Bacteria with increased mutation frequency and antibioticresistance are enriched in the commensal flora of patients with high antibiotic usage

被引:50
作者
Gustafsson, I
Sjölund, M
Torell, E
Johannesson, M
Engstrand, L
Cars, O
Andersson, DI [1 ]
机构
[1] Swedish Inst Infect Dis Control, Dept Bacteriol, SE-17182 Solna, Sweden
[2] Univ Uppsala Hosp, Sect Clin Bacteriol, Dept Med Sci, Antibiot Res Unit, Uppsala, Sweden
[3] Univ Uppsala Hosp, Infect Dis Sect, Uppsala, Sweden
[4] Univ Uppsala Hosp, Dept Womens & Childrens Hlth, Uppsala CF Ctr, Uppsala, Sweden
关键词
human microflora; antibiotic treatment; selection; mutators;
D O I
10.1093/jac/dkg427
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: We examined how prolonged antibiotic treatment affected the resistance and mutation frequency of human microflora isolated from intestine (Escherichia coli, enterococci spp.), pharynx (alpha-streptococci) and nostril (coagulase-negative staphylococci, CoNS). Methods: Samples were collected from patients at the Center of Cystic Fibrosis (n = 18) and the haematology ward (n = 18) of the University Hospital, Uppsala, Sweden. The individually used amount of antibiotics for 1 year was recorded as the defined daily dose (DDD). Primary health care patients (n = 30), with no antibiotic treatment for 1 year before sampling, were used as controls. Three isolates of each bacterium from each patient were examined. Antibiotic susceptibilities were determined by disc diffusion. Mutation frequencies to rifampicin resistance were measured on 30 independent cultures of each bacterial species from each individual by plating on rifampicin agar plates. For alpha-streptococci the mutation frequency to streptomycin resistance was also determined. Results: Isolates from patients with high antibiotic use showed a pronounced shift towards increased resistance and a small but significant increase in the mutation frequency compared with isolates from the controls. For E. coli, enterococci and CoNS the increase in geometric mean mutation frequency in the patient group was 3-, 1.8- and 1.5-fold, respectively (P values 0.0001, 0.016 and 0.012). For alpha-streptococci there was a significant difference in geometric mean mutation frequency between patient and control groups for streptomycin resistance (P = 0.024) but not for rifampicin resistance (P = 0.74). Conclusions: High antibiotic use selected for commensals with highly increased resistance and a slight increase in mutation frequency.
引用
收藏
页码:645 / 650
页数:6
相关论文
共 27 条
[1]   Mutation frequency and biological cost of antibiotic resistance in Helicobacter pylori [J].
Björkholm, B ;
Sjölund, M ;
Falk, PG ;
Berg, OG ;
Engstrand, L ;
Andersson, DI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14607-14612
[2]   High frequency of mutator strains among human uropathogenic Escherichia coli isolates [J].
Denamur, E ;
Bonacorsi, S ;
Giraud, A ;
Duriez, P ;
Hilali, F ;
Amorin, C ;
Bingen, E ;
Andremont, A ;
Picard, B ;
Taddei, F ;
Matic, I .
JOURNAL OF BACTERIOLOGY, 2002, 184 (02) :605-609
[3]   Evolutionary implications of the frequent horizontal transfer of mismatch repair genes [J].
Denamur, E ;
Lecointre, G ;
Darlu, P ;
Tenaillon, O ;
Acquaviva, C ;
Sayada, C ;
Sunjevaric, I ;
Rothstein, R ;
Elion, J ;
Taddei, F ;
Radman, M ;
Matic, I .
CELL, 2000, 103 (05) :711-721
[4]   DNA gyrase, topoisomerase IV, and the 4-quinolones [J].
Drlica, K ;
Zhao, XL .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1997, 61 (03) :377-+
[5]   NORFLOXACIN BINDS TO HUMAN FECAL MATERIAL [J].
EDLUND, C ;
LINDQVIST, L ;
NORD, CE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1988, 32 (12) :1869-1874
[6]   Mutator bacteria as a risk factor in treatment of infectious diseases [J].
Giraud, A ;
Matic, I ;
Radman, M ;
Fons, M ;
Taddei, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :863-865
[7]   The rise and fall of mutator bacteria [J].
Giraud, A ;
Radman, M ;
Matic, I ;
Taddei, F .
CURRENT OPINION IN MICROBIOLOGY, 2001, 4 (05) :582-585
[8]   Costs and benefits of high mutation rates: Adaptive evolution of bacteria in the mouse gut [J].
Giraud, A ;
Matic, I ;
Tenaillon, O ;
Clara, A ;
Radman, M ;
Fons, M ;
Taddei, F .
SCIENCE, 2001, 291 (5513) :2606-2608
[9]   Excretion of ciprofloxacin in sweat and multiresistant Staphylococcus epidermidis [J].
Holby, N ;
Jarlov, JO ;
Kemp, M ;
Tvede, M ;
Bangsborg, JM ;
Kjerulf, A ;
Pers, C ;
Hansen, H .
LANCET, 1997, 349 (9046) :167-169
[10]   MAPPING AND SEQUENCING OF MUTATIONS IN THE ESCHERICHIA-COLI RPOB GENE THAT LEAD TO RIFAMPICIN RESISTANCE [J].
JIN, DJ ;
GROSS, CA .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 202 (01) :45-58