A phenylalanine-arginine β-naphthylamide sensitive multidrug efflux pump involved in intrinsic and acquired resistance of Campylobacter to macrolides

被引:48
作者
Mamelli, L
Amoros, JP
Pagès, JM
Bolla, JM
机构
[1] Univ Mediterranee, Fac Med, IFR 48, EA 2197, F-13385 Marseille 05, France
[2] Univ Corse, Fac Sci & Tech, F-20250 Corte, France
关键词
Campylobacter; macrolides; multidrug resistance; efflux pump; intrinsic resistance; acquired resistance;
D O I
10.1016/S0924-8579(03)00199-7
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The macrolide erythromycin is the antibiotic of choice in the management of Campylobacter infections. Although mutation has been reported to account for resistance to the antibiotic, resistance may also be due to an efflux pump that extrudes the drug prior to reaching its target. Moreover, the efflux pump may be one that accommodates resistance to other related or unrelated drugs (multidrug resistance). We examined the possibility that resistance to erythromycin may involve an efflux pump whose presence may be identified by the use of the unique commercial inhibitor of the previously described efflux pumps phenylalanine-arginine beta-naphtylamide (PAbetaN). We showed that PAbetaN is able to significantly increase the susceptibility of the reference strain NCTC 11168 to erythromycin, suggesting that an efflux pump functions at a basal level in the reference wild type strain. Erythromycin-resistant isolates were tested for their response to PAbetaN treatment. Among the strains tested, resistance of three isolates to erythromycin was reduced to a level comparable to that of the susceptible strain when the strains were grown in the presence of this inhibitor. To conclude, besides mutations, erythromycin resistance in Campylobacter may also be due to an efflux mechanism sensitive to PAbetaN. (C) 2003 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:237 / 241
页数:5
相关论文
共 20 条
[1]   Antimicrobial susceptibility patterns of thermophilic Campylobacter spp. from humans, pigs, cattle, and broilers in Denmark [J].
Aarestrup, FM ;
Nielsen, EM ;
Madsen, M ;
Engberg, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) :2244-2250
[2]  
Aarestrup FM, 2001, VET RES, V32, P311, DOI 10.1051/vetres:2001127
[3]  
Allos BM, 2001, CLIN INFECT DIS, V32, P1201, DOI 10.1086/319760
[4]  
CARRET G, 2002, COMITE ANTIBIOGRAMME
[5]   Quinolone and macrolide resistance in Campylobacter jejuni and C-coli:: Resistance mechanisms and trends in human isolates [J].
Engberg, J ;
Aarestrup, FM ;
Taylor, DE ;
Gerner-Smidt, P ;
Nachamkin, I .
EMERGING INFECTIOUS DISEASES, 2001, 7 (01) :24-34
[6]   CmeABC functions as a multidrug efflux system in Campylobacter jejuni [J].
Lin, J ;
Michel, LO ;
Zhang, QJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (07) :2124-2131
[7]   Identification and characterization of inhibitors of multidrug resistance efflux pumps in Pseudomonas aeruginosa:: Novel agents for combination therapy [J].
Lomovskaya, O ;
Warren, MS ;
Lee, A ;
Galazzo, J ;
Fronko, R ;
Lee, M ;
Blais, J ;
Cho, D ;
Chamberland, S ;
Renau, T ;
Leger, R ;
Hecker, S ;
Watkins, W ;
Hoshino, K ;
Ishida, H ;
Lee, VJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (01) :105-116
[8]   Inhibitors of antibiotic efflux pump in resistant Enterobacter aerogenes strains [J].
Malléa, M ;
Chevalier, J ;
Eyraud, A ;
Pagès, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (05) :1370-1373
[9]   Bioenergetics of the staphylococcal multidrug export protein QacA - Identification of distinct binding sites for monovalent and divalent cations [J].
Mitchell, BA ;
Paulsen, IT ;
Brown, MH ;
Skurray, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) :3541-3548
[10]   Campylobacter species and Guillain-Barre syndrome [J].
Nachamkin, I ;
Allos, BM ;
Ho, T .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (03) :555-+