Postpartum Beef Cows Research Articles

100 Impact of luteal blood perfusion and estrus expression on pregnancy rates of beef cows exposed to embryo transfer

Abstract This study aimed to evaluate the impact of luteal blood perfusion and estrus expression on pregnancy rates of beef cows exposed to fixed-timed embryo transfer (FTET). Postpartum beef cows (n = 763) from 22 locations were exposed to a 7-d Select Synch + controlled internal drug releasing (CIDR) and breeding indicator patches were affixed upon CIDR removal. Estrus expression was assessed twice daily for 72 h and a 100-µg injection of gonadotropin-releasing hormone was administered to cows that failed to express estrus 72 h after CIDR removal. Brightness mode ultrasonography of the corpus luteum (CL) was conducted to select recipients for FTET 9 d after CIDR removal. Suitable recipients were assigned to receive a single fresh or frozen embryo derived from either in vitro (IVF) or in vivo (IVD) method. After embryo recipient selection, CL morphometries and blood perfusion (BP) were then assessed at the time of embryo transfer via transrectal ultrasonography. Embryo recipients were categorized according to CL area [small (< 3 cm²), medium (3 to 4 cm²), or large (> 4 cm²)] and based on the percentage of luteal area with blood perfusion signals [low (< 25%), medium (25 to 45%), or high (> 45%)]. Pregnancy diagnoses were performed between d 60 and 90 of gestation. Cows that failed to express estrus prior FTET had decreased (P ≤ 0.02) luteal area, luteal diameter, and pregnancy rates compared with cows that expressed estrus. Luteal area category had no effect (P = 0.61) on pregnancy rates. Embryo recipients that expressed estrus had similar (P = 0.12) luteal blood perfusion compared with recipients that failed to express estrus. Embryo recipients with high (P = 0.02) and medium (P = 0.05) BP had greater pregnancy rates compared with embryo recipients with low BP. There was no interaction between estrus expression and luteal BP (P = 0.84). In summary, estrus expression and luteal BP positively impacted pregnancy rates to embryo transfer and may be used to facilitate embryo recipient selection.

Influence of early progesterone removal on follicular development, expression of estrus, and pregnancy rates in presynchronized postpartum beef cows

The objective of this study was to evaluate the impact of early progesterone removal on pregnancy rates to fixed-time artificial insemination (FTAI) in presynchronized beef cows. Postpartum beef cows (n = 882) were randomly assigned to 1 of 2 treatments: 1) 7&7 Synch: cows received a controlled internal drug release insert (CIDR) and a 25-mg injection of prostaglandin F2α on day 0, 100 μg of GnRH on day 7, a second injection of prostaglandin F2α (PG2) at CIDR removal on day 14, and a second injection of GnRH at FTAI 60–66 h after PG2 (day 17); 2) 7&6 Synch: cows received the same treatment as 7&7 Synch; however, CIDR removal occurred in conjunction with PG2 on day 13, while FTAI remained at 60–66 h after CIDR removal (day 16). Ovarian ultrasonography was performed to determine follicle diameter at PG2 and FTAI in a subset of cows (n = 40). Cows exposed to the 7&7 Synch tended to have larger follicle diameter at PG2 compared with 7&6 Synch cows (P = 0.09); however, there were no differences in follicle diameter at FTAI. No differences were determined between treatments for the expression of estrus (7&7 Synch: 61.6 ± 5.30; 7&6 Synch: 54.1 ± 5.45; P = 0.31) or pregnancy rates to FTAI (7&7 Synch: 60.8 ± 3.83; 7&6 Synch: 57.0 ± 3.84; P = 0.42). In conclusion, early removal of progesterone did not impact pregnancy rates in presynchronized beef cows.

PSIII-7 7&7 Synch improved pregnancy rates in beef cows experiencing estrus over 24 h before fixed-time insemination

Abstract Our objectives were to compare estrus response and pregnancy rates between two different estrus synchronization protocols and between cows that experienced estrus more than 24 h before appointment breeding and those that experienced estrus less than 24 h before breeding. Over each of 2 yr, postpartum beef cows (n = 1,108) from two different locations were ranked by days postpartum and randomly selected to receive either; 1) 7-d CO-Synch + CIDR (CO-Synch, n = 547), or; 2) 7 & 7 Synch (7&7, n = 561). For the CO-Synch treatment, cows received a controlled internal drug release insert (CIDR; 1.38g progesterone) and 100 µg gonadotropin-releasing hormone (GnRH) i.m., followed in 7 d by CIDR removal and 25 mg prostaglandin F2alpha (PGF) i.m., followed in 60 to 66 h with AI and 100 µg GnRH i.m. For the 7&7 Synch protocol, cows received a CIDR (1.38g progesterone) and 25 mg PGF i.m., followed in 7 d by 100 µg GnRH i.m., followed in 7 d by CIDR removal and 25 mg PGF i.m., followed in 60 to 66 h with AI and 100 µg GnRH i.m. Heat detection patches were applied at the time of CIDR removal to determine estrus response by the time of AI, with cows having patches ≥ 50% activated defined as being in estrus and cows with patches < 50% activated defined as not experiencing estrus. In yr 2, an additional heat detection was performed 24 h before breeding, at which time cows with ≥ 50% activated heat detection patches were defined as having an early estrus (i.e., estrus more than 24 h before breeding) and cows with activated patches first observed at the time of AI were defined as having an on-time estrus. Pregnancy status was determined via transrectal ultrasonography 35 d after AI. Data were analyzed using the GLIMMIX procedure of SAS. As expected, cows in the 7&7 treatment had greater (P ≤ 0.005) estrus response and pregnancy rates than those in the CO-Synch treatment (83% vs. 62% and 65% vs. 55%, respectively). The proportion of cows experiencing early estrus was similar (P > 0.60) between treatments (20.4 and 22.9 for Co-Synch and 7&7, respectively). Interestingly, pregnancy rate was impacted by a treatment × estrus timing interaction (P = 0.04), where cows in the Co-Synch treatment that experienced an early estrus (52.9%) had reduced pregnancy rates compared with 7&7 cows that experienced early estrus (74.0%), Co-Synch cows that experienced on-time estrus (73.7%) and 7&7 cows that experienced on-time estrus (70.5%). Our results indicate the 7&7 Synch protocol can effectively increase pregnancy rates to fixed-time AI, and that pregnancy rates of cows experiencing early estrus are influenced by synchronization protocol.

Classification of postpartum beef cows as estrous cycling or anestrous through the use of estrus detection patches prior to the start of the breeding season

Classification of postpartum beef cows as estrous cycling or anestrous through the use of estrus detection patches prior to the start of the breeding season

15 Influence of early progesterone removal on follicular development, estrus expression, and pregnancy rates in presynchronized beef cows

Abstract The objective of this study was to evaluate the impact of early progesterone removal on pregnancy rates to fixed-time artificial insemination (FTAI) in presynchronized beef cows. Postpartum beef cows (n = 922; body condition score = 4.9 ± 0.77; days postpartum = 77.3 ± 20.77 d) from 7 locations were enrolled in a completely randomized design. Within location, cows were stratified by parity and days postpartum before being randomly assigned to 1 of 2 treatments: 1) 7&7 Synch: Cows received a controlled internal drug release insert (CIDR) and a 25-mg injection of prostaglandin F2α (PG1; d 0). Cows received 100 μg of GnRH on d 7 and the CIDR was removed 7 d later, concurrently with a second prostaglandin F2α (PG2) injection (d 14). Cows received a second injection of GnRH and were FTAI 60-66 h after PG2 (d 17); 2) 7&6 Synch: Cows received the same treatment as 7&7 Synch cows; however, CIDR removal and PG2 were performed on d 13, and cows were FTAI 60-66 h after CIDR removal. Ovarian ultrasonography was performed to determine follicle diameter and CL presence at PG2 and FTAI in a subset of cows (n = 40). Estrus detection patches were utilized to evaluate estrus expression between PG2 and FTAI. Pregnancy diagnosis was performed 28-35 d after FTAI. Cows exposed to the 7&7 Synch tended to have larger follicle diameter at PG2 compared with 7&6 Synch cows (P = 0.09); however, there were no differences in follicle diameter at FTAI. Cows that expressed estrus tended to have larger follicle diameter at FTAI compared with cows that failed to express estrus (P = 0.10). Follicular growth between PG2 and FTAI, percentage of cows with a corpus luteum at PG2, and ovulation rate were not impacted by treatment (P ≥ 0.56). No differences were determined between treatments for estrus expression (7&7 Synch: 77.1 ± 5.91; 7&6 Synch: 74.6 ± 6.28; P = 0.50) or pregnancy rates to FTAI (7&7 Synch: 60.1 ± 4.32; 7&6 Synch: 58.2 ± 4.26; P = 0.69). In conclusion, early removal of progesterone did not impact pregnancy rates in presynchronized beef cows. Thus, the 7&6 Synch protocol described herein may be used as an alternative to the conventional 7&7 Synch protocol without compromising fertility.

154 Characterization of anovular phenotypes in postpartum beef cows

154 Characterization of anovular phenotypes in postpartum beef cows

PSXIV-5 Classification of Postpartum Beef Cows as Estrous Cycling Or Anestrous Through the Use of Estrus Detection Patches

Abstract Application of estrus detection patches for an extended period of time was evaluated as a means of classifying postpartum beef cows as estrous cycling or anestrous at the start of the breeding season. Estrus detection patches (Estrotect Breeding Indicators; Hermitage, TN) were applied to 269 primiparous and multiparous postpartum beef cows in three locations 24 days prior to the start of an estrus synchronization protocol. At the start of the protocol, patches were scored using a 1 to 4 scale (1 = 0-25%; 2 = 25-50%; 3 = 50-75%; 4 = 75-100%), with scores of 3 or 4 considered activated. Estrous cyclicity status was determined via transrectal ovarian ultrasonography performed by experienced technicians coincident with the start of an estrus synchronization protocol. Cows were classified as cycling based on the presence of a corpus luteum (CL). Based on transrectal ovarian ultrasonography, 59% (161/269) of cows were cycling at the start of estrus synchronization. Of cows receiving patches, 95% (256/269) of cows retained patches for the full 24-day period. Among cows retaining patches, 67% (171/256) of cows presented with activated patches, and 33% (85/256) of cows presented with non-activated patches at the start of the synchronization protocol. Among these, 139 cows presented with activated patches and were observed to have CL via ultrasound, therefore being considered true positives (i.e., estrous cycling). A total of 69 cows presented with non-activated patches and were observed to have no CL via ultrasound, therefore, being considered true negatives (i.e., anestrous). Among cows for which patch score did not result in the same classification as an ultrasound-based characterization of CL status, 32 were considered false positives (i.e., activated patch but no CL observed via ultrasound), and 16 were considered false negatives (i.e., non-activated patch but CL observed via ultrasound). Based on these observations, use of activated patches to infer cyclicity resulted in 89% sensitivity, 68% specificity, and a positive predictive value of 78%. When retained, estrus detection patches are a sensitive tool to classify postpartum cows as cycling prior to the start of an estrus synchronization protocol.

291 Impact of Early Resynchronization in Combination with Color Doppler Ultrasonography on Cumulative Pregnancy Rates in Postpartum Beef Cows

Abstract The objective of this study is to evaluate a GnRH and progesterone-based early resynchronization strategy combined with color Doppler ultrasonography for early pregnancy diagnosis. Postpartum Bos taurus beef cows (n = 375) from four locations were enrolled in a completely randomized design, where cows were randomly assigned to 1 of the 2 treatments: 1) Natural Service (NS), cows were exposed to a 7-d CO-Synch + CIDR protocol followed by fixed-time artificial insemination (day 0). On day 15, cows were exposed to natural service for the remainder of the study; or 2) Early Resynchronization (ER), cows were exposed to a 7-d CO-Synch + CIDR protocol followed by fixed-time artificial insemination (day 0). On day 15, a controlled internal drug release (CIDR) device was inserted. On day 20, CIDR was removed, and pregnancy was estimated based on luteal blood perfusion using color Doppler ultrasonography. Non-pregnant cows received a 25-mg injection of prostaglandin F2α at CIDR removal and were fixed-timed-AI concurrently with a 100-μg injection of GnRH 60 to 66 h later. Pregnancy diagnosis and fetal aging were performed on day 53 using conventional ultrasonography. Pregnancy rate to the first AI was greater (P = 0.03) for NS compared with ER (70.25% vs 59.29%, respectively). Pregnancy rates for the second service were also greater (P = 0.01) for NS compared with ER (65.67 vs 42.93%, respectively). Cumulative pregnancy rates to AI did not differ between treatments (P = 0.38); however, cumulative pregnancy rates (first and second service) were greater (P < 0.01) for NS compared with ER (90 vs 77.73%, respectively). In conclusion, the proposed early resynchronization strategy using color Doppler ultrasonography resulted in fewer pregnancies compared with natural service as the second service strategy. Moreover, the proposed ER decreased pregnancy rates to the first insemination, indicating a detrimental effect of ER on pregnancy establishment.

GnRH34 with or without estradiol cypionate in timed AI in Bos indicus beef cows

Two experiments were performed to evaluate the effects of GnRH treatment on the fertility of suckled Nelore beef cows treated with an estradiol/progesterone (E2/P4)-based protocol for timed artificial insemination (TAI). Experiment 1 focused on determining the effects of estradiol cypionate (EC) on ovulation in TAI cows treated with GnRH 34 h after removal of the intravaginal P4 device (IPD). Suckled cows (n = 26) were treated with 2 mg estradiol benzoate (EB) and IPD containing 1 g P4. After 8 days, IPDs were removed, and all cows were treated with 150 μg of d-cloprostenol (prostaglandin F2 alpha analog) and 300 IU of equine chorionic gonadotropin (eCG), then separated into two treatment groups consisting of cows who received 1) saline 0.9% i.m. (GnRH34 group) or 2) 0.6 mg i.m. of EC (EC-GnRH34 group). On day 9 (05:00 p.m.), all cows were given GnRH (10.5 μg of buserelin acetate) i.m. No differences were observed between the groups (P > 0.05) in the time of ovulation after IPD removal or in the proportion of cows ovulating. Experiment 2 focused on determining the effects of GnRH34 along with or in the absence of EC on day 8 on pregnancy per AI (P/AI) in postpartum beef cows. Cows (n = 981) were treated similarly to those in Experiment 1, but an additional group, the EC-GnRH48 group, was included, in which cows received EC on day 8 whereas those that did not show estrus received GnRH at TAI. Thus, in this experiment, groups consisted of GnRH34 (n = 322), EC-GnRH34 (n = 335), and EC-GnRH48 (n = 324). A higher rate of estrus expression was observed in cows treated with EC following IPD removal (EC-GnRH34: 69%, EC-GnRH48: 64.8%) than in cows in the GnRH34 group (45.6%). No difference in P/AI was observed between the treatment groups (P = 0.45), but P/AI in cows in the EC-GnRH34 group (64.2%) tended to be greater (P = 0.1) than in cows in the GnRH34 group (58%). In summary, although ovulation synchrony did not differ among the groups, P/AI in cows treated with EC and GnRH 34 h after IPD removal tended to be greater than in cows treated solely with GnRH; this was most likely due to a shorter proestrus/estrus period, considering the lower proportion of cows that displayed estrus in the GnRH34 group. Finally, given that P/AI did not differ between the EC-GnRH34 and EC-GnRH48 groups, our results suggest that, for cows not displaying estrus, administration of EC at the time of IPD removal followed by treatment with GnRH 48 h afterward represents the most cost-efficient TAI strategy for South American Zebu-based beef operations.

31 Correlation of the Reproductive Microbiome and Cytokine Profiles with Plasma Progesterone Concentrations in Postpartum Beef Cows Prior to Timed Artificial Insemination

Abstract Female sex steroid hormones have been shown to interact with cytokines within the immune system to help influence fertility. Previous research has indicated that shifts in commensal bacteria are associated with compromised reproductive performance during the postpartum period, yet evaluation of how the female sex hormone progesterone (P4) influences these microbial shifts is not fully understood. The objectives of this study were to determine 1) the relationship between P4 concentrations and cytokine concentrations, and 2) the relationship between P4 concentrations and the reproductive microbiome. Twenty Bos indicus-influenced beef cows (~60 days postpartum and free of health issues) were weighed, body condition scored and then subjected to the Bos indicus prostaglandin 5 day (d) + CIDR protocol beginning on d -8 and timed artificially inseminated on d 0. Blood samples were collected on d-3, -1, 0, and 28. Cytokines and reproductive microbiome were evaluated using vaginal and uterine flushes collected on d -3 and d-1. Experimental groups were assigned by d 28 pregnancy status, determined by transrectal ultrasonography, resulting in Open (n = 13) and Pregnant (n = 7) females. Bacterial community analyses were conducted targeting the V4 hypervariable region of the 16S rRNA gene. Plasma P4 concentrations on d -3 and d -1 were quantified per manufacturers’ instructions using a double-antibody RIA kit. Cytokine analyses of plasma and flushes were conducted using the RayBiotech Quantibody Bovine Cytokine Array Q1 kit per the manufacturer’s instructions. Statistical analyses were conducted using the GLM procedure and CORR procedure in SAS. Plasma P4 concentrations did not differ by pregnancy status (P > 0.05) but did decrease from d -3 to d -1 (0.89 vs. 0.08 ± 0.23 ng/mL, respectively; P = 0.02). There were no significant correlations between plasma P4 and plasma cytokines (P > 0.05). Interferon-alpha (IFNα) and P4 concentrations were positively correlated in Open and Pregnant uterine flushes (r = 0.41; P = 0.01). Concentrations of P4 interleukin (IL)-1F5 were negatively correlated in Open and Pregnant vaginal flushes (r = -0.32; P = 0.04). The relative abundance of genus Methanobrevibacter in uterine flushes was positively correlated with P4 concentrations in both experimental groups (r = 0.35; P = 0.02). Within vaginal flushes, there was a tendency for a negative correlation between the relative abundance of genus Bacteroides and P4 concentrations (r = -0.31; P = 0.05). Alternatively, there is a positive correlation between P4 concentration and relative abundance of genus Streptococcus (r = 0.47; P = 0.01) and genus Methanobrevibacter (r = 0.37; P = 0.02) in vaginal flushes. These results suggest there may be relationships between several cytokines and circulating P4 concentrations; therefore, potentially suggesting immunomodulatory activities of P4. Overall, this research alludes to P4 having a vital role in reproductive microbial shifts and associated immune responses. Further investigation on the local effects of P4 within the reproductive tract on immune responses and bacterial shifts could provide greater insight into mechanisms to improve fertility in beef cattle.

Reproductive microbiome and cytokine profiles associated with fertility outcomes of postpartum beef cows.

Shifts from commensal bacteria (for example, Lactobacillus in the phylum Firmicutes) within the reproductive tract have been associated with changes in local reproductive immune responses and decreased fertility in humans. The objective of this study was to characterize the microbiome and cytokine concentrations before artificial insemination (AI) in vaginal and uterine flushes from postpartum beef cows. Twenty Bos indicus-influenced beef cows (approximately 60 d postpartum and free of reproductive, health, or physical issues) were enrolled. The B. indicus prostaglandin (PG) 5-d + controlled intervaginal drug-releasing estrus synchronization protocol was initiated on day -8 of the study with timed AI on d0. Blood samples were collected on days -3, -1, and 28 via coccygeal venipuncture. Vaginal and uterine flushes were collected on days -3 and -1. Based on days 28 pregnancy status determined by transrectal ultrasonography, cows were identified as either Open (n = 13) or Pregnant (n = 7). Bacterial community analyses were conducted targeting the V4 hypervariable region of the 16S rRNA gene. Cytokine analyses were performed using the RayBiotech Quantibody Bovine Cytokine Array Q1 and MyBioSource ELISA kits per the manufacturer's instructions. Statistical analyses for bacteria relative abundance were conducted using PROC NPAR1WAY and for cytokine concentrations using PROC GLM in SAS 9.4. Uterine concentrations of interferon γ, interleukin (IL)1α, and IL21 were greater in Open than in Pregnant cows (P < 0.05). Regardless of pregnancy status, uterine IL13 increased from days -3 to -1 (9.76 vs. 39.48 ± 9.28 pg/mL, respectively; P < 0.05). Uterine relative abundance of the phylum Firmicutes decreased from days -3 to -1 in Open cows (60.4% ± 0.9% vs. 48.5% ± 3.2%; P = 0.004). In Open cows, the genus Blautia decreased in relative abundance within the uterus from days -3 to -1 (2.1% ± 0.2% vs. 0.9% ± 0.1%; P = 0.002). Uterine relative abundance of the phylum Tenericutes increased from days -3 to -1 in Pregnant cows (1.0% ± 0.1% vs. 7.6% ± 4.1%; P = 0.002). In Pregnant cows, the genus Ureaplasma tended to increase within the uterus from days -3 to -1 (0.08% ± 0.06% vs. 7.3% ± 4.1%; P = 0.054). These findings suggest a distinct difference in the reproductive microbiome and cytokine profiles before AI for resulting Open vs. Pregnant cows.

PSIII-14 Reproductive Microbiome and Cytokine Profiles of Postpartum Beef Cows in Relation to Fertility

Abstract Shifts in commensal bacteria (i.e., Firmicutes) in the human microbiome are associated with compromised fertility. The objectives of this study were to characterize 1) the reproductive microbiome and 2) the cytokine concentrations prior to artificial insemination (AI) in vaginal and uterine flushes from postpartum beef cows. Twenty Bos indicus-influenced beef cows (~60 days postpartum and free of health issues) were weighed, body condition scored (BCS) then subjected to the Bee Synch II synchronization protocol on d-8 and timed AI on d0. Blood samples were collected on d-3, -1, 0, and 28. Vaginal and uterine flushes were collected on d-3 and d-1. On d28, pregnancy was determined by transrectal ultrasonography (Open, n=13 and Pregnant, n=7). Bacterial community analyses were conducted targeting the V4 hypervariable region of the 16S rRNA gene. Cytokine analyses were conducted using the RayBiotech Quantibody® Bovine Cytokine Array Q1 kit per manufacturer's instructions. Weight, BCS, and vaginal bacterial communities by phyla were not different (P &amp;gt;0.05). In open cows, the uterine relative abundance of Firmicutes decreased between d-3 and -1 (60.4% ± 0.9% vs. 48.5% ± 3.2%, respectively; P&amp;lt; 0.05). In pregnant cows, the uterine relative abundance of Tenericutes significantly increased between d-3 and -1 (1.0% ± 0.1% vs. 7.6% ± 4.1%, respectively; P&amp;lt; 0.05). Additionally, the genus Ureaplasma tended to increase in relative abundance from d-3 to -1 (0.1% ± 0.1% vs. 7.3% ± 4.9%, respectively; P=0.06). Uterine concentrations of Interferon (IFN)-γ, Interleukin (IL)-1α and IL-21 were greater in open females compared to pregnant. Vaginal concentrations for IFN-α and chemokine ligand (CXCL)-10 were greater in open females compared to pregnant. Regardless of treatment, IL-13 increased from d-3 to d-1. These results suggest a distinct difference in the uterine microbiome and cytokine profiles prior to AI for resulting pregnant and open cows.

PSV-B-16 Correlation between Plasma, Uterine, and Vaginal Cytokine Concentrations in Postpartum Beef Cows Prior to Artificial Insemination

Abstract Cytokines have a vital role in reproductive immune environment during the postpartum period. Previous data evaluated uterine and vaginal cytokine concentrations prior to insemination; however, was unable to correlate these data with plasma cytokine concentrations. The objective of this study was to determine relationships between uterine, vaginal, and plasma pro- and anti-inflammatory cytokine concentrations in postpartum beef cows prior to timed artificial insemination (TAI). Bos indicus-influenced beef cows (n=20) free of any physical, health or reproductive-related issues were subjected to the Bee Synch II protocol 8 days prior (d-8) to TAI (d0). Uterine and vaginal flushes and blood were collected on d-3 and d-1. Pregnancy was determined by transrectal ultrasonography on d28 (Pregnant, n=7; Open, n=13). Using the RayBiotech Quantibody Bovine Cytokine Array 1 the following cytokines concentrations were determined: interferon (IFN)-α, IFN-γ, interleukin (IL)-13, IL-1α, IL-1-F5, IL-21, tumor necrosis factor (TNF)-α, chemokine ligand (CXCL)-9, CXCL-10, and chemokine ligand 4 (CCL4). Concentration data were analyzed using PROC GLM and correlations using Pearson correlation in SAS. For plasma samples, 8 pro-inflammatory cytokines (IFN-α, IFN-γ, IL-13, IL-1α, IL-1-F5, IL-21, CXCL-9, and TNF-α) had greater (P&amp;lt; 0.05) concentrations in open cows compared with pregnant cows. For uterine flushes, 3 pro-inflammatory cytokines (IFN-γ, IL-1α, and IL-21) had greater (P&amp;lt; 0.05) concentrations in open cows compared with pregnant cows. For vaginal flushes, IFN-α concentrations were greater (P&amp;lt; 0.05) in open cows, while CXCL-10 concentrations were greater in pregnant cows. There were no significant correlations between plasma and uterine or vaginal samples (P&amp;gt;0.05). Interestingly, for open cows there were correlations for IFN-α (r=0.46; P=0.02), IFN-γ (r=0.58; P=0.002), and IL-21 (r=0.54; P=0.004) between uterine and vaginal samples; however, no correlations were observed for pregnant cows. These results suggest a greater abundance of pro-inflammatory cytokines within the uterus, vagina, and in peripheral circulation for resulting open cows prior to TAI.

Effect of calving to timed artificial insemination interval on fertility of beef cows.

The objectives of this study were to determine the effect of calving to timed artificial insemination (C-TAI) interval on fertility of Bos taurus and Bos indicus cows and to determine the best C-TAI interval to include postpartum cows in TAI programs in each genotype (B. taurus and B. indicus). In experiment 1, a retrospective study was performed, with data from 2,709 TAI in Bos taurus and Bos indicus cows with different C-TAI intervals. There was a positive linear effect of C-TAI interval on the pregnancy probability (p < .0001). However, there was no effect or interaction with the genotype. When C-TAI intervals were grouped in classes, pregnancy rate differed in groups (p < .05). Receiver operating characteristic (ROC) analysis was performed, and it was observed that 52 days would be the better C-TAI interval to maximize fertility in beef cows. According to the previous result, we further stratified into two C-TAI interval groups (≤ 52 days or > 52 days). Cows with C-TAI longer than 52 days (C-TAI > 52) had greater pregnancy rate (56%) than cows with short C-TAI (46%; p < .01). In experiment 2, 18 postpartum beef cows were subjected to TAI protocol at different C-TAI intervals (n=6 cows per group): 40, 60 or 80 days postpartum. Cows with 60 days of C-TAI had a greater preovulatory follicle diameter than cows with 80 days postpartum (p < .05). The C-TAI interval did not affect (p > .05) the ovulation rate nor the proportion of endometrial polymorphonuclear leucocytes. We conclude that C-TAI interval affects pregnancy rate in both Bos taurus and Bos indicus. We recommend a C-TAI interval longer than 52 days to increase fertility of beef cows included in TAI programs.

Luteal color doppler ultrasonography and pregnancy-associated glycoproteins as early pregnancy diagnostic tools and predictors of pregnancy loss in Bos taurus postpartum beef cows.

The objective of this study was to evaluate the use of luteal color doppler (CD) ultrasonography and plasma concentrations of pregnancy-associated glycoproteins (PAG) for early pregnancy diagnosis in Bos taurus beef cows. Additionally, CD and PAG were evaluated as potential predictors of late embryonic/early fetal mortality (LEM). Postpartum beef cows (n = 212) were exposed to estrus synchronization followed by fixed-time artificial insemination (day 0). On days 20 and 22, B-mode and CD ultrasonography were performed to evaluate corpus luteum (CL) morphometries and blood perfusion. Moreover, blood samples were collected on days 25 and 29 to quantify circulating concentrations of PAG. Conventional ultrasonography on days 29 and 100 was utilized as the gold-standard method for pregnancy diagnosis. Cows that experienced pregnancy loss between days 29 and 100 were classified as LEM. Pregnant cows had larger and more vascularized CL compared with nonpregnant cows on days 20 and 22 (P < 0.001 for all response variables). Accuracy for CD on days 20 and 22 were 87% and 92%, respectively. Accuracy for PAG on days 25 and 29 were 84% and 99%, respectively. No false negative (FN) results were observed for CD on both days 20 and 22; however, there were 7.1% FN results for PAG on day 25. Cows that experienced LEM had decreased (P = 0.04) circulating PAG on day 29 of gestation compared with cows that maintained pregnancy; however, there were no differences in luteal blood perfusion on days 20 and 22 (P ≥ 0.53) or circulating PAG on day 25 (P = 0.46) between LEM cows and cows that maintained pregnancy. Sensitivity and specificity of PAG on day 29 as predictors of LEM were 83% and 77%, respectively. In conclusion, CD resulted in accurate pregnancy diagnosis in B. taurus beef cows on both days 20 and 22 of gestation, while having no FN results. Circulating concentrations of PAG were decreased in cows that experienced LEM; however, further research is required to utilize PAG as a predictor of LEM commercially.

244 Fertility Outcomes Associated with Reproductive Tract Cytokines and Microbiota in Postpartum Beef Cows

Abstract Local immune activity in the reproductive tract is crucial in the response to uterine diseases, normal reproductive functions, and establishing pregnancy. Few studies have evaluated the influence of the local immune environment of the reproductive tract on fertility outcomes. The objectives were to 1) evaluate reproductive cytokine concentrations in postpartum cows undergoing estrus synchronization followed by timed artificial insemination (TAI) and 2) correlate reproductive bacterial communities with cytokine concentrations. Angus cows (n = 20) were subjected to a 7-Day Co-Synch protocol with pre-synchronization beginning 21 days prior (d -21) to TAI (d 0). Uterine and vaginal flushes were collected on d -21 and -2. Pregnancy was determined by transrectal ultrasound on d 30. Bacterial community profiling and analyses were conducted targeting the V1 to V3 hypervariable regions of the 16S rRNA gene. Cytokine concentrations for interleukin (IL)-1b, IL-6, IL-10, and transforming growth factor beta (TGF-β) were determined by commercial ELISA kits. Concentration data were analyzed using PROC MIXED and correlations using Pearson correlation in SAS. No differences were detected in vaginal samples (P &amp;gt;0.05). No differences in IL-10 or IL-1b concentrations were detected in uterine samples (P &amp;gt;0.05). Uterine TGF-β concentrations were greater in resulting pregnant than non-pregnant cows (44.0 ± 13.4 pg/mL vs 14.7 ± 4.9 pg/mL; P = 0.05). Uterine TGF-β was negatively correlated with the relative abundance of genera Treponema (r = -0.668; P = 0.05) in resulting non-pregnant cows on d -21. Uterine IL-6 concentrations were greater in resulting non-pregnant than pregnant cows (198.7 ± 21.8 pg/mL vs 144.3 ± 16.1 pg/mL; P = 0.05). Uterine IL-6 and the relative abundance of genera Butyrivibrio were positively correlated (r = 0.742; P = 0.02) in resulting non-pregnant cows on d -21. These results suggest possible relationships between uterine bacterial communities and cytokines prior to TAI that may ultimately affect fertility outcomes in beef cattle.

PSXII-15 Evaluation of later timing of fixed-time artificial insemination for beef cows when using sex-sorted semen following the 7 &amp; 7 Synch protocol

Abstract An experiment was designed to evaluate later timing of fixed-time artificial insemination (FTAI) with sex-sorted semen among postpartum beef cows following the 7 &amp; 7 Synch protocol, with the hypothesis that later timing would result in increased pregnancy rates (P/AI) among cows that expressed estrus prior to FTAI. Beef cows (n = 414) were blocked based on age and days postpartum (DPP) and randomly assigned to receive FTAI at 66 or 72 h after administration of prostaglandin F2α (PG). Estrus was synchronized using the 7 &amp; 7 Synch protocol, which consists of administration of PG (500 μg cloprostenol) and insertion of an intravaginal progesterone-releasing insert (CIDR; 1.38 g progesterone) on Day 0, gonadotropin-releasing hormone (GnRH; 100 μg gonadorelin) on Day 7, and PG coincident with CIDR removal on Day 14. Estrus detection aids (EstrotectTM) were applied to all cows on Day 14, and activation status was recorded at fixed-time artificial insemination (FTAI) on Day 17. All cows that expressed estrus prior to FTAI received sex-sorted semen (4 × 106 cells per unit; SexedULTRA 4MTM). The proportion of cows expressing estrus prior to FTAI did not differ between treatments at this power of test [66 h: 71% (146/205); 72 h: 76% (158/209)]. Additionally, P/AI of estrous cows inseminated with sex-sorted semen did not differ between treatments [66 h: 44% (90/205); 72 h: 39% (82/209)]. In conclusion, later timing of FTAI following the 7 &amp; 7 Synch protocol failed to improve P/AI of estrous cows inseminated with sex-sorted semen.

239 Increased Preovulatory Estradiol Improves Pregnancy Success of Embryo Transfer in Beef Cows

Abstract Preovulatory estradiol concentrations and expression of estrus have been associated with greater pregnancy rates in beef cattle following AI, thus an experiment was designed to determine if supplemental estradiol (E2) at GnRH-induced ovulation would improve pregnancy retention in postpartum beef cows after embryo transfer. Cows were synchronized with the 7-d CO-Synch + CIDR® protocol. On d0 (48h post-prostaglandin) cows were grouped by estrual status (Estrual; n=198, nonestrual; n=406). Nonestrual cows were administered GnRH and randomly assigned to either no treatment (Control; n=204) or administration of 0.1 mg (IM) estradiol 17-β (Estradiol; n=202). In a preliminary study, 0.1 mg (IM) estradiol 17-β increased plasma estradiol (17.11±3.4 pg/mL; P &amp;lt; 0.01) and remained elevated above baseline for approximately 8h compared to control (1.70±0.58 pg/mL). All cows received an in vivo produced embryo on d7. Embryos were matched by grade, stage, and flush across treatments. Pregnancy was classified on d30 by either plasma pregnancy-associated glycoproteins analysis (Year 1) or ultrasonography (Year 2). Plasma estradiol concentrations (d-2, d0h0, d0h2) were analyzed by PROC MIXED as repeated measures in SAS(9.4), while GLIMMIX procedures were used to analyze differences in pregnancy rates with treatment, group, year, and their interactions as fixed effects. There was a treatment by time interaction (P &amp;lt; 0.001) in E2 concentration. There was no difference in plasma E2 concentrations on d0h0 (P &amp;gt;0.30) between treatments. At d0h2, Estradiol cows (15.7±0.25 pg/mL) had greater plasma E2 compared to Estrual (4.0±0.13 pg/mL) or Control (3.4±0.25 pg/mL) cows (P &amp;lt; 0.001), and Estrual cows had greater plasma E2 than Control cows (P = 0.02). Control cows had decreased (26%) pregnancy rates compared to both Estradiol (37%; P = 0.03) and Estrual (40%; P = 0.01) cows. Pregnancy rates did not differ (P = 0.51) between the Estrual and Estradiol cows. In conclusion, elevated preovulatory concentrations of estradiol are critical for improved pregnancy retention following embryo transfer.

238 Luteal Color Doppler Ultrasonography for Early Pregnancy Diagnosis in Postpartum Bos Taurus Beef Cows

Abstract The objective of this study was to evaluate the use of corpus luteum (CL) color doppler ultrasonography (CD) for early pregnancy diagnosis in Bos taurus beef cows and evaluate differences in CL blood perfusion among cows that experience late embryonic/early fetal mortality (LEM). Postpartum Bos taurus beef cows (n = 214) from three locations were exposed to a 7-d CO-Synch + CIDR protocol followed by fixed-time artificial insemination (day 0). On days 20 and 22, B-mode and CD ultrasonography were performed to evaluate CL morphometries and blood perfusion, respectively. Cows were considered non-pregnant when CL area was &amp;lt; 20 mm2 or estimated blood perfusion was ≤ 25%. Conventional ultrasonography on day 29 was utilized as the gold standard method. Pregnant cows had greater CL diameter, CL area, and CL volume when compared to non-pregnant cows on day 20 and 22 (P &amp;lt; 0.001; Table 1). Additionally, percentage of central, peripheral, and total luteal blood perfusion, as well as the respective blood perfusion scores were greater (P &amp;lt; 0.001) in pregnant compared with non-pregnant cows on both day 20 and 22. Sensitivity, specificity, positive predicted value (PPV), negative predicted value (NPV), and accuracy for the CD on day 20 were 100, 74, 81, 100, and 88%, respectively. Sensitivity, specificity, PPV, NPV, and accuracy for CD on day 22 were 100, 86, 89, 100, and 93%, respectively. Pairwise comparison of receiver operating characteristics curve analysis indicated no differences between CD on days 20 and 22 (P = 0.12). No differences in luteal blood perfusion were observed on day 20 or 22 among cows that maintained pregnancies compared with LEM cows (P ≥ 0.27). In conclusion, CD successfully detected most non-pregnant cows (81 and 89% on day 20 and 22, respectively) and false negative results were absent (NPV = 100%).

Evaluation of Reproductive Tract Cytokines in Post-partum Beef Cows Relating to Reproductive Microbiota and Fertility Outcomes

The activity of the immune system in the reproductive tract has been proven to be crucial in the response to uterine diseases, normal reproductive functions, and tolerance to the allogeneic fetus during pregnancy. The objectives of the current study were to (1) evaluate uterine and vaginal cytokine concentrations in postpartum cows undergoing estrus synchronization followed by timed artificial insemination (TAI) and (2) correlate bacterial communities with cytokine concentrations. Postpartum Angus cows (n = 20) were subjected to a 7-Day Co-Synch protocol with pre-synchronization beginning 21 days prior (d −21) to TAI (d 0). Uterine and vaginal flushes were collected on d −21 and −2. Pregnancy was determined by transrectal ultrasound on d 30. Cytokines include interleukin (IL)-1b, IL-6, IL-10, transforming growth factor beta (TGF-β), and immunoglobin A (IgA) and concentrations were determined by commercial ELISA kits. No differences by day or pregnancy status in cytokine concentrations were detected in vaginal samples. No differences by day or pregnancy status in IgA, IL-10, or IL-1b concentrations were detected in uterine samples. Overall TGF-β concentrations in the uterus were greater in resulting pregnant than non-pregnant cows (44.0 ± 13.4 pg/mL vs. 14.7 ± 4.9 pg/mL; P = 0.047). Uterine TGF-β was correlated with the relative abundance of genera Treponema (r = −0.668; P = 0.049) in resulting non-pregnant cows on d −21 and with the relative abundance of genera Ureaplasma (r = 0.901; P = 0.0004) in resulting pregnant cows on d −2. In resulting pregnant animals, a tendency for a strong correlation was detected between d −2 progesterone concentrations and uterine TGF-β concentrations (r = 0.591, P = 0.07). Overall IL-6 concentrations in the uterus were greater in resulting non-pregnant than pregnant cows (198.7 ± 21.8 pg/mL vs. 144.3 ± 16.1 pg/mL; P = 0.045). A correlation was also detected between uterine IL-6 concentrations and the relative abundance of genera Butyrivibrio (r = 0.742; P = 0.022) in resulting non-pregnant cows on d −21. These results suggest possible relationships between different bacterial communities and cytokine concentrations within the uterus of beef cattle prior to TAI that may ultimately affect fertility outcomes.