Transcriptomic Profiling Suggests That Promysalin Alters the Metabolic Flux, Motility, and Iron Regulation in Pseudomonas putida KT2440

被引:8
作者
Giglio, Krista M. [1 ]
Keohane, Colleen E. [2 ]
Stodghill, Paul, V [1 ]
Steele, Andrew D. [2 ]
Fetzer, Christian [3 ]
Sieber, Stephan A. [3 ]
Filiatrault, Melanie J. [1 ,4 ]
Wuest, William M. [2 ,5 ]
机构
[1] ARS, Emerging Pests & Pathogens Res, USDA, 538 Tower Rd, Ithaca, NY 14853 USA
[2] Emory Univ, Dept Chem, 1515 Dickey Dr, Atlanta, GA 30322 USA
[3] Tech Univ Munich, CIPSM, Dept Chem, Lichtenbergstr 4, D-85747 Garching, Germany
[4] Cornell Univ, Plant Pathol & Plant Microbe Biol Sect, Sch Integrat Plant Sci, 236 Tower Rd, Ithaca, NY 14853 USA
[5] Emory Univ, Emory Antibiot Resistance Ctr, 201 Dowman Dr, Atlanta, GA 30322 USA
基金
美国国家科学基金会;
关键词
Pseudomonas putida; RNA-Seq; promysalin; surface motility; iron; metabolism; TRANSPORT; GENES; PATHWAYS; SYSTEM;
D O I
10.1021/acsinfecdis.8b00041
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Promysalin, a secondary metabolite produced by P. putida RW10S1, is a narrow-spectrum antibiotic that targets P. aeruginosa over other Pseudomonas spp. P. putida KT2440, a nonproducing strain, displays increased swarming motility and decreased pyoverdine production in the presence of exogenous promysalin. Herein, proteomic and transcriptomic experiments were used to provide insight about how promysalin elicits responses in PPKT2440 and rationalize its species selectivity. RNA-sequencing results suggest that promysalin affects PPKT2440 by (1) increasing swarming in a flagella-independent manner; (2) causing cells to behave as if they were experiencing an iron-deficient environment, and (3) shifting metabolism away from glucose conversion to pyruvate via the EntnerDoudoroff pathway. These findings highlight natures ability to develop small molecules with specific targets, resulting in exquisite selectivity.
引用
收藏
页码:1179 / +
页数:17
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