Staphylococcus aureus biofilm as a target for single or repeated doses of oxacillin, vancomycin, linezolid and/or lysostaphin

被引:39
作者
Walencka, E.
Sadowska, B.
Rozalska, S.
Hryniewicz, W.
Rozalska, B. [1 ]
机构
[1] Univ Lodz, Inst Microbiol & Immunol, Dept Immunol & Infect Biol, PL-90131 Lodz, Poland
[2] Univ Lodz, Inst Microbiol & Immunol, Dept Ind Microbiol & Biotechnol, PL-90131 Lodz, Poland
[3] Natl Inst Publ Hlth, Warsaw, Poland
关键词
D O I
10.1007/BF02931580
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Due to high resistance, standard chemotherapy of biofilm-associated staphylococcal infections is ineffective and a number of alternative approaches to antimicrobial treatment have been proposed. Minimum inhibitory concentration (MIC) and biofilm inhibitory concentration (BIC) of oxacillin (Oxa), vancomycin (Van), linezolid (Lzd) and lysostaphin (Lss) as well as the possible synergistic effect of the antibiotics and lysostaphin were determined. The Lss susceptibility of Staphylococcus aureus planktonic and biofilm cultures varied and was strain-dependent. The synergistic effect of sub-BICLss+Oxa was observed for methicillin-sensitive S. aureus (M(s)Sa) and methicillin-resistant S. aureus (M(r)Sa), but not for heterogeneously vancomycin-resistant S. aureus (V(h)Sa) biofilm. Van with sub-BICLss was effective against MsSa and MrSa biofilm, when applied in three subsequent doses. Only sub-BICLss+Lzd combination, given as three cycles therapy, was effective in disruption of all 3 (M(s)Sa, M(r)Sa, V(h)Sa) biofilms.
引用
收藏
页码:381 / 386
页数:6
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