Abstract

Simple SummaryThe mRNA expression of Interferon-τ (IFNT), IFN stimulated genes (ISG15, CTSL1, RSAD2, SLC2A1, CXCL10, and SLC27A6), Peroxisome proliferator-activated receptors (PPARA, D, and G), and Retinoid X receptors (RXRA, B, and G) genes and proteins (IFNT, ISG15, CXCL10, PPARG, RXRG, SLC2A1, and SLC27A6) were lower and MUC1 at mRNA and protein levels, was greater in gestation day (GD) 16 embryo and corresponding endometrium of subclinical endometritis cows, and in cows following transfer of poor quality embryo (Grade 3). All genes and proteins but MUC1 expression was lower in GD16 tubular conceptus and corresponding endometrium vs. GD16 filamentous conceptus and matching endometrium in cows with SCE and in cows following the transfer of Grade 3 embryo. Disrupted embryo-uterine communication by altered expression of candidate genes in SCE cows, and in cows following the transfer of poor GD7 embryo negatively programs the conceptus development and plausibly affects the conceptus survival. Effect of the gestational day (GD) 7 embryo quality grade (QG) and subclinical endometritis (SCE) on mRNA and protein expressions of candidate genes [Interferon-τ (IFNT), IFN stimulated genes (ISG15, CTSL1, RSAD2, SLC2A1, CXCL10, and SLC27A6), Peroxisome proliferator activated receptors (PPARA, D, and G), Retinoid X receptors (RXRA, B, and G), and Mucin-1 (MUC1)] in GD16 conceptus and corresponding endometrium were evaluated. After screening of performance records (n = 2389) and selection of repeat breeders (n = 681), cows with SCE (≥6% polymorphonuclear neutrophils—PMN; n = 180) and no-SCE (<6%PMN; n = 180) received GD7 embryos of different QGs. Based on GD16 conceptus recovery, cows with SCE (n = 30) and No- SCE (n = 30) that received GD7 embryos QG1 (good, n = 20), 2 (fair, n = 20), and 3 (poor, n = 20) were included for gene analysis. mRNA and protein expressions (IFNT, ISG15, CXCL10, PPARG, RXRG, SLC2A1, and SLC27A6) differed between SCE and embryo QG groups. All genes but MUC1 and all proteins but MUC1 expression was greater in filamentous conceptus and corresponding endometrium vs. tubular conceptus and matching endometrium in SCE and embryo QG groups. In conclusion, disrupted embryo-uterine communication by altered expression of candidate genes in SCE cows, and in cows following the transfer of poor embryo negatively programs the conceptus development and plausibly affects conceptus survival.

Highlights

  • Proper conceptus development in early gestation is crucial for the successful implantation and maintenance of pregnancy

  • The objective of this study was to investigate the effects of subclinical endometritis (SCE) and gestational day (GD) 7 embryo quality on the mRNA expression of candidate genes [IFNT, IFN stimulated genes (ISG15, CTSL1, RSAD2, SLC2A1, CXCL10, and SLC27A6), Peroxisome proliferator activated receptors (PPARA, D, and G), Retinoid X receptors (RXRA, B, and G), and Mucin-1 (MUC1)] and their proteins expressions in GD 16 conceptus and corresponding endometrium with and without SCE following the transfer of GD 7 embryos with Quality Grades (QG) 1, 2 and 3 in repeat breeder dairy cows

  • In our previous study, following artificial insemination, we observed mRNA abundances of candidate genes were greater in the filamentous conceptus and corresponding endometrium in cows without SCE than in the tubular conceptus and corresponding endometrium in cows with SCE on GD 16, with the exception that RSAD2, PPARA, and RXRA did not differ between the filamentous conceptus and corresponding endometrium in cows without SCE and the tubular conceptus and corresponding endometrium in cows with SCE [21]

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Summary

Introduction

Proper conceptus development in early gestation is crucial for the successful implantation and maintenance of pregnancy. Pregnancy loss is high during initial embryo elongation and this is considered as a crucial developmental period. Significant early embryonic loss occurs during the period between fertilization and gestational day (GD) 16 [2,3,4,5,6,7,8]. The cause of failure of the embryo to survive and establish pregnancy is multifaceted by paternal, maternal, and embryonic factors [12,13,14], many of the embryonic losses are attributed to maternal factors, such as failure of the uterus to support the conceptus growth and implantation

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