<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">ARSci</journal-id><journal-title-group><journal-title>Advances in Reproductive Sciences</journal-title></journal-title-group><issn pub-type="epub">2330-0744</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/arsci.2020.81005</article-id><article-id pub-id-type="publisher-id">ARSci-97873</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Relationship of Anti-Mullerian Hormone to Reproductive Traits in Katahdin Ewes Bred in Late Spring or Fall
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohan</surname><given-names>Acharya</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Joan</surname><given-names>M. Burke</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Amanda</surname><given-names>J. Ashworth</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Rick</surname><given-names>W. Rorie</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff3"><addr-line>Poultry Production and Product Safety Research, Agricultural Research Service, US Department of Agriculture, Fayetteville, 
AR, USA</addr-line></aff><aff id="aff1"><addr-line>Department of Animal Science, University of Arkansas, Fayetteville, AR, USA</addr-line></aff><aff id="aff2"><addr-line>Dale Bumpers Small Farm Research Center, Agricultural Research Service, US Department of Agriculture, Booneville, AR, USA</addr-line></aff><pub-date pub-type="epub"><day>18</day><month>12</month><year>2019</year></pub-date><volume>08</volume><issue>01</issue><fpage>48</fpage><lpage>56</lpage><history><date date-type="received"><day>12,</day>	<month>December</month>	<year>2019</year></date><date date-type="rev-recd"><day>13,</day>	<month>January</month>	<year>2020</year>	</date><date date-type="accepted"><day>16,</day>	<month>January</month>	<year>2020</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Anti-Mullerian hormone (AMH) is an endocrine marker for fertility in many species. This study investigated possible correlations between serum AMH concentrations, mean number of lambs born (out-of-season in spring or fall), and estimated breeding values (EBVs) for number of lambs born (NLB), number of lambs weaned (NLW), maternal weaning weight (MWWT), weaning weight (WWT), and maternal index (determined by Sheep Genetics Australia). Blood was collected at breeding from Katahdin ewes between 0.7 and 7 years of age in 2015 (n = 163) for the analysis of serum concentrations of AMH. Anti-Mullerian hormone concentration was either expressed quantitatively or divided into quartiles (AMH Q1 through Q4, with Q1 the lowest and Q4 the highest, pg/ml). Data were analyzed by PROC CORR, GLM or chi-squared using SAS. Mean serum AMH was 182 &#177; 11 pg/ml and ranged from 0 to 1112 pg/ml. There was no correlation between serum AMH and EBVs for NLB, NLW, MWWT, WWT and the maternal index. Serum AMH concentration was similar in ewes in different age categories (
  <em>P</em> = 0.157). There was a correlation between EBV for NLB (0.29; 
  <em>P</em> = 0.0002) and NLW (0.19; 
  <em>P</em> = 0.013) with average number of lambs born. Ewes in the lowest AMH quartile (Q1) had a lower mean number of offspring born from spring breeding compared with ewes in other AMH quartiles (Q2, Q3, and Q4; 
  <em>P</em> &lt; 0.05). Further study is needed to determine the effectiveness of using serum AMH for selecting ewes for out-of-season (spring) breeding.
 
</p></abstract><kwd-group><kwd>Anti-Mullerian Hormone</kwd><kwd> Estimated Breeding Values</kwd><kwd> Out-of-Season Breeding</kwd><kwd> Reproductive Performance</kwd><kwd> Sheep</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Anti-Mullerian hormone (AMH) is a dimeric glycoprotein that belongs to a member of the transforming growth factor-β (TGF-β) family [<xref ref-type="bibr" rid="scirp.97873-ref1">1</xref>]. This hormone is produced by granulosa cells of pre-antral and small antral follicles of 1 - 3 mm diameter [<xref ref-type="bibr" rid="scirp.97873-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref3">3</xref>]. Anti-Mullerian hormone facilitates follicle recruitment and growth of young follicles [<xref ref-type="bibr" rid="scirp.97873-ref4">4</xref>]. However, when a follicle increases in size, AMH limits the number of follicles developing from the gonadotropin responsive to the gonadotropin dependent stage [<xref ref-type="bibr" rid="scirp.97873-ref5">5</xref>]. Although AMH limits the number of ovulatory follicles, studies have positively correlated plasma AMH with fertility in sheep [<xref ref-type="bibr" rid="scirp.97873-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref7">7</xref>]. Studies with cattle have shown that AMH concentration remains constant in an individual throughout the estrous cycle and during active reproductive age [<xref ref-type="bibr" rid="scirp.97873-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref10">10</xref>].</p><p>It is well understood that individual ewes vary in reproductive performance, which is the basis for estimated breeding values (EBVs). Estimated breeding values (EBVs) are the mathematical predictions of the genetic merit of an animal for specific traits including reproduction. These values are calculated based on an individual animal’s performance for a trait compared with animals within a contemporary group, and animals in other genetically connected flocks. Estimated breeding values are useful to select for reproductive or maternal traits used in breeding or commercial Katahdins, including prolificacy or number of lambs born (NLB) or weaned (NLW), or maternal weaning weight (MWWT), weaning weight (WWT), and maternal index (http://www.nsip.org/). As lambs, EBVs are an estimate of the parent’s genetic potential until sufficient data is collected on an individual and siblings. Similarly, the ability to conceive out-of-season also varies among ewes [<xref ref-type="bibr" rid="scirp.97873-ref11">11</xref>], but to date there is no way to predict whether an animal is likely to breed out-of-season. It is useful to predict reproductive performance of ewes early in life to minimize costs to rear the most efficient ewes.</p><p>Studies are lacking on relationship between serum concentrations of AMH and maternal EBVs in ewes, or out-of-season breeding success. Therefore, the objective of this study was to examine the relationship between serum AMH, mean number of lambs born (in spring, out-of-season or fall), and EBV for NLB, NLW, MWWT, WWT, and the maternal index.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>The experiment was conducted at USDA, Agriculture Research Service (ARS), Dale Bumpers Small Farms Research Center (DBSFRC) in Booneville, AR, USA (35.08˚N, 93.98˚W). All animal procedures were approved by ARS Institutional Animal Care and Use Committee (protocol # 170103).</p><sec id="s2_1"><title>2.1. Animal Management</title><p>Katahdin ewes were raised at USDA, ARS, DBSFRC in Booneville, AR. A total of 163 ewes ranging from 0.7 to 7 years of age were categorized into 5 age groups: less than 1 (n = 17), 1 to 2 (n = 57), 2 to 3 (n = 23), 3 to 4 (n = 34), and more than 4 years of age (n = 32). Ewes were maintained on predominantly tall fescue (Schedonorus arundinacea) and/or bermudagrass (Cynodon dactylon) overseeded with winter annuals [Wheat (Triticum aestivum L.) and rye (Lolium multiforum L.)] and were supplemented with corn/soybean meal (17% CP, 82% TDN on DM basis). Rams passed breeding soundness evaluation before breeding, and ewes were over 6 months of age and weighed at least 35 kg. Ewes were exposed to rams for approximately 30 days either in fall (August/September) or spring (April/May) at a ram to ewe ratio of 1:20 to 1:30. Body weight of ewes was recorded on first day of ram exposure, and offspring were weighed at birth and approximately 60 days of age.</p><p>In some years ewes that would have been eligible to breed in fall were held over for spring to increase number of ewes available at that time. Pregnancy rate was determined (approximately 28 days after ram removal) by ultrasound examination (Aloka SSD 500 V ultrasound scanner equipped with a 7.5 MHz linear array prostrate transducer; Hitachi Aloka Medical Ltd., Japan). Ewes that did not conceive to two consecutive breedings were removed from the flock. Other management criteria for culling ewes included problems of foot scald and internal parasites. Data on lambs, including pedigrees, body weight at birth, 60 and 90 - 120 days of age were entered in the US National Sheep Improvement Program (NSIP; http://www.nsip.org/) between 2008 and 2017 to generate EBVs in the flock. The EBVs included MWWT, WWT, NLB, NLW, and a Katahdin maternal index (0.246 &#215; WWT EBV + 2.226 &#215; MWWT EBV + 0.406 &#215; NLW EBV − 0.035 &#215; NLB EBV; Notter, 2011). Accuracies of EBVs for NLB for ewes used in the current study ranged from 35% to 72%, 31% to 67% for NLW, 57% to 79% for MWWT, and 55% to 81% for WWT. A definition of all EBVs is at http://nsip.org/wp-content/uploads/2015/03/NSIP-EBV-Descriptions-FINAL-1.16.15.pdf (accessed February 19, 2019).</p><p>Blood was collected in July 2015 by jugular venipuncture into 10 ml BD Vacutainer SS Plus Blood Collection Tubes (Becton, Dickson, Franklin Lakes, NJ). Blood tubes were inverted to mix several times and allowed to clot for 30 min at room temperature. After clotting, the tubes were held on ice until centrifuged (Beckman Coulter T J6 refrigerated centrifuge, Fullerton, CA) at 2500 &#215;g for 25 min. Serum was collected and stored in 5 ml polypropylene tubes at −20˚C until analysis.</p></sec><sec id="s2_2"><title>2.2. Ovine AMH ELISA Immunoassay</title><p>The equine and ovine AMH ELISA kit used was a quantitative three-step sandwich type immunoassay (AL-115, AnshLabs, Webster, TX). Analysis was performed as described by the manufacturer (http://www.anshlabs.com/). Before analysis, all the kit reagents were warmed to room temperature and serum samples were thawed overnight at 4˚C. Solutions were mixed as recommended. Calibrators were serially diluted from 50 pg/ml to 13,600 pg/ml of AMH. Fifty microliters of duplicate calibrators, control or serum samples were added to appropriate wells of the 96-well assay plate. Fifty microliters of AMH assay buffer was added to each well using a repeater pipette. Plate was shaken at 700 rpm on an orbital microplate shaker (Lab-Line Instrument Inc. Melrose Park, IL) for 2 h at room temperature. The plate was removed and washed 5 times with wash solution in microplate strip washer (ELP40 Bio-Tek Instruments, New York, NY). Antibody-Biotin Conjugate RTU (100 &#181;l) was added using a repeater pipette, incubated at 700 rpm on orbital microplate shaker (Lab-Line Instrument Inc. Melrose Park, IL) for 1 h and washed 5 times with wash solution using the microplate strip washer. Streptavidin-enzyme conjugate-RTU (100 &#181;l) was added after washing, incubated in the orbital microplate shaker at 700 rpm for 30 min, and washed 5 times using microplate washer. TBM chromogen (100 &#181;l) was added to each well using a repeated pipette and incubated in orbital microplate shaker at 700 rpm for 20 min. Finally, 100 &#181;l of stopping solution was added to each well and absorbance was read using a model 1420-040 Victor3 Multilabel Counter (Perkin Elmer, USA) at 450 nm.</p></sec><sec id="s2_3"><title>2.3. Statistical Analysis</title><p>For analysis, pregnancy rate is defined as the proportion of ewes that were pregnant approximately 28 days after ram was removed from breeding groups. One ewe did not lamb after being diagnosed as pregnant, but all other ewes determined pregnant post-breeding lambed. Mean number of lambs born was the number of live lambs born per ewe exposed to ram. Parity was the number of times individual ewes were used for breeding. Anti-Mullerian hormone concentrations were expressed either quantitatively or categorically into quartiles (Q1 through Q4, with Q1 lowest and Q4 highest; pg/ml). Quartiles were assigned using Excel Quartile function on raw data.</p><p>Pearson correlation coefficients between AMH, EBVs, and number of lambs born were analyzed using the PROC CORR procedure of SAS (version 9.4; SAS Inst. Inc., Cary, NC, USA). For remaining data, continuous variables were analyzed by PROC GLM, and categorical variables were analyzed by chi-squared using SAS. For categorical data AMH concentrations were divided into four quartiles: Q1 = 0 - 80 pg/ml, Q2 = 81 - 104 pg/ml, Q3 = 105 - 248 pg/ml, and Q = 249 - 1112 pg/ml. Data were expressed as least squares means and standard error. Means were compared using Tukey’s test.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Intra-assay variability of AMH assays ranged from 6.6% to 8.3%. Inter-assay variability between standards was 4.3%. Least square mean serum concentration of AMH was 182 &#177; 11 pg/ml and ranged from 0 to 1112 pg/ml.</p><sec id="s3_1"><title>3.1. Correlation of EBVs with AMH Concentrations and Average Number of Lambs Born</title><p>Serum AMH concentrations were not correlated with EBVs for NLB (−0.02; P = 0.793), NLW (−0.09; P = 0.252), MWWT (−0.02; P = 0.712), WWT (−0.02; P = 0.757), and the maternal index (0.072; P = 0.355). Average number of lambs born was significantly correlated with EBV for NLB (0.29; P = 0.0002) and NLW (0.19; P = 0.013). However, EBV for WWT (−0.09; P = 0.242), MWWT (−0.11; P = 0.138), and maternal index (0.04; P = 0.547) were not correlated with average number of lambs born.</p></sec><sec id="s3_2"><title>3.2. Relationship between AMH Quartiles and Mean Number of Lambs Born from Spring (Out-of-Season) or Fall Breeding</title><p>There was no correlation between AMH quartiles with mean number of lambs born from fall breeding (P &gt; 0.05; <xref ref-type="table" rid="table1">Table 1</xref>). However, there was a significant correlation between mean number of lambs born from spring breeding with AMH quartiles (P &lt; 0.05). Ewes in lowest quartile (Q1) had lower number of lambs born from spring breeding than ewes in other quartiles (Q2, Q3, Q4; P &lt; 0.05).</p></sec><sec id="s3_3"><title>3.3. Influence of Ewe Age on Serum AMH Concentration</title><p>Mean AMH concentration in age groups of less than 1, 1 to 2, 2 to 3, 3 to 4, and more than 4-years was 129 &#177; 20, 148 &#177; 10, 159 &#177; 20, 195 &#177; 10, 166 &#177; 10 pg/ml, respectively. There was no difference in serum AMH concentration among age categories (P = 0.157).</p></sec><sec id="s3_4"><title>3.4. Pregnancy and Lambing Rate of Exposed Ewes between Breeding Seasons</title><p>Overall pregnancy rate was higher (P &lt; 0.01) in fall bred ewes (79.0%) compared with spring bred (48.0%). Mean number of lambs born from fall breeding (1.44 &#177; 0.05) was higher (P &lt; 0.01) compared with mean number of lambs born from spring breeding (0.78 &#177; 0.05) per ewes used for breeding.</p></sec><sec id="s3_5"><title>3.5. Lambing Rate per Parity</title><p>Lambing rate was highest in third parity ewes and lowest in first parity ewes (P &lt; 0.05). Mean numbers of lambs born at first, second, third, fourth, fifth, and sixth</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Relationship between AMH quartiles and mean number of lambs born from different spring or fall breeding. Data expressed in mean &#177; standard error (SE)</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >AMH Quartiles</th><th align="center" valign="middle" >AMH Range (pg/ml)</th><th align="center" valign="middle" >n</th><th align="center" valign="middle" >Fall</th><th align="center" valign="middle" >Spring</th><th align="center" valign="middle" >Overall</th></tr></thead><tr><td align="center" valign="middle" >AMHQ1 AMHQ2 AMHQ3 AMHQ4</td><td align="center" valign="middle" >0 - 80 81 - 104 105 - 248 249 - 1112</td><td align="center" valign="middle" >37 34 39 36</td><td align="center" valign="middle" >1.48 &#177; 0.11 1.54 &#177; 0.11 1.38 &#177; 0.11 1.43 &#177; 0.10</td><td align="center" valign="middle" >0.41 &#177; 0.12<sup>b</sup> 0.92 &#177; 0.11<sup>a</sup> 0.89 &#177; 0.10<sup>a</sup> 0.90 &#177; 0.10<sup>a</sup></td><td align="center" valign="middle" >0.65 &#177; 0.10 0.81 &#177; 0.11 0.87 &#177; 0.10 0.71 &#177; 0.11</td></tr></tbody></table></table-wrap><p>Means with different superscripts in the same column differ (P &lt; 0.05). n = number of ewes in each AMH Quartiles category.</p><p>parity are 0.81 &#177; 0.07, 1.06 &#177; 0.08, 1.52 &#177; 0.09, 1.34 &#177; 0.10, 1.09 &#177; 0.14, and 1.33 &#177; 0.21, respectively.</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>The mathematical calculations of EBVs are complex, taking into account of phenotypic (body weights, type of birth) and genetic (using data from relatives entered into NSIP) parameters. The EBV is the best estimate of the true genetic merit of any individual for a specific genetic trait measured (http://www.nsip.org/). The more data or genetic connections within the breed, the greater the accuracy of the EBV [<xref ref-type="bibr" rid="scirp.97873-ref12">12</xref>]. In the current study, there was no correlation between serum AMH concentrations and any of the EBVs. The priority selection criteria of the flock was parasite resistance followed by maternal traits (maternal milk and number of lambs weaned). Among the ewes in the flock, there was a wide range of EBV for maternal traits. Accuracy of some of these traits, especially in younger ewes may be low enough to impact correlations. Estimated breeding values for NLB as well as NLW in the current study were correlated with mean number of lambs born. The flock also had a higher value correlation between NLB and NLW, implying that there is low voluntary lamb removal (i.e., artificial rearing of lamb or fostering of lambs to other ewes) [<xref ref-type="bibr" rid="scirp.97873-ref13">13</xref>]. However, other EBVs, WWT, MWWT, and maternal index were not correlated. The EBVs, NLW and MWWT are related to mothering ability, which physiologically is related to functional hormones post-lambing such as prolactin. Thus, EBVs for NLB and NLW can be further explored to select highly prolific ewes in the flock with good mothering ability.</p><p>Ovarian follicular population, an indicator for fertility, was positively correlated with plasma AMH concentration in young lambs [<xref ref-type="bibr" rid="scirp.97873-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref7">7</xref>]. A positive correlation between plasma AMH concentrations during the prepubertal period and occurrence of ovulation in response to eCG was also reported [<xref ref-type="bibr" rid="scirp.97873-ref6">6</xref>]. A higher number of embryos were found in synchronized ewes with higher plasma AMH concentrations [<xref ref-type="bibr" rid="scirp.97873-ref14">14</xref>]. Ewes with a high plasma AMH (&gt;97 pg/ml) had a higher number of lambs born per ewe per year until 3.5 years of age compared with low (&lt;97 pg/ml) plasma AMH concentrations measured at 3.5 months of age [<xref ref-type="bibr" rid="scirp.97873-ref7">7</xref>]. Because, AMH concentration remains constant throughout the estrous cycle and during active reproductive age [<xref ref-type="bibr" rid="scirp.97873-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref10">10</xref>], we chose to examine this hormone in a range of age groups of sexually mature ewes. In the current study, when ewes were compared, based on serum AMH measurement after puberty, AMH hormone concentration was not correlated with mean number of lambs born. Similar results were obtained when ewes were compared by quartiles, based on serum AMH measurement after puberty with mean number of lambs born (not shown in the result). However, when number of lambs born from spring and fall breeding were separately correlated with AMH quartiles, ewes in lowest quartiles (Q1) had lower number of lambs born from spring breeding than ewes in other quartiles. Low reproductive performance of ewes in lowest quartiles (Q1) during spring in the current study is similar to the result we recently reported in cattle [<xref ref-type="bibr" rid="scirp.97873-ref15">15</xref>]. In our previous study, we reported AMH concentration of heifers at breeding, with the lowest quartiles (Q1) had lower AI pregnancy rate and conceived at a later estrus cycle in breeding compared with heifers in higher quartiles [<xref ref-type="bibr" rid="scirp.97873-ref15">15</xref>].</p><p>Out-of-season breeding during long days is beneficial to the sheep industry for several reasons. First, breeding in the spring results in late-gestation and lactation coinciding with rise in high quality cool-season forage in the southeastern US [<xref ref-type="bibr" rid="scirp.97873-ref16">16</xref>]. Second, weather in early fall is ideal for pasture lambing, reducing chances of weather related deaths in young [<xref ref-type="bibr" rid="scirp.97873-ref17">17</xref>]. Third, lambs can be marketed in spring when demand is high and the lamb supply is low [<xref ref-type="bibr" rid="scirp.97873-ref18">18</xref>]. In much of the US, pregnancy and lambing rates are higher during fall breeding compared with spring, and Katahdins in the Southeastern US are no exception [<xref ref-type="bibr" rid="scirp.97873-ref11">11</xref>]. Katahdin ewe lambs or yearlings have more pregnancy losses, and lower lamb birth weights when bred during spring compared with fall [<xref ref-type="bibr" rid="scirp.97873-ref11">11</xref>]. In order to increase spring breeding success, it will be useful to identify ewes that are capable of out-of-season breeding. In the current study, ewes in lowest AMH hormone quartiles had lower number of lambs born from spring (out-of-season) breeding, thus further study can be done to select ewes that can breed out-of-season by using AMH endocrine marker.</p><p>Anti-Mullerian hormone is high during the fetal stage compared with postnatal concentrations [<xref ref-type="bibr" rid="scirp.97873-ref2">2</xref>]. Similarly, plasma AMH concentrations in 40 d old ewes are higher than 3.6-month old ewes [<xref ref-type="bibr" rid="scirp.97873-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref19">19</xref>]. Lahoz found a vast difference between 1 and 5-month-old ewes, decreasing with age [<xref ref-type="bibr" rid="scirp.97873-ref20">20</xref>]. Serum AMH concentrations of ewes after puberty, at different reproductive ages has not been reported. In the current study, serum AMH concentrations was similar in different age groups (less than one, 1 - 2, 2 - 3, 3 - 4, and more than 4 year old) ewes. Age did not influence serum AMH concentrations as previously reported in cattle [<xref ref-type="bibr" rid="scirp.97873-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.97873-ref9">9</xref>].</p></sec><sec id="s5"><title>5. Conclusion</title><p>In conclusion, serum AMH concentration was similar among age groups. Ewes in the lowest quartile (Q1) had lower number of offspring born from spring breeding compared with ewes in other AMH quartiles (Q2, Q3, and Q4). However, AMH was not useful in predicting fertility or maternal traits based on EBV of the ewes. Further research can be done to select ewes that are capable of out-of-season breeding using endocrine markers.</p></sec><sec id="s6"><title>Acknowledgements</title><p>This research was supported by the University of Arkansas Division of Agriculture, and the USDA Agriculture Research Service. The authors acknowledge Lauretta Ngere, Chad Lee, Erin Wood, Toby Lester, and Samuel Tabler for their technical help. Mention of trade names or commercial products in this manuscript is solely for providing specific information and does not imply recommendations or endorsement by the authors or sponsoring organizations.</p></sec><sec id="s7"><title>Conflicts of Interest</title><p>The authors declare no conflict of interest regarding this publication.</p></sec><sec id="s8"><title>Cite this paper</title><p>Acharya, M., Burke, J.M., Ashworth, A.J. and Rorie, R.W. (2020) Relationship of Anti-Mullerian Hormone to Reproductive Traits in Katahdin Ewes Bred in Late Spring or Fall. Advances in Reproductive Sciences, 8, 48-56. https://doi.org/10.4236/arsci.2020.81005</p></sec></body><back><ref-list><title>References</title><ref id="scirp.97873-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Cate, R.L., Mattaliano, R.J., Hession, C., Tizard, R., Farber, N.M., Cheung, A., et al. (1986) Isolation of the Bovine and Human Genes for Müllerian Inhibiting Substance and Expression of the Human Gene in Animal Cells. Cell, 45, 685-698. https://doi.org/10.1016/0092-8674(86)90783-X</mixed-citation></ref><ref id="scirp.97873-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Bézard, J., Vigier, B., Tran, D., Mauléon, P. and Josso, N. (1988) Anti-Müllerian Hormone in Sheep Follicles. Reproduction Nutrition Development, 28, 1105-1112. https://doi.org/10.1186/1746-6148-8-118</mixed-citation></ref><ref id="scirp.97873-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Monniaux, D., Drouilhet, L., Rico, C., Estienne, A., Jarrier, P., Touzé, J.L., et al. (2012) Regulation of Anti-Müllerian Hormone Production in Domestic Animals. Reproduction Fertility and Development, 25, 1-16. https://doi.org/10.1071/RD12270</mixed-citation></ref><ref id="scirp.97873-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Scaramuzzi, R.J., Baird, D.T., Campbell, B.K., Driancourt, M.A., Dupont, J., Fortune, J.E., et al. (2011) Regulation of Folliculogenesis and the Determination of Ovulation Rate in Ruminatns. Reproduction Fertility Development, 23, 444-467. https://doi.org/10.1071/RD09161</mixed-citation></ref><ref id="scirp.97873-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Campbell, B.K., Clinton, M. and Webb, R. (2012) The Role of Anti-Müllerian Hormone (AMH) during Follicle Development in a Monovulatory Species (Sheep). Endocrinology, 153, 4533-4543. https://doi.org/10.1210/en.2012-1158</mixed-citation></ref><ref id="scirp.97873-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Lahoz, B., Alabart, J.L., Monniaux, D., Mermillod, P. and Folch, J. (2012) Anti-Mullerian Hormone Plasma Concentration in Prepubertal Ewe Lambs as a Predictor of Their Fertility at a Young Age. BMC Veterinary Research, 8, 2-9. https://doi.org/10.1186/1746-6148-8-118</mixed-citation></ref><ref id="scirp.97873-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Lahoz, B., Alabart, J.L. and Folch, J. (2016) Relationship between Anti-Müllerian Hormone (AMH) and the Ovulatory Response Measured in Three-Month Old Ewe Lambs with Their Reproductive Efficiency in Adulthood. Associatión Interprofesional para el Desarrollo Agrario, 112, 392-404. https://doi.org/10.12706/itea.2016.024</mixed-citation></ref><ref id="scirp.97873-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Rico, C., Fabre, S., Médigue, C., Clemente, N., Clément, F., Bontoux, M., et al. (2009) Anti-Müllerian Hormone Is an Endocrine Marker of Ovarian Gonadotropin-Responsive Follicles and Can Help to Predict Superovulatory Responses in the Cow. Biology of Reproduction, 80, 50-59. https://doi.org/10.1095/biolreprod.108.072157</mixed-citation></ref><ref id="scirp.97873-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Ireland, J.J., Smith, G.W., Scheetz, D., Jimenez-Krassel, F., Folger, J.K., Ireland, J.L.H., et al. (2010) Does Size Matter in Females? An Overview of the Impact of the High Variation in the Ovarian Reserve on Ovarian Function and Fertility, Utility of Anti-Mullerian Hormone as a Diagnostic Marker for Fertility and Causes of Variation in the Ovarian Reserve in Cattle. Reproduction Fertility and Development, 23, 1-14. https://doi.org/10.1071/RD10226</mixed-citation></ref><ref id="scirp.97873-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Mossa, F., Jimenez-Krassel, F., Scheetz, D., Weber-Nielsen, M., Evans, A.C.O. and Ireland, J.J. (2017) Anti-Mullerian Hormone (AMH) and Fertility Management in Agricultural Species. Reproduction, 154, R1-R11. https://doi.org/10.1530/REP-17-0104</mixed-citation></ref><ref id="scirp.97873-ref11"><label>11</label><mixed-citation publication-type="journal" xlink:type="simple"><name name-style="western"><surname>Burke</surname><given-names> J.M. </given-names></name>,<etal>et al</etal>. (<year>2005</year>)<article-title>Lamb Production of Dorper, Katahdin, and St. Croix Bred in Summer, Winter, or Spring in the Southeastern US</article-title><source> Sheep and Goat Research Journal</source><volume> 20</volume>,<fpage> 51</fpage>-<lpage>59</lpage>.<pub-id pub-id-type="doi"></pub-id></mixed-citation></ref><ref id="scirp.97873-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Kuehn, L.A., Lewis, R.M. and Notter, D.R. (2007) Managing the Risk of Comparing Estimated Breeding Values across Flocks or Herds through Connectedness: A Review and Application. Genetics Selection Evolution, 39, 225-247. https://doi.org/10.1051/gse:2007001</mixed-citation></ref><ref id="scirp.97873-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Notter, D.R., Lauretta, L., Burke, J.M., Miller, J.E. and Morgan, J.L. (2018) Genetics Parameters for Ewe Reproductive Performance and Peri-Parturient Fecal Egg Counts and Their Genetic Relationships with Lamb Body Weights and Fecal Egg Count in Katahdin Sheep. Journal of Animal Science, 96, 1579-1589. https://doi.org/10.1093/jas/sky100</mixed-citation></ref><ref id="scirp.97873-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Pinto, P.H.N., Balaro, M.F.A., Souza-Fabjan, J.M.G., Ribeiro, L.S., Braganca, G.M., Leite, et al. (2018) Anti-Mullerian Hormone and Antral Follicle Count Are More Effective for Selecting Ewes with Good Potential for in Vivo Embryo Production than the Presence of FecGE Mutation or eCG Pre-Selection Tests. Theriogenology, 113, 146-152. https://doi.org/10.1016/j.theriogenology.2018.02.018</mixed-citation></ref><ref id="scirp.97873-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Rorie, R., Newberry, H., Lester, T.D., Acharya, M. and Hansen, C. (2016) Anti-Müllerian Hormone at Weaning and Breeding as a Predictor of Beef Heifer Fertility. Reproduction Fertility and Development, 29, 111-112. https://doi.org/10.1071/RDv29n1Ab8</mixed-citation></ref><ref id="scirp.97873-ref16"><label>16</label><mixed-citation publication-type="other" xlink:type="simple">Volesky, J.D., Anderson, B.E. and Nichols, J.T. (2010) Perennial Forages for Irrigated Pasture. Nebraska Extension. http://extensionpublications.unl.edu/assets/html/g1502/build/g1502.htm</mixed-citation></ref><ref id="scirp.97873-ref17"><label>17</label><mixed-citation publication-type="other" xlink:type="simple">USDA-APHIS-VS-CEAH-NAHMS (2014) Sheep and Lamb Death Loss in the United States, 2011. National Animal Health Monitoring System. Animal and Plant Health Inspection Service, Fort Collins. https://www.aphis.usda.gov/animal_health/nahms/sheep/downloads/sheep11/Sheep11_is_DeathLoss.pdf</mixed-citation></ref><ref id="scirp.97873-ref18"><label>18</label><mixed-citation publication-type="other" xlink:type="simple">American Lamb Board (2018) National Lamb Check-Off Program. https://www.americanlamb.com</mixed-citation></ref><ref id="scirp.97873-ref19"><label>19</label><mixed-citation publication-type="other" xlink:type="simple">Torres-Rovira, L., Gonzalez-Bulnes, A., Succu, S., Spezzigu, A., Manca, M.E., Leoni, G.G., et al. (2014) Predictive Value of Antral Follicle Count and Anti-Müllerian Hormone for Follicle and Oocyte Developmental Competence during the Early Prepubertal Period in a Sheep Model. Reproduction Fertility and Development, 26, 1094-1106. https://doi.org/10.1071/RD13190</mixed-citation></ref><ref id="scirp.97873-ref20"><label>20</label><mixed-citation publication-type="other" xlink:type="simple">Lahoz, B., Fabre S., Calvo, J.H., Drouilhet, L., Sanchez, P., Sarto, P., et al. (2016) Assessing the Age-Related Relationship between Plasma Anti-Mullerian Hormone (AMH) and Ovarian Follicle Population in Prepubertal Ewes. 18th International Congress on Animal Reproduction (ICAR), Tours, 26-30 June 2016, 41. https://araid.es/en/content/assessing-age-related-relationship-between-plasma-anti-m%C3%BCllerian-hormone-amh-and-ovarian</mixed-citation></ref></ref-list></back></article>