PESQUISA VETERINÁRIA BRASILEIRA

Abstract in English:

Zlotowski P., Nakazato L., Dutra V., Barros S.S., Gimeno E.J., Göcks M., Colodel E.M. & Driemeier D. 2005. [Inherited glycogenosis in Brahman cattle in Brazil.] Glicogenose hereditária em bovinos Brahman no Brasil. Pesquisa Veterinária Brasileira 25(4):210-214. Setor de Patologia Veterinária, Departamento de Patologia Clínica Veterinária, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Bairro Agronomia, Cx. Postal 15094, Porto Alegre, RS 91540-000. Brazil. E-mail: davetpat@ufrgs.br An inherited disease of cattle, characterized by lysosomal storage of glycogen in several tissues, is reported. The disease was diagnosed in a Brahman herd in the municipality of Porto Lucena, Rio Grande do Sul, Brazil. Affected calves, after one month of age, showed progressive difficulty to follow their mother, retarded growth, muscular weakness and tremors, lethargy and poor body condition. All affected calves were sired by the same bull. Necropsy was performed on three affected calves. The only gross lesion detected was paleness of the skeletal muscles of the trunk and limbs. Cytoplasmic vacuoles, the main histological lesion, were particularly evident in skeletal muscles, myocardium and Purkinje fibers, in neurons of the brain and spinal cord. Large amounts of periodic acid Schiff (PAS) positive granules were also observed in these most severely affected tissues. Pretreatment with diastase completely abolished the PAS reactivity. The 1057?TA, a lethal mutation in the gene of the acid alpha-glucosidase, which causes generalized glycogenosis in Brahman cattle, was detected by PCR in paraffin embedded tissues of affected animals on which post-mortem examination was performed. Clinical, histological and molecular findings were similar to previous descriptions of generalized glycogenosis in Brahman cattle in Australia. No previous indexed reports about generalized glycogenosis of Brahman cattle in Brazil could be found.

• Glycogenosis inherited disease Brahman cattle.

Abstract in Portuguese:

Zlotowski P., Nakazato L., Dutra V., Barros S.S., Gimeno E.J., Göcks M., Colodel E.M. & Driemeier D. 2005. [Inherited glycogenosis in Brahman cattle in Brazil.] Glicogenose hereditária em bovinos Brahman no Brasil. Pesquisa Veterinária Brasileira 25(4):210-214. Setor de Patologia Veterinária, Departamento de Patologia Clínica Veterinária, Faculdade de Veterinária, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves 9090, Bairro Agronomia, Cx. Postal 15094, Porto Alegre, RS 91540-000. Brazil. E-mail: davetpat@ufrgs.br An inherited disease of cattle, characterized by lysosomal storage of glycogen in several tissues, is reported. The disease was diagnosed in a Brahman herd in the municipality of Porto Lucena, Rio Grande do Sul, Brazil. Affected calves, after one month of age, showed progressive difficulty to follow their mother, retarded growth, muscular weakness and tremors, lethargy and poor body condition. All affected calves were sired by the same bull. Necropsy was performed on three affected calves. The only gross lesion detected was paleness of the skeletal muscles of the trunk and limbs. Cytoplasmic vacuoles, the main histological lesion, were particularly evident in skeletal muscles, myocardium and Purkinje fibers, in neurons of the brain and spinal cord. Large amounts of periodic acid Schiff (PAS) positive granules were also observed in these most severely affected tissues. Pretreatment with diastase completely abolished the PAS reactivity. The 1057?TA, a lethal mutation in the gene of the acid alpha-glucosidase, which causes generalized glycogenosis in Brahman cattle, was detected by PCR in paraffin embedded tissues of affected animals on which post-mortem examination was performed. Clinical, histological and molecular findings were similar to previous descriptions of generalized glycogenosis in Brahman cattle in Australia. No previous indexed reports about generalized glycogenosis of Brahman cattle in Brazil could be found.

Abstract in English:

A radiological study of the fore and hind limb lymphatic system was performed in seven calves with hereditary hypoplasia. Four healthy calves from an unrelated Hereford herd were used as a contrai group. Sixteen calves, without signs of disease, from an experimental affected herd were also studied to detect subclinical cases of lymphedema. After sedation and local anaesthesia a trian-guiar flap of skin was reflected over the lateral aspect of the metacaÍpus and metatarsus to expose the subcutaneous lymphatics, which were previously stained by methylene blue injected subcutaneously into the interdigital space. The contrast medium was injected into the stained lymph vessels and lymphographies were taken in the anatomical regions where the popliteal and prescapular lymph nades are located. The lymphangiograms obtained were used to determine the caliber of lymph vessels and the cranio-caudal and proximo-distal dimensions of the popliteal lymph nades. It was demonstrated that direct lymphography is a suitable method to study the peripheral lymphatic system in the hind limbs of cattle with hereditary lymphatic hypoplasia. The lesions were hypoplasia and/or aplasia of the peripheral lymphatic system, characterized by decreased number and enlargement or absence of peripheral lymph vessels and decreased size or absence of popliteal lymph nodes. In calves without clinical signs the peripheral lymphatic lesions which would allow to detect subclinical cases were not observed.

• Lymphatic hypoplasia hereditary diseases heriditary lymphedema

Abstract in Portuguese:

Hipoplasia linfática heriditária foi estudada através do exame radiológico do sistema linfático periférico de sete bovinos da raça Hereford com diagnóstico clínico da doença. Quatro bovinos sadios, da mesma raça, pertencentes a um rebanho livre da doença foram utilizados como controle. Dezesseis bovinos sem sinais clínicos, pertencente a um rebanho experimental, no qual a doença foi reproduzida, foram, também, estudados com o objetivo de detectar-se casos subclínicos da enfermidade. Após a sedação dos animais e anestesia local, foi feita uma incisão na pele, no terço médio da face lateral dos ossos metacarpo e metatarso para exposição dos vasos linfáticos, marcados previamente por azul de metileno. Nos vasos linfáticos foi injetado meio de contraste e foram tomadas radiografias nas regiões anatômicas onde estão localizados os linfonodos pré-escapulares e poplíteos. Nas radiografias eram medidos o calibre dos vasos linfáticos e as dimensões dorso-ventral e crâneo-caudal dos linfonodos. Este estudo demonstrou ser a linfografia direta eficiente para a avaliação do sistema linfático periférico dos membros posteriores de bovinos com hipoplasia linfática. As lesões observadas, de hipoplasia e/ou aplasia do sistema linfático periférico, caracterizaram-se por redução no número e aumento do diâmetro ou ausência de vasos linfáticos e diminuição do tamanho ou ausência dos linfonodos poplíteos. Nos animais que não apresentavam sinais clínicos não foram observadas alterações no sistema linfático periférico que permitissem a detecção de casos subclínicos da enfermidade.

• Hipoplasia linfática doenças hereditárias linfoedema hereditário