O presente trabalho investigou os efeitos hematológicos, respiratórios e cardiocirculatórios de eqüinos PSI submetidos a três diferentes protocolos de indução anestésica. Os grupos (G1, G2 e G3), constituídos de 10 animais cada, receberam: acepromazina 0,1 mg/kg, guaifenesina 113 mg/kg e tiopental sódico 2 g (G1); levomepromazina 0,2 mg/kg, midazolam 0,1 mg/kg e cloridrato de cetamina 2,0 mg/kg (G2); e cloridrato de detomidina 20 µg/kg e tiletamina-zolazepam 1,1 mg/kg (G3). As avaliações realizadas constaram de exame clínico, análise hematológica, hemogasometria arterial e avaliação eletrocardiográfica. As colheitas de dados foram procedidas antes da administração de qualquer fármaco e quinze minutos após a administração do último. Os resultados mostraram que os três protocolos utilizados são efetivos como indutores da anestesia geral em eqüinos. A avaliação da função respiratória não permite destaque positivo ou negativo para nenhum dos protocolos. As alterações cardiocirculatórias observadas foram de caráter temporário e sem significado clínico. As principais diferenças observadas foram a preparação laboriosa da combinação usada no G1, a necessidade mais freqüente de suplementação anestésica no G2 e a ocorrência de dificuldade de manejo do animal após a pré-anestesia no G3, em virtude das dificuldades de deambulação. | This research studied the hematological, respiratory and cardiocirculatory effects in thoroughbred equine subjects after the administration of 3 different induction protocols for general anesthesia. The animals were distributed in 3 groups. The animals from group 1 (G1) received acepromazine (0.1 mg/kg), guaiphenesin (113 mg/kg) and thiopental (2 g). The animals from group 2 (G2) received levomepromazin (0.2 mg/kg), midazolam (0.1 mg/kg) and ketamine (2.0 mg/kg). The animals from group 3 (G3) received detomidine (20 µg/kg) and tiletamine-zolazepam (1.1 mg/kg). The evaluation included clinical examination, venous blood samples for hematological analysis, arterial blood samples for gasometric analysis and eletrocardiographic records. Clinical parameters were observed, samples were taken and the ECG was recorded before any drug administration and 15 minutes after the last medication. The 3 protocols showed to be adequate when used before general anesthesia. Respiratory parameters showed no differences among the 3 groups. The cardiocirculatory events were transient and without clinical significance. The differences among the groups were related to the preparation of solutions (G1), frequency in drug supplementation (G2) and handling the animals (G3).

A presença de anticorpos contra Herpesvírus Bovino tipo 1 (HBV-1) foi avaliada em bovinos jovens provenientes de quinze municípios diferentes, distribuídos nas regiões Norte, Sul e Central do estado da Bahia. Foram coletadas amostras de sangue de bovinos de 1 a 4 anos de idade, não vacinados contra HBV-1 e sem prévio diagnóstico de infecção pelo vírus HBV-1. O total de amostras correspondeu a 558 soros, equivalente a 10% da população bovina de cada fazenda. Os 558 soros foram submetidos à técnica de Microssoroneutralização (MSN) em microplacas, utilizando-se monocamadas de células MDBK e a cepa de HBV-1 Los Angeles, e ao teste de ELISA comercialmente adquirido: HerdCheck-IDDEX. Os resultados da amostragem feito pelo teste de ELISA mostraram que 56% (314/558) dos soros foram positivos e 44% (244/558), negativos. A técnica de MSN mostrou que 48% (269/558) dos soros foram negativos e 52% (289/558) foram positivos. Destes soros positivos, 54% tiveram títulos soroneutralizantes entre 4-16, 35% entre 32-64, e 11% >; ou = 64. Os resultados sugerem que o HBV-1 esteja circulando ativamente na população bovina jovem. Por outra parte, a alta difusão do vírus em animais jovens representaria uma fonte contínua de infecção viral para o rebanho. | The presence of antibodies against BHV-1 was evaluated in young bovines from fifteen different counties distributed along North, South and Central regions of the state of Bahia. Bovines with age ranged from 1 to 4 years old, non-vaccinated against BHV-1 and without diagnostic of BHV-1 infection were chosen for blood collection. A total of 558 serum samples were collected equivalent to 10% of the population in each farm. The sera were submitted to ELISA (HerdCheck-IDDEX) and Microserum neutralization (MSN) tests. The MSN was performed in monolayers of MDBK cells in microplates using Los Angeles BHV-1 strain. The results of serum samples by ELISA showed that 56% (314/558) were positive and 44% (244/558) were negative. The sera assayed by MSN showed that 48% (269/558) were negative and 52% (289/558) were positive. These positive sera demonstrated that 54% had serumneutralization titer between 4-16, 35% between 32-64 and 11% >; or = 64. Our results suggest that the virus is circulating actively in herds. Furthermore, the high diffusion of the BHV-1 in young bovines could represent a constant source of viral infection in the herd.

Esta pesquisa avaliou a habilidade de zangões da abelha africanizada (Apis mellifera L.) em detectar cera de abelha adulterada usando o reflexo da extensão da probóscide (PER). Duzentos e quarenta zangões foram divididos em 12 grupos contendo níveis diferentes de cera de abelha adulterada (100% cera de abelha, 90% cera de abelha, 10% cera de abelha, 0% cera de abelha). Um estímulo de ar foi incluído como testemunha devido à possível influência do fluxo de ar per se. Os animais foram mantidos em tubos de metal, acondicionados com fita adesiva Ducktape® entre a cabeça e o tórax. Os resultados da performance dos zangões no condicionamento olfativo do PER indicam que esses animais são capazes de detectar níveis diferentes de cera de abelha adulterada. Os zangões mostraram melhor resposta ao tratamento contendo 100% de cera de abelha. Esse bioensaio pode servir de ferramenta alternativa na seleção de lotes de cera de abelha na apicultura e indústria. | This research evaluated the ability of Africanized honey bee (Apis mellifera L.) drones to detect adulterated beeswax using the proboscis extension reflex (PER). Two hundred and forty drones were divided into 12 groups containing different levels of adulterated beeswax (100% beeswax, 90% beeswax..., 10% beeswax, 0% beeswax). An air stimulus was included as a control for the possible influence of the air flux per se. The animals were maintained in metal tubes, harnessed with Ducktape® between the head and thorax. The results of the drones performance in PER olfactive conditioning indicate that these animals are able to detect different levels of adulterated beeswax. The drones shown a better response to the treatment containing 100% of beeswax. This bioassay can serve as an alternative tool in the screening of beeswax in beekeeping and industry.

Four calves were exposed via aerosol to 1 of 2 strains of foot-and-mouth disease virus. Two animals received virus derived from an infectious clone virus (A12-IC) and 2 received virus derived from the same clone but which lacked the leader coding region (A12-LLV2) that codes for a protein responsible for turning off host protein synthesis. Animals were euthanized at 24 and 72 h post exposure. Cattle receiving A12-IC had a rapid course of disease with more virus in tissues while A12-LLV2-infected cattle did not develop clinical signs of disease. Formalin-fixed, paraffin-embedded tissue sections were probed with digoxigenin-labeled riboprobes corresponding to the coding sequence for bovine interferon (IFN) alpha and IFNbeta. Staining for IFNalpha mRNA was noted in mononuclear cells of the lungs of all animals and in respiratory lymph nodes of cattle receiving A12-IC. Staining for IFNbeta mRNA was confined to bronchiolar epithelium and present only in the animals infected with A12-IC. Inability of the A12-LLV2 virus to achieve levels of spread seen with A12-IC may be related to translation of IFNalpha in A12-LLV2-infected cells, which renders adjacent cells less susceptible to productive infection.

Blood glycated hemoglobin concentration reflects long-term serum glucose levels in dogs. In this study, the effects of several diseases on blood glycated hemoglobin levels have been evaluated. For this study, blood samples were drawn from 93 unhealthy dogs. The animals were distributed into 10 groups according to pathological process (group 1, digestive problems; group 2, leishmaniasis; group 3, anemia; group 4, dermatological disorders; group 5, urinary problems; group 6, cardiorespiratory problems; group 7, diabetes mellitus; group 8, insulinoma; group 9, general diseases; group 10, control group). Blood glucose and glycated hemoglobin concentrations and hemoglobin and hematocrit values were analyzed in all the animals. In diabetic dogs, a strong increase in blood glycated hemoglobin was observed when compared with the other groups (P < 0.01). In contrast, dogs with insulinoma showed a decrease in blood glycated hemoglobin, though significant differences were not reported in all cases. No change in blood glycated hemoglobin concentrations were reported in dogs affected by other diseases. So, we can suppose that only the chronic alterations in glucose metabolism (chronic hyper- or hypoglycemia) can induce significant changes on the blood glycated hemoglobin concentrations in dogs.

Two agar gel immunodiffusion (AGID) kits for the serodiagnosis of bovine leukemia virus (BLV) were imported from Europe and were compared with North American kits. The BLV AGID kits from North America and from Europe differed significantly. The punches were different, as were the pattern distribution in the agar of the reference and the test sera, resulting in differences in the reading of the immunoprecipitation lines. Based on the testing of 1200 serum samples from cattle, the European kits gave a good correlation with the American kits, as indicated by their respective kappa values. However, the European kits were found to be less sensitive when evaluated against weakly positive samples from field specimens or following a dilution trial. Only 65% and 50% of the weakly positive samples detected by the American kit #1 were detected by the European kits #2 and #3, respectively. The American kit was also capable of detecting BLV antibodies in 45% of strongly positive samples diluted 1/50 in negative sera, while antibodies were detected in only 15% of the samples with the European kit #2 and in none of the samples with the European kit #3. False negatives were also detected with the European kits. Among the false negatives, the degree of expected reactions was weak (European kit #2) or of varying degrees of positivity (European kit #3). Besides the differences in format and performance, the BLV-AGID kits in Europe are evaluated with the National Standard Serum E4 while a proficiency panel composed of a quadruplicate set of 10 reference sera is used in Canada to monitor the kits. Based on the overall observations, we noted a lack of standardization between the BLV-AGID kits used in North America and in Europe.

This is the first extensive survey of metazoan parasites (particularly of the roundworm Baylisascaris procyonis) from the intestines of raccoons in British Columbia. The sample collected in 1997-1998 consisted of 82 raccoons that had been sick or had been killed accidentally by automobiles. Fifteen parasite taxa were found: 3 nematodes, 9 digenetic trematodes, 2 acanthocephalans and 1 cestode. Ten of these parasites constitute new host records for raccoons, including 4 digenetic trematodes that have been reported in marine birds and mammals on the Pacific Coast of North America. Baylisascaris procyonis infected 61% of the raccoons with a mean intensity of 27. The high rate of infection indicates a large potential for environmental contamination and, thus, human and animal exposure to infectious eggs. Prevention of larva migrans is discussed, particularly for people in contact with raccoons in wildlife rehabilitation centers.