This paper aimed to determine the excretion period of B19 vaccine strain during a complete reproductive cycle (from estrus synchronization, artificial insemination, pregnancy and until 30 days after parturition) of dairy cows from 3 to 9 years old that were previously vaccinated from 3 to 8 months. Three groups were monitored with monthly milk and urine collection during 12 months: G1 with seven cows from 3 to 4 years old; G2 with three cows from 5 to 6 years old; and G3 with four cows from 7 to 9 years old. Urine and milk samples were submitted to bacteriological culture and urine and PCR reactions for detection of Brucella spp. and PCR-multiplex for B19 strain identification. Ring test (RT) was also performed in the milk samples, and serum samples were tested by buffered acidified plate antigen test (BAPA). All animals were serologically negative at BAPA and Brucella spp. was not isolated from both urine and milk samples. RT revealed 13/210 (6.2%) positive milk samples. PCR reactions detected DNA of Brucella spp. in 86/420 (20.5%) samples. In urine it was found a significantly higher frequency (35.2%; 74/210) than in milk (5.7%; 12/210), more frequently from the estrus to 150 days of pregnancy and after parturition (6.7%; 10/150), and from 150 days of pregnancy to parturition (3.4%; 2/60), and they were all identified as B19 strain. In three groups, intermittent excretion of B19 strain was detected mainly in urine samples, which confirmed its multiplication and persistence in cows for until 9 years.

Objetivou-se com este estudo calcular a prevalência e identificar os fatores de risco associados à infecção por Chlamydophila abortus em suínos criados em granjas tecnificadas no Estado de Alagoas, Brasil. Para compor a amostra do estudo foram utilizados 342 suínos, sendo 312 matrizes e 30 varrões oriundos de sete granjas de ciclo completo e distribuídas em cinco municípios do Estado de Alagoas. O diagnóstico sorológico da infecção por C. abortus foi realizado através da microtécnica de Fixação do Complemento (RFC). A análise dos fatores de risco foi realizada por meio da aplicação de questionários investigativos, constituídos por perguntas objetivas referentes ao criador, às características gerais da propriedade, ao manejo produtivo, reprodutivo e sanitário. Observou-se prevalência de 10,5% (36/342) de suínos soropositivos para a infecção por C. abortus, com 85,8% das granjas analisadas com animais positivos. As variáveis que demonstraram associação significativa foram: utilização de bebedouros comuns para jovens e adultos (p=0,024; OR=10,83; IC=1,36-86,03) e método de cobertura de monta natural associada à inseminação artificial (p=0,05; OR=7,62; IC=1,00-58,31). Relata-se a primeira ocorrência de anticorpos anti-C. abortus em suínos no Brasil. Fatores como a introdução de reprodutores nos plantéis e a forma de fornecimento de água foram evidenciados como facilitadores da infecção das matrizes neste estudo. Dessa forma, medidas de controle da infecção devem ser enfocadas nesse aspecto para evitar a disseminação do agente nas granjas suinícolas e em outros plantéis da região.

The objective of this study was to determine the prevalence and identify risk factors associated with Chlamydophila abortus infection in commercial swine farms on the state of Alagoas, Brazil. To compose the study sample 342 pigs were used, with 312 sows and 30 boars from seven swine farms and distributed in five districts of the Alagoas. The serological diagnosis of infection by C. abortus was performed by fixation of complement microtechnique (RFC). The analysis of risk factors were performed by the application of research questionnaires, consisting of objective questions relating to the designer, the general characteristics of the property, the production, reproductive and health management. I was observed a prevalence of 10.5% (36/342) of pigs seropositive for infection by C. abortus with 85.8% of farms with positive animals analyzed. The variables that showed significant association were use of common drinker for young and adults pigs (p=0.024, OR=10.83, CI=1.36-86.03) and associated the natural mount with artificial insemination (p=0.05, OR=7.62, CI=1.00-58.31). This work reports the first occurrence of anti-C. abortus in pigs in Brazil. Factors as the introduction of boars in herds and the form of water supply were seen as facilitators of infection on sows in this study. Thus measures of infection control should be focused on this aspect to prevent the spread of the agent in pig farms and other herds in the region.

Foram analisadas 192 amostras de queijo clandestinas provenientes de várias regiões do Estado de São Paulo e Minas Gerais, Brasil, para isolamento e detecção de DNA de Brucella spp. através das técnicas de cultivo microbiológico e reação da polimerase em cadeia (PCR), respectivamente. Para as amostras positivas foi pesquisada a ocorrência da espécie Brucella abortus (biovares 1, 2 e 4), além da diferenciação do DNA em cepa vacinal B19 ou de campo por PCR. Não foi possível isolar o microrganismo de nenhuma amostra, porém, na PCR, 37 amostras (19,27%) foram positivas na reação com primers gênero específicos e destas, todas (100%) foram comprovadas como sendo Brucella abortus. A diferenciação da cepa revelou que 30/37 amostras (81,08%) eram cepa vacinal B19 e sete (18,92%) eram cepas de Brucella abortus de campo. Os resultados mostraram uma maior sensibilidade diagnóstica da PCR em relação ao cultivo microbiológico, e a padronização da reação de diferenciação da cepa em vacinal ou campo permitiu que todas as amostras positivas para Brucella abortus fossem analisadas, sendo uma metodologia confiável e aplicável a infecções naturais pelo microrganismo.

A total of 192 samples of illegal cheese from different regions of the states of São Paulo and Minas Gerais, Brazil, were analyzed for the isolation and detection of Brucella spp. DNA by means of microbiological culture and polymerase chain reaction (PCR), respectively. Samples that yielded positive results were submitted to the analysis of the occurrence of Brucella abortus (biovars 1, 2 e 4), as well as to the differentiation of DNA in B19 vaccinal strain or Brucella abortus field strain using PCR. Although the microorganism was not isolated from any sample, PCR detected 37 positive samples (19.27%) using genus-specific primers. From these, all (100%) were Brucella abortus. Differentiation of the strain showed that 30/37 samples (81.08%) were vaccinal strain B19 and seven (18.92%) were Brucella abortus field strains. Results showed that diagnostic sensitivity of PCR was greater than that of microbiological culture. The standardization of the reaction for the differentiation of vaccinal and field strains enabled the analysis of all samples positive for Brucella abortus. It is, therefore, a reliable method, also applicable to natural infections caused by the microrganism.

A polymerase chain reaction (PCR) assay to detect Clostridium perfringens alpha toxin gene (cpa) was used to identify eighty-nine C. perfringens strains obtained from bovine clinical material. The strains were biochemically characterized as C. perfringens. The isolated strains were cultured on plates containing brain heart infusion agar with 5% sheep blood under anaerobic conditions. DNA extraction was performed by boiling. The 324 bp amplification product of cpa was observed in all isolates. C. sordellii, C. botulinum, C. novyi, and C. septicum were also tested but did not produce any alpha toxin gene amplification. These findings suggest that PCR is a useful assay in identifying C. perfringens toxin types.