Linezolid is a specific inhibitor of 50S ribosomal subunit formation in Staphylococcus aureus cells

被引:29
作者
Champney, WS [1 ]
Miller, M [1 ]
机构
[1] E Tennessee State Univ, James H Quillen Coll Med, Dept Biochem & Mol Biol, Johnson City, TN 37614 USA
关键词
D O I
10.1007/s00284-001-0023-7
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Linezolid is an oxazolidinone compound that has been shown to have impressive antimicrobial activity against a number of Grain-positive bacteria. It inhibits an initiation step of protein synthesis, and its binding site has been shown to be on the 50S ribosomal subunit. Linezolid was tested to see whether would interfere with the formation of the 50S subunit in Staphylococcus aureus cells, since a number of other 50S-specific antibiotics have this second inhibitory function. Linezolid inhibited protein synthesis in S. aureus cells with an IC50 of 0.3 mug/ml. A concentration-dependent decline in cell number with an increase in generation time was found. Pulse-chase labeling studies revealed a specific inhibitory effect on 50S particle formation, with no effect on 30S subunit assembly. The compound inhibited 50S synthesis with an IC50 of 0.6 mug/ml, indicating an equivalent effect on translation and particle assembly. A postantibiotic effect of 1 h was found when cells were initially treated with the drug at 2 mug/ml. 50S particle numbers recovered more rapidly than translational capacity, consistent with the increase in viable cell numbers. The inhibitory activities of this novel antimicrobial agent in cells are discussed.
引用
收藏
页码:350 / 356
页数:7
相关论文
共 37 条
[1]  
AMABILECUEVAS CF, 1995, AM SCI, V83, P320
[2]   Gram-positive resistance: challenge for the development of new antibiotics [J].
Baquero, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 39 :1-6
[3]   Ketolides lack inducibility properties of MLSB resistance phenotype [J].
Bonnefoy, A ;
Girard, AM ;
Agouridas, C ;
Chantot, JF .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1997, 40 (01) :85-90
[4]  
Bryskier A, 1997, INFEC DIS T, V21, P39
[5]  
Champney W. S., 2001, Current Drug Targets - Infectious Disorders, V1, P19, DOI 10.2174/1568005013343281
[6]   A comparison of the inhibition of translation and 50S ribosomal subunit formation in Staphylococcus aureus cells by nine different macrolide antibiotics [J].
Champney, WS ;
Tober, CL ;
Burdine, R .
CURRENT MICROBIOLOGY, 1998, 37 (06) :412-417
[7]   Inhibition of translation and 50S ribosomal subunit formation in Staphylococcus aureus cells by 11 different ketolide antibiotics [J].
Champney, WS ;
Tober, CL .
CURRENT MICROBIOLOGY, 1998, 37 (06) :418-425
[8]   50S ribosomal subunit synthesis and translation are equivalent targets for erythromycin inhibition in Staphylococcus aureus [J].
Champney, WS ;
Burdine, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1301-1303
[9]   Azithromycin and clarithromycin inhibition of 50S ribosomal subunit formation in Staphylococcus aureus cells [J].
Champney, WS ;
Burdine, R .
CURRENT MICROBIOLOGY, 1998, 36 (02) :119-123
[10]   Specific inhibition of 50S ribosomal subunit formation in Staphylococcus aureus cells by 16-membered macrolide, lincosamide, and streptogramin B antibiotics [J].
Champney, WS ;
Tober, CL .
CURRENT MICROBIOLOGY, 2000, 41 (02) :126-135