Seasonal Infertility Research Articles

IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: Systemic and ovarian impacts of heat stress in the porcine model.

This review describes how heat stress causes systemic endocrine and metabolic alterations that contribute to intracellular ovarian perturbations, resulting in female infertility. Heat stress (HS) in mammals results from an imbalance in heat accumulation and dissipation. Fertility impairments consequential to HS have been recognized for decades in production animals, and more recently, observations have been extended to other species, including women. There are several systemic impacts of HS that can independently affect reproduction, including metabolic endotoxemia, reduced plane of nutrition, and endocrine disruption. At the level of the ovary, molecular pathways are altered by HS, such as inflammation, JAK-STAT, PI3K, oxidative stress, cell death, and heat shock response. Taken together, impaired ovarian function contributes to seasonal infertility that results from HS. This review paper describes the physiological and endocrine systemic impacts of HS that may independently and collaboratively impair fertility in the porcine model. The review then details ovarian intracellular events that are altered during HS and finally determines future needs in this area of research.

Factors and mechanisms influencing seasonal disorders in pig reproduction

The problem of unsatisfactory reproductive results in pigs is visible in a significant percentage of herds, especially during summer months and early autumn (seasonal summer infertility). This is reflected mainly in the reduced percentage of sows entering estrus after weaning and the effectiveness of mating/insemination. The consequence is a significantly lower number of births in November, December and sometimes even in January, compared to other seasons. There are many causes of seasonal summer infertility. The first things mentioned are usually the length of the light day and the high temperature in the pigs environment. An important reason that is not often discussed is the daily temperature fluctuations which usually occur at the end of summer and the beginning of autumn. Persistent unfavorable conditions are responsible for long-term stress. Hormonal disorders related to stress, leading to reproductive disorders, result from connections taking place in the hypothalamus between the hypothalamus-pituitary-gonadal axis (HPG), which regulates, among others, the reproductive functions of the ovaries, and the hypothalamus – pituitary – adrenal axis – HPA which governs organism reaction to stress. Under stressful conditions, glucocorticoids (cortisol, corticosterone) secreted in large amounts by the adrenal glands, as well as adrenaline, norepinephrine and, in small amounts, dopamine, may inhibit reproductive functions at the level of the hypothalamus, reducing the secretion of GnRH. At the same time, by reaching the pituitary gland, these hormones limit the sensitivity of the cells of this endocrine gland to GnRH. As a consequence, the maturation of follicles slows down, the number of ovulating and rupturing follicles decreases, and the secretion of estrogen is reduced. The consequence is the absence of heat or, more often, the so-called “silent heat”. Another problem is the uneven maturation of the follicles, which leads to a delayed appearance of estrus and its longer duration: 3-4 days. The final effect of these is a decrease in the rate of females presenting heat after weaning of piglets, a deterioration in the mating/insemination success rate, an increase in the rate of early abortions and percentage of litters with a small number of piglets in a litter. The summary stated that despite the identification of various seasonal causes of reproductive disorders in pigs, depending on both sows and boars, and the availability of various “tools” to reduce phenomenon of seasonal infertility, the presented problem has not been solved in a large percentage of swine farms. Its intensity varies and depends primarily on awareness, knowledge of ways to eliminate unfavorable conditions and determination in this regard. The first step, as always, is to objectively assess the situation. The assessment can be made through a detailed analysis of production data.

Impact of heat stress on prolactin-mediated ovarian JAK-STAT signaling in postpubertal gilts.

Heat stress (HS) compromises almost every aspect of animal agriculture including reproduction. In pigs, this infecundity is referred to as seasonal infertility (SI), a phenotype including ovarian dysfunction. In multiple species, HS-induced hyperprolactinemia has been described; hence, our study objectives were to characterize and compare HS effects on circulating prolactin (PRL) and ovarian Janus kinase/signal transducer and activator of transcription (JAK-STAT) signaling during the follicular (FOL) or luteal (LUT) phases of the estrous cycle in postpubertal gilts. Gilts were estrus synchronized using altrenogest and environmental treatments began immediately after altrenogest withdrawal. For the FOL study: postpubertal gilts were allocated to constant thermoneutral (TN; n = 6; 20 ± 1.2 °C) or cyclical HS (n = 6; 25 to 32 ± 1.2 °C) conditions for 5 d. In the LUT study: postpubertal gilts were assigned to either TN (n = 7; 20 ± 2.6 °C) or cyclical HS (n = 7; 32 to 35 ± 2.6 °C) conditions from 2 to 12 days postestrus (dpe). Blood was collected by jugular venipuncture for PRL quantification on day 5 in the FOL and on day 0 and day 12 in the LUT gilts. Ovaries and corpora lutea (CL) were obtained from euthanized FOL and LUT gilts on day 5 and day 12, respectively. Western blotting was performed to quantify prolactin receptor (PRLR) and JAK/STAT pathway protein abundance. In the FOL phase, no difference (P = 0.20) in circulating PRL between thermal groups was observed. There was no effect (P ≥ 0.34) of HS on PRLR, signal transducer and activator of transcription 3 (STAT3), signal transducer and activator of transcription 5α (STAT5α), and phosphorylated signal transducer and activator of transcription α/β tyrosine 694/699 (pSTAT5α/βTyr694/699) abundance and Janus kinase 2 (JAK2), phosphorylated janus kinase 2 tyrosine 1007/1008 (pJAK2Tyr1007/1008), STAT1, phosphorylated signal transducer and activator of transcription 1 tyrosine 701 (pSTAT1Tyr701), phosphorylated signal transducer and activator of transcription 1 serine 727 (pSTAT1Ser727), and phosphorylated signal transducer and activator of transcription 3 tyrosine 705 (pSTAT3Tyr705) were undetectable in FOL gilt ovaries. Ovarian pSTAT5α/βTyr694/699 abundance tended to moderately increase (4%; P = 0.07) in FOL gilts by HS. In the LUT phase, circulating PRL increased progressively from 2 to 12 dpe, but no thermal treatment-induced difference (P = 0.37) was noted. There was no effect (P ≥ 0.16) of HS on CL abundance of PRLR, pJAK2Tyr1007/1008, JAK2, STAT1, pSTAT1Tyr701, pSTAT1Ser727, pSTAT3Tyr705, STAT5α, or pSTAT5α/βTyr694/699. In LUT phase, CL STAT3 abundance was increased (11%; P < 0.03) by HS. There was no impact of HS (P ≥ 0.76) on levels of pJAK2Tyr1007/1008 and pSTAT5α/βTyr694/699 in LUT gilts; however, the CL pSTAT3Tyr705:STAT3 ratio tended to be decreased (P = 0.10) due to HS. These results indicate an HS-induced estrous cycle-stage-dependent effect on the ovarian JAK/STAT pathway, establishing a potential role for this signaling pathway as a potential contributor to SI.

Porcine endometrial heat shock proteins are differentially influenced by pregnancy status, heat stress, and altrenogest supplementation during the peri-implantation period.

Heat stress (HS) deleteriously affects multiple components of porcine reproduction and is causal to seasonal infertility. Environment-induced hyperthermia causes a HS response (HSR) typically characterized by increased abundance of intracellular heat shock proteins (HSP). Gilts exposed to HS during the peri-implantation period have compromised embryo survival, however if (or how) HS disrupts the porcine endometrium is not understood. Study objectives were to evaluate the endometrial HSP abundance in response to HS during this period and assess the effect of oral progestin (altrenogest; ALT) supplementation. Postpubertal gilts (n = 42) were artificially inseminated during behavioral estrus (n = 28) or were kept cyclic (n = 14), and randomly assigned to thermal neutral (TN; 21 ± 1 °C) or diurnal HS (35 ± 1 °C for 12 h/31.6 ± 1 °C for 12 h) conditions from day 3 to 12 postestrus (dpe). Seven of the inseminated gilts from each thermal treatment group received ALT (15 mg/d) during this period. Using quantitative PCR, transcript abundance of HSP family A (Hsp70) member 1A (HSPA1A, P = 0.001) and member 6 (HSPA6, P < 0.001), and HSP family B (small) member 8 (HSB8, P = 0.001) were increased while HSP family D (Hsp60) member 1 (HSPD1, P = 0.01) was decreased in the endometrium of pregnant gilts compared to the cyclic gilts. Protein abundance of HSPA1A decreased (P = 0.03) in pregnant gilt endometrium due to HS, while HSP family B (small) member 1 (HSPB1) increased (P = 0.01) due to HS. Oral ALT supplementation during HS reduced the transcript abundance of HSP90α family class B member 1 (HSP90AB1, P = 0.04); but HS increased HSP90AB1 (P = 0.001), HSPA1A (P = 0.02), and HSPA6 (P = 0.04) transcript abundance irrespective of ALT. ALT supplementation decreased HSP90α family class A member 1 (HSP90AA1, P = 0.001) protein abundance, irrespective of thermal environment, whereas ALT only decreased HSPA6 (P = 0.02) protein abundance in TN gilts. These results indicate a notable shift of HSP in the porcine endometrium during the peri-implantation period in response to pregnancy status and heat stress.

Effects of increased ambient temperature and supplemental altrenogest before pregnancy establishment in gilts.

Heat stress (HS) mitigation strategies are critically needed to combat the substantial economic effects on animal agriculture. The manifestations of seasonal infertility include delayed puberty onset, reduced conception rates, decreased litter size, and increased wean to estrus interval. To assess the effects of HS during early gestation and evaluate the benefit of supplemental altrenogest (ALT) as a mitigation strategy, 30 crossbred postpubertal gilts (157 ± 11 kg body weight) were subjected to estrous synchronization via 14 d oral administration of ALT. Artificial insemination during estrus was performed, and gilts were then placed into one of four treatment groups: HS (35 ± 1 °C for 12 h/31.60 ± 1 °C for 12 h) with (HSALT, n = 7) or without (HSCON, n = 7) 15 mg/d ALT supplementation or thermal neutral (TN; 20 ± 1 °C) conditions with (TNALT, n = 8) or without (TNCON, n = 8) 15 mg/d ALT supplementation until 12 d post-estrus (dpe). Administrating ALT occurred at 0600 hours from 3 to 12 dpe, and rectal temperatures (TR) and respiration rates (RR) were recorded. Blood was collected via jugular venipuncture on 0, 4, 8, and 12 dpe. Gilts were euthanized humanely at 12 dpe followed by the collection of ovarian tissue, and uterine flushing for conceptus collection. In HS compared with TN gilts, RR and TR were increased (P < 0.01) but unaffected by ALT supplementation. Feed intake was reduced (P < 0.01) by HS but unaltered by the ALT treatment. Corpora lutea (CL) weight was reduced (P < 0.01) in HSCON gilts when compared with TNCON and HSALT gilts despite progesterone concentrations in serum and luteal tissue not being affected by treatment (P ≥ 0.10). CL diameter was reduced (P ≤ 0.05) in HSALT gilts compared with other treatments. Interleukin-1β (IL1B) uterine flush concentration was not affected (P > 0.20) by environment or ALT supplementation, although moderate (P = 0.06) interaction between environment and ALT existed, as IL1B concentration in TNALT was increased (P = 0.03) compared with TNCON gilts. While environment did not affect conceptus development (P = 0.90), ALT supplementation advanced conceptus elongation (P < 0.01). Collectively, these data demonstrate that HS may affect luteal development before pregnancy establishment, and ALT increases conceptus elongation by 12 dpe.

Current status of assisted reproductive technologies in buffaloes.

Buffaloes are raised by small farm holders primarily as source of draft power owing to its resistance to hot climate, disease, and stress conditions. Over the years, transformation of these animals from draft to dairy was deliberately carried out through genetic improvement program leading to the development of buffalo-based enterprises. Buffalo production is now getting more attention and interest from buffalo raisers due to its socioeconomic impact as well as its contribution to propelling the livestock industry in many developing countries. Reproduction of buffaloes, however, is confronted with huge challenge and concern as being generally less efficient to reproduce compared with cattle due to both intrinsic and extrinsic factors such as poor estrus manifestation, silent heat, marked seasonal infertility, postpartum anestrus, long calving interval, delayed puberty, inherently low number of primordial follicles in their ovaries, high incidence of atresia, and apoptosis. Assisted reproductive technologies (ARTs) are major interventions for the efficient utilization of follicle reserve in buffaloes. The present review focuses on estrus and ovulation synchronization for fixed time artificial insemination, in vitro embryo production, intracytoplasmic sperm injection, cryopreservation of oocytes and embryos, somatic cell nuclear transfer, the factors affecting utilization in various ARTs, and future perspectives in buffaloes.

The Suinfort® Semen Supplement Counters Seasonal Infertility in Iberian Sows.

Simple SummaryEfficient pork production relies on a predictable supply of market pigs. Seasonal infertility caused by heat stress decreases fertility in sows during the summer months, impacting breeding targets and decreasing the efficiency of pork production. The present study examined the effect of a seminal additive containing caffeine, oxytocin, and lecirelin on the fertility and prolificacy of Iberian sows during two consecutive years. The results confirmed that inclusion of the additive in semen prior to AI decreased the seasonality effect, increasing the percentage of pregnant Iberian sows throughout the year.Suinfort®, a commercial semen supplement demonstrated to increase fertility and litter size in commercial sows, was tested to improve reproductive performance in Iberian sows. A total of 1430 Iberian sows were artificially inseminated (AI) with semen from Duroc boars and assigned by parity to receive the seminal additive Suinfort® containing 2 IU oxytocin, 5 µg lecirelin, and 2 mM caffeine (SF; n = 1713 AI), or to serve as non-supplemented controls (CON; n = 2625 AI). CON showed a lower fertility comparing to winter for spring (p = 0.001) and summer (p < 0.001); summer was lower than autumn (p = 0.012). SF removed this seasonal effect (p > 0.05). Fertility was significantly higher for SF sows during summer (p = 0.025) and autumn (p = 0.004). Total born, live-born, stillborn, and mummified piglets did not differ between CON and SF but were impacted by the season, with total and live-born decreasing in summer compared with autumn (p < 0.001) and winter (p = 0.005). In conclusion, seminal supplementation with Suinfort® improved the fertility of Iberian sows during periods of seasonal infertility.

Characterization of the effects of heat stress on autophagy induction in the pig oocyte

BackgroundHeat stress (HS) occurs when body heat accumulation exceeds heat dissipation and is associated with swine seasonal infertility. HS contributes to compromised oocyte integrity and reduced embryo development. Autophagy is a potential mechanism for the oocyte to mitigate the detrimental effects of HS by recycling damaged cellular components.MethodsTo characterize the effect of HS on autophagy in oocyte maturation, we utilized an in vitro maturation (IVM) system where oocytes underwent thermal neutral (TN) conditions throughout the entire maturation period (TN/TN), HS conditions during the first half of IVM (HS/TN), or HS conditions during the second half of IVM (TN/HS).ResultsTo determine the effect of HS on autophagy induction within the oocyte, we compared the relative abundance and localization of autophagy-related proteins. Heat stress treatment affected the abundance of two well described markers of autophagy induction: autophagy related gene 12 (ATG12) in complex with ATG5 and the cleaved form of microtubule-associated protein 1 light chain 3 beta (LC3B-II). The HS/TN IVM treatment increased the abundance of the ATG12-ATG5 complex and exacerbated the loss of LC3B-II in oocytes. The B-cell lymphoma 2 like 1 protein (BCL2L1) can inhibit autophagy or apoptosis through its interaction with either beclin1 (BECN1) or BCL2 associated X, apoptosis regulator (BAX), respectively. We detected colocalization of BCL2L1 with BAX but not BCL2L1 with BECN1, suggesting that apoptosis is inhibited under the HS/TN treatment but not autophagy. Interestingly, low doses of the autophagy inducer, rapamycin, increased oocyte maturation.ConclusionsOur results here suggest that HS increases autophagy induction in the oocyte during IVM, and that artificial induction of autophagy increases the maturation rate of oocytes during IVM. These data support autophagy as a potential mechanism activated in the oocyte during HS to recycle damaged cellular components and maintain developmental competence.

Latest Advances in Sow Nutrition during Early Gestation.

Simple SummaryThe first month of gestation in the pig is characterised by many changes, such as entry of the embryos into the uterus, increased secretion of the pregnancy hormone, progesterone, and the implantation of the embryos into the uterus. Before implantation, embryos have not yet attached to the uterus, and are reliant on nutrients and signals in the uterine fluids, which are controlled by progesterone, among others. High feed intake has a positive effect on progesterone secretion and supports the establishment and development of pregnancy. Very low feed intakes, such as in sows competing for feed in group housing, can be detrimental to embryo survival and even the maintenance of pregnancy. After implantation, specific nutrients that improve the vascularisation of the placenta, such as arginine, can support the capacity of the uterus to support a litter of developing embryos since in this stage competition between embryos starts to play a role.In the pig, the establishment and maintenance of luteal function in early gestation is crucial to endometrial function, embryo development, and survival. The level of feed intake has a positive effect on formation of luteal tissue and progesterone secretion by the ovaries in the pre-implantation period, which is important for endometrial remodeling and secretion. These effects are independent of luteinising hormone (LH) and probably driven by metabolic cues, such as insulin and insulin-like growth factor (IGF-1), and seem to support progesterone secretion and delivery to the endometrium, the latter which occurs directly, bypassing the systemic circulation. Even after implantation, a high feed intake seems to improve embryo survival and the maintenance of pregnancy. In this stage, luteal function is LH-dependent, although normal variations in energy intake may not result in pregnancy failure, but may contribute to nutrient supply to the embryos, since in this phase uterine capacity becomes limiting. Feed incidents, however, such as unintended fasting of animals or severe competition for feed, may result in embryo or even pregnancy loss, especially in periods of seasonal infertility. Specific nutrients such as arginine have a role in the vascularisation of the placenta and can improve the uterine capacity in the period after implantation.

81 Zearalenone Affects the Ovarian Proteome During Heat Stress in Prepubertal Gilts

Abstract Zearalenone (ZEA), an estrogenic mycotoxin, causes hormonal disruption and reproductive dysfunction in pigs. Heat stress (HS) occurs when exogenous and metabolic heat accumulation exceeds heat dissipation; a scenario negatively impacting gilt reproduction. Our objective was to identify differentially abundant ovarian proteins in gilts exposed to HS +/- ZEA. We hypothesized that ZEA exposure would negatively impact the prepubertal gilt ovarian proteome and HS would be additive to ZEA-induced toxicity. Prepubertal gilts (n = 38) were assigned to one of six treatment groups: thermoneutral (TN) ad libitum control (TNCtl; n = 6); TN + ZEA (TNZea; 2 ppm; n = 6); pair-fed (PF) control (PFCtl; n = 6); PF+ ZEA (PFZea; 2 ppm; n = 6); cyclical HS control (HSCtl; n = 7); and HS + ZEA (HSZea; 2 ppm; n = 7). Gilts were subjected to TN (20 ± 1°C) or cyclic HS (35 ± 1°C for 12 h/31.6° for 12 h) conditions for 7 d. Liquid chromatography-mass spectrometry (LC-MS/MS) was performed on ovarian protein homogenates. Exposure to ZEA altered (P &amp;lt; 0.05) abundance of 93 proteins in TN gilts (48 increased and 45 decreased). In PF gilts, ZEA increased 50 and decreased 47 proteins (P &amp;lt; 0.05). During HS, ZEA differentially affected (P &amp;lt; 0.05) 126 proteins: 58 increased and 68 increased. Pathways impacted by either HS or ZEA alone or in combination included cellular stress, metabolic pathways, and estrogenic pathways. Thus, ZEA and HS, either alone or in combination, impact the ovarian proteome in prepubertal gilts in ways that could contribute to seasonal infertility. This project was supported by the Iowa Pork Producers Association.

Susceptibility of boar spermatozoa to heat stress using in vivo and in vitro experimental models.

Induction of heat stress as an experimental procedure in animals is commonly used to examine heat-related impacts on sperm quality. This study aimed to develop potential heat stress models that could be used at any time of the year, to advance the study of seasonal infertility in the pig under controlled conditions. Heat stress was induced by either housing boars (n = 6) at 30°C inside a hot room for 42days (55-65% humidity; LD 12:12h; in vivo), or by heating boar semen (n = 7) for 30min at various temperatures (35.5, 38.8, 40, 42, 46, 50, 54 and 60°C; in vitro). Sperm motility was then characterized by computer-assisted sperm analysis (CASA; IVOS version 10: Hamilton Thorne, USA), and DNA integrity was evaluated by terminal deoxynucleotidyl transferase dUTP nick-end labelling (TUNEL) and flow cytometry. Our in vivo hot room model induced biologically meaningful levels of DNA damage in boar spermatozoa (10.1 ± 1.9 hot room vs. 6.7 ± 1.7% control; P > 0.05), although not statistically significant from controls. Moreover, sperm concentration and motility parameters did not differ between treatments (P > 0.05). Compared to the 38.8°C control, our in vitro heat shock model significantly increased sperm DNA damage after incubation at 54 and 60°C (3.0 ± 1.0, 2.9 ± 1.0, 1.2 ± 0.3, 2.5 ± 0.7, 9.0 ± 3.7, 16.2 ± 7.1, 14.2 ± 5.8 and 41.8 ± 18.6% respectively; P ≤ 0.05). However, these temperatures rendered sperm completely immotile or dead, with most motility parameters declining rapidly to zero above 40 or 42°C. In conclusion, our results suggest that temperature combined with individual factors may contribute to a boar's overall susceptibility to heat stress. Refinement of these models particularly of the in vitro heat shock model could be further pursued to overcome environmental variability, reduce whole animal experiments and provide a putative diagnostic fertility screening tool to evaluate heat tolerance in the boar.

Seasonal effects on fertility in gilts and sows

The ancestral wild pig is a short day length seasonal breeder. The domestic pig appears to have retained some of this seasonality as evidenced by a reduction in fertility during the summer—autumn period. The most important aspect of this seasonality is a reduction in the number of mated sows that farrow. Many of these sows conceive and embryos develop normally for 20 - 25 days before pregnancy is terminated and the sow returns to oestrus (25 - 35 days after mating). In other species, transduction of photoperiodic information is achieved by release of melatonin during the dark period. In the pig, the pattern of melatonin secretion and the subsequent hypothalamo—pituitary—gonadal responses appear to be more complex. A relatively high light intensity is required for pigs to generate a distinct diurnal melatonin rhythm and they appear unable to respond appropriately to abrupt changes in photoperiod. Pigs on restricted feeding and maintained under long photoperiods (but not under short photoperiods) have higher concentrations of melatonin than do similarly maintained pigs fed ad libitum. Continuous release melatonin implants have a deleterious effect on farrowing rate, suggesting that the abnormally high melatonin concentrations observed in sows in summer—autumn play a role in the pathogenesis of seasonal infertility. Ad libitum feeding of sows during the first few weeks of pregnancy may prevent the increase in melatonin concentrations and so remove the seasonal influence on fertility. The pituitary response to different photoperiods is also somewhat confusing. Although there is some evidence of increased sensitivity to the negative feedback of ovarian steroids in the prepubertal gilts and weaned sows during summer—autumn, LH concentrations are increased in early pregnant sows. It is proposed that the failure of sows to maintain pregnancy in summer—autumn results from disruption of maternal recognition of pregnancy causing regression of the corpora lutea, loss of pregnancy and return of the sow to oestrus.

Effect of parity number, year and season farrowing on reproductive performance in Large White pigs

This study examines certain identifiable non-genetic sources of variation (parity number, year and season farrowing) for their effects on Large White sow litter performance traits, such as litter size, mortality and weight of piglets at birth and at weaning. The population used for the present study is from a pig farm managed by Tavriys’ki svyni, LLC, located in Skadovsky district (Kherson Oblast, Ukraine). Reproductive performance records on 280 Large White (LW) sows were used. A total of 633 litters were farrowed from January 2007 to July 2017. The litter records included information on the total number of piglets born (TNB), number of piglets born alive (NBA), number of stillborn piglets (NSB), frequency of stillborn piglets (FSB), average weight of piglets at birth (AWPB), litter size at weaning (NW), piglet pre-weaning mortality (PWM) and average weight of piglets at weaning (AWPW). To determine the effect of parity number, year and month farrowing on reproductive performance traits, the analysis of variance (ANOVA) was used. Results obtained showed significant influence of parity number on most of the reproductive parameters studied, apart from AWPB, PWM and AWPW. The total litter size at birth was the lowest in primiparous sows and in cases second-parity sows, but significantly exceeded the overall average population estimation during the fourth-sixth parities farrowing. The least squares estimates of the mortality rate of piglets at birth were significantly lower than in second parity sows, however they significantly increased in sows at eighth parity. The year of the sow's farrowing had the most significant influence on the weight of piglets at birth and at weaning. Moreover, a clear upward trend can be noted in relation to the weight of piglets at birth, which is accompanied by a gradual increase of the corresponding least squares estimates during 2007-2015. Late summer and early autumn (August-October) are the seasons when the litter size traits in the LW sows consistently show the lowest values, indicating a ‘seasonal infertility period’. Thus, all the analysis performed in the present work shows that in the LW sows, as in other pig breeds, the parity number, year and season farrowing influence the reproductive and developmental processes.

Effect of seasonal infertility period on boar sperm proteins and quality characteristics

Swine seasonal infertility reduces the productivity and profitability of a pig farm. The main causes of this condition are elevated environmental temperatures and long photoperiod during the summer season. The aim of this study was to investigate which sperm proteins and parameters are affected during the period of seasonal infertility. Depending on the environmental temperatures, the period from October to June was considered as cold and the period from July to September as warm season. A total of 65 ejaculates from 18 boars were collected over a year. Each semen sample was evaluated for kinetics (Computer Assisted Semen Analyzer), morphology (Sperm Blue stain), viability (Propidium Iodide - Calcein AM stain), mitochondrial membrane potential (Rhodamine 123 – Propidium Iodide stain), membrane integrity and functionality (Hypo-osmotic swelling test) and sperm DNA integrity (Acridine Orange Test). Moreover, selected proteins (HSP90, GPX5, OPN) were detected and quantified. The kinetic parameters VSL, LIN and the midpiece abnormalities were significantly higher in the warm compared to the cold season (p&lt;0.05), while a strong tendency towards higher values for HSP90 and GPX5 was observed in warm compared to cold season (p=0.07and p=0.06, respectively). In conclusion, among the boar sperm characteristics tested in our study, seasonal infertility period negatively affected VSL and LIN kinetics, while GPX5 seminal plasma enzyme and HSP90 sperm surface protein increased their sperm protective effects.

Effect of Dextrose Supplementation in the Pre-Ovulatory Sow Diet to Reduce Seasonal Influences on Litter Birth Weight Variation.

Simple SummarySeasonal infertility manifests in either pregnancy failure, or reduced litter size, or both in sows bred during summer. What is less clear is whether season influences piglet traits important for post-natal survival and growth, such as birth weight variation. Sows fed a diet with dextrose before ovulation gave birth to litters with reduced birth weight variation. Thus, this experiment had two aims: first, to identify if sows bred during summer would give birth to litters with higher birth weight variation, and second, to test if feeding sows dextrose before mating would reduce birth weight variation, especially during summer months. This experiment identified that there is evidence for increased birth weight variation in sows bred during the summer months despite the observed reduced litter size, suggesting that this is another way seasonal infertility can manifest. The 5% inclusion of dextrose in the pre-ovulatory sow diet increased litter size without compromising litter homogeneity at birth and resulted in higher piglet growth rates in those born to sows mated in winter (lactated in summer). Dextrose can be used successfully in a ‘wean to mate’ diet to boost the reproductive performance of sows.In this experiment, we proposed two hypotheses: birth weight variation would increase in litters from sows bred in summer, and dextrose supplementation during the wean to mate period would ameliorate this manifestation of seasonal infertility. Five hundred and ninety-one multiparous sows were allocated to Control; standard diet, or Dextrose; control +5% dextrose diets from weaning until insemination during summer and winter. Dextrose sows farrowed 1.0 and 1.4 more total pigs born and pigs born alive than Control sows, respectively (p < 0.05). There was a tendency for a higher co-efficient of variation (CV) birth weight in summer than winter (16.6 ± 0.4 versus 15.8 ± 0.4; p = 0.1), but no effect of treatment or interaction between treatment and season was observed. Piglet average daily gain was unaffected in those born to sows bred in summer, but when born to sows bred in winter, Dextrose piglets grew 23 g per day faster than Control (p < 0.05). This experiment identified evidence for increased birth weight CV in sows bred during the summer months despite the reduced litter size, suggesting that this is another way seasonal infertility can manifest.

Seasonality of reproduction in gilts and sows

In the wild, the pig adapts her reproductive functions according to the seasonal changes in the environment, such as the ambient temperature and availability of food. Like in other short day seasonal breeders, breeding season is favoured in the mid winter in order to provide the offspring with the best chances to survive four months later. Seasonal changes in environment are perceived mainly by the ability of the pig to recognise seasonal changes in photoperiod. This information is mediated through changes in the activity of the pineal gland to secret melatonin, essentially by the same mechanism as reported for other mammals. Stimulation of melatonin receptors located in the hypothalamus has a significant role for the release of GnRH and subsequent gonadotrophin release from the pituitary. Management and nutrition related factors determine the degree of seasonal effects on reproduction in the commercial piggery environment. Significant improvements in fertility in herds suffering from seasonal infertility are achievable by providing gilts and sows with abundant feed after mating. Attempts to alleviate the seasonal effects on fertility by applying light programs are underway and may lead to significant improvements in productivity of the domestic pig in the long run. Hormonal treatments may be somewhat effective, but not a sustainable solution to seasonal infertility. In conclusion, seasonal infertility is a photoperiod induced phenomenon that can be manipulated by changes in photoperiod and by accounting for season as a significant factor when feeding strategies are applied in commercial piggeries.

Heat stress during the luteal phase decreases luteal size but does not affect circulating progesterone in gilts1.

Heat stress (HS) occurs when heat dissipation mechanisms are insufficient to maintain euthermia, and it is associated with seasonal infertility (SI), which manifests as smaller litters, longer wean-to-estrus interval, increased abortions, and reduced conception rates. To understand HS-induced mechanisms underlying SI, crossbred post-pubertal gilts (167 ± 10 kg; n = 14) experienced either thermal neutral (TN, 20 ± 1 °C, n = 7) or cyclical HS (35 ± 1 °C for 12 h and 31.6 °C for 12 h, n = 7) conditions from 2 to 12 d post-estrus (dpe). Estrous cycles were synchronized via altrenogest administration for 14 d, phenotypic manifestation of estrus was observed and gilts were assigned to experimental treatment. Gilts were limit fed 2.7 kg daily with ad libitum water access. Blood was collected at 0, 4, 8, and 12 dpe via jugular venipuncture and animals were humanely euthanized at 12 dpe. The corpora lutea (CL) width were measured via digital calipers on both ovaries, and CL from one ovary were excised, weighed, and protein and steroid abundance analyzed via western blotting and ELISA, respectively. Relative to TN, HS increased (P < 0.01) rectal temperature and respiration rates and reduced (P < 0.01) feed intake. The CL from HS ovaries were reduced in diameter (P < 0.05) and weight (P < 0.01) relative to those from TN animals. No difference (P = 0.38) in CL or serum progesterone concentrations between groups was observed at any time point, though at 12 dpe the serum progesterone:CL weight was increased (P < 0.10) by HS. No treatment differences (P = 0.84) in circulating insulin were observed. Luteal protein abundance of steroid acute regulatory protein, 3 beta-hydroxysteroid, or prostaglandin F2α receptor were not different between treatments (P = 0.73). Taken together, these data demonstrate that the CL mass is HS sensitive, but this phenotype does not appear to be explained by the metrics evaluated herein. Regardless, HS-induced decreased CL size may have important implications to pig SI and warrants additional attention.

208 Molecular mechanisms through which heat stress compromises reproduction in pigs

Abstract Seasonal variations in environmental temperatures impose added stress on domestic species bred for economically important production traits. These heat-mediated stressors vary on a seasonal, daily, or spatial scale, and negatively impact behavior and reduce feed intake and growth rate, which inevitably leads to reduced herd productivity. The seasonal infertility observed in domestic swine is primarily characterized by depressed reproductive performance manifesting as delayed puberty onset, reduced farrowing rates, and extended weaning-to-estrus intervals. Understanding the effects of heat stress at the organismal, cellular, and molecular level is a prerequisite to identifying mitigation strategies that could reduce the economic burden of compromised reproduction. Additionally, hyperthermia experienced in utero influences industry-relevant postnatal phenotypes. Understanding tissue-specific molecular mechanisms through which heat stress confers suppressed reproductive ability is essential to the development of mitigation focused hypothesis driven solutions. This work was supported by the National Pork Board and the Iowa Pork Producers Association.

Effect of altering the ratio of exogenous gonadotropins on reproductive performance of primiparous sows during the seasonal infertility period

At weaning, 150 primiparous sows were assigned sequentially to receive 400 IU equine chorionic gonadotropin (eCG) with 200 IU human chorionic gonadotropin (hCG) (Gn600), or 400 IU eCG with 400 IU hCG (Gn800), or served as untreated controls. Compared with control and Gn600, the Gn800 had increased estrus response by day 7 and reduced wean-to-estrus intervals (P &lt; 0.05). Compared with controls, both Gn600 and Gn800 increased numbers of large follicles (≥6 mm) at estrus detection (P &lt; 0.05) and the subsequent farrowing rates (P &lt; 0.05). Litter size was unaffected. These data demonstrate the efficacy of supplemental hCG for alleviating effects of seasonal infertility in primiparous sows.

Tropical summer induces DNA fragmentation in boar spermatozoa: implications for evaluating seasonal infertility.

Summer infertility continues to undermine pig productivity, costing the pig industry millions in annual losses. The boar's inefficient capacity to sweat, non-pendulous scrotum and the extensive use of European breeds in tropical conditions, can make the boar particularly vulnerable to the effects of heat stress; however, the link between summer heat stress and boar sperm DNA damage has not yet been demonstrated. Semen from five Large White boars was collected and evaluated during the early dry, late dry and peak wet seasons to determine the effect of seasonal heat stress on the quality and DNA integrity of boar spermatozoa. DNA damage in spermatozoa during the peak wet was 16-fold greater than during the early dry and nearly 9-fold greater than during the late dry season. Sperm concentration was 1.6-fold lower in the peak wet than early dry whereas no difference was found across several motility parameters as determined by computer-assisted sperm analysis. These results demonstrate that tropical summer (peak wet season) induces DNA damage and reduces concentration without depressing motility in boar spermatozoa, suggesting that traditional methods of evaluating sperm motility may not detect inherently compromised spermatozoa. Boar management strategies (such as antioxidant supplementation) need to be developed to specifically mitigate this problem.