MODULATION OF THE MUTAGENIC RESPONSE IN PROKARYOTES

被引:51
作者
DEFLORA, S
CAMOIRANO, A
DAGOSTINI, F
BALANSKY, R
机构
[1] Institute of Hygiene and Preventive Medicine, University of Genoa
来源
MUTATION RESEARCH | 1992年 / 267卷 / 02期
关键词
PROKARYOTES; ANTIMUTAGENICITY; DNA DAMAGE; MODULATION;
D O I
10.1016/0027-5107(92)90062-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Short-term tests investigating genetic end-points in prokaryotes have been extensively used worldwide not only for risk assessment purposes but also for evaluating the modulation of the mutagenic response. In spite of some intrinsic limitations, such as the lack of cell compartmentalization or the need for an exogenous metabolic system working extracellularly, experimental systems in bacteria can provide useful preliminary indications and some information on the mechanisms involved. In the large majority of studies the putative modulator is mixed with a known mutagen and then assayed in target bacteria, with suitable controls. However, under natural conditions exposure of target cells to modulators may either precede, co-exist with, or follow exposure to mutagens. Therefore, a variety of methodological variations, involving pre-treatment, co-treatment, or post-treatment of bacteria with the putative modulator, have been designed. Application of these procedures showed that the effects of modulators can be completely upset, from inhibition to enhancement, or vice versa, by changing the experimental conditions. Use of methodological variations may provide more complete information on the spectrum of possible effects in bacteria as well as a better insight into modulation mechanisms. Several examples illustrating the flexibility of the Salmonella test in this field of research are available. On the other hand, the widespread use of these relatively simple techniques, yet requiring skillfulness and experience, may lead to some misuse or oversimplifications. A rather common inadequacy is to use excessive amounts of test mutagens, or to express the results in terms of revertants/survivors, rather than revertants/plate. In fact, in the Salmonella test the number of revertants is rather unrelated to the initial number of plated bacteria, provided a normal background lawn of bacterial growth is formed. Thus, a 50% killing of bacteria will not appreciably influence the number of revertants/plate, but expressed as revertants/survivors the effect will look twice as large.
引用
收藏
页码:183 / 192
页数:10
相关论文
共 25 条
  • [1] BALANSKY RM, 1985, NEOPLASMA, V32, P313
  • [2] THE INFLUENCE OF SELENIUM AND CAFFEINE ON CHEMICAL CARCINOGENESIS IN RATS, MUTAGENESIS IN BACTERIA, AND UNSCHEDULED DNA-SYNTHESIS IN HUMAN-LYMPHOCYTES
    BALANSKY, RM
    BLAGOEVA, PM
    MIRTCHEVA, Z
    [J]. BIOLOGICAL TRACE ELEMENT RESEARCH, 1983, 5 (4-5) : 331 - 343
  • [3] CAMOIRANO A, 1988, LIFE SCI ADV EXP ONC, V7, P21
  • [4] ANTI-MUTAGENESIS IN MICROBIAL SYSTEMS
    CLARKE, CH
    SHANKEL, DM
    [J]. BACTERIOLOGICAL REVIEWS, 1975, 39 (01) : 33 - 53
  • [5] PURE EXOGENOUS SINGLET OXYGEN - NONMUTAGENICITY IN BACTERIA
    DAHL, TA
    MIDDEN, WR
    HARTMAN, PE
    [J]. MUTATION RESEARCH, 1988, 201 (01): : 127 - 136
  • [6] De Flora S, 1984, Toxicol Pathol, V12, P337
  • [7] MUTAGENICITY OF ACTIVE OXYGEN SPECIES IN BACTERIA AND ITS ENZYMATIC OR CHEMICAL INHIBITION
    DEFLORA, S
    BENNICELLI, C
    ZANACCHI, P
    DAGOSTINI, F
    CAMOIRANO, A
    [J]. MUTATION RESEARCH, 1989, 214 (01): : 153 - 158
  • [8] DEFLORA S, 1985, CARCINOGENESIS, V6, P1735
  • [9] PREVENTION BY N-ACETYLCYSTEINE OF BENZO[A]PYRENE CLASTOGENICITY AND DNA ADDUCTS IN RATS
    DEFLORA, S
    DAGOSTINI, F
    IZZOTTI, A
    BALANSKY, R
    [J]. MUTATION RESEARCH, 1991, 250 (1-2): : 87 - 93
  • [10] INVITRO EFFECTS OF N-ACETYLCYSTEINE ON THE MUTAGENICITY OF DIRECT-ACTING COMPOUNDS AND PROCARCINOGENS
    DEFLORA, S
    BENNICELLI, C
    ZANACCHI, P
    CAMOIRANO, A
    MORELLI, A
    DEFLORA, A
    [J]. CARCINOGENESIS, 1984, 5 (04) : 505 - 510