Fitness benefits in fluoroquinolone-resistant Salmonella Typhi in the absence of antimicrobial pressure

被引:89
作者
Baker, Stephen [1 ,2 ,3 ]
Pham Thanh Duy [1 ]
Tran Vu Thieu Nga [1 ]
Tran Thi Ngoc Dung [1 ]
Voong Vinh Phat [1 ]
Tran Thuy Chau [1 ]
Turner, A. Keith [4 ]
Farrar, Jeremy [1 ,2 ]
Boni, Maciej F. [1 ,2 ]
机构
[1] Oxford Univ Clin Res Unit, Wellcome Trust Major Overseas Programme, Ho Chi Minh City, Vietnam
[2] Univ Oxford, Nuffield Dept Clin Med, Ctr Trop Med, Oxford, England
[3] London Sch Hyg & Trop Med, London WC1, England
[4] Wellcome Trust Sanger Inst, Hinxton, England
来源
ELIFE | 2013年 / 2卷
基金
英国惠康基金;
关键词
ENTERICA SEROVAR TYPHI; ANTIBIOTIC-RESISTANCE; MULTIDRUG-RESISTANT; ESCHERICHIA-COLI; REDUCED SUSCEPTIBILITY; BIOLOGICAL COST; IN-VIVO; EXPERIMENTAL POPULATIONS; CLINICAL-RESPONSE; MUTATIONS;
D O I
10.7554/eLife.01229
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fluoroquinolones (FQ) are the recommended antimicrobial treatment for typhoid, a severe systemic infection caused by the bacterium Salmonella enterica serovar Typhi. FQ-resistance mutations in S. Typhi have become common, hindering treatment and control efforts. Using in vitro competition experiments, we assayed the fitness of eleven isogenic S. Typhi strains with resistance mutations in the FQ target genes, gyrA and parC. In the absence of antimicrobial pressure, 6 out of 11 mutants carried a selective advantage over the antimicrobial-sensitive parent strain, indicating that FQ resistance in S. Typhi is not typically associated with fitness costs. Double-mutants exhibited higher than expected fitness as a result of synergistic epistasis, signifying that epistasis may be a critical factor in the evolution and molecular epidemiology of S. Typhi. Our findings have important implications for the management of drug-resistant S. Typhi, suggesting that FQ-resistant strains would be naturally maintained even if fluoroquinolone use were reduced.
引用
收藏
页数:17
相关论文
共 59 条
[51]   Fitness costs of fluoroquinolone resistance in Streptococcus pneumoniae [J].
Rozen, Daniel E. ;
McGee, Lesley ;
Levin, Bruce R. ;
Klugman, Keith P. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (02) :412-416
[52]   Use of mixed infections to study cell invasion and intracellular proliferation of Salmonella enterica in eukaryotic cell cultures [J].
Segura, I ;
Casadesús, J ;
Ramos-Morales, F .
JOURNAL OF MICROBIOLOGICAL METHODS, 2004, 56 (01) :83-91
[53]   Pervasive Sign Epistasis between Conjugative Plasmids and Drug-Resistance Chromosomal Mutations [J].
Silva, Rui F. ;
Mendonca, Silvia C. M. ;
Carvalho, Luis M. ;
Reis, Ana M. ;
Gordo, Isabel ;
Trindade, Sandra ;
Dionisio, Francisco .
PLOS GENETICS, 2011, 7 (07)
[54]   Cost of Antibiotic Resistance and the Geometry of Adaptation [J].
Sousa, Ana ;
Magalhaes, Sara ;
Gordo, Isabel .
MOLECULAR BIOLOGY AND EVOLUTION, 2012, 29 (05) :1417-1428
[55]   Safety of live oral Salmonella typhi vaccine strains with deletions in htrA and aroC aroD and immune response in humans [J].
Tacket, CO ;
Sztein, MB ;
Losonsky, GA ;
Wasserman, SS ;
Nataro, JP ;
Edelman, R ;
Pickard, D ;
Dougan, G ;
Chatfield, SN ;
Levine, MM .
INFECTION AND IMMUNITY, 1997, 65 (02) :452-456
[56]   Positive Epistasis Drives the Acquisition of Multidrug Resistance [J].
Trindade, Sandra ;
Sousa, Ana ;
Xavier, Karina Bivar ;
Dionisio, Francisco ;
Ferreira, Miguel Godinho ;
Gordo, Isabel .
PLOS GENETICS, 2009, 5 (07)
[57]   The acquisition of full fluoroquinolone resistance in Salmonella Typhi by accumulation of point mutations in the topoisomerase targets [J].
Turner, Arthur K. ;
Nair, Satheesh ;
Wain, John .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (04) :733-740
[58]   Quinolone-resistant Salmonella typhi in Viet Nam:: Molecular basis of resistance and clinical response to treatment [J].
Wain, J ;
Hoa, NTT ;
Chinh, NT ;
Vinh, H ;
Everett, MJ ;
Diep, TS ;
Day, NPJ ;
Solomon, T ;
White, NJ ;
Piddock, LJV ;
Parry, CM .
CLINICAL INFECTIOUS DISEASES, 1997, 25 (06) :1404-1410
[59]   Biological cost of rifampin resistance from the perspective of Staphylococcus aureus [J].
Wichelhaus, TA ;
Böddinghaus, B ;
Besier, S ;
Schäfer, V ;
Brade, V ;
Ludwig, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (11) :3381-3385