Transferable mechanisms of quinolone resistance

被引:84
作者
Ruiz, Joaquim [1 ]
Pons, Maria J. [1 ]
Gomes, Claudia [1 ]
机构
[1] Univ Barcelona, Ctr Recerca Salut Int Barcelona CRESIB, Hosp Clin, Barcelona 08036, Spain
关键词
Quinolone resistance; Qnr; Qep; OqxAB; AAC(6 ')-Ib-cr; Natural transformation; 16S RIBOSOMAL-RNA; PENTAPEPTIDE REPEAT PROTEINS; MULTIDRUG EFFLUX PUMP; PLASMID-MEDIATED RESISTANCE; NALIDIXIC-ACID-RESISTANT; ESCHERICHIA-COLI; FLUOROQUINOLONE RESISTANCE; STENOTROPHOMONAS-MALTOPHILIA; ANTIMICROBIAL RESISTANCE; HYDROPHILIC FLUOROQUINOLONES;
D O I
10.1016/j.ijantimicag.2012.02.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Quinolones were introduced into clinical practice in the late 1960s. Although quinolone resistance was described early, no transferable mechanism of quinolone resistance (TMQR) was confirmed until 1998. To date, five different TMQRs have been described in the literature, including target protection (Qnr), quinolone modification (AAC(6')-Ib-cr), plasmid-encoded efflux systems (e.g. QepA or OqxAB, amongst others), effect on bacterial growth rates and natural transformation. Although TMQRs usually only result in a slight increase in the minimum inhibitory concentrations of quinolones, they possess an additive effect and may facilitate the acquisition of full quinolone resistance. The emergence of new related genes may continue in the next years. (C) 2012 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:196 / 203
页数:8
相关论文
共 116 条
[1]   Trends in bacterial resistance to fluoroquinolones [J].
Acar, JF ;
Goldstein, FW .
CLINICAL INFECTIOUS DISEASES, 1997, 24 :S67-S73
[2]   Zoo animals as reservoirs of gram-negative bacteria harboring integrons and antimicrobial resistance genes [J].
Ahmed, Ashraf M. ;
Motoi, Yusuke ;
Sato, Maiko ;
Maruyama, Makito ;
Watanabe, Hitoshi ;
Fukumoto, Yukio ;
Shimamoto, Tadashi .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2007, 73 (20) :6686-6690
[3]   Cloning and characterization of SmeDEF, a novel multidrug efflux pump from Stenotrophomonas maltophilia [J].
Alonso, A ;
Martínez, JL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (11) :3079-3086
[4]   Salmonella ovarian abscess following travel diarrhoea episode [J].
Alonso D. ;
Muñoz J. ;
Ruiz J. ;
Carmona F. ;
Nadal A. ;
Gascón J. .
Archives of Gynecology and Obstetrics, 2007, 276 (5) :551-553
[5]   Design, synthesis and activity against Toxoplasma gondii, Plasmodium spp., and Mycobacterium tuberculosis of new 6-fluoroquinolones [J].
Anquetin, Guillaume ;
Greiner, Jacques ;
Mahmoudi, Nassira ;
Santillana-Hayat, Maud ;
Gozalbes, Rafael ;
Farhati, Khemais ;
Derouin, Francis ;
Aubry, Alexandra ;
Cambau, Emmanuelle ;
Vierling, Pierre .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2006, 41 (12) :1478-1493
[6]   Ciprofloxacin concentrations in lung tissue following a single 400 mg intravenous dose [J].
Birmingham, MC ;
Guarino, R ;
Heller, A ;
Wilton, JH ;
Shah, A ;
Hejmanowski, L ;
Nix, DE ;
Schentag, JJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 43 :43-48
[7]   TEMAFLOXACIN SYNDROME - REVIEW OF 95 CASES [J].
BLUM, MD ;
GRAHAM, DJ ;
MCCLOSKEY, CA .
CLINICAL INFECTIOUS DISEASES, 1994, 18 (06) :946-950
[8]   In Vitro Effect of qnrA1, qnrB1, and qnrS1 Genes on Fluoroquinolone Activity against Isogenic Escherichia coli Isolates with Mutations in gyrA and parC [J].
Briales, A. ;
Rodriguez-Martinez, J. M. ;
Velasco, C. ;
Diaz de Alba, P. ;
Dominguez-Herrera, J. ;
Pachon, J. ;
Pascual, A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (03) :1266-1269
[9]   In-vitro mutagenesis of qnrA and qnrS genes and quinolone resistance in Escherichia coli [J].
Cattoir, V. ;
Poirel, L. ;
Nordmann, P. .
CLINICAL MICROBIOLOGY AND INFECTION, 2007, 13 (09) :940-943
[10]   Plasmid-mediated quinolone resistance pump QepA2 in an Escherichia coli isolate from France [J].
Cattoir, Vincent ;
Poirel, Laurent ;
Nordmann, Patrice .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (10) :3801-3804