Factors influencing pre-ovulatory follicle diameter and weaning-to-ovulation interval in spontaneously ovulating sows in tropical environment.

Follicle development and timing of ovulation are indicators of the reproductive performance of sows. The present study aimed to determine factors influencing pre-ovulatory follicle diameter and weaning-to-ovulation interval (WOI) in spontaneously ovulating sows in tropical climates with special emphasis on breed, parity and backfat thickness at weaning. In total, 80 sows were included in the study. Follicle development was determined by using transrectal real-time B-mode ultrasonography every 6 hr after standing oestrus. Weaning-to-oestrous interval (WEI), oestrous-to-ovulation interval (EOI), WOI and the diameter of graafian follicles were investigated in relation to breed, parity number (1, 2-3 and 4-7) and backfat thickness (low, moderate and high) of sows. Overall, WEI, EOI, WOI and the pre-ovulatory follicle diameter were 92.5 ± 21.6 hr, 64.3 ± 19.3 hr, 156.3 ± 29.1 hr and 10.3 ± 2.0 mm, respectively. Pre-ovulatory follicle size was smaller in primiparous sows compared with sows of greater parity, 4-7 (9.7 ± 0.51 and 11.7 ± 0.52 mm, respectively, p < .05). Weaning-to-ovulation interval was positively correlated with WEI (r = 0.75, p < .001) and EOI (r = 0.66, p < .001), but negatively correlated with size of the graafian follicle (r = -0.34, p < .01). Sows with a shorter WEI had a larger pre-ovulatory follicle diameter (at 64 hr after oestrus) (r = -0.37, p < .01). Sows with low backfat thickness had a WOI 23.4 hr longer than those with moderate backfat thickness (p < .05) and 17.6 hr longer than sows with a high backfat thickness (p = .140). The follicle diameter in primiparous sows with high backfat thickness (11.7 ± 1.1 mm) was higher than in those with low (8.9 ± 0.7 mm, p < .05) or moderate (8.6 ± 0.8, p < .05) backfat thickness. In conclusion, factors influencing follicle diameter and WOI in sows included parity number and backfat thickness at weaning. The impact of backfat thickness on follicle diameter, WEI and WOI was most pronounced in primiparous sows.

Hepatitis E virus genotype 3f sequences from pigs in Thailand, 2011-2012.

Phylogenetic analysis of partial ORF1 and ORF2 genes of Hepatitis E virus (HEV) strains from pigs in Thailand during 2011-2012 was performed. The result indicated that the current Thai strains belonged to the genotype 3 subgroup 3f, which were similar to the previous HEVs circulating in humans in Thailand.

Gilt reproductive performance in a tropical environment after oestrus synchronization and fixed-time artificial insemination.

The present study was performed to evaluate the reproductive performance of gilts inseminated using fixed-time artificial insemination (FTAI) protocol. A total of 408 Landrace × Yorkshire crossbred gilts were included in the experiment. Gilts at 8 months of age were randomly allocated into three groups: control AI (n = 192), treatment 1-TAI (n = 117) and treatment 2-FTAI (n = 99). Gilts in the control AI group were inseminated 2-3 times during standing oestrus at 0, 12 and 24 h after the onset of oestrus. Gilts in the treatment 1-TAI group were orally administered 20 mg per day of altrenogest for 18 days and then inseminated 2-3 times during standing oestrus by conventional AI. Gilts in the treatment 2-FTAI group were synchronized like gilts in treatment 1-TAI group but then GnRH (10 µg of buserelin) was administered 120 h after the end of altrenogest treatment and fixed time artificial inseminated twice at 24 and 32 h after GnRH irrespective of the presence of oestrus or not. Conception rate of gilts in treatment 2-FTAI (87.9%) was similar to the treatment 1-TAI (94.9%) and control AI (83.3%) (P > 0.05). Conception rate in treatment 1-TAI (94.9%) was higher compared to control AI group (83.3%, P = 0.040). Farrowing rate of gilts in treatment 2-FTAI (83.8%) was similar to treatment 1-TAI (89.7%) and control AI (76.0%) (P > 0.05). Farrowing rate of treatment 1-TAI (89.7%) was higher than control AI gilts (76.0%, P = 0.033). In treatment 2-FTAI, the conception and farrowing rate of the nine gilts that were inseminated even if they were not detected in oestrus (all during warm season) was 44.4% and 44.4%, respectively. Regular return to oestrus was similar between groups (9.4%, 0.9% and 4.1% for control AI, treatment 1-TAI and treatment 2-FTAI, respectively, P > 0.05). The total number of piglets born per litter in treatment 1-TAI group was higher than control AI (13.1 ± 0.2 versus 11.6 ± 0.2, respectively, P < 0.001) and treatment 2-FTAI groups (12.2 ± 0.3, P = 0.019). The number of piglets born alive was higher in treatment 1-TAI (12.1 ± 0.3) compared to treatment 2-FTAI (11.3 ± 0.2) and control AI group (11.2 ± 0.3). The percentage of stillbirth and mummified foetus were not different between groups (P > 0.05). The present study indicated that fixed-time AI in gilts can be successfully performed by administration of altrenogest for 18 days, GnRH at 120 h after altrenogest withdrawal and then double fixed-time AI at 24 and 32 h after the administration of GnRH. Fertility metrics such as conception rate, farrowing rate and litter performances using this method were similar to gilts inseminated at oestrus with conventional AI.

Reproductive performance of weaned sows after single fixed-time artificial insemination under a tropical climate: Influences of season and insemination technique.

We evaluated the reproductive performance of sows after single fixed-time AI under a tropical climate and investigated the influences of season and insemination technique on the efficacy of single fixed-time AI. After weaning, the sows were divided into CONTROL (n = 212) and FIXED-TIME (n = 212) groups. Sows in the CONTROL group were inseminated at 12 and 36 h after the onset of oestrus, while sows in the FIXED-TIME group were administered 10 µg of GnRH at 72 h after weaning and were inseminated 32 h later. Reproductive performance parameters, including total born, born alive, mummified foetuses and stillborn piglets per litter, piglet birth weight, variation of piglet birth weight within litter, regular return-to-oestrus and farrowing rate, were compared between the two groups. Season was classified into two groups: cool (n = 170) and hot (n = 254), and insemination technique was classified into two groups: conventional AI (n = 171) and intra-uterine insemination (IUI) with a reduced number of spermatozoa (n = 253). On average, regular return-to-oestrus (3.3 vs. 5.6%, P > 0.05) and farrowing rates (92.8 vs. 88.1%, P > 0.05) did not differ between CONTROL and FIXED-TIME groups. However, the total born and born alive piglets per litter in the FIXED-TIME were lower than in the CONTROL group (12.0 vs. 12.8 piglets/litter; P = 0.030 and 11.3 vs. 12.2 piglets/litter, P = 0.007). Interestingly, the number of total born piglets in the FIXED-TIME group was lower than in the CONTROL group only in the sows inseminated in the hot season (11.7 ±â€¯0.32 and 12.9 ±â€¯0.31, respectively, P = 0.005). Piglet birth weight, variation of piglet birth weight within litter, number of piglets at weaning and body weight of piglets at weaning did not differ between groups, irrespective of the season (P > 0.05). The total number of piglets born per litter in the FIXED-TIME group was lower than that in the CONTROL group in sows inseminated via IUI (11.7 ±â€¯0.32 and 12.9 ±â€¯0.32, respectively, P = 0.013), but not in sows inseminated using conventional AI (12.7 ±â€¯0.42 and 12.5 ±â€¯0.41, respectively, P = 0.772). Single fixed-time AI could be successfully performed in sows under a tropical climate, with a promising reproductive performance. However, a decreased litter size at birth after single fixed-time AI was observed when insemination was performed in the hot season. Moreover, single fixed-time AI using IUI with a reduced number of spermatozoa also decreased litter size at birth.