EVOLUTION OF RESISTANCE IN MICROORGANISMS OF HUMAN-ORIGIN

被引:6
作者
KAYSER, FH
机构
[1] Institute of Medical Microbiology, University of Zürich
关键词
D O I
10.1016/0378-1135(93)90150-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Resistance to antimicrobials in bacteria results from either evolution of ''new'' DNA or from variation in existing DNA. Evidence suggests that new DNA did not originate since the use of antibiotics in medicine, but evolved long ago in soil bacteria. This evidence is based on functional and structural homologies of resistance proteins in human pathogens, and resistance proteins or physiological proteins of soil bacteria. Variation in existing DNA has been shown to comprise variations in structural or regulatory genes of the normal chromosome or mutations in already existing plasmid-mediated resistance genes modifying the resistance phenotype. The success of R-determinants in human pathogens was due to their horizontal spread by transformation, transduction and conjugation. Furthermore, transposition has enabled bacteria to efficiently distribute R-determinants between independent DNA-molecules. Since the genetic processes involved in the development of resistance are rare events, the selective pressure exerted by antibiotics has significantly contributed to the overall evolutionary picture. With few exceptions, experimental data about the role of antibiotic usage outside human medicine with respect to the resistance problem in human pathogens are missing. Epidemiological data about the occurrence of resistance in human pathogens seem to indicate that the major contributing factor to the problem we face today was the extensive use of antibiotics in medicine itself.
引用
收藏
页码:257 / 267
页数:11
相关论文
共 34 条
[21]   EXTREMELY HIGH-INCIDENCE OF ANTIBIOTIC-RESISTANCE IN CLINICAL ISOLATES OF STREPTOCOCCUS-PNEUMONIAE IN HUNGARY [J].
MARTON, A ;
GULYAS, M ;
MUNOZ, R ;
TOMASZ, A .
JOURNAL OF INFECTIOUS DISEASES, 1991, 163 (03) :542-548
[22]  
Murphy E, 1989, MOBILE DNA-UK, P269
[23]   DOES PROLONGED EXPOSURE TO ANTIBIOTIC-RESISTANT BACTERIA INCREASE THE RATE OF ANTIBIOTIC-RESISTANT INFECTION [J].
PARSONNET, KC ;
KASS, EH .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (06) :911-914
[24]   EPIDEMIC OF HOSPITAL-ACQUIRED INFECTION DUE TO METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS IN MAJOR VICTORIAN HOSPITALS [J].
PAVILLARD, R ;
HARVEY, K ;
DOUGLAS, D ;
HEWSTONE, A ;
ANDREW, J ;
COLLOPY, B ;
ASCHE, V ;
CARSON, P ;
DAVIDSON, A ;
GILBERT, G ;
SPICER, J ;
TOSOLINI, F .
MEDICAL JOURNAL OF AUSTRALIA, 1982, 1 (11) :451-454
[25]   GONORRHEA AND THE STORY OF RESISTANT NEISSERIA-GONORRHOEAE [J].
SEHGAL, VN ;
SRIVASTAVA, G .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 1987, 26 (04) :206-214
[26]   CONTINUOUS NON-THERAPEUTIC USE OF ANTIBACTERIAL DRUGS IN FEED AND DRUG-RESISTANCE OF GRAM-NEGATIVE ENTERIC FLORAE OF FOOD-PRODUCING ANIMALS [J].
SIEGEL, D ;
HUBER, WG ;
ENLOE, F .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1974, 6 (06) :697-701
[27]   LOCALIZED SEX IN BACTERIA [J].
SMITH, JM ;
DOWSON, CG ;
SPRATT, BG .
NATURE, 1991, 349 (6304) :29-31
[28]   HYBRID PENICILLIN-BINDING PROTEINS IN PENICILLIN-RESISTANT STRAINS OF NEISSERIA-GONORRHOEAE [J].
SPRATT, BG .
NATURE, 1988, 332 (6160) :173-176
[29]   RECRUITMENT OF A PENICILLIN-BINDING PROTEIN GENE FROM NEISSERIA-FLAVESCENS DURING THE EMERGENCE OF PENICILLIN RESISTANCE IN NEISSERIA-MENINGITIDIS [J].
SPRATT, BG ;
ZHANG, QY ;
JONES, DM ;
HUTCHISON, A ;
BRANNIGAN, JA ;
DOWSON, CG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8988-8992
[30]   SURVEY OF METHICILLIN-RESISTANT CLINICAL STRAINS OF COAGULASE-NEGATIVE STAPHYLOCOCCI FOR MECA GENE DISTRIBUTION [J].
SUZUKI, E ;
HIRAMATSU, K ;
YOKOTA, T .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (02) :429-434