Younis Ahmed, Krifucks Oleg, Fleminger Gideon, Heller Elimelech D, Gollop Natan, Saran Arthur, Leitner Gabriel
National Mastitis Reference Center, Kimron Veterinary Institute, PO Box 12, Bet-Dagan 50250, Israel.
J Dairy Res. 2005 May;72(2):188-94. doi: 10.1017/s002202990500083x.
The involvement of Staphylococcus aureus exosecretions in bovine udder infection (Younis et al. 2003) suggests that four different monomer protein bands appearing between 36 and 31 kDa, are associated with the severity of the cow's infection response. Three out of these four bands have been identified by means of protein sequencing. Band B, with a MW of 35 kDa was identified as Panton-Valentaine leucocidin LukF'-PV chain- Staph. aureus; band C, with a MW of 32 kDa was identified as leucocidin chain LukM precursor- Staph. aureus; and band D was found to be similar, but not identical, to phosphatidylinositol-specific phospholipase-C-X. Bands B and C were purified by gel filtration using FPLC. The ability of these proteins to induce udder inflammation in vivo, and proliferation response in vitro and cytokine secretion were tested for both the crude exosecretions and purified bands. Three cows were inoculated intracisternally, with three quarters receiving either 0.007-0.008 mg (as total proteins) of Staph. aureus FR2449/1 bacterial exosecretion, pooled fraction 39-41 (bands B and C), or culture broth medium. The fourth quarter was left free as a control. Quarters that received fraction 39-41 of Staph. aureus FR2449/1, exhibited induced inflammation, which was indicated by increased somatic cell count and enhanced NAGase activity that was significantly higher than that of the original Staph. aureus FR2449/1 bacterial exosecretion. Proliferation tests of bovine blood lymphocytes in vitro showed that the pooled fraction 39-41 stimulated bovine proliferation of mononuclear cells much more than the original Staph. aureus FR2449/1 bacterial exosecretion. Secretion of TNF-alpha, IL-1beta, IL-6 and IL-8 was in accordance with the contents of LukF'-PV and LukM precursor in the exosecretions. The results suggest that LukM/ LukF' induce inflammation into the udder by a mechanism similar to that of LPS or by a unique mechanism(s) which requires further investigation.
金黄色葡萄球菌外分泌物与牛乳房感染的关系(尤尼斯等人,2003年)表明,在36至31 kDa之间出现的四条不同的单体蛋白带与奶牛感染反应的严重程度相关。这四条带中的三条已通过蛋白质测序鉴定。分子量为35 kDa的B带被鉴定为杀白细胞素Panton-Valentaine LukF'-PV链 - 金黄色葡萄球菌;分子量为32 kDa的C带被鉴定为杀白细胞素链LukM前体 - 金黄色葡萄球菌;D带被发现与磷脂酰肌醇特异性磷脂酶C-X相似,但不完全相同。B带和C带通过使用FPLC的凝胶过滤进行纯化。对粗外分泌物和纯化带测试了这些蛋白质在体内诱导乳房炎症、体外增殖反应和细胞因子分泌的能力。给三头奶牛进行乳池内接种,四分之三的乳房分别接受0.007 - 0.008 mg(作为总蛋白)的金黄色葡萄球菌FR2449/1细菌外分泌物、合并的39 - 41组分(B带和C带)或培养基肉汤。第四季度作为对照不接种。接受金黄色葡萄球菌FR2449/1的39 - 41组分的乳房表现出诱导的炎症,这通过体细胞计数增加和NAGase活性增强来表明,该活性显著高于原始的金黄色葡萄球菌FR2449/1细菌外分泌物。体外牛血淋巴细胞增殖试验表明,合并的39 - 41组分比原始金黄色葡萄球菌FR2449/1细菌外分泌物更能刺激牛单核细胞的增殖。TNF-α、IL-1β、IL-6和IL-8的分泌与外分泌物中LukF'-PV和LukM前体的含量一致。结果表明,LukM/LukF'通过与LPS类似的机制或需要进一步研究的独特机制诱导乳房炎症。