Antibiotic resistance in the absence of selective pressure

被引:68
作者
Gillespie, SH [1 ]
机构
[1] UCL Royal Free & Univ Coll, Sch Med, London NW3 2PF, England
关键词
antibiotic resistance; selective pressure; evolution; multiple drug resistant tuberculosis;
D O I
10.1016/S0924-8579(00)00340-X
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Antibiotic resistance poses a serious threat to modern medical practice making treatment more difficult and is associated with increased mortality among patients infected with resistant organisms. There is clear evidence that acquisition of resistance is associated with a decrease in the fitness of the organisms at least in the short term. Evidence from in vitro experiments indicates that bacteria have the ability to adapt to this deficit and recover fitness on serial passage. More recent results show that identical organisms isolated from patients in outbreaks have an initial deficit but that adaptation occurs in vivo. Strategies directed towards controlling resistance must move beyond wishful thinking that supposes that these organisms will disappear merely with control of prescribing. In some cases, resistance will not disappear because there is no evolutionary disadvantage in being resistant once adaptation has taken place. It is important. therefore. that we direct out efforts towards preventing primary resistance emerging and in limiting the spread of resistant strains. Ultimately, we must look again to new drug discovery to improve our therapeutic armoury. (C) 2001 Elsevier Science B.V. and International Society of Chemotherapy All rights reserved.
引用
收藏
页码:171 / 176
页数:6
相关论文
共 50 条
  • [21] ALTERED PEPTIDOGLYCAN STRUCTURE IN A PNEUMOCOCCAL TRANSFORMANT RESISTANT TO PENICILLIN
    GARCIABUSTOS, JF
    CHAIT, BT
    TOMASZ, A
    [J]. JOURNAL OF BACTERIOLOGY, 1988, 170 (05) : 2143 - 2147
  • [22] GHUYSEN JM, 1991, NEW COMPREHENSIVE BI, V2
  • [23] Gillam Stuart L., 1998, CONTINUING MED ED J, V2, P4
  • [24] Acquisition of five high-Mr penicillin-binding protein variants during transfer of high-level β-lactam resistance from Streptococcus mitis to Streptococcus pneumoniae
    Hakenbeck, R
    König, A
    Kern, I
    van der Linden, M
    Keck, W
    Billot-Klein, D
    Legrand, R
    Schoot, B
    Gutmann, L
    [J]. JOURNAL OF BACTERIOLOGY, 1998, 180 (07) : 1831 - 1840
  • [25] HANDSMAN D, 1967, LANCET, V2, P264
  • [26] HANDSMAN D, 1974, MD J AUST, V2, P353
  • [27] ALTERATIONS IN KINETIC-PROPERTIES OF PENICILLIN-BINDING PROTEINS OF PENICILLIN-RESISTANT STREPTOCOCCUS-PNEUMONIAE
    HANDWERGER, S
    TOMASZ, A
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1986, 30 (01) : 57 - 63
  • [28] TRANSFER OF ERYTHROMYCIN RESISTANCE FROM CLINICALLY ISOLATED LYSOGENIC STRAINS OF STREPTOCOCCUS-PYOGENES VIA THEIR ENDOGENOUS PHAGE
    HYDER, SL
    STREITFELD, MM
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1978, 138 (03) : 281 - 286
  • [29] EMERGENCE OF MULTIPLY RESISTANT PNEUMOCOCCI
    JACOBS, MR
    KOORNHOF, HJ
    ROBINSBROWNE, RM
    STEVENSON, CM
    VERMAAK, ZA
    FREIMAN, I
    MILLER, GB
    WITCOMB, MA
    ISAACSON, M
    WARD, JI
    AUSTRIAN, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1978, 299 (14) : 735 - 740
  • [30] Invasive pneumococcal disease in the immunocompromised host
    Janoff, EN
    Rubins, JB
    [J]. MICROBIAL DRUG RESISTANCE, 1997, 3 (03) : 215 - 232