Efficacy of Calcium-EDTA as an Inhibitor for Metallo-β-Lactamase in a Mouse Model of Pseudomonas aeruginosa Pneumonia

被引:61
作者
Aoki, Nobumasa [2 ]
Ishii, Yoshikazu [1 ]
Tateda, Kazuhiro [1 ]
Saga, Tomoo
Kimura, Soichiro
Kikuchi, Yoshiaki
Kobayashi, Tetsuo [2 ]
Tanabe, Yoshinari [2 ]
Tsukada, Hiroki [2 ]
Gejyo, Fumitake [2 ]
Yamaguchi, Keizo
机构
[1] Toho Univ, Fac Med, Dept Microbiol & Infect Dis, Sch Med,Ota Ku, Tokyo 1438540, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Div Infect Control & Prevent, Niigata 9518510, Japan
关键词
VENTILATOR-ASSOCIATED PNEUMONIA; INTENSIVE-CARE UNITS; CHELATION-THERAPY; NOSOCOMIAL INFECTIONS; CLINICAL ISOLATE; COMBINATIONS; LEAD; CARBAPENEMASES; SURVEILLANCE; PERMEABILITY;
D O I
10.1128/AAC.00511-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study, we have evaluated the efficacy of calcium-EDTA (Ca-EDTA) as an inhibitor of bacterial metalloenzymes, such as metallo-beta-lactamase (MBL) and other proteases, in a mouse model of Pseudomonas aeruginosa pneumonia. The simultaneous presence of Ca-EDTA (32 mu g/ml) reduced the MICs of imipenem (IPM) in all MBL-producing P. aeruginosa isolates (IMP-1, -2, -7, and -10 and VIM-2) but not non-MBL-producing strains. In the pneumonia model, mice were intranasally infected with MBL-producing P. aeruginosa and then kept under conditions of hyperoxia to mimic ventilator-associated pneumonia. With both intranasal and subcutaneous administrations, Ca-EDTA significantly potentiated survival benefits of IPM compared to those of IPM alone. Ca-EDTA combination therapy induced a significant reduction of the bacterial burden in the lungs (P < 0.05). Furthermore, the inhibition activity of Ca-EDTA against MBL activity was confirmed by using the purified IMP-1 enzyme, which was characterized by a 50% inhibitory concentration (IC50) of 55 +/- 8.2 mu M. Finally, the protective effects of Ca-EDTA were demonstrated by culture supernatant-induced epithelial cell damage and acute lung injury in mice. These data suggest the therapeutic potential of Ca-EDTA not only by the blocking of MBLs but also by neutralizing tissue-damaging metalloproteases in P. aeruginosa infections.
引用
收藏
页码:4582 / 4588
页数:7
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