Effects of Feeding Bt MON810 Maize to Pigs for 110 Days on Peripheral Immune Response and Digestive Fate of the cry1Ab Gene and Truncated Bt Toxin

peer-reviewedBackground: The objective of this study was to evaluate potential long-term (110 days) and age-specific effects of feeding genetically modified Bt maize on peripheral immune response in pigs and to determine the digestive fate of the cry1Ab gene and truncated Bt toxin. Methodology/Principal Findings: Forty day old pigs (n = 40) were fed one of the following treatments: 1) isogenic maize-based diet for 110 days (isogenic); 2) Bt maize-based diet (MON810) for 110 days (Bt); 3) Isogenic maize-based diet for 30 days followed by Bt maize-based diet for 80 days (isogenic/Bt); and 4) Bt maize-based diet (MON810) for 30 days followed by isogenic maize-based diet for 80 days (Bt/isogenic). Blood samples were collected during the study for haematological analysis, measurement of cytokine and Cry1Ab-specific antibody production, immune cell phenotyping and cry1Ab gene and truncated Bt toxin detection. Pigs were sacrificed on day 110 and digesta and organ samples were taken for detection of the cry1Ab gene and the truncated Bt toxin. On day 100, lymphocyte counts were higher (P<0.05) in pigs fed Bt/isogenic than pigs fed Bt or isogenic. Erythrocyte counts on day 100 were lower in pigs fed Bt or isogenic/Bt than pigs fed Bt/isogenic (P<0.05). Neither the truncated Bt toxin nor the cry1Ab gene were detected in the organs or blood of pigs fed Bt maize. The cry1Ab gene was detected in stomach digesta and at low frequency in the ileum but not in the distal gastrointestinal tract (GIT), while the Bt toxin fragments were detected at all sites in the GIT. Conclusions/Significance: Perturbations in peripheral immune response were thought not to be age-specific and were not indicative of Th 2 type allergenic or Th 1 type inflammatory responses. There was no evidence of cry1Ab gene or Bt toxin translocation to organs or blood following long-term feeding.The research leading to these results has received funding from the European Union’s Seventh Framework Programme (FP7/2007-2013) under grant agreement n° 211820 and the Teagasc Walsh Fellowship programme

SLC10A7 mutations cause a skeletal dysplasia with amelogenesis imperfecta mediated by GAG biosynthesis defects.

Skeletal dysplasia with multiple dislocations are severe disorders characterized by dislocations of large joints and short stature. The majority of them have been linked to pathogenic variants in genes encoding glycosyltransferases, sulfotransferases or epimerases required for glycosaminoglycan synthesis. Using exome sequencing, we identify homozygous mutations in SLC10A7 in six individuals with skeletal dysplasia with multiple dislocations and amelogenesis imperfecta. SLC10A7 encodes a 10-transmembrane-domain transporter located at the plasma membrane. Functional studies in vitro demonstrate that SLC10A7 mutations reduce SLC10A7 protein expression. We generate a Slc10a7-/- mouse model, which displays shortened long bones, growth plate disorganization and tooth enamel anomalies, recapitulating the human phenotype. Furthermore, we identify decreased heparan sulfate levels in Slc10a7-/- mouse cartilage and patient fibroblasts. Finally, we find an abnormal N-glycoprotein electrophoretic profile in patient blood samples. Together, our findings support the involvement of SLC10A7 in glycosaminoglycan synthesis and specifically in skeletal development

Redução de proteína e fósforo em dietas com fitase para frangos de corte dos 22 aos 42 dias de idade

Avaliou-se o efeito da inclusão de fitase em dietas com proteína bruta (PB) e fósforo disponível (Pd) reduzidos sobre o desempenho, rendimento de carcaça e cortes e quantidade de poluentes na cama de frangos dos 22 aos 42 dias de idade. Foram utilizados 1200 pintos aos 21 dias, média de peso inicial de 646±8g, distribuídos em blocos ao acaso em esquema fatorial 3x3+1 (três porcentagens de Pd - 0,2, 0,3 e 0,4% - e três de PB - 14, 16 e 18% - e um tratamento adicional, padrão) em seis repetições de 20 aves cada. A fitase (500FTU/kg) foi adicionada nas dietas com fósforo reduzido (0,2 e 0,3%). Aos 42 dias as aves foram abatidas e amostras das camas foram encaminhadas para análise. Em dietas com reduzido teor de PB, melhor desempenho e rendimento de carcaça e menor quantidade de fósforo, cálcio, potássio e zinco nas camas foram obtidos com 0,3% Pd+fitase. Menor quantidade de nitrogênio e potássio, porém com maior deposição de gordura abdominal e maior excreção de cobre, foram obtido com 14% de PB. Comparadas ao controle, dietas com 14% de PB e 0,3% de Pd reduziram a excreção de fósforo em 34%. Conclui-se que dietas com 14% de PB e 0,3% de Pd, suplementadas com fitase e aminoácidos cristalinos, podem ser utilizadas para frangos de corte dos 22 aos 42 dias