11 PREGNANCY RATES AND ATP1A1 POLYMORPHISM IN THERMOTOLERANT HOLSTEIN COWS DURING SUMMER IN BRAZIL
T. F. Lacerda A , R. B. G. C. Carvalho A , M. G. Favoreto A and B. Loureiro AUniversidade Vila Velha, Vila Velha, Espírito Santo, Brazil
Reproduction, Fertility and Development 29(1) 113-113 https://doi.org/10.1071/RDv29n1Ab11
Published: 2 December 2016
Abstract
Maximum body temperatures (BT) registered in dairy cows have been used as an indicator of heat stress (HS). However, some studies have shown that the variation in BT, which represents energy requirements for BT regulation, is more representative of HS. Cows that show less variation in BT can be considered thermotolerant. The ATP1A1 gene is critical for maintaining homeostasis through the fluctuation of plasma K+ and Na+. Thus, this experiment was designed to (1) test the correlation between the coefficient of variation (CV) in BT and pregnancy rate after artificial insemination (AI) in the summer, and (2) identify polymorphisms in the ATP1A1 gene. Seventy lactating Holstein cows kept in a freestall system were used. To measure BT, an automatic thermometer coupled to a placebo intravaginal implant was kept in the cows, for 3 days, measuring the temperature every 5 min. The temperature CV for each animal was calculated as the ratio of the standard deviation to the mean. Each animal’s daily milk production was registered on the day of implant insertion. The animals used in the experiment were AI without hormonal synchronization, 12 h after presenting oestrus. Semen from Holstein and Gir breeds were used. After 30 days, pregnancy was diagnosed using an ultrasound. Animals were re-inseminated as they showed oestrus until they became pregnant. The number of AI necessary for each animal to become pregnant was calculated. DNA was extracted from tail hair from sixty cows used in the experiment. For polymorphism detection, primers from a fragment of the ATP1A1 gene (forward 5′-AGTGCTGCGTGAAACCTG-3′, reverse 5′-GTGATGTGTGGAATGGTGC-3′) were used. PCR reactions were performed and PCR products were electrophoresed on 1% agarose gel for visualisation of the fragment sizes. Then, the PCR products were purified and sequenced. The obtained sequences were analysed and edited using the BioEdit Software (