Laboratory Evolution of Antimicrobial Resistance in Bacteria to Develop Rational Treatment Strategies

被引:12
作者
Maeda, Tomoya [1 ,2 ]
Furusawa, Chikara [2 ,3 ]
机构
[1] Hokkaido Univ, Res Fac Agr, Lab Microbial Physiol, Kita 9,Nishi 9,Kita ku, Sapporo 0608589, Japan
[2] RIKEN, Ctr Biosyst Dynam Res, 6-2-3 Furuedai, Suita 5650874, Japan
[3] Univ Tokyo, Universal Biol Inst, 7-3-1 Hongo, Tokyo 1130033, Japan
来源
ANTIBIOTICS-BASEL | 2024年 / 13卷 / 01期
基金
日本学术振兴会;
关键词
antimicrobial resistance; laboratory evolution; collateral sensitivity; TRANSFER-RNA SYNTHETASE; ANTIBIOTIC-RESISTANCE; MYCOBACTERIUM-TUBERCULOSIS; COMBINATION THERAPY; ANTIFUNGAL AGENT; TOLERANCE; DISCOVERY; PERSISTENCE; INHIBITORS; EMERGENCE;
D O I
10.3390/antibiotics13010094
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Laboratory evolution studies, particularly with Escherichia coli, have yielded invaluable insights into the mechanisms of antimicrobial resistance (AMR). Recent investigations have illuminated that, with repetitive antibiotic exposures, bacterial populations will adapt and eventually become tolerant and resistant to the drugs. Through intensive analyses, these inquiries have unveiled instances of convergent evolution across diverse antibiotics, the pleiotropic effects of resistance mutations, and the role played by loss-of-function mutations in the evolutionary landscape. Moreover, a quantitative analysis of multidrug combinations has shed light on collateral sensitivity, revealing specific drug combinations capable of suppressing the acquisition of resistance. This review article introduces the methodologies employed in the laboratory evolution of AMR in bacteria and presents recent discoveries concerning AMR mechanisms derived from laboratory evolution. Additionally, the review outlines the application of laboratory evolution in endeavors to formulate rational treatment strategies.
引用
收藏
页数:24
相关论文
共 124 条
[81]   Collateral sensitivity of antibiotic-resistant microbes [J].
Pal, Csaba ;
Papp, Balazs ;
Lazar, Viktoria .
TRENDS IN MICROBIOLOGY, 2015, 23 (07) :401-407
[82]   Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase [J].
Palencia, Andres ;
Li, Xianfeng ;
Bu, Wei ;
Choi, Wai ;
Ding, Charles Z. ;
Easom, Eric E. ;
Feng, Lisa ;
Hernandez, Vincent ;
Houston, Paul ;
Liu, Liang ;
Meewan, Maliwan ;
Mohan, Manisha ;
Rock, Fernando L. ;
Sexton, Holly ;
Zhang, Suoming ;
Zhou, Yasheen ;
Wan, Baojie ;
Wang, Yuehong ;
Franzblau, Scott G. ;
Woolhiser, Lisa ;
Gruppo, Veronica ;
Lenaerts, Anne J. ;
O'Malley, Theresa ;
Parish, Tanya ;
Cooper, Christopher B. ;
Waters, M. Gerard ;
Ma, Zhenkun ;
Ioerger, Thomas R. ;
Sacchettini, James C. ;
Rullas, Joaquin ;
Angulo-Barturen, Inigo ;
Perez-Herran, Esther ;
Mendoza, Alfonso ;
Barros, David ;
Cusack, Stephen ;
Plattner, Jacob J. ;
Alley, M. R. K. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2016, 60 (10) :6271-6280
[83]   beta lactam monotherapy versus beta lactam-aminoglycoside combination therapy for sepsis in immunocompetent patients: systematic review and meta-analysis of randomised trials [J].
Paul, M ;
Benuri-Silbiger, I ;
Soares-Weiser, K ;
Leibovici, L .
BMJ-BRITISH MEDICAL JOURNAL, 2004, 328 (7441) :668-672F
[84]   Proton-dependent multidrug efflux systems [J].
Paulsen, IT ;
Brown, MH ;
Skurray, RA .
MICROBIOLOGICAL REVIEWS, 1996, 60 (04) :575-+
[85]   Exogenous Alanine and/or Glucose plus Kanamycin Kills Antibiotic-Resistant Bacteria [J].
Peng, Bo ;
Su, Yu-bin ;
Li, Hui ;
Han, Yi ;
Guo, Chang ;
Tian, Yao-mei ;
Peng, Xuan-xian .
CELL METABOLISM, 2015, 21 (02) :249-261
[86]   Conserved collateral antibiotic susceptibility networks in diverse clinical strains of Escherichia coli [J].
Podnecky, Nicole L. ;
Fredheim, Elizabeth G. A. ;
Kloos, Julia ;
Sorum, Vidar ;
Primicerio, Raul ;
Roberts, Adam P. ;
Rozen, Daniel E. ;
Samuelsen, Orjan ;
Johnsen, Pal J. .
NATURE COMMUNICATIONS, 2018, 9
[87]   Overexpression of the mexC-mexD-oprJ efflux operon in nfxB-type multidrug-resistant strains of Pseudomonas aeruginosa [J].
Poole, K ;
Gotoh, N ;
Tsujimoto, H ;
Zhao, QX ;
Wada, A ;
Yamasaki, T ;
Neshat, S ;
Yamagishi, JI ;
Li, XZ ;
Nishino, T .
MOLECULAR MICROBIOLOGY, 1996, 21 (04) :713-724
[88]   Five rules for resistance management in the antibiotic apocalypse, a road map for integrated microbial management [J].
Raymond, Ben .
EVOLUTIONARY APPLICATIONS, 2019, 12 (06) :1079-1091
[89]   An antifungal agent inhibits an aminoacyl-tRNA synthetase by trapping tRNA in the editing site [J].
Rock, Fernando L. ;
Mao, Weimin ;
Yaremchuk, Anya ;
Tukalo, Mikhail ;
Crepin, Thibaut ;
Zhou, Huchen ;
Zhang, Yong-Kang ;
Hernandez, Vincent ;
Akama, Tsutomu ;
Baker, Stephen J. ;
Plattner, Jacob J. ;
Shapiro, Lucy ;
Martinis, Susan A. ;
Benkovic, Stephen J. ;
Cusack, Stephen ;
Alley, M. R. K. .
SCIENCE, 2007, 316 (5832) :1759-1761
[90]   The challenge of antimicrobial resistance: What economics can contribute [J].
Roope, Laurence S. J. ;
Smith, Richard D. ;
Pouwels, Koen B. ;
Buchanan, James ;
Abel, Lucy ;
Eibich, Peter ;
Butler, Christopher C. ;
Tan, Pui San ;
Walker, A. Sarah ;
Robotham, Julie V. ;
Wordsworth, Sarah .
SCIENCE, 2019, 364 (6435) :41-+