Siderophore Cephalosporin Cefiderocol Utilizes Ferric Iron Transporter Systems for Antibacterial Activity against Pseudomonas aeruginosa

被引:255
作者
Ito, Akinobu [1 ]
Nishikawa, Toru [1 ]
Matsumoto, Shuhei [1 ]
Yoshizawa, Hidenori [1 ]
Sato, Takafumi [1 ]
Nakamura, Rio [1 ]
Tsuji, Masakatsu [1 ]
Yamano, Yoshinori [1 ]
机构
[1] Shionogi & Co Ltd, Drug Discovery & Dis Res Lab, Osaka, Japan
关键词
VITRO ANTIMICROBIAL ACTIVITY; METALLO-BETA-LACTAMASES; CONJUGATED MONOCARBAM; RESISTANCE; S-649266; CARBAPENEMASES; MECHANISMS; EMERGENCE; PROTEINS; EFFICACY;
D O I
10.1128/AAC.01405-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Cefiderocol (S-649266) is a novel parenteral siderophore cephalosporin conjugated with a catechol moiety at the third-position side chain. The in vitro activity of cefiderocol against Pseudomonas aeruginosa was enhanced under iron-depleted conditions, whereas that of ceftazidime was not affected. The monitoring of [thiazole-C-14] cefiderocol revealed the increased intracellular accumulation of cefiderocol in P. aeruginosa cells incubated under iron-depleted conditions compared with those incubated under iron-sufficient conditions. Cefiderocol was shown to have potent chelating activity with ferric iron, and extracellular iron was efficiently transported into P. aeruginosa cells in the presence of cefiderocol as well as siderophores, while enhanced transport of extracellular ferric iron was not observed when one of the hydroxyl groups of the catechol moiety of cefiderocol was replaced with a methoxy group. We conclude that cefiderocol forms a chelating complex with iron, which is actively transported into P. aeruginosa cells via iron transporters, resulting in potent antibacterial activity of cefiderocol against P. aeruginosa.
引用
收藏
页码:7396 / 7401
页数:6
相关论文
共 36 条
[1]  
[Anonymous], 2015, CLSI DOCUMENT M07 A1
[2]  
[Anonymous], 2014, 54 INTERSCIENCE C AN
[3]   Mechanisms of multidrug resistance in Acinetobacter species and Pseudomonas aeruginosa [J].
Bonomo, Robert A. ;
Szabo, Dora .
CLINICAL INFECTIOUS DISEASES, 2006, 43 :S49-S56
[4]   Iron uptake regulation in Pseudomonas aeruginosa [J].
Cornelis, Pierre ;
Matthijs, Sandra ;
Van Oeffelen, Liesbeth .
BIOMETALS, 2009, 22 (01) :15-22
[5]   IRON-REGULATED OUTER-MEMBRANE PROTEINS OF ESCHERICHIA-COLI-K-12 AND MECHANISM OF ACTION OF CATECHOL-SUBSTITUTED CEPHALOSPORINS [J].
CURTIS, NAC ;
EISENSTADT, RL ;
EAST, SJ ;
CORNFORD, RJ ;
WALKER, LA ;
WHITE, AJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (12) :1879-1886
[6]   Antimicrobial susceptibility among Gram-positive and Gram-negative isolates collected in Europe between 2004 and 2010 [J].
Denis, Olivier ;
Nonhoff, Claire ;
Dowzicky, Michael J. .
JOURNAL OF GLOBAL ANTIMICROBIAL RESISTANCE, 2014, 2 (03) :155-161
[7]  
Drechsel H., 1997, TRANSITION METALS MI, V1, P1
[8]   Role of outer membrane protein OprD and penicillin-binding proteins in resistance of Pseudomonas aeruginosa to imipenem and meropenem [J].
Farra, Anna ;
Islam, Sohidul ;
Stralfors, Annelie ;
Sorberg, Mikael ;
Wretlind, Bengt .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2008, 31 (05) :427-433
[9]   Targeting iron assimilation to develop new antibacterials [J].
Foley, Timothy L. ;
Simeonov, Anton .
EXPERT OPINION ON DRUG DISCOVERY, 2012, 7 (09) :831-847
[10]   HIGHLY SENSITIVE, SIMPLE DETERMINATION OF SERUM IRON USING CHROMAZUROL-B [J].
GARCIC, A .
CLINICA CHIMICA ACTA, 1979, 94 (02) :115-119