Ocorrência de aflatoxina em amendoim, no estado de São Paulo, durante os anos de 1988 e 1989

Este trabalho teve o escopo de dar a público os resultados das análises efetuadas num total de 625 amostras de amendoim descascado, na sua maioria HPS ("hand pick selected"), durante os anos de 1988 (517) e 1989 (108). Considerando que a legislação brasileira permite um máximo de 30 /¼g/kg, somadas as aflatoxinas B1 e G1, os resultados mostraram que em 1988, 52% das amostras (correspondentes a lotes), estavam contaminadas e em 1989, 34%. Os níveis médios de aflatoxina nas amostras contaminadas foram de 13 3,8 ¼g/kg em 1988 e 414,8 ¼g/kg em 1989, que podem ser considerados elevados. O contingente de lotes utilizáveis pela indústria foi de 67% em 1988 e 76% em 1989 (correspondentes às amostras com níveis não detectáveis e abaixo de 30 ¼g/kg).

Does a spontaneous cure for chagas' disease exist?

Six Costa Rican Chagas' disease patients, with wellknown acute phase history and no specific treatment were examined in several occasions during 39, 24, 32, 16 and 14 years, respectively, from the onset. Nome of the patients presented heart abnormalities as revealed by the conventional EKG and ergometry, exceptfor one of them with an incomplete block of the right bundle branch. Also, no alterations of the oesophagus motility was detected manometrically except for another patient who presented a slight hypersensivity reaction to a pharmacological test (Mecholyl). Three out of six patients became serologically negative in 1981, remaining as such until 1986. Besides the conventional serology, the search of protective ("lytic") antibodies was also performed in 1985 and 1986, being completely negative in one of the "cured" patients and dubious in the other two. The hypothesis that these three patients had as spontaneous cure, based on the clinical, serological and parasitologica l findings is discussed.

Biologia e controle microbiano de Urbanus acawoios (Williams, 1926) (Lepidoptera: Hesperiidae): II. patologia e susceptibilidade em larvas infectadas por Bacillus thuringiensis Var. kurstaki (H-3a:3b)

Devido à falta de informações sobre Urbanus acawoios (Williams, 1926) (Lepidoptera: Hesperiidae), e pelos danos severos por ele causados em árvores de Clitoria racemosa, o presente trabalho foi desenvolvido sob condições de laboratório para verificar a possibilidade de utilizar Bacillus thuringiensis var. kurstaki (H-3a:3b) como agente microbiano para o seu controle. O pH do intestino médio do hesperídeo mostrou ser bastante alcalino, variando de 8,4 a 9,2 (média de 8,7), indicando a possibilidade das larvas serem susceptíveis ao patógeno. Os ensaios confirmaram a alta susceptibilidade a dosagens equivalentes a 110 g / ha, resultando em tempos letais medianos (TL50) de 42,28, 37,18, 28,00 e 51,87 horas para larvas de 3o, 4°, início e final do 5º ínstares, respectivamente. Três outras dosagens (80, 150 e 280 g/h) foram aplicadas para larvas do 3º ínstar, resultando em TLs50 de 42,62, 30,77 e 30,06 horas, respectivamente. Descrições detalhadas sobre os sintomas externos nas larvas infectadas foram dadas. As alterações histológicas do intestino médio afetado pela d-endotoxina de B. thuringiensis foram descritas. Os resultados obtidos no presente trabalho revelam a grande possibilidade de controlar esta praga utilizando-se produtos e formulados à base desta bactéria.

Expression and purification of the immunogenically active fragment B of the Park Williams 8 Corynebacterium diphtheriae strain toxin

The construction of a hexahistidine-tagged version of the B fragment of diphtheria toxin (DTB) represents an important step in the study of the biological properties of DTB because it will permit the production of pure recombinant DTB (rDTB) in less time and with higher yields than currently available. In the present study, the genomic DNA of the Corynebacterium diphtheriae Park Williams 8 (PW8) vaccine strain was used as a template for PCR amplification of the dtb gene. After amplification, the dtb gene was cloned and expressed in competent Escherichia coli M15™ cells using the expression vector pQE-30™. The lysate obtained from transformed E. coli cells containing the rDTB PW8 was clarified by centrifugation and purified by affinity chromatography. The homogeneity of the purified rDTB PW8 was confirmed by immunoblotting using mouse polyclonal anti-diphtheria toxoid antibodies and the immune response induced in animals with rDTB PW8 was evaluated by ELISA and dermonecrotic neutralization assays. The main result of the present study was an alternative and accessible method for the expression and purification of immunogenically reactive rDTB PW8 using commercially available systems. Data also provided preliminary evidence that rabbits immunized with rDTB PW8 are able to mount a neutralizing response against the challenge with toxigenic C. diphtheriae.