The objective of this study was to identify and characterize species of Eimeria in broiler chickens using traditional morphological and pathological plus molecular (DNA amplification) diagnostic methodologies. Using a combination of those techniques it was possible to identify the presence of multiple circulating species in the flock as well as higher frequencies for some of them, especially Eimeria praecox and Eimeria maxima, which were identified in 100% of the flocks. The frequencies of the other species were Eimeria mitis and Eimeria necatrix (93.3%), Eimeria tenella (76,7%), Eimeria acervulina (56.7%) and Eimeria brunetti (16.7%). However using the lesion score, the most common species were E. maxima (46.7%), E. acervulina (30%), E. tenella (23.3%), and E. necatrix (10%). E. brunetti and E. praecox were not identified by using lesion score. DNA amplification had detection sensitivity for Eimeria species in the field samples of at least 20 oocysts. The implementation of DNA amplification as a routine diagnostic technique in aviaries can assist Eimeria population.

BackgroundChickens are animals that are sensitive to thermal stress, which may decrease their production level in terms that it affects feed intake and thus, decreasing body weight gain. The Heat Shock Factors (HSF) and Heat Shock Proteins (HSP) genes are involved in the key cellular defense mechanisms during exposure in hot environments. Aimed with this study to analyze the expression of HSF1, HSF3, HSP70 and HSP90 genes in two local breeds (Peloco and Caneluda) and a commercial broiler line (Cobb 500®) to verify differences in resistance of these chicken to Heat stress treatment. Chicken were submitted to heat stress under an average temperature of 39°C ± 1.ResultsUnder stress environment, the HSP70 and HSP90 genes were more expressed in backyard chickens than in broiler. There was a difference in HSP70 and HSP90 expression between Caneluda and Cobb and between Peloco and Cobb under stress and comfort environment respectively. HSP70 expression is higher in local breeds during heat stress than in a commercial broiler line. No significant differences were observed in the expression of HSF1 and HSF3 genes between breeds or environments.ConclusionsHSP70 and HSP90 genes are highly expressed, HSF1 and HSF3 genes did not have high expression in all genetic groups. HSP70 and HSP90 are highly expressed in Peloco and Caneluda within heat stress, these breeds proved to be very resistant to high temperature.

Bovine babesiosis and anaplasmosis complex: diagnosis and evaluation of the risk factors from Bahia, BrazilComplexo tristeza parasitária bovina: diagnóstico e avaliação dos fatores de risco na Bahia, Brasil AbstractDirect diagnoses were made by using -blood smears and nested PCR (nPCR) tests on 309 blood samples from crossbred dairy cattle in the municipality of Ibicaraí, Bahia. From diagnostic blood smear slides, the observed parasitic frequencies were 31.1% for Anaplasma marginale and 20.4% for Babesia sp. From nPCR diagnoses, they were 63% for A. marginale, 34% for Babesia bigemina and 20.4% for Babesia bovis. There were significant differences (P < 0.01) between the two diagnostic methods (nPCR and blood smear slides). The compliance obtained from the kappa test was 0.41 and 0.48 for A. marginale and Babesia sp., respectively. The tick samples from the six farms analyzed using nPCR were only positive for A. marginale. Evaluation of the risk factors relating to the presence of ticks and the age of the animals showed that there was a significant association (P < 0.01) with the frequency of animals infected with both pathogens. Therefore, under the conditions studied, nPCR proved to be a good tool for diagnosing the agents of the bovine babesiosis and anaplasmosis complex because of its sensitivity and specificity in comparison with blood smears. The municipality of Ibicaraí is an area with endemic prevalence of bovine babesiosis and anaplasmosis confirmed by nPCR and A. marginale is the main agent of the disease.Keywords: Bovine Babesiosis and Anaplasmosis Complex, blood smear, nPCR, risk factors. ResumoRealizou-se o diagnóstico direto por esfregaço sanguíneo e nested PCR (nPCR) em 309 amostras de sangue de bovinos mestiços leiteiros provenientes do município de Ibicaraí, Bahia. A frequência observada no diagnóstico por lâminas de esfregaço sanguíneo foi 31,1% para Anaplasma marginale e 20,4% para Babesia sp. Enquanto que no diagnóstico por nPCR foi 63% para A. marginale, 34% para Babesia bigemina e 20,4% Babesia bovis. Verificaram-se diferenças significativas (P<0,01) na comparação entre os dois métodos de diagnósticos (nPCR e esfregaço sanguíneo). A concordância ao teste KAPPA obtida foi de 0,41 e 0,48 para A. marginale e Babesia sp., respectivamente. As amostras de carrapatos das seis propriedades analisadas por nPCR foram positivas apenas para A. marginale. Na avaliação dos fatores de risco verificou-se que a presença de carrapato e idade dos animais apresentaram associação significativa (P<0,01) com a frequência de animais infectados por ambos os patógenos analisados por nPCR. Portanto, nas condições estudadas, a nPCR revelou-se uma boa ferramenta para diagnóstico dos agentes do complexo tristeza parasitária bovina (TPB) devido a sensibilidade e especificidade, quando comparado ao esfregaço sanguíneo. O município de Ibicaraí

RESUMO -Utilizaram-se 153.963 controles mensais de produção de leite e 13.273 primeiras lactações de vacas da raça Holandesa, com partos entre 1989 a 1998, com o objetivo de estimar parâmetros genéticos, fenotípicos e de meio ambiente para produção de leite no dia do controle (PLDC) e produção até 305 dias de lactação (P305), bem como verificar a conveniência de se utilizar a PLDC em avaliações genéticas, em substituição à P305. Foram utilizados quatro modelos (modelo animal). Em dois, modelos 1 e 2, consideraramse os controles mensais de produção, coletados ao longo da lactação, como medidas repetidas de um animal, diferenciados segundo o critério de formação de grupos de animais contemporâneos. No modelo 1 (PLDCM01), as produções dos animais foram agrupadas segundo o rebanho-ano-estação de controle de produção, enquanto, no modelo 2 (PLDCM02), o agrupamento considerou o rebanho-ano-estação de parto. No modelo 3, analisaram-se os controles mensais de produção, como características individuais (C01 até C10); e no modelo 4, analisou-se a tradicional P305. As análises foram realizadas utilizando-se o método da Máxima Verossimilhança Restrita, por meio do sistema MTDFREML. As estimativas de herdabilidade para PLDC, com o uso do modelo 1, modelo 2 e para P305, foram de 0,27, 0,15 e 0,25, respectivamente. As herdabilidades para os controles mensais variaram de 0,11±0,02 (C01) a 0,21±0,03 (C08), e os maiores valores ocorreram a partir do quarto mês. A correlação de ordem entre os valores genéticos obtidos, para P305 e para PLDC (modelo 1), foi de 0,62, para touros, e de 0,78, para vacas. Concluiu-se que é viável a utilização da PLDC em estudos envolvendo a produção de leite e que os controles do meio da lactação, se usados para seleção, podem apresentar vantagens em relação à P305.Palavras-chave: controle mensal, método REML, modelo animal, produção de leite, raça Holandesa Genetic Evaluation of Holstein Cattle Using Test Day Milk YieldABSTRACT -153,963 test day milk yield records and 13,273 first lactations of Holstein cows calving between 1989 and 1998, were used with the objective of estimating genetic, phenotypic and environmental parameters for test day milk yield (PLDC) and 305 day milk yield (P305) and to study the convenience of using test day yields in genetic evaluations to replace P305. Four models were used. Models 1 and 2 differed according contemporary grouping and monthly milk records were considered as repeated measures. In model 1 (PLDCM01) records were grouped by herd-year-season of test day yield and in model 2 (PLDCM02) by herd-year-season of calving. In a third (model 3), monthly yield records were analyzed as individual traits (C01 to C10); and the fourth (model 4) was the traditional 305-day model. Restricted Maximum Likelihood methodology was used with the MTDFREML system. The estimates of heritability for PLDC, using model 1, model 2 and for P305 were 0.27, 0.15 and 0.25, respectively. Heritabilities for monthly milk records ranged from 0.11+0.02 (C01) to 0.21+0.03 (C08), with the largest valu...

Ehrlichiosis is a zoonotic disease that is caused by bacteria of the genus Ehrlichia. The aims of this study were to detect the presence of Ehrlichia spp. in the blood of dogs in Ituberá, Bahia, and to compare the sensitivities and specificities of blood smear, serological, and molecular examinations. Furthermore, this study identified factors associated with exposure to the agent in dogs in this locality. Blood samples were collected from 379 dogs and submitted for indirect immunofluorescent assay and polymerase chain reaction testing for the detection of Ehrlichia spp. antibodies and DNA, respectively. Additionally, a peripheral blood smear was obtained from the ear tip for parasite identification. Of the 379 animals, 12.4%, 32.7%, and 25.6% were identified as positive on the blood smear, serological, and molecular tests, respectively. The dogs positive in one of the three techniques were considered exposed (46.9%). Younger dogs and rural habitat were protective factors and presence of ticks and contact with other dogs were the risk factors associated with exposure to the agent. It was concluded that dogs of Ituberá have high positivity for Ehrlichia spp. and that the diagnostic methods used for detection are complementary.Keywords: Diagnosis, dog, Ehrlichia canis, Indirect Immunofluorescence, nested PCR. ResumoErliquiose é uma doença zoonótica causada por bactérias do gênero Ehrlichia. O objetivo desse estudo foi detectar a presença de Ehrlichia spp. no sangue de cães em Ituberá-BA, e comparar as sensibilidades e especificidades do esfregaço sanguíneo, e testes sorológico e molecular. Além disso, esse estudo identificou fatores associados com a exposição ao agente em cães desta localidade. Amostras de sangue foram coletadas de 379 cães e submetidas à Reação de Imunofluorescência Indireta e Reação em Cadeia de Polimerase para detecção de anticorpos e DNA de Ehrlichia spp., respectivamente. Adicionalmente, sangue periférico de ponta de orelha foi coletado para identificação do parasita. Dos 379 animais, 12,4%, 32,7% e 25,6% foram identificados como positivos no esfregaço sanguíneo, teste sorológico e molecular, respectivamente. Cães positivos em uma das três técnicas foram considerados expostos (46,9%). Cães mais novos e hábitat rural foram fatores de proteção e presença de carrapatos e contato com outros cães foram os fatores de risco associados à exposição ao agente. Foi concluído que, os cães do município de Ituberá têm alta positividade para Ehrlichia spp. e que os diferentes métodos diagnósticos utilizados para sua detecção são complementares.