Anti-staphylococcal activity and cytocompatibility of lysostaphin

E. M. Gordina, S. Bozhkova, D. Labutin, D. Goncharuk, E. N. Tkach
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Abstract

Objective. To study the antibacterial activity of lysostaphin against staphylococci various species, as well as its effect on the viability of Vero cells. Materials and Methods. Lysostaphin was obtained by genetic engineering. Purification of the protein was carried out on SP-sepharose, the purity was determined by electrophoresis in PAGE by Lamley. The susceptibility to lysostaphin of 9 species 175 strains of staphylococci was studied. Identification was performed by MALDI-TOF MS, antibiotic susceptibility by EUCAST (v. 11.0). The MIC of lysostaphin was studied by the method of serial dilutions with concentrations between 0.015 and 512 mg/l. For 72 hours, the viability of Vero cells with lysostaphin at concentrations of 0.5-32.0 mg/l was determined by the MTT method with counting of living cells according to their growth curve. The results were analyzed by ANOVA followed by Dunnett’s test. Results. A kinetic study of S. aureus growth in the presence of revealed an inhibitory effect of endopeptidase (MIC 0.06 mg/l). Lysostaphin was characterized by pronounced activity against clinical methicillinsensitive S. aureus. The MIC ranged between 0.03 and 0.5 mg/l and the MIC50/90 was 0.125⁄0.5 mg/l. For methicillin-resistant S. aureus MIC50/90 0.25⁄0.5 mg/l. The MIC50 for MRSE was 2 times higher than for MSSE – 1 mg/l. The maximum MIC value was determined against isolates of S. warneri and S. hominis – 64 mg/l, the lowest for S. saprophyticus – 0.5 mg/l. MIC50 of lysostaphin against MRSA was 4 times lower than that of vancomycin, MIC90 was 3 times lower. Differences in viable cells depending on the concentration of lysostaphin were not found. Conclusions. Significant activity of lysostaphin against staphylococci was revealed, which is several times higher than vancomycin against MRSA. Lysostaphin was also effective against methicillin-resistant S. aureus. The high anti-staphylococcal activity and cytocompatibility of lysostaphin are promising for its further study in the prevention and treatment of staphylococcal orthopedic infections.
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溶葡萄球菌蛋白的抗葡萄球菌活性和细胞相容性
目标。研究溶葡萄球菌素对不同葡萄球菌的抑菌活性及其对Vero细胞活力的影响。材料与方法。通过基因工程获得溶葡萄球菌素。用SP-sepharose对蛋白进行纯化,用Lamley在PAGE电泳检测纯度。研究了9种葡萄球菌175株对溶葡萄球菌素的敏感性。鉴定采用MALDI-TOF质谱,药敏采用EUCAST (v. 11.0)。采用浓度为0.015 ~ 512 mg/l的连续稀释法研究溶葡萄球菌素的MIC。采用MTT法测定溶葡萄球菌素浓度为0.5 ~ 32.0 mg/l的Vero细胞72h后的活力,根据细胞生长曲线计数活细胞。结果:对金黄色葡萄球菌生长的动力学研究表明,内肽酶(MIC为0.06 mg/l)对金黄色葡萄球菌的生长有抑制作用。溶葡萄球菌蛋白具有明显的抗甲氧西林不敏感金黄色葡萄球菌活性。MIC为0.03 ~ 0.5 mg/l, MIC50/90为0.125 / 0.5 mg/l。耐甲氧西林金黄色葡萄球菌MIC50/90 0.25 / 0.5 mg/l。MRSE的MIC50是MSSE - 1 mg/l的2倍。对沃纳氏链球菌和人型链球菌的MIC值最高为64 mg/l,对腐生链球菌的MIC值最低为0.5 mg/l。溶葡萄球菌素对MRSA的MIC50比万古霉素低4倍,MIC90比万古霉素低3倍。结论:溶葡萄球菌素对葡萄球菌的抑菌活性明显高于万古霉素对MRSA的抑菌活性数倍。溶葡萄球菌素对耐甲氧西林金黄色葡萄球菌也有效。溶葡萄球菌蛋白具有较高的抗葡萄球菌活性和细胞相容性,在预防和治疗骨科葡萄球菌感染方面具有广阔的应用前景。
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