Assessment of sow herd frequency of PCV-2 using placental umbilical cord serum and serology in 18 breeding farms in Brazil.

Porcine circovirus type 2 (PCV-2) is the agent of one of the most important diseases in the swine industry. Although it has been controlled through vaccination, viremic piglets at birth may represent a risk by reducing vaccination efficacy. Since there are few reports on the viremic status of pre-suckling piglets regarding PCV-2 infection, we assessed the PCV-2 frequency in sows housed in 18 breeding farms with no history of clinical PCVAD in Brazil, using placental umbilical cord serum (PUCS). The selection criteria were: breeding farms with more than 1,000 sows; sows not vaccinated for PCV-2 at least for 2 years prior to the study; farms with no history of PCV-2 clinical disease in the last 12 months; and production systems with a maximum of two sites. Blood from the umbilical cords in sow placenta or directly from piglet's immediately after birth was collected from 30 litters on each farm for PCR. In addition, blood from 538 sows was collected for PCV-2 antibody detection. A total of 17.29% of the PUCS tested positive. The PCV-2 DNA was detected in PUCS from 94.4% of all farms. A total of 94.8% of the sows was positive for PCV-2 antibodies. However, seronegative sows were detected in 44.4% of farms. All 18 farms had at least 46.9% seropositive dams. A higher percentage of seronegative sows was observed for farms with more than 10% of PCV-2-positive litters compared to those with ≤10% of PCV-2 positive litters (8.9 +/-1.7% vs. 1.5 +/- 0.7%, p < 0.01, respectively).

L-cysteine improves boar semen motility at 5 ºC but does not affect the oxidative status.

Hypothermic storage has been proposed as a method to reduce bacterial loads and promoting prudent use of antibiotics. Reducing temperature, however, can lead to cold shock damage and oxidative stress in boar semen. This study verified the effect of L-cysteine on the quality of semen stored at 5 °C for 120 h. Twenty-one normospermic ejaculates were diluted in Beltsville Thawing Solution into five treatments: Positive control (Pos_Cont, storage at 17 °C without L-cysteine) and groups with 0, 0.5, 1, and 2 mmol/L of L-cysteine supplementation stored at 5 °C. Variables were analyzed as repeated measures, considering treatment, storage time, and interaction as main factors. The effects of different L-cysteine concentrations were also evaluated using polynomial orthogonal contrasts. Sperm motility and pH were higher in the Pos_Cont compared to the groups stored at 5 °C (P < 0.05). In polynomial orthogonal contrast models, total motility was affected by the interaction between L-cysteine and storage time (P = 0.04), with a linear increase in motility when increasing the amount of L-cysteine at 72 and 120 h. Progressive motility increased quadratically as the L-cysteine reached 1 mmol/L (P < 0.01). In the thermoresistance test at 120 h, sperm motility increased quadratically up to an L-cysteine dose of 1 mmol/L (P < 0.05). Sulfhydryl content linearly increased with L-cysteine supplementation (P = 0.01), with no effect on intracellular ROS and sperm lipid peroxidation (P ≥ 0.06) in 5ºC-stored doses. In conclusion, L-cysteine supplementation has a positive effect on sperm motility up to 120 h of storage at 5 °C.

Managing Reproduction in Hyperprolific Sow Herds.

The rearing of large litters from hyperprolific sows is a characteristic of modern genotypes. However, these sows have body and reproductive characteristics that differentiate them from the genotypes of the past decades, making it necessary to adopt different management strategies. This review describes the main care and challenges associated with the hyperprolificity of sows during the period in which replacement gilts are selected, along with gestation, parturition, lactation, and the weaning-estrus interval. It describes the challenges that these sows' piglets will face during the lactation period and includes some strategies adopted to develop these surplus piglets. In addition, it identifies areas where more research is needed to understand the reproductive management of modern genotypes.

Sperm concentration of boar semen doses and sperm quality: Novel perspectives based on the extender type and sperm resilience.

This study evaluated the effect of sperm concentration of boar semen doses on their capacity to maintain its motility over the thermo-resistance test (TRT; sperm resilience) and verified if the extender type (short or long-term) could influence this effect. Thirty ejaculates from five crossbred mature PIC® boars were used, and a factorial design was followed to produce semen doses with 1.5 billion cells in 45 or 90 mL, using Beltsville Thawing Solution (BTS) or Androstar® Plus (APlus). Then, low-concentration doses (16.7 × 106 cells/mL in 90 mL) and higher-concentration doses (33.3 × 106 cells/mL in 45 mL) with BTS or APlus were produced and stored at 17 °C for 168 h. At 72 h, during the TRT, the low-concentration doses (16.7 × 106 cells/mL) lost three-fold less motility than doses with 33.3 × 106 cells/mL (P < 0.01), regardless of the extender type (11. 5% vs. 30.5% of initial motility, respectively). Similar results were found when the TRT was carried out at 168 h, with low-concentration doses losing two-fold less motility (11.4%) than highly concentrated doses (25.9%; P < 0.01). No sperm concentration effect was observed on membrane integrity or mitochondrial membrane potential (P ≥ 0.23). The osmolarity was not affected by the sperm concentration (P = 0.56), only by the extender and the storage time (P < 0.01). In conclusion, the sperm concentration effect on sperm quality was not influenced by extender type, and the data suggest that a low concentration of semen doses positively affects sperm resilience.

Does a single fixed-time insemination in weaned sows affect gestation and lactation length, and piglet performance during lactation compared with multiple insemination protocols in a commercial production setting?

This study evaluated the effect of different single fixed-time artificial insemination (FTAI) protocols on gestation length, farrowing distribution (synchrony), and piglet performance. In Study 1, 866 sows were assigned to two groups: Multiple AI (n = 484) - multiple artificial insemination (AI) at 24 h intervals during estrus; and FTAI+MultAI (n = 382) - OvuGel® 96 h post-weaning and single FTAI 22-24 h later. In Study 2, FTAI protocols were retrospectively analyzed: pLH - sows received 2.5 mg (Exp.1, n = 184) or 5 mg (Exp.2, n = 362) of porcine luteinizing hormone (pLH) at estrus onset, and single FTAI 24 h later. The FTAI+MultAI resulted in shorter gestation length (P < 0.01) and greater synchrony of farrowing on days 114-115 of gestation (P < 0.01) than Multiple AI. Longer lactation length (21.2 vs. 20.9 d; P = 0.02) and greater piglet weaning weight (5378.9 ± 73.1 vs. 5153.2 ± 74.4 g; P = 0.03) for FTAI+MultAI compared to Multiple AI were observed. In Study 2, the gestation length based on the first AI record was shorter for FTAI and resulted in greater synchrony of farrowing on days 114-115 of gestation, compared with Multiple AI (P ≤ 0.05). Gestation length did not differ between groups (P > 0.05) when measured based on most probable AI responsible for fertilization (ultrasound evaluation). In conclusion, FTAI resulted in shorter gestation length and greater farrowing synchrony compared with Multiple AI. Longer lactation length and greater piglet weaning weight were observed for FTAI compared with multiple insemination protocols.

Altrenogest treatment during the last week of lactation on ovarian traits and subsequent reproductive performance of primiparous and multiparous sows.

High-quality follicles result in larger corpora lutea (CL), producing more progesterone, and having a fundamental role in pregnancy maintenance. For some sows, follicular growth takes place during lactation, and follicle selection occurs under a catabolic environment. As altrenogest inhibits follicular development, this study aimed to evaluate follicular growth, CL size, estrus expression, and subsequent reproductive performance of sows treated with altrenogest during the last seven days of a three-week lactation. A total of 81 primiparous and 319 multiparous sows were allocated to two treatments: CONT (control group) and ALT (20 mg of altrenogest/day during the last seven days of lactation). Subsamples of 20 primiparous sows and 97 multiparous were randomly selected to evaluate follicular growth and 26 multiparous sows for serum progesterone analysis at day 21 of gestation. On day 21 of pregnancy, CL measurement was performed by ultrasound. Once in estrus, sows were post-cervically inseminated with pooled semen doses with 1.5 × 109 sperm cells at estrus onset and every 24 h during the standing reflex period. Sows not showing estrus until 10 days after weaning were considered in anestrus. The variables weaning-to-estrus interval, CL size, litter size in the subsequent cycle, and piglet birth weight were evaluated using the GLIMMIX procedure and compared using the Tukey-Kramer test. Anestrus, pregnancy, farrowing, and adjusted farrowing rate were evaluated as binary responses using logistic regression. Follicular size was analyzed as a repeated measure during treatment and after weaning. Treatment was considered as a fixed effect. During the treatment period, follicular size was smaller in ALT sows than CONT sows (3.29 vs. 3.52 mm; P < 0.001). However, after treatment, ALT sows showed a larger follicular size than CONT sows (5.30 vs. 5.03 mm; P ≤ 0.01). There were less ALT sows showing estrus than CONT sows on days three (1.03 vs. 4.57%) and four (55.38 vs. 68.02%) after weaning (P ≤ 0.05), respectively. At 21 days after insemination, ALT sows showed larger CL size and lower CL size variation (P < 0.01) than CONT sows. Anestrus rate, pregnancy rate, farrowing rate, adjusted farrowing rate, litter size in the subsequent cycle, piglet birth weight, litter birth weight, and birth weight variation did not differ between treatments (P ≥ 0.14). In conclusion, altrenogest treatment during the last week of lactation concentrated estrus expression on day five after weaning, larger follicle and CL sizes; however, with no improvement in reproductive performance.

Adjusted method of penis fixation during boar semi-automatic semen collection aiming to reduce bacterial contamination.

Semen collection has an essential role in the initial bacterial load in boar ejaculates and extended semen. The study aimed to explore the efficacy of an adjusted penis fixation in a semi-automatic collection system on reducing bacterial contamination of ejaculates in two-boar studs with different scenarios. Historically, stud A had low levels of bacterial load in raw semen, while stud B had a high level of contamination. A total of 56 mature boars had their semen collected using two methods of penis fixation: (a) Traditional: The penis was fixed directly with the artificial cervix and transferred to the adjustable clamp; (b) Adjusted: The fixation was performed with one gloved-hand, and after exteriorization, the penis was gripped using the artificial cervix with the other gloved-hand and transferred to the adjustable clamp. The bacterial load (p = .0045) and the occurrence of ejaculates >231 CFU/ml (p = .0101) were reduced in the Adjusted compared to the Traditional method. Bacterial load was reduced when using the Adjusted method in stud B (p = .0011), which showed a greater occurrence of critical factors for bacterial contamination (p ≤ .0034). The Adjusted method reduced the occurrence of ejaculates >231 CFU/ml when the preputial ostium was dirty (p = .016) and the duration of semen collection was >7 min (p = .022) compared to the Traditional method. In conclusion, the Adjusted penis fixation was efficient in reducing bacterial load of ejaculates, mainly in boar stud B, which had high contamination challenges.

Reproductive performance in gilts following applications of different insemination doses and techniques.

This study evaluated the applicability of intrauterine artificial insemination (IUAI) in gilts and the impact of age at insemination and different body characteristics of gilts on the success rate for cannula insertion. Additionally, reproductive performance was evaluated for IUAI and cervical artificial insemination (CAI), considering different semen dose sizes. A total of 636 gilts were assigned in a 2 × 2 factorial design: two artificial insemination techniques (CAI and IUAI) and two semen dose sizes (1.5 × 109 sperm cells/50 mL or 2.5 × 109 sperm cells/80 mL). In those gilts assigned to IUAI (n = 319) the success rate for intrauterine cannula insertion was evaluated according to weight at first detected estrus, body condition score (BCS), and age at insemination. Reproductive performance, occurrence of bleeding, and semen backflow during all inseminations were compared among groups (2 × 2). Two subgroups were evaluated regarding the time expended to perform insemination (n = 380), and the semen backflow collected during 1 h after insemination (n = 114). The success rate for intrauterine cannula insertion, based on a successful insertion in all inseminations performed during estrus, was 58.9%. Additionally, greater possibility (>60%; P ≤ 0.04) of cannula insertion was observed in heavier gilts (≥124 kg), as well as in older gilts (≥225 d) and those with greater BCS (>3). There were no differences among the groups in pregnancy rate (≥95.3%; P = 0.23), farrowing rate (≥93.7%; P = 0.54), total piglets born (≥14.5; P = 0.45), as well as, bleeding (P = 0.48) and backflow (P = 0.48) during insemination. However, the percentage of semen backflow volume and percentage of sperm cells in the backflow were lower in gilts inseminated by CAI with 1.5 billion sperm cells/50 mL (P < 0.01) than in the other groups. There was no expressive reduction in time expended to perform IUAI compared to CAI. However, gilts inseminated with 1.5 billion sperm cells/50 mL showed a lower total time to inseminate than all other groups (P < 0.01). In conclusion, higher weight, BCS, and age increased the success rate for cannula insertion. However, IUAI did not optimize the insemination procedure, and remains limited for gilts due to the low success rate for cannula insertion. Reproductive performance was not affected by IUAI or CAI using 1.5 or 2.5 billion sperm cells in 50 or 80 mL, respectively, suggesting the possibility of using CAI with 1.5 billion sperm cells/50 mL in gilts.

Effects of the classification of boars according to progressive sperm motility and the extender type on the reproductive performance of a single fixed-time insemination.

The study aimed to evaluate the fertility of boars according to the resistance of their semen to storage using dilution in either Short- or Long-term extender for single fixed-time insemination. From a total of 32 boars, twelve boars were classified during three semen collection (one collection/boar/week) as Low- (64.5%) or High-preservation (83.9%) capacity for maintaining progressive motility (PM) at 120 h of storage using Short-term extender. After the selection period, six ejaculates (weekly collected) from the Low- and High-preservation boars were diluted in Short- or Long-term extender (2 × 2 factorial design) for insemination and evaluation of fertility. A total of 519 weaned sows were submitted to induction of ovulation with triptorelin (OvuGel®) at 96 h post-weaning. Twenty-four hours later, estrus sows were single fixed-time inseminated (FTAI) with semen doses from the different groups of evaluation. The SAS® software was used for statistical analysis considering the class of boar, type of extender, and interaction as fixed effects. The GLIMMIX procedure was used, considering a binomial distribution for total motility (TM) and PM, binary distribution for pregnancy (PR), and farrowing rate (FR), and the total born (TB) was analyzed assuming a normal distribution with the comparison of means by Tukey-Kramer test. An interaction of class of boars and type of extender was observed for TM and PM at insemination (P < 0.001). Long-term extender increased TM in Low-preservation boars, with no effect in High-preservation boars. The ejaculates from High-preservation boars diluted in Short- or Long-term extender showed higher PM at insemination (86.8 and 87.8%, respectively) compared to those from Low-preservation boars in Short- or Long-term extender (73.2% and 77.9%, respectively). There was no effect of the interaction of boar preservation class and type of extender (P ≥ 0.163) on PR, FR or TB. However, Low-preservation boars presented lower TB (14.1 ± 0.2) compared to High-preservation boars (15.0 ± 0.2; P < 0.01). The PR (93.3 vs. 90.1) and FR (88.8 vs. 88.2) were not affected by class of Low- or High-preservation boars, respectively (P ≥ 0.187). The type of extender did not affect PR, FR, or TB (P ≥ 0.440). In conclusion, Low-preservation boars impaired the reproductive performance of single-FTAI sows by reducing TB with no apparent effect on PR or FR.

Follicular dynamic and reproductive performance of gilts submitted to estrous cycle synchronization using two different progestogen sources.

This study evaluated reproductive indicators of gilts treated with altrenogest or an intravaginal device (IVD) containing medroxyprogesterone acetate (MPA) for estrous cycle synchronization, starting the protocol on different days of the estrous cycle or replacing the IVD in the middle of treatment. In Experiment 1, 126 gilts were assigned, according to the day of treatment onset (Day 5 or 10 of the estrous cycle), to the following treatments: Control-5 (no hormone); Control-10 (no hormone); IVD-5 (IVD with MPA); IVD-10 (IVD with MPA); ALT-5 (altrenogest); or ALT-10 (altrenogest). The first day of the previous estrus was considered as Day 0 of the estrous cycle, and progestogen groups were treated for 14 d. In Experiment 2, 63 gilts were assigned to Control, ALT, or IVD groups. Progestogen treatment started on Day 10 of the estrous cycle, and the IVD was replaced after 7 d of treatment. In both experiments, no gilts expressed estrus during progestogen administration. In Experiment 1, the interval hormonal withdrawal-to-estrus (IHE) tended to be shorter when treatment started on Day 10 than on Day 5 (3.6 vs. 4.1 d, respectively; P = 0.09). The percentage of gilts expressing estrus after hormone withdrawal was lower for IVD-gilts (76.3%) compared to ALT (100%) and Control-gilts (92.9%; P ≤ 0.07). The percentage of persistent follicles (PFOL) was greater in IVD-10 (60.0%) and ALT-10 (33.3%) than CONT-10 (0.0%; P ≤ 0.06). The adjusted farrowing rate (AFR) was lower in IVD (65.5%) and ALT (80.5%) compared with CONT (97.4%; P ≤ 0.08). In Experiment 2, the IHE was longer for ALT than IVD (4.9 vs. 3.9 d, respectively; P < 0.01). No difference among groups was observed in the percentage of gilts expressing estrus (overall 86.4%), but the occurrence of PFOL was higher in IVD (61.5%) compared to ALT (5.3%), and Control groups (10.5%; P < 0.01). The AFR was lower in IVD (53.8%) than in ALT (88.2%) and Control (94.7%; P ≤ 0.05). The total number of piglets born was not affected by hormonal treatments in either experiment. Estrous expression was delayed in gilts treated with altrenogest or IVD-MPA. However, the reproductive performance of IVD-gilts was compromised, which was not circumvented by IVD replacement in the middle of treatment. Therefore, further studies are necessary to understand MPA pharmacodynamics and investigate alternative devices for a steady release of progestogens in gilts.

Reproductive performance of sows inseminated with semen doses stored for up to seven days in long-term extender in a field condition.

This study aimed to evaluate the reproductive performance of sows inseminated with semen doses preserved at 15-18 °C for up to seven days in long-term extender (Duragen®). Parity one (PO1) to PO7 sows were randomly assigned to the following groups: AI1-3 (n=190), insemination with semen doses stored between one and three days; and AI5-7 (n=124), insemination with semen doses stored between five and seven days. Sows were submitted to estrus detection twice a day. Post-cervical insemination according to weaning-to-estrus interval was performed. The farrowing rate (FR) did not differ between the groups (AI1-3=83.2%; AI5-7=82.2%; p>0.05) nor did the total number of piglets born (TPB; AI1-3=14.2±0.3; AI5-7=14.5±0.3; p>0.05). Considering the semen dose most likely responsible for fertilization according to its storage time (1, 2-3, 5, and 6-7 days), the FR (72.7%, 87.8%, 85.7%, and 79%, respectively) and TPB (14.4, 14.0, 14.9, and 13.5, respectively) were similar among the groups (p>0.05). In conclusion, the use of semen doses extended with long-term extender stored for up to seven days did not impair the reproductive performance of sows. Therefore, it's using could optimize production efficiency and logistics of semen dose deliveries to sow farms.

Antibiotic-free extended boar semen preserved under low temperature maintains acceptable in-vitro sperm quality and reduces bacterial load.

This study aimed to assess the sperm quality and number of colony-forming units (CFU mL-1) in extended boar semen stored at low temperatures with or without antibiotics. Normospermic ejaculates (n = 34) were diluted in split samples with Androstar® Premium with or without antibiotics (ampicillin and apramycin sulfate). The extended semen doses were stored for 120 h under three storage temperatures (5, 10, and 17 °C). Variables were analyzed as repeated measures using the GLIMMIX procedure, in a factorial design. The extended semen doses under low-temperature storage (5 and 10 °C) had total motility above 75% throughout the storage. The interaction antibiotic × temperature was significant for total (P = 0.004) and progressive motility (P = 0.005). In extended boar semen doses with antibiotics, the total and progressive motility increased as the storage temperature increased (80.2%, 84.5%, and 89.1%; 70.5%, 76.0%, and 82.9% for total and progressive motility at 5, 10, and 17 °C, respectively; P < 0.05). In extended semen doses without antibiotics, the total and progressive motility were lower when stored at 5 °C than at 10 °C and 17 °C (81.8%, 85.4% and 86.6% and 71.9%, 76.7%, 78.9% for total and progressive motility at 5, 10, and 17 °C, respectively; P < 0.05). After the thermoresistance test, total and progressive motility of doses with antibiotics were higher at 17 °C than 5 °C (P < 0.05); however, they were not affected (P > 0.05) by storage temperature in extended semen doses without antibiotics. The number of CFU mL-1 was lower in extended semen doses without antibiotics stored at 5 and 10 °C than at 17 °C (P < 0.05); however, in extended semen doses with antibiotics, no effect of storage temperature was observed (P > 0.05). The bacterial load was greater in extended semen without antibiotics than with antibiotics, regardless of the storage temperature (P < 0.05). The acrosome and sperm membrane integrity were not influenced (P > 0.05) by using antibiotics. A higher percentage of normal acrosomes was observed as the storage temperature increased (93.6%, 94.3%, and 96.8% at 5, 10, and 17 °C, respectively; P < 0.0001). The membrane integrity was higher (P < 0.0001) in extended semen doses stored at 17 °C than at 10 or 5 °C. The pH rose throughout the storage in all the treatments, except in extended semen doses stored at 17 °C without antibiotics, in which a decrease in the pH occurred at 120 h (P < 0.05). Although the sperm quality being negatively affected by low temperatures, the storage of extended boar semen doses at 5 °C is possible since the sperm viability in vitro was maintained for up to 5 days, fulfilling the requirements of semen quality to be used in artificial insemination. Nevertheless, the use of extended semen doses without antibiotics requires the optimization of hygiene procedures during semen dose processing.

Differential seminal plasma proteome signatures of boars with high and low resistance to hypothermic semen preservation at 5°C.

BACKGROUND: Hypothermic storage at 5°C has been investigated as an alternative to promote the prudent use of antibiotics for boar artificial insemination doses. However, this temperature is challenging for some ejaculates or boars. OBJECTIVE: The present study aimed to identify putative biomarkers for semen resistance to hypothermic storage at 5°C by comparing the seminal plasma proteomes of boars with high and low seminal resistance to preservation at 5°C. MATERIALS AND METHODS: From an initial group of 34 boars, 15 were selected based on the following criteria: ejaculate with ≤20% abnormal spermatozoa and at least 70% progressive motility at 120 hours of storage at 17°C. Then, based on the response to semen hypothermic storage at 5°C, boars were classified into two categories: high resistance-progressive motility of >75% in the three collections (n = 3); and low resistance-progressive motility of <75% in the three collections (n = 3). Seminal plasma proteins were analyzed in pools, and differential proteomics was performed using Multidimensional Protein Identification Technology. RESULTS: Progressive motility was lower at 120 hours of storage in low resistance, compared to high resistance boars (P < .05). Acrosome and plasma membrane integrity were not affected by the boar category, storage time, or their interaction (P ≥ .104). Sixty-five proteins were considered for differential proteomics. Among the differentially expressed and exclusive proteins, the identification of proteins such cathepsin B, legumain, and cystatin B suggests significant changes in key enzymes (eg, metalloproteinases) involved in spermatogenesis, sperm integrity, and fertilizing potential. DISCUSSION AND CONCLUSION: Differences in the seminal plasma suggest that proteins involved in the proteolytic activation of metalloproteinases and proteins related to immune response modulation could disrupt key cellular pathways during spermatogenesis and epididymal maturation, resulting in altered resistance to chilling injury. Further in vivo studies focusing on the immunological crosstalk between epithelial cells and gametes might explain how the immune regulators influence sperm resistance to hipothermic storage.

Effects of intravaginal devices containing different dosages of medroxyprogesterone acetate for the control of the estrous cycle in gilts.

This aim of this study was to investigate the effectiveness of intravaginal devices (IVDs), containing medroxyprogesterone acetate (MPA), for controlling the estrous cycle in pubertal gilts. Gilts were assigned to four treatments: Control (no IVD); IVD containing 100 (IVD100), 200 (IVD200) or 400 mg (IVD400) of MPA. The IVDs were inserted on day 12 of the estrous cycle and maintained intra-vaginally for 14 days. The percentage of gilts in estrus, interval between IVD removal and estrous onset, adjusted farrowing rate (AFR), total number of piglets born (TPB), follicle size and serum progesterone (P4) were recorded. None of the gilts expressed estrus during the IVD treatment period. All gilts of the control group expressed estrus (15/15; 100%) which was greater (P =  0.03) than all IVD-treated gilts (33/44; 75%); however, there were no treatment differences (P =  0.09). The interval between IVD removal and estrous onset was shorter for IVD100 (3.8 ± 0.6 d) compared to IVD400 (5.3 ± 0.6 d; P = 0.05). The IVD400-treated gilts had smaller follicles than the IVD100-treated gilts (P =  0.05). The P4 concentrations were similar among treated groups (P =  0.99). The AFR did not differ among treatment groups (P = 0.37); however, the control group had a greater TPB than the other treatment groups (P =  0.04). The gilts treated with IVDs had longer interval to estrous expression. The most effective dosage was 400 mg of MPA, considering both the minimal follicular growth during the IVD treatment period and the lesser numbers of persistent follicles.

Reproductive performance of fixed-time artificial insemination in swine and factors for the technology success / Desempenho reprodutivo da inseminação artificial em tempo fixo em suínos e fatores para o sucesso da tecnologia

ABSTRACT: Fixed-time artificial insemination (FTAI) is a reproductive technology that aids in obtaining an appropriate time to perform single artificial insemination (AI), thus reducing the number of inseminations per sow bred. FTAI protocols can either be based on estrus detection or day of weaning, aiming to synchronize ovulation using ovulation inducers. The protocols involving estrus detection usually employ porcine luteinizing hormone (pLH) as an inducer and, in general, satisfactory reproductive performance is observed. For protocols based on weaning day, the main hormone used is analog of gonadotropin-releasing hormone such as triptorelin and buserelin. Regardless of the protocol, the number of piglets born is usually not affected by FTAI. However, a possible compromise in the farrowing rate should be considered. The FTAI in gilts requires progestogen treatment for estrus synchronization, increasing the labor requirement and cost of protocol. Some of the benefits of FTAI are a reduced number of semen doses required, advantage of planning the breeding time and; consequently, optimizing labor involved. However, the limitations include a slight reduction in the fertility index due to the compromised farrowing rate in some cases, costs incurred by following the protocol, and difficulty in measuring all the conceptual benefits under commercial conditions. The aim of this review is to approach the reproductive performance of the current protocols of FTAI, considering the benefits and limitations of this technology in swine production.

RESUMO: A inseminação artificial em tempo fixo (IATF) surge como uma biotecnologia para definir o melhor momento para realizar uma única IA, reduzindo o número de células espermáticas por fêmea inseminada. Os protocolos de IATF podem se basear na detecção do estro ou na data de desmame e têm como objetivo sincronizar a ovulação a partir do uso de indutores da ovulação. Protocolos baseados na detecção de estro comumente utilizam o hormônio luteinizante suíno (pLH) como indutor e, de maneira geral, resultados satisfatórios têm sido observados quanto à performance reprodutiva. No caso dos protocolos baseados na data de desmame, os principais hormônios utilizados são os análogos do hormônio liberador de gonadotrofina: triptorelina e buserelina. Independentemente do protocolo, o número de nascidos totais normalmente não é afetado pelo uso da IATF. Porém, um possível comprometimento na taxa de parto deve ser considerado. Já a aplicação da IATF em leitoas requer o fornecimento de um progestágeno, para sincronização do estro, aumentando o manejo e o custo do protocolo. A IATF pode proporcionar diversos benefícios para a indústria suinícola, uma vez que é possível reduzir o número de doses de sêmen produzidas, melhorar o planejamento de coberturas e, consequentemente, otimizar a mão de obra. No entanto, essa biotecnologia apresenta limitações devendo ser considerado a redução nos dados de fertilidade, uma vez que a taxa de parto pode ser comprometida em alguns casos e, o custo do protocolo e a dificuldade de estimar todos os benefícios conceituais da IATF quando aplicada sob condições comerciais. O objetivo dessa revisão é abordar o desempenho reprodutivo dos mais recentes protocolos de IATF, considerando os benefícios e as limitações dessa tecnologia na produção de suínos.

Porcine luteinising hormone given at oestrus onset by intramuscularroute does not advance ovulation in gilts / Hormônio luteinizante suíno aplicado no início do estro pela via intramuscular não antecipa a ovulação em leitoas

This study aimed to evaluate the use of porcine luteinising hormone (pLH) given at oestrus onset in gilts to synchronise ovulation. A total of 120 gilts (40/treatment) were assigned in three treatments: control - application of placebo by intramuscular (i.m.) route at oestrus onset; pLH2.5 - application of 2.5mg of pLH by i.m. route at oestrus onset; pLH5 - application of 5mg of pLH by i.m. route at oestrus onset. On average, the interval onset of oestrus to ovulation did not differ (P>0.05) among treatments (control - 28.7±1.6h; pLH2.5 - 28.2±1.6h; pLH5 - 27.5±1.6h). The frequency distribution of gilts ovulated in different moments after oestrus detection was not affected (P>0.05) by the treatment. In conclusion, the use of 2.5mg or 5mg of pLH given at oestrus onset in gilts by i.m. route does not advance and synchronises the interval onset of oestrus to ovulation.

Este estudo teve como objetivo avaliar o uso do hormônio luteizante suíno (pLH) aplicado no início do estro em leitoas para sincronização da ovulação. Um total de 120 leitoas (40/tratamento) foram distribuídas em três tratamentos: controle - aplicação de placebo por via intramuscular (i.m.) no início do estro; pLH2,5 - aplicação de 2,5mg de pLH por via i.m. no início do estro; pLH5 - aplicação de 5mg de pLH por via i.m. no início do estro. Em média, o intervalo início do estro e a ovulação não diferiu (P>0,05) entre os tratamentos (controle - 28,7±1,6 h; pLH2,5 - 28,2±1,6h; pLH5 - 27,5±1,6h). A distribuição de frequência de leitoas ovuladas em diferentes momentos após a detecção de estro não foi afetada pelos tratamentos (P>0,05). Assim, o uso de 2,5mg ou 5mg de pLH aplicado no início do estro por via i.m. em leitoas não antecipa nem sincroniza o intervalo início do estro e a ovulação.

Effects of different litter depths on environmental parameters and growth performance of growing finishing pigs / Efeito de diferentes profundidades de cama usada para suínos em crescimento e em terminação sobre parâmetros ambientais e desempenho de crescimento

Deep litter systems represent low cost alternatives to raise growing-finishing pigs, reducing slurry accumulation, although pig's thermal comfort may be negatively affected by the heat produced inside the litter. This study compared environmental and performance parameters for growing-finishing pigs raised on deep litter systems having distinct depths and on solid floor. The experiment was conducted in a region of temperate climate of Brazil, comparing three treatments: litter having rice husk 0.5m (T1); and 0.25m deep (T2); and solid concrete floor (T3). The first litter was used in two lots and replaced by a second litter used in other two lots, during 52 weeks. Each lot included five pigs in a 7m² pen, from 60 to 145 d of age. Environmental parameters were determined at weekly intervals, including: atmospheric temperature; relative humidity; temperature at the center of the pen, in the surface (TSF); and at half of the depth (THD), only for T1 and T2. Feed consumption and weight of pigs were measured every four weeks. Atmospheric temperature and relative humidity were not influenced by the treatments (P>0.05). Mean TSF was 22.8 ± 3.6°C, being lower for T3 (P<0.05), but with no difference between T1 and T2 (P>0.05). TSF was higher for new than for used litters (P<0.001) and for the first than for the second litter (P=0.03), apparently increasing in lots raised during termophilic phases. Mean THD was 33.8±10.8°C, being higher for T1 than for T2 (P<0.05). THD was also higher for new than for used litters (P<0.001) and for the first than for the second litters (P<0.05). No growth performance parameter differed across treatments (P>0.05). Despite the potential unfavorable thermal comfort under high temperatures, deep litter systems can be used to raise pigs in the growing-finishing phases due to the absence of negative effects for growth performance.

O uso de cama representa uma alternativa de baixo custo para a criação de suínos em crescimento e em terminação, promovendo redução do acúmulo de dejetos, embora o conforto térmico dos animais possa ser prejudicado pelo calor produzido no interior da cama. Este estudo compara os parâmetros ambientais e o desempenho de crescimento de suínos em sistemas de criação sobre cama, com profundidades distintas, e sobre piso concreto. O experimento foi realizado em uma região de clima temperado na região Sul do Brasil, comparando três tratamentos: cama de casca de arroz com 0,5m (T1), com 0,25m de profundidade (T2) e piso de concreto (T3). A primeira cama foi usada em dois lotes de animais e foi substituída por uma segunda, usada em outros dois lotes, compreendendo 52 semanas. Cada lote foi constituído por cinco animais criados dos 60 aos 145 dias de idade, em uma baia de 7m². Os seguintes parâmetros ambientais foram medidos semanalmente: temperatura ambiente, umidade relativa e temperatura no centro da baia, na superfície (TSF) e na metade da profundidade da cama (TMP), apenas em T1 e T2. O consumo de ração e o peso dos animais foram aferidos a cada quatro semanas. A temperatura ambiente e a umidade relativa não foram influenciadas pelos tratamentos (P>0,05). A TSF média foi de 22,8±3,6°C, sendo menor no T3 (P<0,05), mas sem diferir entre T1 e T2 (P>0,05). A TSF foi mais alta nas camas novas do que nas usadas (P<0,001) e nas primeiras camas em comparação com as segundas (P=0,03), aparentemente sendo mais alta nos lotes criados durante as fases termofílicas. A TMP média foi de 33,8 ± 10,8°C, sendo mais alta no T1 do que no T2 (P<0,05). A TMP também foi mais alta nas camas novas do que nas usadas (P<0,001) e nas primeiras camas em comparação com as segundas (P<0,05). Nenhum dos parâmetros de crescimento diferiu entre os tratamentos (P<0,05). Ainda que possam ocorrer condições de conforto térmico desfavoráveis aos animais, principalmente ...

Inseminação artificial intra-uterina em leitoas com sêmen criopreservado com dimetilacetamida e glicerol / Intrauterine artificial insemination of gilts using cryopreserved boar semen with dimetilacetamide and glycerol

Este estudo teve por objetivo avaliar o uso da dimetilacetamida (DMA) e de glicerol na criopreservação de sêmen suíno sobre as taxas de concepção e fertilização in vivo, utilizando o método de inseminação artificial pós-cervical. Foram sincronizadas 60 leitoas pré-púberes e inseminadas com o uso de sêmen congelado com glicerol 3 por cento (30 fêmeas) e DMA 5 por cento (30 fêmeas). O método de inseminação utilizado foi o pós-cervical, com concentração de 1 x 10(9) espermatozóides vivos por dose. Após 36 a 40h da inseminação, as fêmeas foram abatidas, sendo realizada a contagem de corpos hemorrágicos (CH) nos ovários. Foi realizada a lavagem dos ovidutos das fêmeas, verificando o número de estruturas recuperadas (oócitos e embriões), calculando-se as taxas de concepção e fertilização. A média de CH nas fêmeas do grupo glicerol 3 por cento não diferiu (P>0,05) daquelas do grupo DMA 5 por cento (10,4 x 10,2, respectivamente). Não houve diferença (P>0,05) nas taxas de recuperação de estruturas entre os grupos glicerol 3 por cento (68,9 por cento) e DMA 5 por cento (66,9 por cento). Os resultados obtidos nos grupos glicerol 3 por cento e DMA 5 por cento para as taxas de concepção (73,3 x 76,6 por cento) e fertilização (48,6 x 59,4 por cento) não apresentaram diferença (P>0,05). Conclui-se que não há diferenças nas taxas de concepção e fertilização in vivo utilizando-se sêmen congelado com o uso de dimetilacetamida ou de glicerol.

The objective of this study was to evaluate the use of dimethylacetamide (DMA) and glycerol in boar semen cryopreservation on the conception and fertility rates.Sixty pre-pubertal gilts were synchronized and inseminated with semen including either glycerol 3 percent or DMA 5 percent as cryoprotectants (n=30 for both groups). Artificial insemination was conducted with the intrauterine method using doses with 1 x 10(9) viable spermatozoa. The gilts were slaughtered 36-40h after the insemination and the hemorrhagic bodies (CH) in the ovaries were counted. The oviducts were washed, so oocytes and embryos could be recovered to determine the conception and fertility rates. The average CH obtained with glycerol 3 percent did not differ (P>0.05) from those observed with DMA (10.4 x 10.2, respectively). Recovery rates also did not differ (P>0.05) between groups (68.9 percent with glycerol and 66.9 percent with DMA). Conception (73.3 x 76.6 percent) and fertility rate (48.6 x 59.4 percent) were also similar (P>0.05) for glycerol and DMA, respectively. Those results indicate that DMA 5 percent can replace glycerol 3 percent in the composition of extenders for frozen boar semen.