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Registro completo
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Biblioteca (s) : |
INIA Tacuarembó. |
Fecha : |
10/06/2015 |
Actualizado : |
13/05/2020 |
Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
Autor : |
DE BARBIERI, I.; HEGARTY, R.S.; SILVEIRA, C.; GULINO, L.M.; ODDY, V.H.; GILBERT, R.A.; KLIEVE, A.V.; OUWERKERK, D. |
Afiliación : |
LUIS IGNACIO DE BARBIERI ETCHEBERRY, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; ROGER STEPHEN HEGARTY, School of Environmental and Rural Science, University of New England, Armidale, NSW, Australia.; CAROLINA INES SILVEIRA ROJAS, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; LISA MAREE GULINO, Rumen Ecology Unit, Queensland Department of Agriculture, Fisheries and Forestry, Brisbane, QLD, Australia. Centre for Animal Science, Queensland Alliance for Agriculture and Food Innovation, Brisbane, QLD, Australia.; VICTOR H. ODDY, Beef Industry Centre, Department of Primary Industries NSW, Armidale, NSW, Australia.; ROSALIND A. GILBERT, Rumen Ecology Unit, Queensland Department of Agriculture, Fisheries and Forestry, Brisbane, QLD, Australia; Centre for Animal Science, Queensland Alliance for Agriculture and Food Innovation, Brisbane, QLD, Australia; ATHOL V. KLIEVE, Rumen Ecology Unit, Queensland Department of Agriculture, Fisheries and Forestry, Brisbane, QLD, Australia;f School of Agriculture and Food Sciences, University of Queensland, Gatton, QLD, Australia; DIANE J. OUWERKERK, Rumen Ecology Unit, Queensland Department of Agriculture, Fisheries and Forestry, Brisbane, QLD, Australia. Centre for Animal Science, Queensland Alliance for Agriculture and Food Innovation, Brisbane, QLD, Australia. |
Título : |
Programming rumen bacterial communities in newborn Merino lambs. |
Fecha de publicación : |
2015 |
Fuente / Imprenta : |
Small Ruminant Research, Volume 129, August 2015, Pages 48-59. DOI: https://doi.org/10.1016/j.smallrumres.2015.05.015 |
DOI : |
10.1016/j.smallrumres.2015.05.015 |
Idioma : |
Inglés |
Notas : |
Article history: Received 5 December 2014; Received in revised form 19 May 2015; Accepted 21 May 2015; Available online 3 June 2015. Acknowledgments:
The authors thank David Paul and Drew Ferguson of CSIRO for their support. Additionally we want to thank Graeme Bremner, Andrew Blakely, Gary Taylor, Dave Lockrey, Andrew Eichorn, Victoire de Raphelis-Soissan, Anita Maguire, Cathy Minchin, and Scott Godwin, for their contributions during the field or lab part of the research. Ignacio De Barbieri was supported by National Institute for Agricultural Research (INIA Uruguay). This work was supported in part by the Australian Government?s the Rumen Pangenome project within Filling the Research Gap (FTRG- 1194147-75) program. |
Contenido : |
Establishment of the rumen microbiome can be affected by both early-life dietary measuresand rumen microbial inoculation. This study used a 2 × 3 factorial design to evaluate theeffects of inclusion of dietary fat type and the effects of rumen inoculum from differentsources on ruminal bacterial communities present in early stages of the lambs? life. Twodifferent diets were fed ad libitum to 36 pregnant ewes (and their lambs) from 1 month pre-lambing until weaning. Diets consisted of chaffed lucerne and cereal hay and 4% molasses,with either 4% distilled coconut oil (CO) provided as a source of rumen-active fat or 4%Megalac®provided as a source of rumen-protected fat (PF). One of three inoculums wasintroduced orally to all lambs, being either (1) rumen fluid from donor ewes fed the PF diet;(2) rumen fluid from donor ewes fed CO; or (3) a control treatment of MilliQ-water. Afterweaning at 3 months of age, each of the six lamb treatment groups were grazed in spatiallyseparated paddocks. Rumen bacterial populations of ewes and lambs were characterisedusing 454 amplicon pyrosequencing of the V3/V4 regions of the 16S rRNA gene. Speciesrichness and biodiversity of the bacterial communities were found to be affected by thediet in ewes and lambs and by inoculation treatment of the lambs. Principal coordinateanalysis and analysis of similarity (ANOSIM) showed between diet differences in bacterialcommunity groups existed in ewes and differential bacterial clusters occurred in lambsdue to both diet and neonatal inoculation. Diet and rumen inoculation acted together toclearly differentiate the bacterial communities through to weaning, however the micro-biome effects of these initial early life interventions diminished with time so that rumenbacterial communities showed greater similarity 2 months after weaning. These resultsdemonstrate that ruminal bacterial communities of newborn lambs can be altered by mod-ifying the diet of their mothers. Moreover, the rumen microbiome of lambs can be changedby diet while they are suckling or by inoculating their rumen, and resulting changes in therumen bacterial microbiome can persist beyond weaning MenosEstablishment of the rumen microbiome can be affected by both early-life dietary measuresand rumen microbial inoculation. This study used a 2 × 3 factorial design to evaluate theeffects of inclusion of dietary fat type and the effects of rumen inoculum from differentsources on ruminal bacterial communities present in early stages of the lambs? life. Twodifferent diets were fed ad libitum to 36 pregnant ewes (and their lambs) from 1 month pre-lambing until weaning. Diets consisted of chaffed lucerne and cereal hay and 4% molasses,with either 4% distilled coconut oil (CO) provided as a source of rumen-active fat or 4%Megalac®provided as a source of rumen-protected fat (PF). One of three inoculums wasintroduced orally to all lambs, being either (1) rumen fluid from donor ewes fed the PF diet;(2) rumen fluid from donor ewes fed CO; or (3) a control treatment of MilliQ-water. Afterweaning at 3 months of age, each of the six lamb treatment groups were grazed in spatiallyseparated paddocks. Rumen bacterial populations of ewes and lambs were characterisedusing 454 amplicon pyrosequencing of the V3/V4 regions of the 16S rRNA gene. Speciesrichness and biodiversity of the bacterial communities were found to be affected by thediet in ewes and lambs and by inoculation treatment of the lambs. Principal coordinateanalysis and analysis of similarity (ANOSIM) showed between diet differences in bacterialcommunity groups existed in ewes and differential bacterial clusters occurred in lambsdue ... Presentar Todo |
Palabras claves : |
COCONUT OIL; EARLY-LIFE INTERVENTION; PROTECTED FAT; RUMEN FLUID INOCULATION; RUMEN MICROBIOME. |
Thesagro : |
MERINO; OVINOS; RUMEN. |
Asunto categoría : |
L01 Ganadería |
Marc : |
LEADER 03812naa a2200325 a 4500 001 1052756 005 2020-05-13 008 2015 bl uuuu u00u1 u #d 024 7 $a10.1016/j.smallrumres.2015.05.015$2DOI 100 1 $aDE BARBIERI, I. 245 $aProgramming rumen bacterial communities in newborn Merino lambs. 260 $c2015 500 $aArticle history: Received 5 December 2014; Received in revised form 19 May 2015; Accepted 21 May 2015; Available online 3 June 2015. Acknowledgments: The authors thank David Paul and Drew Ferguson of CSIRO for their support. Additionally we want to thank Graeme Bremner, Andrew Blakely, Gary Taylor, Dave Lockrey, Andrew Eichorn, Victoire de Raphelis-Soissan, Anita Maguire, Cathy Minchin, and Scott Godwin, for their contributions during the field or lab part of the research. Ignacio De Barbieri was supported by National Institute for Agricultural Research (INIA Uruguay). This work was supported in part by the Australian Government?s the Rumen Pangenome project within Filling the Research Gap (FTRG- 1194147-75) program. 520 $aEstablishment of the rumen microbiome can be affected by both early-life dietary measuresand rumen microbial inoculation. This study used a 2 × 3 factorial design to evaluate theeffects of inclusion of dietary fat type and the effects of rumen inoculum from differentsources on ruminal bacterial communities present in early stages of the lambs? life. Twodifferent diets were fed ad libitum to 36 pregnant ewes (and their lambs) from 1 month pre-lambing until weaning. Diets consisted of chaffed lucerne and cereal hay and 4% molasses,with either 4% distilled coconut oil (CO) provided as a source of rumen-active fat or 4%Megalac®provided as a source of rumen-protected fat (PF). One of three inoculums wasintroduced orally to all lambs, being either (1) rumen fluid from donor ewes fed the PF diet;(2) rumen fluid from donor ewes fed CO; or (3) a control treatment of MilliQ-water. Afterweaning at 3 months of age, each of the six lamb treatment groups were grazed in spatiallyseparated paddocks. Rumen bacterial populations of ewes and lambs were characterisedusing 454 amplicon pyrosequencing of the V3/V4 regions of the 16S rRNA gene. Speciesrichness and biodiversity of the bacterial communities were found to be affected by thediet in ewes and lambs and by inoculation treatment of the lambs. Principal coordinateanalysis and analysis of similarity (ANOSIM) showed between diet differences in bacterialcommunity groups existed in ewes and differential bacterial clusters occurred in lambsdue to both diet and neonatal inoculation. Diet and rumen inoculation acted together toclearly differentiate the bacterial communities through to weaning, however the micro-biome effects of these initial early life interventions diminished with time so that rumenbacterial communities showed greater similarity 2 months after weaning. These resultsdemonstrate that ruminal bacterial communities of newborn lambs can be altered by mod-ifying the diet of their mothers. Moreover, the rumen microbiome of lambs can be changedby diet while they are suckling or by inoculating their rumen, and resulting changes in therumen bacterial microbiome can persist beyond weaning 650 $aMERINO 650 $aOVINOS 650 $aRUMEN 653 $aCOCONUT OIL 653 $aEARLY-LIFE INTERVENTION 653 $aPROTECTED FAT 653 $aRUMEN FLUID INOCULATION 653 $aRUMEN MICROBIOME 700 1 $aHEGARTY, R.S. 700 1 $aSILVEIRA, C. 700 1 $aGULINO, L.M. 700 1 $aODDY, V.H. 700 1 $aGILBERT, R.A. 700 1 $aKLIEVE, A.V. 700 1 $aOUWERKERK, D. 773 $tSmall Ruminant Research, Volume 129, August 2015, Pages 48-59. DOI: https://doi.org/10.1016/j.smallrumres.2015.05.015
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 | Acceso al texto completo restringido a Biblioteca INIA Las Brujas. Por información adicional contacte bibliolb@inia.org.uy. |
Registro completo
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Biblioteca (s) : |
INIA Las Brujas. |
Fecha actual : |
21/02/2014 |
Actualizado : |
28/07/2023 |
Tipo de producción científica : |
Capítulo en Libro Técnico-Científico |
Autor : |
DE LA FUENTE, L.; BAJSA, N.; QUAGLIOTTO, L.; FABIANO, E.; PÉREZ, C.; ALTIER, N.; ARIAS, A. |
Afiliación : |
L. DE LA FUENTE, Departamento de Bioquímica, IIBCE, Montevideo Facultad de Ciencias, Montevideo; N. BAJSA, Departamento de Bioquímica, IIBCE, Montevideo; L. QUAGLIOTTO, Departamento de Bioquímica, IIBCE, Montevideo; E. FABIANO, Departamento de Bioquímica, IIBCE, Montevideo; C. PÉREZ, Facultad de Agronomía, Paysandú; NORA ADRIANA ALTIER MANZINI, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; A. ARIAS, Departamento de Bioquímica, IIBCE, Montevideo. |
Título : |
Interactions among Rhizobia and biocontrol agents in forage legumes. |
Complemento del título : |
Proceedings of the 12 th International Congress on Nitrogen Fixation, Foz do Iguaçu, Paraná, Brazil, September 12?17, 1999. |
Fecha de publicación : |
2002 |
Fuente / Imprenta : |
In: Pedrosa, F.O., Hungria, M., Yates, G., Newton, W.E. (eds). Nitrogen Fixation: From Molecules to Crop Productivity. Current Plant Science and Biotechnology in Agriculture, vol 38. Springer, Dordrecht. p. 552. https://doi.org/10.1007/0-306-47615-0_311 |
DOI : |
10.1007/0-306-47615-0_311 |
Idioma : |
Inglés |
Notas : |
This work was partially supported by PEDECIBA, The European Union, and CSIC. |
Contenido : |
Forage legumes play an important role in the agriculture of Uruguay as a major source of high quality feed for livestock. Their nitrogen fixation capability in symbiotic association with rhizobia confers them a beneficial carryover effect in crop rotation. Nevertheless, important losses in pasture
production are due to soilborne fungal pathogens (Altier 1996). The utilization of rhizospheric fluorescent pseudomonads as biocontrol agents is a feasible alternative to solve this problem. © 2002 Kluwer Academic Publishers. |
Palabras claves : |
Biocontrol Agent; Forage Legume; Rhizoctonia Solani. |
Asunto categoría : |
F01 Cultivo |
Marc : |
LEADER 01486nam a2200241 a 4500 001 1010795 005 2023-07-28 008 2002 bl uuuu u01u1 u #d 024 7 $a10.1007/0-306-47615-0_311$2DOI 100 1 $aDE LA FUENTE, L. 245 $aInteractions among Rhizobia and biocontrol agents in forage legumes.$h[electronic resource] 260 $aIn: Pedrosa, F.O., Hungria, M., Yates, G., Newton, W.E. (eds). Nitrogen Fixation: From Molecules to Crop Productivity. Current Plant Science and Biotechnology in Agriculture, vol 38. Springer, Dordrecht. p. 552. https://doi.org/10.1007/0-306-47615-0_311$c1007 500 $aThis work was partially supported by PEDECIBA, The European Union, and CSIC. 520 $aForage legumes play an important role in the agriculture of Uruguay as a major source of high quality feed for livestock. Their nitrogen fixation capability in symbiotic association with rhizobia confers them a beneficial carryover effect in crop rotation. Nevertheless, important losses in pasture production are due to soilborne fungal pathogens (Altier 1996). The utilization of rhizospheric fluorescent pseudomonads as biocontrol agents is a feasible alternative to solve this problem. © 2002 Kluwer Academic Publishers. 653 $aBiocontrol Agent 653 $aForage Legume 653 $aRhizoctonia Solani 700 1 $aBAJSA, N. 700 1 $aQUAGLIOTTO, L. 700 1 $aFABIANO, E. 700 1 $aPÉREZ, C. 700 1 $aALTIER, N. 700 1 $aARIAS, A.
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