[Baes C., Brand B., Mayer M., Kühn Ch., Liu Z., Reinhardt F., Reinsch N. (2009). Refined positioning of a quantitative trait locus affecting somatic cell score on chromosome 18 in the German Holstein using linkage disequilibrium. J. Dairy Sci., 92: 4046–4054.]Search in Google Scholar
[Bennewitz J., Reinsch N., Grohs C., Leveziel H., Malafosse A., Thomsen H., Xu N., Looft C. (2003). Combined analysis of data from two granddaughter designs: A simple strategy for QTL confirmation and increasing experimental power in dairy cattle. Genet. Sel. Evol., 35: 319–338.]Search in Google Scholar
[Brand B., Baes C., Mayer M., Reinsch N., Kühn C. (2009). Identification of a two-marker-haplotype on Bos taurus autosome 18 associated with somatic cell score in German Holstein cattle. BMC Genet., 10: 1–13.]Search in Google Scholar
[Clancey E., Kiser J.N., Moraes J.G.N., Dalton J., Spencer T.E., Neibergs H.L. (2019) Genome-wide association analysis and gene set enrichment analysis-SNP identify genes associated with 305-day milk yield in Holstein dairy cows. Anim. Genet., 50: 254–258.10.1111/age.1279230994194]Search in Google Scholar
[Cole J.B., Wiggans G.R., Ma L., Sonstegard T.S., Lawlor T.J. Jr., Crooker B.A., Van Tassell C.P., Yang J., Wang S., Matukumalli L.K., Da Y. (2011). Genome-wide association analysis of thirty one production, health, reproduction and body conformation traits in contemporary U.S. Holstein cows. BMC Genomics, 12: 408.]Search in Google Scholar
[Detilleux J., Kastelic J.P., Barkema H.W. (2015). Mediation analysis to estimate direct and indirect milk losses due to clinical mastitis in dairy cattle. Prev. Vet. Med., 118: 449–456.]Search in Google Scholar
[Dziarski R. (2004). Peptidoglycan recognition proteins (PGRPs). Mol. Immunol., 40: 877–886.]Search in Google Scholar
[Dziarski R., Gupta D. (2006). The peptidoglycan recognition proteins (PGRPs). Genome Biol., 7: 232.]Search in Google Scholar
[Gao J., Yu F.Q,. Luo L.P., He J.Z., Hou R.G., Zhang H.Q., Li S.M., Su J.L., Han B. (2012). Antibiotic resistance of Streptococcus agalactiae from cows with mastitis. Vet. J., 194: 423–424.]Search in Google Scholar
[Guterbock W.M., Van Eenennaam A.L., Anderson R.J., Gardner I.A., Cullor J.S., Holmberg C.A. (1993). Efficacy of intramammary antibiotic therapy for treatment of clinical mastitis caused by environmental pathogens. J. Dairy Sci., 76: 3437–3444.]Search in Google Scholar
[Ibeagha-Awemu E.M., Peters S.O., Akwanji K.A., Imumorin I.G., Zhao X. (2016). High density genome wide genotyping-by-sequencing and association identifies common and low frequency SNPs, and novel candidate genes influencing cow milk traits. Sci. Rep., 6: 31109.]Search in Google Scholar
[Kang D., Liu G., Lundstrom A., Gelius E., Steiner H. (1998). Isolation, characterization, and antimicrobial properties of bovine oligosaccharide-binding. P. Natl. Acad. Sci. USA, 95: 10078–10082.]Search in Google Scholar
[Kossaibati M.A., Esslemont R.J. (1997). The costs of production diseases in dairy herds in England. Vet. J., 154: 41–51.]Search in Google Scholar
[Koressaar T., Lepamets M., Kaplinski L., Raime K., Andreson R., Remm M. (2018). Primer3_masker: integrating masking of template sequence with primer design software. Bioinformatics, 34: 1937–1938.]Search in Google Scholar
[Kühn C., Bennewitz J., Reinsch N., Xu N., Thomsen H., Looft C., Brockmann G.A., Schwerin M., Weimann C., Hiendleder S., Erhardt G., Medjugorac I., Förster M., Brenig B., Reinhardt F., Reents R., Russ I., Averdunk G., Blümel J., Kalm E. (2003). Quantitative trait loci mapping of functional traits in the German Holstein cattle population. J. Dairy Sci., 86: 360–368.]Search in Google Scholar
[Kurz J.P., Yang Z., Weiss R.B., Wilson D.J., Rood K.A., Liu G.E., Wang Z. (2019). A genome-wide association study for mastitis resistance in phenotypically well-characterized Holstein dairy cattle using a selective genotyping approach. Immunogenetics, 71: 35–47.]Search in Google Scholar
[Litwińczuk Z., Król J., Brodziak A. (2015). Factors determining the susceptibility of cows to mastitis and losses incurred by producers due to the disease – a review. Ann. Anim. Sci., 15: 819–831.]Search in Google Scholar
[Liu C., Gelius E., Liu G., Steiner H., Dziarski R. (2000). Mammalian peptidoglycan recognition protein binds peptidoglycan with high affinity, is expressed in neutrophils, and inhibits bacterial growth. J. Biol. Chem., 275: 24490–24499.]Search in Google Scholar
[Marete A., Sahana G., Fritz S., Lefebvre R., Barbat A., Lund M.S., Guldbrandtsen B., Boichard D. (2018). Genome-wide association study for milking speed in French Holstein cows. J. Dairy Sci., 101: 6205–6219.]Search in Google Scholar
[Martin P., Szymanowska M., Zwierzchowski L., Leroux C. (2002). The impact of genetic polymorphisms on the protein composition of ruminant milks. Reprod. Nutr. Dev., 425: 433–459.]Search in Google Scholar
[McConnel C.S., Crisp S.A., Biggs T.D., Ficklin S.P., Parrish L.M., Trombetta S.C., Sischo W.M., Adams-Progar A. (2020). A fixed cohort field study of gene expression in circulating leukocytes from dairy cows with and without mastitis. Front. Vet. Sci., 7: 559279.]Search in Google Scholar
[Meredith B.K., Kearney F.J., Finlay E.K., Bradley D.G., Fahey A.G., Berry D.P., Lynn D.J. (2012). Genome-wide associations for milk production and somatic cell score in Holstein-Friesian cattle in Ireland. BMC Genet., 13: 21.]Search in Google Scholar
[Moore S.G., Pryce J.E., Hayes B.J., Chamberlain A.J., Kemper K.E., Berry D.P., McCabe M., Cormican P., Lonergan P., Fair T., Butler S.T. (2016). Differentially expressed genes in endometrium and corpus luteum of Holstein cows selected for high and low fertility are enriched for sequence variants associated with fertility. Biol. Reprod., 94: 1–11.]Search in Google Scholar
[Pant S.D., Verschoor C.P., Schenkel F.S., You Q., Kelton D.F., Karrow N.A. (2011). Bovine PGLYRP1 polymorphisms and their association with resistance to Mycobacterium avium ssp. paratuberculosis. Anim. Genet., 42: 354–360.]Search in Google Scholar
[Puckowska P., Borowska A., Szwaczkowski T., Oleński K., Kamiński S. (2019). Effects of a novel missense polymorphism within the SIGLEC5 gene on fertility traits in Holstein-Friesian cattle. Reprod. Domest. Anim., 54: 1163–1168.]Search in Google Scholar
[Raina V.S., Kour A., Chakravarty A.K., Vohra V. (2020) Marker-assisted selection vis-à-vis bull fertility: coming full circle-a review. Mol. Biol. Rep., 47: 9123–9133.]Search in Google Scholar
[Ruegg P.L. (2017). A 100-year review: Mastitis detection, management, and prevention. J. Dairy Sci., 100: 10381–10397.]Search in Google Scholar
[Seabury C.M., Womack J.E. (2008). Analysis of sequence variability and protein domain architectures for bovine peptidoglycan recognition protein 1 and Toll-like receptors 2 and 6. Genomics, 92: 235–245.]Search in Google Scholar
[Seabury C.M., Seabury P.M., Decker J.E., Schnabel R.D., Taylor J.F., Womack J.E. (2010). Diversity and evolution of 11 innate immune genes in Bos taurus taurus and Bos taurus indicus cattle. P. Natl. Acad. Sci. USA, 107: 151–156.]Search in Google Scholar
[Seegers H., Fourichon C., Beaudeau F. (2003). Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet. Res., 34: 475–491.]Search in Google Scholar
[Sender G., Korwin-Kossakowska A., Pawlik A., Galal Abdel Hameed K., Oprządek J. (2013). Genetic basis of mastitis resistance in dairy cattle – a review. Ann. Anim. Sci., 13: 663–673.]Search in Google Scholar
[Siatka K., Sawa A., Krężel-Czopek S. (2018). Effect of postpartum endocrine function, metabolism, and mastitis on fertility in high-yielding cows – a review. Ann. Anim. Sci., 18: 351–359.]Search in Google Scholar
[Trevisi E., Zecconi A., Cogrossi S., Razzuoli E., Grossi P., Amadori M. (2014). Strategies for reduced antibiotic usage in dairy cattle farms. Res. Vet. Sci., 96: 229–233.]Search in Google Scholar
[Tydell C.C., Yount N., Tran D., Yuan J., Selsted M.E. (2002). Isolation, characterization, and antimicrobial properties of bovine oligosaccharide-binding protein. A microbicidal granule protein of eosinophils and neutrophils. J. Biol. Chem., 277: 19658–19664.]Search in Google Scholar
[Tydell C.C., Yuan J., Tran P., Selsted M.E. (2006). Bovine peptidoglycan recognition protein-S: antimicrobial activity, localization, secretion, and binding properties. J. Immunol., 176: 1154–1162.]Search in Google Scholar
[Venselaar H., Te Beek T.A., Kuipers R.K., Hekkelman M.L., Vriend G. (2010). Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces. BMC Bioinf., 11: 548.]Search in Google Scholar
[Walawski K. (1999). Genetic aspects of mastitis resistance in cattle. J. Appl. Genet., 40: 117–128.]Search in Google Scholar
[Wang H.L., Li Z.X., Wang L.J., He H., Yang J., Chen L., Niu F.B., Liu Y., Guo J.Z., Liu X.L. (2013). Polymorphism in PGLYRP-1 gene by PCR-RFLP and its association with somatic cell score in Chinese Holstein. Res. Vet. Sci., 95: 508–514.]Search in Google Scholar
[Wellnitz O., Bruckmaier R.M. (2012). The innate immune response of the bovine mammary gland to bacterial infection. Vet. J., 192: 148–152.]Search in Google Scholar
[Zabolewicz T., Barcewicz M., Brym P., Puckowska P., Kamiński S. (2014). Association of polymorphism within LTF gene promoter with lactoferrin concentration in milk of Holstein cows. Pol. J. Vet. Sci., 17: 633–641.]Search in Google Scholar