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首页> 外文期刊>Folia Microbiologica >Fatty acid analysis ofStenotrophomonas maltophilia clinical strains showing different susceptibility to antibiotics at 30 and 37°C
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Fatty acid analysis ofStenotrophomonas maltophilia clinical strains showing different susceptibility to antibiotics at 30 and 37°C

机译:嗜麦芽窄食单胞菌临床菌株的脂肪酸分析显示在30和37°C下对抗生素的敏感性不同

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摘要

Isolates ofStenotrophomonas maltophilia species display the feature “temperature-dependent susceptibility” (TDS) to antibiotics. Both 30TDS strains (at least 4 times lower value of minimum inhibitory concentration (MIC) of an antibiotic at 30 than at 37°C) and 37TDS strains (at least 4 times lower value of MIC at 37 than at 30°C) were described. Changes in the distribution of saturated and unsaturated fatty acids (FA) at 30 and 37°C were considered as one of possible causes of the TDS phenomenon. Gas chromatography was used to determine the distribution of individual FA in five 37TDS strains ofS. maltophilia (Group I); in five strains with MIC values unaffected by the cultivation temperature (Group II) and in six 30TDS (four strains) or 30/37TDS (two strains) isolates (Group III). At identical temperatures, no statistically significant differences in the distribution of major FA (iso-15:0,anteiso-15:0, 16:0 and 16:1) were registered between individual groups. Statistically significant (p<0.05) differences between groups were found in minor FA only (iso-16:0,iso-17:0 andiso-17:1). Distribution changes of cellular FA at 30 and 37°C can be considered to play only a minor role in the formation of the TDS phenomenon.
机译:嗜麦芽窄食单胞菌物种的分离物表现出对抗生素的“温度依赖性敏感性”(TDS)特征。描述了30TDS菌株(在30℃时,抗生素的最小抑菌浓度(MIC)的最低值至少比在37°C时低4倍)和37TDS菌株(在37时的MIC值在30°C时,至少低4倍)。 。 30和37°C下饱和和不饱和脂肪酸(FA)的分布变化被认为是TDS现象的可能原因之一。气相色谱法用于确定5种37TDS S菌株中单个FA的分布。嗜麦芽症(第一组);五个MIC值不受培养温度影响的菌株(第二组)和六个30TDS(四个菌株)或30 / 37TDS(两个菌株)分离株(第三组)。在相同的温度下,各组之间的主要脂肪酸分布(iso-15:0,anteiso-15:0、16:0和16:1)在统计学上没有显着差异。仅在较小的FA(iso-16:0,iso-17:0和iso-17:1)中发现了两组之间的统计学差异(p <0.05)。可以认为细胞FA在30和37°C的分布变化在TDS现象的形成中仅起很小的作用。

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  • 来源
    《Folia Microbiologica》 |2002年第6期|742-746|共5页
  • 作者

    P. Hejnar; Z. Chmela; M. Rypka;

  • 作者单位

    Institute of Microbiology Faculty of Medicine Palacký University;

    Institute of Pathological Physiology Faculty of Medicine Palacký University;

    Institute of Pathological Physiology Faculty of Medicine Palacký University;

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  • 正文语种 eng
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