Spectral Snapshots of Bacterial Cell-Wall Composition and the Influence of Antibiotics by Whole-Cell NMR

被引:36
|
作者
Nygaard, Rie [1 ]
Romaniuk, Joseph A. H. [1 ]
Rice, David M. [1 ]
Cegelski, Lynette [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
DOUBLE-RESONANCE CHARACTERIZATION; STAPHYLOCOCCUS-AUREUS STRAIN; IN-VIVO C-13; PEPTIDOGLYCAN; VANCOMYCIN; BINDING; MECHANISM; CHLORAMPHENICOL; BIOSYNTHESIS; RESISTANCE;
D O I
10.1016/j.bpj.2015.01.037
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Gram-positive bacteria surround themselves with a thick cell wall that is essential to cell survival and is a major target of antibiotics. Quantifying alterations in cell-wall composition are crucial to evaluating drug modes of action, particularly important for human pathogens that are now resistant to multiple antibiotics such as Staphylococcus aureus. Macromolecular and whole-cell NMR spectroscopy allowed us to observe the full panel of carbon and nitrogen pools in Staphylococcus aureus cell walls and intact whole cells. We discovered that one-dimensional C-13 and N-15 NMR spectra, together with spectroscopic selections based on dipolar couplings as well as two-dimensional spin-diffusion measurements, revealed the dramatic compositional differences between intact cells and cell walls and allowed the identification of cell-wall signatures in whole-cell samples. Furthermore, the whole-cell NMR approach exhibited the sensitivity to detect distinct compositional changes due to treatment with the antibiotics fosfomycin (a cell-wall biosynthesis inhibitor) and chloramphenicol (a protein synthesis inhibitor). Whole cells treated with fosfomycin exhibited decreased peptidoglycan contributions while those treated with chloramphenicol contained a higher percentage of peptidoglycan as cytoplasmic protein content was reduced. Thus, general antibiotic modes of action can be identified by profiling the total carbon pools in intact whole cells.
引用
收藏
页码:1380 / 1389
页数:10
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