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2.
PLoS One ; 7(5): e36531, 2012.
Article in English | MEDLINE | ID: mdl-22606269

ABSTRACT

The lack of affordable techniques for gene transfer in birds has inhibited the advancement of molecular studies in avian species. Here we demonstrate a new approach for introducing genes into chicken somatic tissues by administration of a lentiviral vector, derived from the feline immunodeficiency virus (FIV), into the chorioallantoic membrane (CAM) of chick embryos on embryonic day 11. The FIV-derived vectors carried yellow fluorescent protein (YFP) or recombinant alpha-melanocyte-stimulating hormone (α-MSH) genes, driven by the cytomegalovirus (CMV) promoter. Transgene expression, detected in chicks 2 days after hatch by quantitative real-time PCR, was mostly observed in the liver and spleen. Lower expression levels were also detected in the brain, kidney, heart and breast muscle. Immunofluorescence and flow cytometry analyses confirmed transgene expression in chick tissues at the protein level, demonstrating a transduction efficiency of ∼0.46% of liver cells. Integration of the viral vector into the chicken genome was demonstrated using genomic repetitive (CR1)-PCR amplification. Viability and stability of the transduced cells was confirmed using terminal deoxynucleotidyl transferase (dUTP) nick end labeling (TUNEL) assay, immunostaining with anti-proliferating cell nuclear antigen (anti-PCNA), and detection of transgene expression 51 days post transduction. Our approach led to only 9% drop in hatching efficiency compared to non-injected embryos, and all of the hatched chicks expressed the transgenes. We suggest that the transduction efficiency of FIV vectors combined with the accessibility of the CAM vasculature as a delivery route comprise a new powerful and practical approach for gene delivery into somatic tissues of chickens. Most relevant is the efficient transduction of the liver, which specializes in the production and secretion of proteins, thereby providing an optimal target for prolonged study of secreted hormones and peptides.


Subject(s)
Chick Embryo , Gene Transfer Techniques , Genetic Vectors , Immunodeficiency Virus, Feline/genetics , Animals , Animals, Genetically Modified , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Base Sequence , Cells, Cultured , Chick Embryo/metabolism , Chick Embryo/virology , Chickens/genetics , Chorioallantoic Membrane/metabolism , Chorioallantoic Membrane/virology , DNA Primers/genetics , Liver/metabolism , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Tissue Distribution , Transduction, Genetic/methods , alpha-MSH/genetics , alpha-MSH/metabolism
3.
Vet J ; 185(2): 130-7, 2010 Aug.
Article in English | MEDLINE | ID: mdl-19546015

ABSTRACT

Four genetically related Improved Awassi sheep flocks had sporadic births of lambs with congenital visual impairments that differed from other known forms of sheep blindness. Pedigree analysis suggested an autosomal recessive mode of inheritance. Behavioural studies of 4-month old affected lambs showed that their day vision (but not night vision) was impaired. Electrophysiological results at this age demonstrated diminished function of cones but not rods. Histopathological and immunohistochemical evaluation of affected retinas from 5-month old lambs revealed both red-green and blue cones, suggesting that the behavioural day blindness and reduced cone electroretinograms reflect cone dysfunction rather than severe cone photoreceptor loss. Awassi day blindness may be a form of achromatopsia.


Subject(s)
Blindness/veterinary , Pedigree , Sheep Diseases , Animals , Animals, Newborn , Blindness/epidemiology , Blindness/genetics , Blindness/pathology , Electroretinography/veterinary , Female , Immunohistochemistry/veterinary , Male , Mutation , Retinal Cone Photoreceptor Cells/metabolism , Retinal Cone Photoreceptor Cells/pathology , Retinal Rod Photoreceptor Cells/metabolism , Retinal Rod Photoreceptor Cells/pathology , Sheep , Sheep Diseases/epidemiology , Sheep Diseases/genetics , Sheep Diseases/pathology
4.
Fertil Steril ; 82(6): 1714-5, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15589891

ABSTRACT

This is the first report of successful cryopreservation and transplantation of an intact ovary in a large animal (sheep). Three of eight transplanted sheep had resumed hormonal cyclicity.


Subject(s)
Cryopreservation , Ovary/transplantation , Animals , Arteriovenous Anastomosis , Estrus/blood , Female , Ovary/blood supply , Ovary/surgery , Progesterone/blood , Regional Blood Flow , Sheep , Veins
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