickens were positive for both protozoa. The results show that backyard chicken can used as indicators of the presenced of the protozoa N. caninum and T. gondii, emphasizing yours importance in the public health. Considering the high prevalence of toxoplasmosis in backyard chickens in the region, control measures should be taken to prevent transmission of the infection to the animals and humans.

Detecção de anticorpos anti -

The aim of the present study was to investigate experimental infections by Rickettsia parkeri in domestic chickens (Gallus gallus domesticus) and to determine the dynamics of antibody production during acute and chronic infection. The animals (n = 64) were allocated into eight groups as follows: G1, inoculated intramuscularly (IM) with 2.5 × 10 5 Vero cells (1 mL) infected with R. parkeri; G2, inoculated IM with 5.0 × 10 5 Vero cells (2 mL) infected with R. parkeri; G3, received 1 mL of the inoculum subcutaneously (SC); G4, received 2 mL of inoculum SC; G5, received 1 mL of the inoculum intraperitoneally (IP); G6, injected with 2 mL of the inoculum IP; G7 and G8, received 1 mL and 2 mL of culture medium IM, respectively (negative control groups). All R. parkeri inocula were viable prior to inoculation in the birds. In order to assess the dynamics of antibody production in acute and chronic infection, sera of chickens were collected 3, 7, 14, and 21 d post infection (PI) and assessed using an immunofluorescence antibody test (IFAT). In addition, PCR (gltA gene) was performed using fragments of spleen and lung from euthanized chickens to detect the replication of R. parkeri in tissues during the experimental period. Animals from the G4 and G3 groups exhibited the highest mean antibody titers, with maximum levels observed at 7 and 14 d PI, respectively. Conversely, G2, G4 and G6 exhibited higher mean antibody titers than G1, G3 and G5, respectively. Antibody titers were dose-dependent. Rickettsial DNA was not detected in either spleen or lung tissue. The present study demonstrated that birds seroconvert after being challenged by R. parkeri. However, there was no replication of the agent in the tissues analyzed and rickettsemia was not observed. (1 ml) infectadas por R. parkeri via intramuscular (IM); G2 -5,0 x 105 células Vero (2 ml) infectadas por R. parkeri via IM; G3 -1 ml do inóculo via subcutânea (SC); G4 -2 ml de inóculo via SC; G5 -1 ml do inóculo via intraperitoneal (IP); G6 -2 ml de inóculo via IP, e G7 e G8 -1 e 2 ml de meio de cultivo de células Vero via IM, respectivamente representando os grupos controles negativos. Ressaltase que todos os inóculos de R. parkeri estavam viáveis no momento da inoculação. Os soros das aves foram coletados aos 3, 7, 14 e 21 dias pós-infecção (PI) e testadas por reação de imunofluorescência indireta (RIFI) para avaliar a dinâmica de anticorpos na infecção aguda e crônica. A identificação da multiplicação de R. parkeri nos tecidos, no mesmo período PI, foi realizada por PCR, para um fragmento do gene gltA, em amostras de baço e pulmão provenientes das galinhas eutanasiadas. As aves do G4 e G3 apresentaram as maiores médias de anticorpos obtendo os níveis mais elevados aos sete e 14 dias PI, respectivamente. G2, G4 e G6 apresentaram médias de anticorpos superiores comparados aos G1, G3 e G5 respectivamente, sendo considerada a infecção dose-dependente. Não foi detectado DNA rickettsial nos tecidos avaliados. No presente trabalho foi possível demonstrar que as aves so...