Development and spread of bacterial resistance to antimicrobial agents: An overview

被引:140
作者
Tenover, FC [1 ]
机构
[1] Ctr Dis Control & Prevent, Nosocomial Pathogens Lab Branch, Hosp Infect Program, Atlanta, GA USA
关键词
D O I
10.1086/321834
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Resistance to antimicrobial agents is emerging in a wide variety of nosocomial and community-acquired pathogens. The emergence and spread of multiply resistant organisms represent the convergence of a variety of factors that include mutations in common resistance genes that extend their spectrum of activity, the exchange of genetic information among microorganisms, the evolution of selective pressures in hospitals and communities that facilitate the development and spread of resistant organisms, the proliferation and spread of multiply resistant clones of bacteria, and the inability of some laboratory testing methods to detect emerging resistance phenotypes. Twenty years ago, bacteria that were resistant to antimicrobial agents were easy to detect in the laboratory because the concentration of drug required to inhibit their growth was usually quite high and distinctly different from that of susceptible strains. Newer mechanisms of resistance, however, often result in much more subtle shifts in bacterial population distributions. Perhaps the most difficult phenotypes to detect, as shown in several proficiency testing surveys, are decreased susceptibility to beta -lactams in pneumococci and decreased susceptibility to vancomycin in staphylococci. In summary, emerging resistance has required adaptations and modifications of laboratory diagnostic techniques, empiric anti-infective therapy for such diseases as bacterial meningitis, and infection control measures in health care facilities of all kinds. Judicious use is imperative if we are to preserve our arsenal of antimicrobial agents into the next decade.
引用
收藏
页码:S108 / S115
页数:8
相关论文
共 110 条
  • [1] [Anonymous], 1995, INFECT CONT HOSP EP, V16, P105
  • [2] [Anonymous], MMWR MORB MORTAL WKL
  • [3] [Anonymous], REP ASM TASK FORC AN
  • [4] [Anonymous], 1975, Infectious Multiple Drug Resistance
  • [5] [Anonymous], 2000, M2A7 NCCLS
  • [6] Antimicrobial resistance in isolates from inpatients and outpatients in the united states: Increasing importance of the intensive care unit
    Archibald, L
    Phillips, L
    Monnet, D
    McGowan, JE
    Tenover, F
    Gaynes, R
    [J]. CLINICAL INFECTIOUS DISEASES, 1997, 24 (02) : 211 - 215
  • [7] Vancomycin in surgical infections due to meticillin-resistant Staphylococcus aureus with heterogeneous resistance to vancomycin
    Ariza, J
    Pujol, M
    Cabo, J
    Peña, C
    Fernández, N
    Liñares, J
    Ayats, J
    Gudiol, F
    [J]. LANCET, 1999, 353 (9164) : 1587 - 1588
  • [8] Risk factors for carriage of drug-resistant Streptococcus pneumoniae among children in Memphis, Tennessee
    Arnold, KE
    Leggiadro, RJ
    Breiman, RF
    Lipman, HB
    Schwartz, B
    Appleton, MA
    Cleveland, KO
    Szeto, HC
    Hill, BC
    Tenover, FC
    Elliot, JA
    Facklam, RR
    [J]. JOURNAL OF PEDIATRICS, 1996, 128 (06) : 757 - 764
  • [9] Emergence of vancomycin-resistant enterococci in Australia: Phenotypic and genotypic characteristics of isolates
    Bell, JM
    Paton, JC
    Turnidge, J
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (08) : 2187 - 2190
  • [10] Presence of Staphylococcus aureus with reduced susceptibility to vancomycin in Germany
    Bierbaum, G
    Fuchs, K
    Lenz, W
    Szekat, C
    Sahl, HG
    [J]. EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1999, 18 (10) : 691 - 696