Breed composition does not influence the performance of Holstein-Gyr crossbred as oocyte donors for OPU/IVP

Holstein-Gyr crossbred cattle are strategic for dairy systems in tropical countries, since they combine milk yield genetics with adaptability to tropical climate. However, Holstein (Bos taurus) and Gyr (Bos indicus) breeds present remarkable differences regarding reproductive physiology. Brazil stands out as the world’s largest user of embryo in vitro production (IVP) in bovine, and the use of this technique is increasing in dairy systems. As Holstein-Gyr crossbreds are important oocyte donors for IVP, the present work aimed at investigating whether increased Gyr or Holstein breed composition influences donor’s performance. Sixteen Holstein-Gyr crossbred females presenting increased (HG, 71.4 to 87.5% Holstein; n = 9) or decreased (GH, 40.2 to 46.6% Holstein; n = 7) Holstein composition were submitted to three ovum pick up (OPU) sessions. We observed similar (P = 0.2946) antral follicle count between HG and GH donors (24.8 ± 3.2 vs 29.4 ± 2.8 respectively; mean ± SEM). Groups also display similar morphological oocyte grading (Grade I: 0.1 ± 0.1 vs 0.1 ± 0.1 – P = 0.9680; Grade II: 0.9 ± 0.5 vs 1.9 ± 0.5 – P = 0.1942; Grade III, 4.0 ± 1.2 vs 7.2 ± 1.4 – P = 0.1047, HG vs GH respectively; mean ± SEM). Additionally, the proportion of viable oocyte was similar between HG and GH groups (27.8% vs 31.9%, respectively, P = 0.3500) and oocyte lipid area fraction (6.8% vs 9.5%, respectively; P = 0.1539). Our results indicate that the individual variation has more influence than breed composition of crossbred oocyte donors.


Introduction
Pantaneiro and Campeiro equine breeds are descendants of Iberian horses, which were introduced into Brazil during the colonization period and are known as naturalized breeds. The main characteristics of these breeds are the abilities to acclimatize and multiply under diverse bioclimatic conditions. In addition, these animals play a fundamental role in the herding livestock at the places to which they are inserted, contributing significantly to the economic development of these regions. However, such horses almost disappeared due to an indiscriminate crossing with other breeds, castration of the best animals to work, and diseases (Santos et al., 2007).
The first step to starting a conservation of genetic material from Campeiro and Pantaneiro breeds is to assemble data on the reproductive traits of these horses. Therefore, assessing different parameters between the breeds becomes of utmost significance for the establishment of references on horse breeds and peculiarities, which helps reproductive management (Sereno et al., 2008;McManus et al., 2013).
One of the management tools is based on gestational age determination by measuring fetal ocular orbit through ultrasonography (Turner et al., 2006). Foal peripartum and hematological profile evaluations before the first feeding until weaning are fundamentally important since each equine species has different hematological values; therefore, studies on these reference intervals and peculiarities of each breed is necessary (Muñoz et al., 2012).
Changes in most age-related blood parameters in equine species make the use of reference values impossible for adult animals and in the clinical evaluation of foals from birth to about six months of age (Medeiros et al., 1971).
The most accurate knowledge of hematological reference values corresponding to the different breeds and age groups is indispensable for an adequate clinical evaluation of newborn foals . Nonetheless, using reference values from adult horses to neonatal foals is ineffective for clinical evaluations as long as several hematological parameters change during the first months of life (Medeiros et al., 1971).
Therefore, this study aimed to carry out a descriptive evaluation of gestational characteristics, such as fetal age determination by measuring fetus ocular orbit of Campeiro and Pantaneiro mares through ultrasonography. Besides that, it also aimed to evaluate the peripartum of these animals -such as the mare behavior during labor, placental weight, foal height at birth, and blood biochemical profile of foals before the first feeding until weaning.
The findings of this study will set the stage for further studies on other equine breeds from centers for genetic resource conservation, such as Baixadeiro, Lavradeiro, and Marajoara.

Material and Methods
The experiment was conducted at the Sucupira experimental field station, Embrapa CENARGEN, in Brasilia -Federal District, Brazil. The area lies at latitude 15º46'46''S and longitude 47º 55'46''W. For that, fifteen horses were used (five Campeiro mares and three stallions, and five Pantaneiro mares and two stallions) between 5 and 20 years old (11.4 ± 3.4). The animals were raised in an extensive fodder-feeding system (Mombaça and Tanzania grass), mineral salt, and water ad libitum.

Fetal ocular orbit diameter
After the breeding of ten mares by one of the five stallions, pregnancies were monitored monthly from the third month until the foaling, determining the gestational age through fetal orbit diameter measuring.
These measurements were obtained by rectal ultrasound from where the entire uterus was examined for ocular orbit location. After the orbit was located, an image was frozen to dimension the size of the vitreous body (between the lateral and medial sclera); it consisted of the average between the lateral-medial and rostro-caudal diameters. As for accuracy, three measures were taken for each evaluation (Turner et al., 2006).
Once all measurements were completed, the relationship between ocular orbit sizes and gestational age was made to create a formula for regression equation, which could be used in the field for more accurate estimates of the gestational age of equine fetuses, especially for the breeds Campeiro and Pantaneiro.

Peripartum evaluation
Near the 11th gestation month, mares were separated within a padock of nearly 2,000 m 2 and evaluated daily for attendance at foaling. In this daily control, the mares were restrained in a stock and evaluated from about 50 cm distance. The filling of the udder and teats was assessed and, some hours before delivery, we observed the waxing of teat orifice, which indicated forthcoming delivery (Silva and Oliveira, 2015).

Placenta weight and foal birth size
At the time of delivery, as soon as neonates stood up in the station, their heights were measured from the front hoof toe to the top of the withers. This measure was obtained using a flexible tape measure. A descriptive evaluation of these values was performed.
Throughout the postpartum period, the mares were monitored through a safe distance of about 10 m for collection and assessment of placenta weight after complete placental delivery. These values were used for a descriptive evaluation of both breeds in this study.

Blood biochemical parameters
Foal blood sampling was performed shortly after birth, with the first being made immediately after foaling and before colostrum ingestion, and the subsequent ones at 24 h after birth, seven days thereafter, and when the foal was one, two, three, four, five, and six months old. On each occasion, an aliquot of 12 ml blood was collected by jugular venipuncture and divided into one tube with anticoagulant (ethylenediaminetetraacetic acid -EDTA, potassium salt) and another without anticoagulant.
At this stage of the study, we evaluated the sequential changes in hematological parameters (red blood cell counts -RBC, globular volume -GV, hemoglobin -Hb, mean corpuscular volume -MCV, and mean corpuscular hemoglobin concentration -MCHC, leukocyte count -Leuk, leukocyte differential counts -LDC, eosinophils -Eos, monocytes -Mon and platelet counts -PC) and blood biochemistry (urea -U, creatinine -Creat, aspartate aminotransferase -AST, alkaline phosphatase -AP, gamma-glutamyltransferase -GGT, albumin -Alb, total plasma proteins -TPP, fibrinogen -Fib, globulins -Glob, and total serum proteins -Pt). The examinations were carried out at the laboratory of Veterinary Clinical Pathology of the University of Brasília (UnB).
RBC, Leuk, PC, and Hb counts were made using a cell counter (ABX Micros ESV 60 -HORIBA Medical), and the GV and Fib were determined using the microhematocrit method (Stockham and Scott, 2008). The MCV and MCHC were obtained through the standard calculation (Stockham and Scott, 2008). TTP was determined through the refractometer (Stockham and Scott, 2008). From the total, blood smears were made and stained with a rapid dye (panoptic) to perform the LDC and the cellular morphological analysis (Stockham and Scott, 2008). Serum biochemistry (Creat, AST, GGT, AP, and Alb) was determined in a semi-automatic device using specific biochemical kits (BioPlus2000 -BioPlus, Brazil 2 Labtest®, Brazil).
Glob values were obtained by subtracting the serum proteins from the Alb (Pt-Alb = Glob) (Stockham and Scott, 2008).

Statistical analysis
In order to obtain the statistical analysis of the relationship between fetal ocular orbital and gestational age, a polynomial regression model was run by R statistical software (RX64 3.3.0), and the comparison between the regression models of both breeds was performed by a covariance analysis test (ANCOVA). This procedure fits up to ten different regression models for two variables: one dependent and one independent.
For the sequential changes in hematological parameters over time, descriptive statistics methods were used, including dispersion, standard deviation, and variance (One-way ANOVA test). The growth curves for each blood parameter, between breeds, were compared through a curve growth analysis, also using R statistical software (RX64 3.3.0). After verifying no significant difference in the results regarding blood parameters between Campeiro and Pantaneiro foals, the dataset of both breeds was combined and comparisons for each sampling time were made through the Welch's two-sample t-test with the same software R (RX64 3.3.0).

Results
The best model to relate fetal ocular orbit measurements and gestation age was a linear regression. For Campeiro, the model was y = -55.802 + 11.1x (R 2 = 0.977; P < 0.05) and for Pantaneiro was y = -49.742 + 10.9x (R 2 = 0.972; P < 0.05), wherein y represents the gestational age in days and x represents the fetal ocular orbit diameter in millimeters, as shown in Figure 1.

Discussion
Our study revealed a direct relationship between fetal ocular orbit diameter and gestation age, which is a reliable parameter to estimate the gestation time in equine species. Moreover, the sameness of results between the two studied breeds can be explained by similarities in origin and size of these animals. Both breeds descend from Iberian breeds introduced into the central-south of Brazil, brought by Spanish expeditions during the 18th century (Santos et al., 1992).
A positive relationship was found between placental weight and foal birth height, corroborating the findings of some authors (Allen et al., 2002;Elliott et al., 2009;Fernandes et al., 2012;Meireles et al., 2017). According to Wilsher and Allen (2003), the birth of heavier and larger foals can be explained by the fact that heavy placentas are more likely to cause uterine distention in mares. Therefore, as equine placentas are classified as diffuse epithelial, it becomes connected to the entire uterine surface, and the larger its mass, the greater the absorption of nutrients and gases; consequently, the greater the size and weight of the foal at birth. Both the mean values of Campeiro and Pantaneiro foal heights and the average values of placenta weights were very close, once again because these animals had similar origins and characteristics.
Regarding the blood variables, for both breeds, GV, MCV, and Hb presented values above the average established by Harvey et al. (1984). These authors created a reference for foals within the studied age range. These high values of GV, MCV, and Hb observed in our study might have been due to dehydration since the studied horses were in a region with a period of intense drought and in extremely large pastures, what makes water intake difficult for younger animals. These high values can also be attributed to possible physiological adaptations of these animals to the region of hot and dry climate, which are distinct from the weather where these breeds originated and are still present today.
Except for MCHC, the erythrogram results for Campeiro and Pantaneiro foals differed from the findings of Ribeiro et al. (2008) andFonteque et al. (2016), who studied juvenile and adult equines of the same breeds. These authors reported low erythrocyte measurements if compared to other breeds. The explanation for this difference between young animals of the same breed may be the differences in climate, temperature, food availability, and animal excitability during the experiment period. The animals studied by Ribeiro et al. (2008) were located in the Pantanal region of the State of Mato Grosso (Brazil), where horses spend much of the year in wetlands with high humidity, abundant food, and water. On the other side, the foals studied here were in the Federal District, a region with a very dry climate, high temperatures, and low food availability for much of the year.
According to Grondin and Dewitt (2010), pure blood horses such as the Andalusian and Lusitano present high erythrocyte, Hb, and average GV values when compared to animals of other breeds. Therefore, again, one possible explanation for the high values of GV, MCV, and Hb in Campeiro and Pantaneiro breeds can be attributed to their Iberian origin -brought during the Brazilian colonization period.
From birth to 180 days of life, the MCHCs were below the references by Harvey et al. (1984). This outcome might be related to a likely iron deficiency since mares grazed pastures poor in minerals during gestation, in addition to a low iron availability within the neonate first days. According to that author, newborn animals and children are prone to develop iron deficiency when compared to adults, as there is a limitation of body iron stores, as well as an increase in iron demand for fast growth of neonates, and a decrease in this element concentration in breast milk.
Campeiro and Pantaneiro foals up to 8 months old presented Leuk and Neu counts above the reference obtained from adult animals over 25 months, being significantly above the results described by other authors who studied foals of the same age (Ribeiro et al., 2008;Fonteque et al., 2016). Among the related causes, the most consistent is due to the stress experienced by these animals throughout the experiment, from postpartum to 6 months of age. In this sense, the increase in the number of leukocytes after exercise, generally ranging from 10 to 30%, is related to an elevation in cortisol levels (Snow et al., 1982).
Lymph counts in locally adapted Brazilian foals, between 30 and 180 days of age, fell below to those reported by Harvey et al. (1984). Lymph data for Brazilian animals are in concordance with those of Jeffcott et al. (1982), who associated an increase in Lymph cell counts within the first months of life to a constant development of the lymphatic system after foal birth.
During the 6 months of the experiment, plasma globulin averages remained higher than the reference values described by Bauer et al. (1990), except for the moment before colostrum ingestion since there are no references in the literature about Glob during this period. Hyperglobulinemia may be observed in uterine antigen stimulation resulting from a possible infection or inflammation (Bauer et al., 1990), but in spite of this finding, no clinical alteration was observed in these animals.
Both breeds presented U measurements higher than the mean established as a reference for foals between 24 h and 180 days described by Harvey et al. (1984). On the other hand, Creat was within the references for foals and adult animals throughout the study. Bauer et al. (1984) assigned the high value of U measurements to a negative energy balance -when body tissues are metabolized to generate energy, especially in young animals -a relatively common finding in foals under some type of stress and/or intrauterine catabolism. This explanation can be attributed to the high U measurements observed in Campeiro and Pantaneiro foals, especially after delivery, since most of the mares went through stress conditions in the days prior to delivery and particularly at the moment of birthing, probably due to the daily evaluation to predict and monitor the delivery.