Leitner G, Krifucks O, Glickman A, Younis A, Saran A
National Mastitis Reference Center, Kimron Veterinary Institute, Ministry of Agriculture and Rural Development, P.O. Box 12, Bet Dagan 50250, Israel.
FEMS Immunol Med Microbiol. 2003 Mar 20;35(2):99-106. doi: 10.1016/S0928-8244(02)00458-3.
Septic arthritis in mice was used as a model to evaluate the virulence of Staphylococcus aureus and coagulase-negative staphylococci (CNS) isolated from cases of bovine mastitis. In addition, the model was used to evaluate the cross protection elicited by heterologous antibodies. Mice were intramuscularly inoculated with serial bacterial doses of different strains of S. aureus or CNS, for virulence determination; they were monitored for arthritis, gangrene or death up to 20 days. Antibody response, cross reactivity and resistance to challenge were tested by subcutaneous inoculation with a low dose of one of the S. aureus or CNS strains followed by challenge with two S. aureus strains. S. aureus alpha-hemolysin isolate was the most virulent, followed by alpha+beta-hemolysin and beta-hemolysin isolates. The least virulent isolates were the non-hemolytic S. aureus strains but even they were more virulent than the CNS strains tested. Antibodies against three different S. aureus antigens were detected by the ELISA in all mice that were inoculated with the S. aureus strains but not in any of those with the CNS strains. Immunoblot test against various S. aureus strains as antigens showed high cross-reactivity among the S. aureus strains but only a slight similarity, restricted to the bands above 36 kDa, with the CNS sera. Low-dose inoculation of alpha or alpha+beta strains before challenge with homologous and heterologous strains protected the mice, whereas the two beta strains provided only partial protection. The inoculations of non-hemolytic S. aureus or the CNS strains did not elicit any protection. Our findings demonstrate that pre-exposure of mice to a low dose of certain S. aureus strains could provide protection and that the antibodies produced could have an important protective role.
小鼠败血症性关节炎被用作模型,以评估从牛乳腺炎病例中分离出的金黄色葡萄球菌和凝固酶阴性葡萄球菌(CNS)的毒力。此外,该模型还用于评估异源抗体引发的交叉保护作用。为了确定毒力,给小鼠肌肉注射不同菌株的金黄色葡萄球菌或CNS的系列细菌剂量;对它们进行长达20天的关节炎、坏疽或死亡监测。通过皮下接种低剂量的一种金黄色葡萄球菌或CNS菌株,随后用两种金黄色葡萄球菌菌株进行攻击,来测试抗体反应、交叉反应性和对攻击的抵抗力。金黄色葡萄球菌α-溶血素分离株的毒力最强,其次是α+β-溶血素和β-溶血素分离株。毒力最弱的分离株是非溶血金黄色葡萄球菌菌株,但即使它们也比所测试的CNS菌株毒力更强。在所有接种金黄色葡萄球菌菌株的小鼠中,通过ELISA检测到针对三种不同金黄色葡萄球菌抗原的抗体,但在接种CNS菌株的小鼠中均未检测到。以各种金黄色葡萄球菌菌株为抗原的免疫印迹试验表明,金黄色葡萄球菌菌株之间具有高交叉反应性,但与CNS血清仅在36 kDa以上的条带存在轻微相似性。在用同源和异源菌株攻击之前,低剂量接种α或α+β菌株可保护小鼠,而两种β菌株仅提供部分保护。接种非溶血金黄色葡萄球菌或CNS菌株未引发任何保护作用。我们的研究结果表明,小鼠预先暴露于低剂量的某些金黄色葡萄球菌菌株可提供保护,并且产生的抗体可能具有重要的保护作用。