First in vitro embryo production in alpacas (Lama pacos).

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dc.contributor Gamarra, G
dc.contributor Huaman, E
dc.contributor Leon, S
dc.contributor Carpio, M
dc.contributor Alvarado, E
dc.contributor Asparrin, M
dc.contributor Vivanco, HW
dc.date.accessioned 2012-01-29T22:38:13Z
dc.date.available 2012-01-29T22:38:13Z
dc.date.issued 2008
dc.identifier.citation Rep. Fert. Dev. (2008) 21(1): 177-178
dc.identifier.issn 1031-3613
dc.identifier.uri http://livestocklibrary.com.au/handle/1234/15084
dc.description.abstract The objective was to produce alpaca embryos in laboratory due to its potential role for the multiplication of genetically superior animals and for conservation purposes. Ovaries were collected from an alpaca abattoir located in the Central Highlands of Peru and transported in a thermos flask with warm saline and antibiotics to the laboratory located 200 km away on the coast. Alpaca epididymal sperm to be used for fertilization was previously frozen by diluting in a TRIS-Fructose based extender with 10% glycerol and frozen as pellets in liquid nitrogen vapor. From 31 ovaries, 262 cumulus&#x2013;oocyte complexes (COCs) were collected (mean of 8.5 COCs per ovary) which were matured in TCM-199 supplemented with 10% heat inactivated FCS plus epidermal growth factor (EGF), FSH, LH, estradiol, and cysteamine for 30 h incubation at 38.5&#xb0;C, 5% CO2 and 90% humidity. The selected oocytes post-maturation were fertilized with the frozen/thawed sperm that was subjected post-thawing to Percoll gradient (90 and 45% Percoll), centrifugation and resuspension in TALP-IVF medium supplemented with 20 &#x3bc;m D-penicillamine, 10 &#x3bc;m hypotaurine, 1 &#x3bc;m epinephrine and 1.1 &#x3bc;g mL-1 of heparin. The oocytes were inseminated with a concentration of 10 &#xd7; 106 spermatozoa per drop of 100 mL of fertilization medium containing 30 oocytes each and incubated for 24 h at 38.5&#xb0;C, 5% CO2 and 90% humidity. The presumptive zygotes were transferred to 200 &#x3bc;L drops (30 zygotes per drop) of SOFaa media supplemented with 5% heat-inactivated FCS which was replaced by SOFaa plus 1% heat-inactivated FCS on day 5 after fertilization. The incubation period post-fertilization was up to day 7 at 38.5&#xb0;C, 5% CO2 and 90% humidity, when the embryos were inspected and graded. The cleavage rate was evaluated at 72 h post-fertilization and embryo development was evaluated on day 5 and 7 post-fertilization. The cleavage rate was 27.1% (71/262) and the percentage of oocytes that reached the stage of morula and blastocyst was 8.0% (21/262). The percentage of blastocyst that hatched when incubated after day 7 was 14.28% (3/21). The in vitro embryo production in alpacas was successful and suggests the possibility for application in intensive reproduction for conservation of South American camelids and for genetic improvement.<fn-group><fn>Research was partially funded by contributions of BIONICHE and SAIS TUPAC AMARU, Junin, Peru.</fn></fn-group>
dc.publisher CSIRO Publishing
dc.source.uri http://www.publish.csiro.au/view/journals/dsp_journal_fulltext.cfm?nid=44&f=RDv21n1Ab157
dc.title First in vitro embryo production in alpacas (Lama pacos).
dc.type Research
dc.description.version Abstract
dc.identifier.volume 21
dc.identifier.page 177-178
dc.identifier.issue 1


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