The macrolide-resistance of multiple-drug resistant strains of Staphylococcus aureus was divided into two types; the decreased sensitivity of ribosomes (type 1) and the decreased uptake (type II). Both types were resistant to erythromycin, tylosin and 3-acetyltylosin, and their resistance was not inducible. 3-Acetyl-4-isovaleryltylosin inhibited the growth of both types. Protein synthesis on ribosomes of type 1 in vitro (S. aureus MS-9610) was inhibited by 3-acetyl-4”-isovaleryltylosin, but little or no inhibition was seen with either tylosin or 3-acetyltylosin. Ribosomes of type II in vitro (S. aureus MS-8710) were sensitive to all macrolides. 3-Acetyl-4“-isovaleryltylosin accumulated about twice as much as 3-acetyltylosin in intact cells of type II. © 1981, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Tsuchiya, M., Suzukake, K., Hori, M., Sawa, T., Takeuchi, T., Umezawa, H., … Inui, T. (1981). Studies on the effects of 3-acetyl-4“-isovaleryltylosin against multiple-drug resistant strains of staphylococcus aureus. Journal of Antibiotics, 34(3), 305–312. https://doi.org/10.7164/antibiotics.34.305
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