Immunopathological Responses to the Bovine Mastitis Associated with Staphylococcus Species Infection

Main Article Content

Agharid A Al-Rasheed
Sana’a S Ahmed
Karim A Al-Jashamy
Bashiru Garba

Abstract

Bovine mastitis is a disease that concerns animals' welfare and increases the economic production losses. Bacterial agents such as Staphylococcus species are the main causative agent of bovine mastitis. This bacterial agent expresses some inflammatory cytokines that might enhance the cell-mediated, which may promote the pathogenesis of mastitis. The objective of the current study was to investigate the bovine innate immune response circulating levels of pro-inflammatory and anti-inflammatory cytokines. A total of 10 mL of milk specimens were collected randomly from 100 clinically mastitic cows, and another 20 clinically healthy cows were considered as a control group for the California Mastitis test. The microbiological cultures of milk specimens were performed. The interleukins (ILs)that involved IL-4, IL-6, and IL-10 were detected using the ELISA test for the evaluation of the
pro-inflammatory bovine mastitis pathophysiology. The results of this study showed that Staphylococcus aureus detection was in 31.2% of mastitic milk and 8.7% of non-mastitic milk specimens; and the coagulase-negative Staphylococcus was detected in 14.8% and 18.7% in the mastitic and non-mastitic milk specimens, respectively. The IL-6 level was shown significantly higher (P<0.05)in the specimens of mastitic milk (194±12.8 pg/mL) compared to the non-mastitic milk (31±2.9 pg/mL). In conclusion, the elevated level of expression of IL-6 cytokine in the milk of cows with mastitis suggested that IL-6 might be used as a potentially suitable biomarker for early bovine mastitis diagnosis

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Immunopathological Responses to the Bovine Mastitis Associated with Staphylococcus Species Infection. (2022). The Iraqi Journal of Veterinary Medicine, 46(2), 7-11. https://doi.org/10.30539/ijvm.v46i2.1398
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How to Cite

Immunopathological Responses to the Bovine Mastitis Associated with Staphylococcus Species Infection. (2022). The Iraqi Journal of Veterinary Medicine, 46(2), 7-11. https://doi.org/10.30539/ijvm.v46i2.1398

References

Murphy MP, Niedziela DA, Leonard FC, Keane OM. The in vitro host cell immune response to bovine-adapted Staphylococcus aureus

varies according to bacterial lineage. Scientific Reports, 2019; 9(1): 6134.

Garba B, Habibullah SA, Saidu B, Suleiman N. Effect of mastitis on some hematological and biochemical parameters of Red Sokoto goats. https://doi.org/10.14202/vetworld.2019.572-577

Veterinary World, 2019; 12(4): 572-577.

Zbinden C, Stephan R, Johler S, Borel N, Bünter J, Bruckmaier RM, Wellnitz O. The inflammatory response of primary bovine mammary

epithelial cells to Staphylococcus aureus strains is linked to the bacterial phenotype. PLoS ONE, 2014; 9(1): e87374. https://doi.org/10.1371/journal.pone.0087374

De Vliegher S, Fox LK, Piepers S, McDougall S, Barkema HW. Invited review: Mastitis in dairy heifers: Nature of the disease, potential

impact, prevention, and control. J Dairy Sci. 2012; 95(3): 1025–1040. https://doi.org/10.3168/jds.2010-4074

Simojoki H, Salomäki T, Taponen S, Iivanainen A, Pyörälä S. Innate immune response in experimentally induced bovine intramammary . https://doi.org/10.1186/1297-9716-42-49

infection with Staphylococcus simulans and S. epidermidis. Vet Res. 2011; 42(1): 49.

França A, Gaio V, Lopes N, Melo LDR. Virulence factors in coagulasenegative Staphylococci. Pathogens, 2021; 10(2): 170. https://doi.org/10.3390/pathogens10020170

Heilmann C, Ziebuhr W, Becker K. Are coagulase-negative Staphylococci virulent? Clin Microbiol Infec. 2019; 25(9): 1071–1080. https://doi.org/10.1016/j.cmi.2018.11.012

Aqib AI, Nighat S, Kulyar FE, Sana S. Drug susceptibility profile of Staphylococcus aureus isolated from mastitic milk of goats and risk

factors associated with goat mastitis in Pakistan. Pakistan J Zoolog.2019; 51(1): 307–315.

Cheung GY, Bae JS, Otto M. Pathogenicity and virulence of Staphylococcus aureus. Virulence. 2021; 12(1): 547–569. https://doi.org/10.1080/21505594.2021.1878688

Gaddafi MS, Yakubu Y, Junaidu AU, Bello MB, Garba B, Bitrus AA, et al. Nasal colonization of pigs and farm attendants by Staphylococcus aureus and methicillin-resistant Staphylococcus aureus (MRSA) in Kebbi, Northwestern Nigeria. Thai J Vet. Med. 2021; 51(1): 119-124. https://doi.org/10.56808/2985-1130.3100

Moussa AA, Abdulahi Abdi A, Awale MA, Garba B. Occurrence and phenotypic characterization of multidrug-resistant bacterial

pathogens isolated from patients in a public hospital in Mogadishu, Somalia. Infec Drug Res. 2021; (14): 825–832. https://doi.org/10.2147/IDR.S275090

Vasileiou NG, Chatzopoulos DC, Gougoulis DA, Sarrou S, Katsafadou AI, Spyrou V, et al. Slime-producing Staphylococci as causal agents of subclinical mastitis in sheep. Vet. Micro. 2018; 224: 93–99. https://doi.org/10.1016/j.vetmic.2018.08.022

Vasileiou NG, Chatzopoulos DC, Sarrou S, Fragkou IA, Katsafadou AI, Mavrogianni VS, Petinaki E, Fthenakis GC. Role of Staphylococci in mastitis in sheep. J Dairy Res. 2019; 86(3): 254–266. https://doi.org/10.1017/S0022029919000591

Tomazi T, Gonçalves JL, Barreiro JR, Arcari MA, dos Santos MV. Bovine subclinical intramammary infection caused by coagulase-negative staphylococci increases somatic cell count but has no effect on milk yield or composition. J Dairy Sci. 2015; 98(5): 3071–3078. https://doi.org/10.3168/jds.2014-8466

Simojoki H, Orro T, Taponen S, Pyorala S. Host response in bovine mastitis experimentally induced with Staphylococcus chromogenes. Vet Micro. 2009; 134(1–2): 95–99. https://doi.org/10.1016/j.vetmic.2008.09.003

Winter P, Colditz I. Immunological responses of the lactating ovine udder following experimental challenge with Staphylococcus

epidermidis. Vet Immunol Immunopathol. 2002; 89(1–2): 57–65. https://doi.org/10.1016/S0165-2427(02)00184-8

Dingwell RT, Leslie KE, Schukken YH, Sargeant JM, Timms LL. Evaluation of the California mastitis test to detect an intramammary

infection with a major pathogen in early lactation dairy cows. Can Vet J. 2003; 44(5): 413.

Hogan JS, Gonzalez RN, Harmon RJ, Nickerson SC, Oliver SP, Pankey JW, et al. Laboratory handbook on bovine mastitis. National Mastitis Council, Madison, WI, 1999; 78(7): 485-488.

Piccart K, Verbeke J, De Visscher A, Piepers S, Haesebrouck F, De Vliegher S. Local host response following an intramammary challenge with Staphylococcus fleurettii and different strains of Staphylococcuschromogenes in dairy heifers. Vet Res. 2016: 47(1): 1–11. https://doi.org/10.1186/s13567-016-0338-9

Alhussien MN, Dang AK. Milk somatic cells, factors influencing their release, future prospects, and practical utility in dairy animals: An overview. Vet World. 2018; 11(5): 562. https://doi.org/10.14202/vetworld.2018.562-577

Mohammed SG, ALMobarak. In vitro efficacy of Tylosin and Enrofloxacin in treatment of bovine mastitis causing bacteria in

Omdurman locality. J World’s Poult Res. 2020; 10(2): 53–58. https://doi.org/10.36380/scil.2020.ojafr7

Ezzat AM, Quintela-Baluja M, BK, Fernández-No I, Caamaño-Antelo S, Calo-Mata P, Barros-Velázquez J. The Immunology of mammary gland of dairy ruminants between healthy and inflammatory conditions. J Vet Med. 2014; 2014: 659801. https://doi.org/10.1155/2014/659801

Ericsson UH, Lindberg A, Persson WK, Ekman T, Artursson K, NilssonÖst M, Bengtsson B. Microbial aetiology of acute clinical mastitis and agent-specific risk factors. Vet Microbiol. 2009; 137(1–2):90–97. https://doi.org/10.1016/j.vetmic.2008.12.005

Andreotti CS, Baravalle C, Sacco SC, Lovato M, Pereyra EAL, Renna MS, et al. Characterization of immune response in Staphylococcus aureus chronically infected bovine mammary glands during active involution. Comp Immunol, Microbiol Inf Dis. 2017; (54): 51–60. https://doi.org/10.1016/j.cimid.2017.08.005

Sakemi Y, Tamura Y, Hagiwara K. Interleukin-6 in quarter milk as a further prediction marker for bovine subclinical mastitis. J Dairy Res.2011; 78(1): 118–121.

Oviedo-Boyso J, Valdez-Alarcón JJ, Cajero-Juárez M, Ochoa-Zarzosa A, López-Meza JE, Bravo-Patiño A, et al. Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis. J Inf. 2007; 54(4): 399–409. https://doi.org/10.1016/j.jinf.2006.06.010

Bannerman DD. Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary

infection of dairy cows. J Anim Sci. 2009; 87(13): 10-25. https://doi.org/10.2527/jas.2008-1187

Bochniarz M, Zdzisińska B, Wawron W, Szczubiał M, Dąbrowski R. Milk and serum IL-4, IL-6, IL-10, and amyloid A concentrations in

cows with subclinical mastitis caused by coagulase-negative Staphylococci. J Dairy Sci. 2017;100(12):9674–9680. https://doi.org/10.3168/jds.2017-13552

Hurdayal R, Brombacher F. Interleukin-4 receptor alpha: From innate to adaptive immunity in murine models of cutaneous

leishmaniasis. Frontiers in Immunology, 2017; (8): 1354.

Abd AH. Immunological response of bovine mammary cell lines in mastitis and milk hygiene. Iraqi J. Vet. Med. 2012; 36(1): 1–13. https://doi.org/10.30539/iraqijvm.v36i1.515

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