Developing new antibacterials through natural product research

被引:49
作者
Kirst, Herbert A.
机构
[1] not available, Indianapolis, IN 46278
关键词
antibacterial; antibiotic; antimicrobial; biosynthesis; fermentation product; infectious disease; natural product; semi-synthetic; DRUG DISCOVERY; PLEUROMUTILIN DERIVATIVES; POLYMYXIN-B; ANTIMICROBIAL AGENTS; PEPTIDE ANTIBIOTICS; RESISTANT-BACTERIA; CHEMICAL SPACE; IN-VITRO; DESIGN; BIOSYNTHESIS;
D O I
10.1517/17460441.2013.779666
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Natural products have long been instrumental for discovering antibiotics, but many pharmaceutical companies abandoned this field and new antibiotics declined. In contrast, microbial resistance to current antibiotics has approached critical levels. Areas covered: This article gives historical perspectives by providing background about present-day economic realities and medical needs for antibiotic research, whose pipeline is mostly focused toward older known agents and newer semi-synthetic derivatives. Future research trends and projected technological developments open many innovative opportunities to discover novel antibacterials and find ways to control pathogenic bacteria without conventional antibiotics that provoke resistance. Expert opinion: The successful registration of daptomycin, retapamulin and fidaxomicin indicate the re-emergence of natural products has already begun. Semi-synthetic derivatives from other under-explored classes are progressing. More effort is being put into approaches such as total synthesis, discovery of new structural scaffolds for synthesis, alterations of biosynthetic pathways, combinatorial biosynthesis, new screening targets and new resources from which to isolate natural products. A return to successful screening of actinomycetes depends on solving the rate-limiting dereplication obstacle. Long-term solutions need to come from greater exploration of the massive numbers of uncultured microbes. An ultimate solution to the antibiotic-promoted microbial resistance cycle may lie in finding ways to control bacteria by non-lethal means.
引用
收藏
页码:479 / 493
页数:15
相关论文
共 165 条
  • [71] Immunotherapies in Infectious Diseases
    Kak, Vivek
    Sundareshan, Vidya
    Modi, Jignesh
    Khardori, Nancy Misri
    [J]. MEDICAL CLINICS OF NORTH AMERICA, 2012, 96 (03) : 455 - +
  • [72] Kanyo Z, 2011, 51 INT C ANT AG CHEM
  • [73] Keasling JD, 2012, NATURE, V492, P188, DOI 10.1038/492188a
  • [74] New approaches for treating staphylococcal biofilm infections
    Kiedrowski, Megan R.
    Horswill, Alexander R.
    [J]. ANTIMICROBIAL THERAPEUTICS REVIEWS: ANTIBIOTICS THAT TARGET THE RIBOSOME, 2011, 1241 : 104 - 121
  • [75] Establishing Molecular Tools for Genetic Manipulation of the Pleuromutilin-Producing Fungus Clitopilus passeckerianus
    Kilaru, Sreedhar
    Collins, Catherine M.
    Hartley, Amanda J.
    Bailey, Andy M.
    Foster, Gary D.
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2009, 75 (22) : 7196 - 7204
  • [76] THE STRUCTURE OF A201A, A NOVEL NUCLEOSIDE ANTIBIOTIC
    KIRST, HA
    DORMAN, DE
    OCCOLOWITZ, JL
    JONES, ND
    PASCHAL, JW
    HAMILL, RL
    SZYMANSKI, EF
    [J]. JOURNAL OF ANTIBIOTICS, 1985, 38 (05) : 575 - 586
  • [77] STRUCTURE OF ALTHIOMYCIN
    KIRST, HA
    SZYMANSKI, EF
    DORMAN, DE
    OCCOLOWITZ, JL
    JONES, ND
    CHANEY, MO
    HAMILL, RL
    HOEHN, MM
    [J]. JOURNAL OF ANTIBIOTICS, 1975, 28 (04) : 286 - 291
  • [78] Kirst HA, 1996, PROGR MED CHEM, V1, P1
  • [79] Recent derivatives from smaller classes of fermentation-derived antibacterials
    Kirst, Herbert A.
    [J]. EXPERT OPINION ON THERAPEUTIC PATENTS, 2012, 22 (01) : 15 - 35
  • [80] Kirst HA, 2010, EXPERT OPIN THER PAT, V20, P1271, DOI [10.1517/13543776.2010.511178, 10.1517/13543776.2010.513908]