Adaptive resistance to biocides in Salmonella enterica and Escherichia coli O157 and cross-resistance to antimicrobial agents

被引:199
作者
Braoudaki, M [1 ]
Hilton, AC [1 ]
机构
[1] Aston Univ, Sch Life & Hlth Sci, Birmingham B4 7ET, W Midlands, England
关键词
D O I
10.1128/JCM.42.1.73-78.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The mechanisms by which bacteria resist killing by antibiotics and biocides are still poorly defined, although repeated exposure to sublethal concentrations of antibacterial agents undoubtedly contributes to their development. This study aimed both to investigate the potential of Salmonella enterica and Escherichia coli O157 for adaptive resistance to commonly used biocides and to determine any cross-resistance to antibiotics. Strains were repeatedly passaged in media containing increasing concentrations of a biocide or antibiotic until adaptive resistance was obtained. A wide panel of antimicrobial agents was then screened by using the adapted strain to determine cross-resistance, if any. Adaptive resistance was readily achieved for both S. enterica and E. coli O157. Cross-resistance in adaptively resistant S. enterica varied with the serotype; Salmonella enterica serovar Enteritidis expressed cross-resistance to chloramphenicol, whereas Salmonella enterica serovar Typhimurium expressed cross- resistance to chlorhexidine. Benzalkonium chloride-resistant Salmonella enterica serovar Virchow showed elevated resistance to chlorhexidine; however, chlorhexidine resistant Salmonella serovar Virchow did not demonstrate reciprocal cross-resistance to benzalkonium chloride, suggesting specific rather than generic resistance mechanisms. E. coli O157 strains acquired high levels of resistance to triclosan after only two sublethal exposures and, when adapted, repeatedly demonstrated decreased susceptibilities to various antimicrobial agents, including chloramphenicol, erythromycin, imipenem, tetracycline, and trimethoprim, as well as to a number of biocides. These observations raise concern over the indiscriminate and often inappropriate use of biocides, especially triclosan, in situations where they are unnecessary, whereby they may contribute to the development of microbial resistance mechanisms.
引用
收藏
页码:73 / 78
页数:6
相关论文
共 29 条
[1]   New trimethoprim-resistant dihydrofolate reductase cassette, dfrXV, inserted in a class 1 integron [J].
Adrian, PV ;
du Plessis, M ;
Klugman, KP ;
Amyes, SGB .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (09) :2221-2224
[2]   The antibacterial activity of triclosan-impregnated storage boxes against Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, Bacillus cereus and Shewanella putrefaciens in conditions simulating domestic use [J].
Braid, JJ ;
Wale, MCJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (01) :87-94
[3]  
*BRIT SOC ANT CHEM, 1991, J ANTIMICROBIAL CHEM, V27
[4]  
BRUMER R, 2000, MICROBIAL RESISTANCE
[5]   Gradient plate method to induce Streptococcus pyogenes resistance [J].
Carsenti-Etesse, H ;
Roger, PM ;
Dunais, B ;
Durgeat, S ;
Mancini, G ;
Bensoussan, M ;
Dellamonica, P .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 44 (04) :439-443
[6]   Cross-resistance between triclosan and antibiotics in Pseudomonas aeruginosa is mediated by multidrug efflux pumps:: Exposure of a susceptible mutant strain to triclosan selects nfxB mutants overexpressing MexCD-OprJ [J].
Chuanchuen, R ;
Beinlich, K ;
Hoang, TT ;
Becher, A ;
Karkhoff-Schweizer, RR ;
Schweizer, HP .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (02) :428-432
[7]  
George AM, 1996, FEMS MICROBIOL LETT, V139, P1, DOI 10.1016/0378-1097(96)00127-9
[8]   CROSS-RESISTANCE TO NALIDIXIC-ACID, TRIMETHOPRIM, AND CHLORAMPHENICOL ASSOCIATED WITH ALTERATIONS IN OUTER-MEMBRANE PROTEINS OF KLEBSIELLA, ENTEROBACTER, AND SERRATIA [J].
GUTMANN, L ;
WILLIAMSON, R ;
MOREAU, N ;
KITZIS, MD ;
COLLATZ, E ;
ACAR, JF ;
GOLDSTEIN, FW .
JOURNAL OF INFECTIOUS DISEASES, 1985, 151 (03) :501-507
[9]  
Hopkins KL, 2001, LETT APPL MICROBIOL, V32, P126, DOI 10.1046/j.1472-765X.2001.00871.x
[10]   Adaptive resistance to benzalkonium chloride, amikacin and tobramycin: the effect on susceptibility to other antimicrobials [J].
Joynson, JA ;
Forbes, B ;
Lambert, RJW .
JOURNAL OF APPLIED MICROBIOLOGY, 2002, 93 (01) :96-107