Antibiotic resistance genes from the environment: a perspective through newly identified antibiotic resistance mechanisms in the clinical setting

被引:141
作者
Canton, R. [1 ,2 ]
机构
[1] Univ Complutense, Fac Farm, Hosp Univ Ramon & Cajal, Microbiol Serv, E-28040 Madrid, Spain
[2] Univ Complutense, Fac Farm, Dept Microbiol, E-28040 Madrid, Spain
关键词
Clinical setting; environment; metagonomic; resistance genes; resistome; MEDIATED QUINOLONE RESISTANCE; 16S RIBOSOMAL-RNA; EFFLUX PUMP; PLASMID; FLUOROQUINOLONES; RESISTOME; AMINOGLYCOSIDES; OXAZOLIDINONES; DETERMINANTS; MOBILIZATION;
D O I
10.1111/j.1469-0691.2008.02679.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Soil bacteria may contain antibiotic resistance genes responsible for different mechanisms that permit them to overcome the natural antibiotics present in the environment. This gene pool has been recently named the 'resistome', and its components can be mobilized into the microbial community affecting humans because of the participation of genetic platforms that efficiently facilitate the mobilization and maintenance of these resistance genes. Evidence for this transference has been suggested or demonstrated with newly identified widespread genes in multidrug-resistant bacteria. These resistance genes include those responsible for ribosomal methylases affecting aminoglycosides (armA, rtmB), methyltransferases affecting linezolid (cfr) or plasmid-mediated efflux pumps conferring low-level fluoroquinolone resistance (qepA), all of which are associated with antibiotic-producing bacteria. In addition, resistance genes whose ancestors have been identified in environmental isolates that are not recognized as antibiotic producers have also been recently detected. These include the qnr and the bla(CTX) genes compromising the activity of fluoroquinolones and extended-spectrum cephalosporins, respectively. The application of metagenomic tools and phylogenetic analysis will facilitate future identification of other new resistance genes and their corresponding ancestors in environmental bacteria, and will enable further exploration of the concept of the resistome as being a unique reservoir of antibiotic resistance genes and genetic elements participating in resistance gene transfer.
引用
收藏
页码:20 / 25
页数:6
相关论文
共 29 条
[1]   High rate of mobilization for blaCTX-Ms [J].
Barlow, Miriam ;
Reik, Rebecca A. ;
Jacobs, Stephen D. ;
Medina, Monica ;
Meyer, Matthew P. ;
McGowan, John E., Jr. ;
Tenover, Fred C. .
EMERGING INFECTIOUS DISEASES, 2008, 14 (03) :423-428
[2]   The CTX-M β-lactamase pandemic [J].
Canton, Rafael ;
Coque, Teresa M. .
CURRENT OPINION IN MICROBIOLOGY, 2006, 9 (05) :466-475
[3]   Unexpected occurrence of plasmid-mediated quinolone resistance determinants in environmental Aeromonas spp. [J].
Cattoir, Vincent ;
Poirel, Laurent ;
Aubert, Camille ;
Soussy, Claude-James ;
Nordmann, Patrice .
EMERGING INFECTIOUS DISEASES, 2008, 14 (02) :231-237
[4]   Vibrio splendidus as the source of plasmid-mediated QnrS-like quinolone resistance determinants [J].
Cattoir, Vincent ;
Poirel, Laurent ;
Mazel, Didier ;
Soussy, Claude-James ;
Nordmann, Patrice .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (07) :2650-2651
[5]   Expanding the soil antibiotic resistome: exploring environmental diversity [J].
D'Costa, Vanessa M. ;
Griffiths, Emma ;
Wright, Gerard D. .
CURRENT OPINION IN MICROBIOLOGY, 2007, 10 (05) :481-489
[6]   Sampling the antibiotic resistome [J].
D'Costa, VM ;
McGrann, KM ;
Hughes, DW ;
Wright, GD .
SCIENCE, 2006, 311 (5759) :374-377
[7]  
DELACRUZ F, 2002, BACTERIAL RESISTANCE, P19
[8]   16S ribosomal RNA methylation: Emerging resistance mechanism against aminoglycosides [J].
Doi, Yohei ;
Arakawa, Yoshichika .
CLINICAL INFECTIOUS DISEASES, 2007, 45 (01) :88-94
[9]   Importance of the efflux pump systems in the resistance of Mycobacterium tuberculosis to Fluoroquinolones and linezolid [J].
Escribano, I. ;
Rodriguez, C. ;
Llorca, B. ;
Garcia-Pachon, E. ;
Ruiz, M. ;
Royo, G. .
CHEMOTHERAPY, 2007, 53 (06) :397-401
[10]   Worldwide disseminated armA aminoglycoside resistance methylase gene is borne by composite transposon Tn1548 [J].
Galimand, A ;
Sabtcheva, S ;
Courvalin, P ;
Lambert, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (07) :2949-2953