Comparative validation using quantitative real-time PCR (qPCR) and conventional PCR of bovine semen centrifuged in continuous density gradient

Author(s)

Resende, M. V. ^[1] ; Lucio, A. C. ^[2] ; Perini, A. P. ^[1] ; Oliveira, L. Z. ^[1] ; Almeida, A. O. ^[1] ; Alves, B. C. A. ^[3] ; Moreira-Filho, C. A. ^[4] ; Santos, I. W. ^[5] ; Hossepian de Lima, V. F. M. ^[1]

Affiliation

^[1] UNESP, FCAV, Dept Med Vet Prevent & Reprod Anim, Jaboticabal, SP - Brazil

^[2] UNESP, FCAV, Dept Zootecnia, Jaboticabal, SP - Brazil

^[3] Inst Israelita Ensino & Pesquisa Albert Einstein, Sao Paulo - Brazil

^[4] Univ Sao Paulo, Fac Med, Dept Pediat, BR-09500900 Sao Paulo - Brazil

^[5] UFPR, Dept Vet Med, Palotina, Parana - Brazil

• Document type: Journal article
• Source: Arquivo Brasileiro de Medicina Veterinária e Zootecnia; v. 63, n. 3, p. 544-551, JUN 2011.
• Web of Science Citations: 1

Abstract

The objective of the present study was to determine the sperm enrichment with X-bearing spermatozoa, after one centrifugation in a Percoll or OptiPrep continuous density gradient, using quantitative real-time polymerase chain reaction (qPCR) of sperm DNA and resultant in vitro-produced bovine embryos by PCR. Frozen/thawed sperm was layered on density gradients and the tubes were centrifuged. Supernatants were gently aspirated and the sperm recovered from the bottom of the tubes. Cleavage and blastocyst rates were determined through in vitro production of embryos and PCR was performed to identify the embryos' genetic sex. A difference in blastocyst rate was found in the Percoll treatment compared to OptiPrep (P<0.05). The percentage of female embryos in the Percoll and OptiPrep groups was 62.0% and 47.1%, respectively. These results were confirmed by qPCR of spermatozoa DNA and underestimation was seen only in the Percoll group. It was possible to sexing sperm using simple approach. (AU)