Single nucleotide polymorphisms, gene expression and serum profile of immune and antioxidant markers associated with postpartum disorders susceptibility in Barki sheep

References

• El-Wakil SI, Shemeis AR, Ahmed AM, Abdallah A. Genetic and phenotypic relationships involving body weight, degree of maturity and measurer of gain rate of Barki sheep without having recourse to fitting growth curves. J Agricult Sci. 2008;33:4835–4848.
   Google Scholar
• El-Sayed AA, Ateya AI, Hamed MF, et al. Gene expression pattern of acetyl-coA carboxylase alpha, fatty acid synthase, and stearoyl-CoA desaturase in pregnant Barki sheep under complete feed deprivation. Mans Vet Med J. 2019;23:8–13.
   Google Scholar
• Manat TD, Chaudhary SS, Singh VK, Patel SB, Tyagi KK. Oxidative stress profile during postpartum period in Surti goats. Indan J Anim Res. 2017;51(5):837–840.
   Web of Science ®Google Scholar
• Tóthová C, Nagy O, Kovác G. Changes in the concentrations of selected acute phase proteins and variables of energetic profile in dairy cows after parturition. J Appl Anim Res. 2014;42(3):278–283.
   Web of Science ®Google Scholar
• Iliev PT, Georgieva TM. Acute phase proteins biomarkers of diseases in small ruminants: an overview. Bulg J Vet Med. 2017; :1311–1477.
   Google Scholar
• Simplício KM, Rocha TG, Sanchez DC, Cotrim FS, Silva PC, Fagliari JJ. Serum concentrations of acute phase proteins in goats and ewes with naturally acquired Staphylococcus aureus mastitis. Arq Bras Med Vet Zootec. 2017;69(2):285–292.
   Google Scholar
• Agarwal A, Gupta S, Sharma RK. Role of oxidative stress in female reproduction. Reprod Biol Endocrinol. 2005;3:28–21.
   PubMed Web of Science ®Google Scholar
• Wang Y, Walsh SW, Guo J, Zhang J. Meternal levels of prostacyclin, thomboxine, vitamin E, and lipid peroxides throughout normal pregnancy. Am J Obstet Gynecol. 1991;165(6):1690–1997.
   PubMed Web of Science ®Google Scholar
• Murtaugh MP, Baarsch MJ, Zhou Y, Scamurra RW, Lin G. Inflammatory cytokines in animal health and disease. Vet Immunol Immunopathol. 1996;54(1-4):45–55.
   PubMed Web of Science ®Google Scholar
• Fossum C, Wattrang E, Fuxler L, Jensen KT, Wallgren P. Evaluation of various cytokines (IL-6, IFNα, IFN-γ, TNF-α) as markers for acute bacterial infection in swine - a possible role for serum interleukin-6. Vet Immunol Immunopathol. 1998;64(2):161–172.
   PubMed Web of Science ®Google Scholar
• Alsemgeest SPM, van't Klooster GAE, van Miert ASJPAM, Hulskamp-Koch CK, Gruys E. Primary bovine hepatocytes in the study of cytokine induced acute-phase protein secretion in vitro. Vet Immunol Immunopathol. 1996;53(1-2):179–184.
   PubMed Web of Science ®Google Scholar
• Berry DP, Bermingham ML, Good M, More SJ. Genetics of animal health and disease in cattle. Ir Vet J. 2011;64 (1):5.
   PubMedGoogle Scholar
• Soller M, Andersson L. Genomic approaches to the improvement of disease resistance in farm animals. Rev Sci Tech. 1998;17(1):329–345.
   PubMed Web of Science ®Google Scholar
• Nicholas FW. Animal breeding and disease. Philos Trans R Soc Lond B Biol Sci. 2005;360(1459):1529–1536.
   PubMed Web of Science ®Google Scholar
• Pugh DG, Baird N. Sheep and Goat Medicine. 2nd ed. Philadelphia, London: W.B. Saunders Company; 2012.
   Google Scholar
• Boom R, Sol CJ, Salimans MM, Jansen CL, Wertheim-van Dillen PM, van der Noordaa J. Van der noord AAJ. Rapid and simple method for purification of nucleic acids. J Clin Microbiol. 1990;28(3):495–503.
   PubMed Web of Science ®Google Scholar
• Boesenberg-Smith KA, Pessarakli MM, Wolk DM. Assessment of DNA yield and purity: an overlooked detail of PCR troubleshooting. Clini Microbiol News. 2012;34(1):1–6.
   Google Scholar
• Sanger F, Nicklen S, Coulson AR. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977;74(12):5463–5467.
   PubMed Web of Science ®Google Scholar
• Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool. J Mol Biol. 1990;215(3):403–410.
   PubMed Web of Science ®Google Scholar
• Tamura K, Dudley J, Nei M, Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol. 2007;24(8):1596–1599.
   PubMed Web of Science ®Google Scholar
• Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods. 2001;25 (4):402–408.
   PubMed Web of Science ®Google Scholar
• Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001;29(9):2002–2007.
   Web of Science ®Google Scholar
• Darwish AA. The clinicopathological picture of some postpartum disorders in Barki Ewes. AJVS. 2019;62(2):16–25.
   Google Scholar
• Ishikawa Y, Nakada K, Hagiwara K, et al. Changes in interleukin-6 concentration in peripheral blood of pre- and post-partum dairy cattle and its relationship to postpartum reproductive diseases. J Vet Med Sci. 2004;66(11):1403–1408.
   PubMed Web of Science ®Google Scholar
• Boby J, Kumar H, Ganesan A, Singh SK, Narayanan K. Pre–partum serum cytokine levels as a potential tool for the prediction of retention of fetal membranes in cross–bred cows. Adv Anim Vet Sci. 2013;1:14–17.
   Google Scholar
• Botos I, Segal DM, Davies DR. The structural biology of toll-like receptors. Structure. 2011;19(4):447–459.
   PubMed Web of Science ®Google Scholar
• White SN, Taylor KH, Abbey CA, Gill CA, Womack JE. Haplotype variation in bovine toll-like receptor 4 and computational prediction of a positively selected ligand-binding domain. Proc Natl Acad Sci U S A. 2003;100(18):10364–10369.
   PubMed Web of Science ®Google Scholar
• Fujita M, Into T, Yasuda M, et al. Involvement of leucine residues at positions 107, 112, and 115 in a leucine-rich repeat motif of human toll-like receptor 2 in the recognition of diacylated lipoproteins and lipopeptides and Staphylococcus aureus peptidoglycans. J Immunol. 2003;171(7):3675–3683.
   PubMed Web of Science ®Google Scholar
• Kruithof EK, Satta N, Liu JW, Dunoyer-Geindre S, Fish RJ. Gene conversion limits divergence of mammalian TLR1 and TLR6. BMC Evol Biol. 2007;7(148):148–110.
   PubMedGoogle Scholar
• Shinkai H, Tanaka M, Morozumi T, et al. Biased distribution of single nucleotide polymorphisms (SNPs) in porcine toll-like receptor 1 (TLR1), TLR2, TLR4, TLR5, and TLR6 genes. Immunogenetics. 2006;58(4):324–330.
   PubMed Web of Science ®Google Scholar
• Marikovsky M, Zi V, Nev N, Harris-Cerruti C, Mahler O. Cu/Zn superoxide dismutase plays important role in immune response. J Immunol. 2003;170(6):2993–3001.
   PubMed Web of Science ®Google Scholar
• Pasupuleti M, Davoudi M, Malmsten M, Schmidtchen A. Antimicrobial activity of a C-terminal peptide from human extracellular superoxide dismutase. BMC Res Notes. 2009;2:136.
   PubMedGoogle Scholar
• Świderek WP, Charon KM, Winnicka A, Gruszczynsk J. Relationship between blood lymphocyte phenotype, DRB1 (MHC CLASS II) gene polymorphism and somatic cell count in ewe milk. Bull Vet Inst Pulawy. 2006;50:73–77.
   Google Scholar
• Wang X, Xu S, Gao X, Ren H, Chen J. Genetic polymorphism of TLR4 gene and correlation with mastitis in cattle. J Genet Genomics. 2007;34(5):406–412.
   PubMedGoogle Scholar
• Sharma BS, Leyva I, Schenkel F, Karrow N. Association of toll-like receptor 4polymorphisms with somatic cell score and lactation persistency in Holstein bulls. J Dairy Sci. 2006;89(9):3626–3635.
   PubMed Web of Science ®Google Scholar
• Raliou M, Dembélé D, Düvel A, et al. Subclinical endometritis in dairy cattle is associated with distinct mRNA expression patterns in blood and endometrium. PLoS One. 2019;14(8):e0220244.
   PubMed Web of Science ®Google Scholar
• Chunyan S, Wang H, Wang X, et al. Characterization of inflammatory responses by cervical cytology, cytokine expression and ultrastructure changes in a goat subclinical endometritis model. J Vet Med Sci. 2017;79(1):197–205.
   PubMed Web of Science ®Google Scholar
• Fagundes NS, Amanda L, Rezende PB, et al. Short communication: proinflammatory gene expression relative to the collection technique of endometrial samples from cows with and without subclinical endometritis. J Dairy Sci. 2019;102(6):5511–5517.
   PubMed Web of Science ®Google Scholar
• Knaapen AM, Seiler F, Schilderman PA, et al. Neutrophils cause oxidative DNA damage in alveolar epithelial cells. Free Radic Biol Med. 1999;27(1-2):234–240.
   PubMed Web of Science ®Google Scholar
• Goff JP. Immune suppression around the time of calving and the impact of metabolic disease. XXV Jubilee World Buiatrics Congress Budapest, Hungary. Hungarian Vet J. 2006;130(1):39–42.
   Google Scholar
• Guerin P, El- Mouatassim S, Menezo Y. Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings. Hum Reprod Update. 2001;7(2):175–189.
   PubMed Web of Science ®Google Scholar
• Takahashi M, Keicho K, Takahashi H, Ogawa H, Schulte RM, Okano A. Effect of oxidative stress on development and DNA damage in in-vitro cultured bovine embryos by comet assay. Theriogenology. 2000;54(1):137–145.
   PubMed Web of Science ®Google Scholar
• Biri A, Bozkurt N, Turp A, Kavutcu M, Himmetoglu Ö, Durak İ. Role of oxidative stress in intrauterine growth restriction. Gynecol Obstet Invest. 2007;64(4):187–192.
   PubMed Web of Science ®Google Scholar
• Bernabucci U, Ronchi B, Lacetera N, Nardone A. Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows. J Dairy Sci. 2005;88(6):2017–2026.
   PubMed Web of Science ®Google Scholar
• Castillo C, Hernàndez J, Valverde I, et al. Plasma malonaldehyde (MDA) and total antioxidant status (TAS) during lactation in dairy cows. Res Vet Sci. 2006;80(2):133–139.
   PubMed Web of Science ®Google Scholar
• Sivarajasingam SP, Imami N, Johnson MR. Myometrial cytokines and their role in the onset of labour. J Endocrinol. 2016;231(3):R101–119.
   PubMed Web of Science ®Google Scholar
• Krakowski L, Zdzisinska B. Selected cytokines and acute phase proteins in heifers during the ovarian cycle course and in different pregnancy periods. Inst Pulaw. 2007;51:31–36.
   Google Scholar
• Thulasiraman P, Mukherjee J, Banerjee D, et al. Acute phase proteins – a potent biomarker for mastitis. Vetscan. 2013;7(2):6–14.
   Google Scholar
• Endler M, Saltvedt S, Eweida M, Åkerud H. Oxidative stress and inflammation in retained placenta: a pilot study of protein and gene expression of GPX1 and NFκB. BMC Pregnancy Childbirth. 2016;16(1):384.
   PubMedGoogle Scholar
• Liu C, Yang Q, Fang G, et al. Collagen metabolic disorder induced by oxidative stress in human uterosacral ligament-derived fibroblasts: a possible pathophysiological mechanism in pelvic organ prolapse. Mol Med Rep. 2016;13(4):2999–3008.
   PubMed Web of Science ®Google Scholar
• Hong S, Hong L, Li B, et al. The role of GPX1 in the pathogenesis of female pelvic organ prolapse. PLoS One. 2017;12(8):e0181896.
   PubMed Web of Science ®Google Scholar
• Mordak R, Nicpoń J, Illek J. Metabolic and mineral conditions of retained placenta in highly productive dairy cows: pathogenesis, diagnostics and prevention – a review. Acta Vet Brno. 2017;86(3):239–248..
   Web of Science ®Google Scholar
• El-Deeb WM. Clinicobiochemical investigations of gangrenous mastitis in does: immunological responses and oxidative stress biomarkers. J Zhejiang Univ Sci B. 2013;14(1):33–39.
   PubMed Web of Science ®Google Scholar
• Kaya S, Merhan O, Kacar C, Colak A, Bozukluhan K. Determination of ceruloplasmin, some other acute phase proteins, and biochemical parameters in cows with endometritis. Vet World. 2016;9(10):1056–1062.
   PubMed Web of Science ®Google Scholar
• Manimaran A, Kumaresan A, Jeyakumar S, et al. Potential of acute phase proteins as predictor of postpartum uterine infections during transition period and its regulatory mechanism in dairy cattle. Vet World. 2016;9(1):91–100.
   PubMed Web of Science ®Google Scholar
• Kaya S, Öğün M, Özen H, et al. The impact of endometritis on specific oxidative stress parameters in cows. J Hellenic Vet Med Soc. 2018;68(2):231–236.
   Web of Science ®Google Scholar
• Hansen VL, Faber LS, Salehpoor AA, Miller RD. A pronounced uterine pro-inflammatory response at parturition is an ancient feature in mammals. Proc R Soc B. 2017;284:20171694. http://dx.doi.org/10.1098/rspb.2017.1694.
   PubMedGoogle Scholar
• Mondal S, Minj A, Pathak MC, Singh DN, Varshney VP. Importance of hormonal changes during the periparturition period in black Bengal goats. Int J Clin Exp Physiol. 2014;1(1):20–26.
   Google Scholar
• Koyuncu M, Yerlikaya H. Effect of selenium-vitamin E injection of ewes on reproduction and growth of their lambs. S Afr J Anim Sci. 2007;37:233–236.
   Web of Science ®Google Scholar
• Kachuee R, Moeini MM, Sour M. The effect of dietary organic and inorganic selenium supplementation on serum Se, Cu, Fe and Zn status during the late pregnancy in Merghoz goats and their kids. Small Rum Res. 2013;110(1):20–27.
   Web of Science ®Google Scholar
• Khan R, Naz S, Nikousefat Z, et al. Effect of vitamin E in heat-stressed poultry. World’s Poultry Sci J. 2011;67(3):469–478. https://doi.org/10.1017/S0043933911000511
   Web of Science ®Google Scholar