Emerging evolutionary paradigms in antibiotic discovery

被引:61
作者
Chevrette, Marc G. [1 ,2 ]
Currie, Cameron R. [2 ]
机构
[1] Univ Wisconsin, Dept Genet, Madison, WI 53706 USA
[2] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
Natural products; Secondary metabolism; Evolution; Ecology; Antibiotics; FUNGUS-GROWING ANTS; MODULAR POLYKETIDE SYNTHASES; BIOSYNTHETIC GENE CLUSTERS; NATURAL-PRODUCTS; SUBINHIBITORY CONCENTRATIONS; ECOLOGICAL DIFFERENTIATION; ANTIBACTERIAL ACTIVITY; STAPHYLOCOCCUS-AUREUS; SYMBIOTIC ASSOCIATION; SECONDARY METABOLISM;
D O I
10.1007/s10295-018-2085-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Antibiotics revolutionized medicine and remain its cornerstone. Despite their global importance and the continuous threat of resistant pathogens, few antibiotics have been discovered in recent years. Natural products, especially the secondary metabolites of Actinobacteria, have been the traditional discovery source of antibiotics. In nature, the chemistry of antibiotic natural products is shaped by the unique evolution and ecology of their producing organisms, yet these influences remain largely unknown. Here, we highlight the ecology of antibiotics employed by microbes in defensive symbioses and review the evolutionary processes underlying the chemical diversity and activity of microbe-derived antibiotics, including the dynamics of vertical and lateral transmission of biosynthetic pathways and the evolution of efficacy, targeting specificity, and toxicity. We argue that a deeper understanding of the ecology and evolution of microbial interactions and the metabolites that mediate them will allow for an alternative, rational approach to discover new antibiotics.
引用
收藏
页码:257 / 271
页数:15
相关论文
共 142 条
  • [61] Prodigal: prokaryotic gene recognition and translation initiation site identification
    Hyatt, Doug
    Chen, Gwo-Liang
    LoCascio, Philip F.
    Land, Miriam L.
    Larimer, Frank W.
    Hauser, Loren J.
    [J]. BMC BIOINFORMATICS, 2010, 11
  • [62] Evolution of metabolic diversity: Insights from microbial polyketide synthases
    Jenke-Kodama, Holger
    Dittmann, Elke
    [J]. PHYTOCHEMISTRY, 2009, 70 (15-16) : 1858 - 1866
  • [63] Global trends in emerging infectious diseases
    Jones, Kate E.
    Patel, Nikkita G.
    Levy, Marc A.
    Storeygard, Adam
    Balk, Deborah
    Gittleman, John L.
    Daszak, Peter
    [J]. NATURE, 2008, 451 (7181) : 990 - U4
  • [64] Combinatorialization of Fungal Polyketide Synthase-Peptide Synthetase Hybrid Proteins
    Kakule, Thomas B.
    Lin, Zhenjian
    Schmidt, Eric W.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (51) : 17882 - 17890
  • [65] Symbiotic bacteria protect wasp larvae from fungal infestation
    Kaltenpoth, M
    Göttler, W
    Herzner, G
    Strohm, E
    [J]. CURRENT BIOLOGY, 2005, 15 (05) : 475 - 479
  • [66] MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
    Katoh, Kazutaka
    Standley, Daron M.
    [J]. MOLECULAR BIOLOGY AND EVOLUTION, 2013, 30 (04) : 772 - 780
  • [67] Katz L., 2016, J IND MICROBIOL BIOT
  • [68] Classification of the Adenylation and Acyl-Transferase Activity of NRPS and PKS Systems Using Ensembles of Substrate Specific Hidden Markov Models
    Khayatt, Barzan I.
    Overmars, Lex
    Siezen, Roland J.
    Francke, Christof
    [J]. PLOS ONE, 2013, 8 (04):
  • [69] Irish contributions to the origins of antibiotics
    Kingston, W.
    [J]. IRISH JOURNAL OF MEDICAL SCIENCE, 2008, 177 (02) : 87 - 92
  • [70] Global increase and geographic convergence in antibiotic consumption between 2000 and 2015
    Klein, Eili Y.
    Van Boeckel, Thomas P.
    Martinez, Elena M.
    Pant, Suraj
    Gandra, Sumanth
    Levin, Simon A.
    Goossens, Herman
    Laxminarayan, Ramanan
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (15) : E3463 - E3470