162
Views
2
CrossRef citations to date
0
Altmetric
Articles

Relationships between novel nucleotide variants within the colony-stimulating factor 1 receptor (CSF1R) gene and mastitis indicators in sheep

, , , &

References

  • Gelasakis AI, Mavrogianni VS, Petridis IG, Vasileiou NGC, Fthenakis GC. Mastitis in sheep—the last 10 years and the future of research. Vet Microbiol. 2015;181(1–2):136–146.
  • Bergonier D, Berthelot X. New advances in epizootiology and control of ewe mastitis. Livestock Product Sci. 2003;79(1):1–16.
  • Chew BP, Hollen LL, Hillers JK, Herlugson ML. Relationship between vitamin A and beta-carotene in blood plasma and milk and mastitis in Holsteins. J Dairy Sci. 1982;65(11):2111–2118.
  • Menzies PI, Ramanoon SZ. Mastitis of sheep and goats. Vet Clin North Am Food Anim Pract. 2001;17(2):333–358.
  • Mork T, Waage S, Tollersrud T, Kvitle B, Sviland S. Clinical mastitis in ewes; bacteriology, epidemiology and clinical features. Acta Vet Scand. 2007;49(1):23.
  • Authority EFS. Scientific opinion on the welfare risks related to the farming of sheep for wool, meat and milk production. EFSA J. 2014;12(12):128.
  • Asselstine V, Miglior F, Suarez-Vega A, et al. Genetic mechanisms regulating the host response during mastitis. J Dairy Sci. 2019;102(10):9043–9059.
  • Jiang Q, Zhao H, Li RL, et al. In silico genome-wide miRNA-QTL-SNPs analyses identify a functional SNP associated with mastitis in Holsteins. BMC Genet. 2019;20(1):46.
  • Khan MZ, Wang D, Liu L, et al. Significant genetic effects of JAK2 and DGAT1 mutations on milk fat content and mastitis resistance in Holsteins. J Dairy Res. 2019;86(4):388–393.
  • Pokorska J, Piestrzyńska-Kajtoch A, Kułaj D, Ochrem A, Radko A. Polymorphism of bovine lipocalin-2 gene and its impact on milk production traits and mastitis in Holstein Friesian cattle. Electron J Biotechnol. 2019;40:17–21.
  • Bergonier D, De Crémoux R, Rupp R, Lagriffoul G, Berthelot X. Mastitis of dairy small ruminants. Vet Res. 2003;34(5):689–716.
  • Burvenich C, Van Merris V, Mehrzad J, Diez-Fraile A, Duchateau L. Severity of E. coli mastitis is mainly determined by cow factors. Vet Res. 2003;34(5):521–564.
  • Rinaldi M, Li RW, Bannerman DD, et al. A sentinel function for teat tissues in dairy cows: dominant innate immune response elements define early response to E. coli mastitis. Funct Integr Genomics. 2010;10(1):21–38.
  • Bishop SC, Axford RFE, Nicholas FW, Owen JB. Breeding for Disease Resistance in Farm Animals. 3rd ed. Wallingford: CABI Publishing; 2010:3–14.
  • Detilleux JC. Genetic factors affecting susceptibility of dairy cows to udder pathogens. Vet Immunol Immunopathol. 2002;88(3–4):103–110.
  • Rupp R, Boichard D. Genetics of resistance to mastitis in dairy cattle. Vet Res. 2003;34(5):671–688.
  • Tolone M, Larrondo C, Yáñez JM, Newman S, Sardina MT, Portolano B. Assessment of genetic variation for pathogen-specific mastitis resistance in Valle del Belice dairy sheep. BMC Vet Res. 2016;12(1):158.
  • Garcia S, Hartkamp LM, Malvar-Fernandez B, et al. Colony-stimulating factor (CSF) 1 receptor blockade reduces inflammation in human and murine models of rheumatoid arthritis. Arthritis Res Ther. 2016;18(1):75.
  • Lin WY, Xu DQ, Austin CD, et al. Function of CSF1 and IL34 in macrophage homeostasis, inflammation, and cancer. Front Immunol. 2019;10:2019.
  • Chitu V, Stanley ER. Colony-stimulating factor-1 in immunity and inflammation. Curr Opin Immunol. 2006;18(1):39–48.
  • Xun QJ, Wang Z, Hu XL, Ding K, Lu XY. Small-molecule CSF1R inhibitors as anticancer agents. Curr Med Chem. 2020;27(23):3944–3966.
  • Qian BZ, Deng Y, Im JH, et al. A distinct macrophage population mediates metastatic breast cancer cell extravasation, establishment and growth. PLoS One. 2009;4(8):e6562.
  • Manthey CL, Johnson DL, Illig CR, et al. JNJ-28312141, a novel orally active colony-stimulating factor-1 receptor/FMS-related receptor tyrosine kinase-3 receptor tyrosine kinase inhibitor with potential utility in solid tumors, bone metastases, and acute myeloid leukemia. Mol Cancer Ther. 2009;8(11):3151–3161.
  • Banos G, Bramis G, Bush SJ, et al. The genomic architecture of mastitis resistance in dairy sheep. BMC Genomics. 2017;18(1):624.
  • Li TT, Gao JF, Zhao XX, Ma YJ. Digital gene expression analyses of mammary glands from meat ewes naturally infected with clinical mastitis. R Soc Open Sci. 2019;6(7):181604.
  • Akhatayeva Z, Mao C, Jiang F, et al. Indel variants within the PRL and GHR genes associated with sheep litter size. Reprod Domest Anim. 2020. doi: https://doi.org/10.1111/rda.13796.
  • Yang Y, Hu H, Mao C, et al. Detection of the 23 bp nucleotide sequence mutation in retinoid acid receptor related orphan receptor alpha (RORA) gene and its effect on sheep litter size. Anim Biotechnol. 2020:1-9.
  • Dekkers JC, Dentine MR. Quantitative genetic variance associated with chromosomal markers in segregating populations. Theor Appl Genet. 1991;81(2):212–220.
  • Rupp R, Boichard D, Rupp R, Boichard D. Genetic parameters for clinical mastitis, somatic cell score, production, udder type traits, and milking ease in first lactation Holsteins. J Dairy Sci. 1999;82(10):2198–2204.
  • Kandeel SA, Morin DE, Calloway CD, Constable PD. Association of California mastitis test scores with intramammary infection status in lactating dairy cows admitted to a veterinary teaching hospital. J Vet Intern Med. 2018;32(1):497–505.
  • Cui Y, Yan HL, Wang K, et al. Insertion/deletion within the KDM6A gene is significantly associated with litter size in goat. Front Genet. 2018;9:91.
  • Wang K, Yan HL, Xu H, et al. A novel indel within goat casein alpha S1 gene is significantly associated with litter size. Gene. 2018;671:161–169.
  • Shi YY, He L. SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci. Cell Res. 2005;15(2):97–98.
  • Dai WQ, Xu YF, Zhu BH. On the edge l(infinity) radius of Saitou and Nei’s method for phylogenetic reconstruction. Theor Comput Sci. 2006;369(1–3):448–455.
  • Zhao HY, Wu XF, Cai HF, et al. Genetic variants and effects on milk traits of the caprine paired-like homeodomain transcription factor 2 (PITX2) gene in dairy goats. Gene. 2013;532(2):203–210.
  • Schober P, Boer C, Schwarte LA. Correlation coefficients: appropriate use and interpretation. Anesth Analg. 2018;126(5):1763–1768.
  • Waage S, Vatn S. Individual animal risk factors for clinical mastitis in meat sheep in Norway. Prev Vet Med. 2008;87(3–4):229–243.
  • Moosavi M, Mirzaei A, Ghavami M, Tamadon A. Relationship between season, lactation number and incidence of clinical mastitis in different stages of lactation in a Holstein dairy farm. Vet Res Forum. 2014;5(1):13–19.
  • Carcangiu V, Vacca GM, Mura MC, et al. Relationship between MTNR1A melatonin receptor gene polymorphism and seasonal reproduction in different goat breeds. Anim Reprod Sci. 2009;110(1–2):71–78.
  • Wang K, Kang Z, Jiang E, et al. Genetic effects of DSCAML1 identified in genome-wide association study revealing strong associations with litter size and semen quality in goat (Capra hircus). Theriogenology. 2020;146:20–25.
  • Wang Z, Zhang X, Jiang E, et al. InDels within caprine IGF2BP1 intron 2 and the 3′-untranslated regions are associated with goat growth traits. Anim Genet. 2020; 51(1):117–121.
  • Dai XM, Ryan GR, Hapel AJ, et al. Targeted disruption of the mouse colony-stimulating factor 1 receptor gene results in osteopetrosis, mononuclear phagocyte deficiency, increased primitive progenitor cell frequencies, and reproductive defects. Blood. 2002;99(1):111–120.
  • Cecchini MG, Dominguez MG, Mocci S, et al. Role of colony stimulating factor-1 in the establishment and regulation of tissue macrophages during postnatal development of the mouse. Development. 1994;120(6):1357–1372.
  • Hamilton JA, Achuthan A. Colony stimulating factors and myeloid cell biology in health and disease. Trends Immunol. 2013;34(2):81–89.
  • Stanley ER, Chitu V. CSF-1 receptor signaling in myeloid cells. Cold Spring Harbor Perspect Biol. 2014;6(6):a021857–a021857.
  • Conway JG, McDonald B, Parham J, et al. Inhibition of colony-stimulating-factor-1 signaling in vivo with the orally bioavailable cFMS kinase inhibitor GW2580. Proc Natl Acad Sci USA. 2005;102(44):16078–16083.
  • Conway JG, Pink H, Bergquist ML, et al. Effects of the cFMS kinase inhibitor 5-(3-methoxy-4-((4-methoxybenzyl)oxy)benzyl)pyrimidine-2,4-diamine (GW2580) in normal and arthritic rats. J Pharmacol Exp Ther. 2008;326(1):41–50.
  • Zhang X, Zhang S, Tang Q, et al. Goat sperm associated antigen 17 protein gene (SPAG17): small and large fragment genetic variation detection, association analysis, and mRNA expression in gonads. Genomics. 2020;112(6):5115–5121.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.