Whole-organism phenotypic screening for anti-infectives promoting host health

被引:16
作者
Clatworthy, Anne E. [1 ,2 ,3 ,4 ]
Romano, Keith P. [2 ,3 ,5 ]
Hung, Deborah T. [1 ,2 ,3 ,4 ]
机构
[1] Broad Inst MIT & Harvard, Cambridge, MA 02142 USA
[2] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02114 USA
[4] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Div Pulm & Crit Care Med, 75 Francis St, Boston, MA 02115 USA
关键词
PSEUDOMONAS-AERUGINOSA INFECTION; DROSOPHILA-MELANOGASTER; MODEL HOST; CAENORHABDITIS-ELEGANS; GENOMIC RESPONSES; ZEBRAFISH EMBRYOS; DRUG DISCOVERY; ANIMAL-MODELS; IDENTIFICATION; BACTERIAL;
D O I
10.1038/s41589-018-0018-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To date, antibiotics have been identified on the basis of their ability to kill bacteria or inhibit their growth rather than directly for their capacity to improve clinical outcomes of infected patients. Although historically successful, this approach has led to the development of an antibiotic armamentarium that suffers from a number of shortcomings, including the inevitable emergence of resistance and, in certain infections, suboptimal efficacy leading to long treatment durations, infection recurrence, or high mortality and morbidity rates despite apparent bacterial sterilization. Conventional antibiotics fail to address the complexities of in vivo bacterial physiology and virulence, as well as the role of the host underlying the complex, dynamic interactions that cause disease. New interventions are needed, aimed at host outcome rather than microbiological cure. Here we review the role of screening models for cellular and whole-organism infection, including worms, flies, zebrafish, and mice, to identify novel therapeutic strategies and discuss their future implications.
引用
收藏
页码:331 / 341
页数:11
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