Title In vitro activity of minocycline combined with fosfomycin against clinical isolates of methicillin-resistant Staphylococcus aureus
Authors Sun, Chunguang
Falagas, Matthew E.
Wang, Rui
Karageorgopoulos, Drosos E.
Yu, Xuhong
Liu, Youning
Cai, Yun
Liang, Beibei
Song, Xiujie
Liu, Zheyuan
Affiliation Chinese Peoples Liberat Army Gen Hosp, Dept Clin Pharmacol, Beijing 100853, Peoples R China.
Peking Univ, Dept Pharm Adm & Clin Pharm, Sch Pharmaceut Sci, Hlth Sci Ctr, Beijing 100871, Peoples R China.
Alfa Inst Biomed Sci, Athens, Greece.
Henry Dunant Hosp, Dept Med, Athens, Greece.
Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA.
Chinese Peoples Liberat Army Gen Hosp, Dept Pulm Dis, Beijing 100853, Peoples R China.
Chinese Peoples Liberat Army Gen Hosp, Dept Clin Pharmacol, 28 Fuxing Rd, Beijing 100853, Peoples R China.
Keywords FICI
fosfomycin
minocycline
MRSA
synergism
HOSPITALIZED-PATIENTS
UNITED-STATES
SUSCEPTIBILITY
TIGECYCLINE
INFECTIONS
EPIDEMIOLOGY
VANCOMYCIN
PROGRAM
SENTRY
MRSA
Issue Date 2011
Publisher journal of antibiotics
Citation JOURNAL OF ANTIBIOTICS.2011,64,(8),559-562.
Abstract This study aimed to evaluate the in vitro activity of minocycline combined with fosfomycin against isolates of methicillin-resistant Staphylococcus aureus (MRSA). A total of 87 clinical isolates of MRSA collected from three Chinese hospitals were included in the study. The checkerboard method with determination of the fractional IC index (FICI) was used to determine whether antibiotic combinations act synergistically against these isolates. The susceptibility results for minocycline and fosfomycin were interpreted according to the most relevant criteria. The results demonstrated the following interactions: 76 isolates (87.4%) showed synergistic interactions (FICI <= 0.5) and 11 isolates (12.6%) showed indifferent interactions (0.5<FICI<4). No antagonistic interactions (FICI >= 4) were observed. The combination of minocycline and fosfomycin can be synergistic against MRSA. Further studies are required to determine the potential clinical role of this combination regimen as a therapeutic alternative for certain types of MRSA infections. The Journal of Antibiotics (2011) 64, 559-562; doi:10.1038/ja.2011.52; published online 20 July 2011
URI http://hdl.handle.net/20.500.11897/323248
ISSN 0021-8820
DOI 10.1038/ja.2011.52
Indexed SCI(E)
Appears in Collections: 药学院

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