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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Flow cytometric investigation of filamentation, membrane patency, and membrane potential in Escherichia coli following ciprofloxacin exposure.
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Flow cytometric investigation of filamentation, membrane patency, and membrane potential in Escherichia coli following ciprofloxacin exposure.

机译:流式细胞仪研究环丙沙星暴露后大肠杆菌中的丝化,膜通透性和膜电位。

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Ninety-eight percent of the cells in a population of Escherichia coli in log-phase growth lost colony-forming ability after being exposed for 3 h to the quinolone antibiotic ciprofloxacin at four times the MIC in nutrient broth, a concentration easily reached in vivo. Flow cytometric analysis, however, demonstrated that only 68% of this bacterial population had lost membrane potential, as judged by the membrane potential-sensitive dye bis-(1,3-dibutylbarbituric acid) trimethine oxonol [DiBAC(4)(3)], and only 30% could no longer exclude the nucleic acid-binding dye propidium iodide (PI), reflecting lost membrane integrity, efflux mechanisms, or both. Subsequent removal of ciprofloxacin and resuspension in nutrient broth resulted in renewed cell division after 2 h, with a calculated postantibiotic effect (PAE) time of 57 min. The proportion of DiBAC- and PI-fluorescent cells in this recovering population remained stable for more than 4 h after antibiotic removal. Eighty percent of cells present at drug removal were filamentous. Their number subsequently decreased with time, and the increase in particle count seen at the end of the PAE resulted from the division of short cells. Exposure to ciprofloxacin in the presence of the protein synthesis inhibitor chloramphenicol increased colony-forming ability to 60% of starting population numbers. In contrast to ciprofloxacin alone, this antibiotic combination resulted in insignificant filamentation and no dye uptake. Subsequent drug removal and resuspension in nutrient broth resulted in the appearance of filaments within 1 h, with 69% of the population forming filaments at 3 h. Dye uptake was also seen, with 20% of the population fluorescing with either dye after 4 h. We were unable to relate dye uptake to the viable count. Cell division resumed 240 min after removal of both drugs, yielding a PAE calculated at 186 min. Inhibition of protein synthesis with chloramphenicol prevented ciprofloxacin-induced changes in bacterial morphology, cell membrane potential, and ability to exclude nucleic acid-binding dye. These changes persisted beyond the end of the classically defined PAE and were not a definite indicator of cell death as defined by loss of colony formation, which related at least in part to filamentation.
机译:在对数生长期的大肠杆菌种群中,有98%的细胞在营养肉汤中MIC的4倍暴露于喹诺酮类抗生素环丙沙星3小时后丧失了集落形成能力,该浓度很容易在体内达到。然而,流式细胞仪分析表明,根据对膜电位敏感的染料双-(1,3-二丁基巴比妥酸)三甲ine肟醇[DiBAC(4)(3)]的判断,该细菌种群中只有68%的膜电位丧失了。 ,只有30%的人无法再排除核酸结合染料碘化丙锭(PI),这反映了丧失的膜完整性和/或流出机理,或两者兼而有之。随后除去环丙沙星并重新悬浮在营养肉汤中,导致2小时后细胞分裂重新开始,计算出的抗生素后作用时间(PAE)为57分钟。去除抗生素后,该恢复群体中DiBAC和PI荧光细胞的比例保持稳定超过4小时。药物去除时存在的细胞中有百分之八十是丝状的。它们的数量随后随时间减少,并且在PAE末端看到的颗粒数增加是由短细胞分裂引起的。在蛋白质合成抑制剂氯霉素的存在下暴露于环丙沙星可将菌落形成能力提高到起始种群数量的60%。与单独的环丙沙星相比,这种抗生素组合导致微不足道的丝状化并且不吸收染料。随后的药物去除和重悬在营养肉汤中导致在1小时内出现细丝,其中69%的人群在3小时内形成细丝。还观察到了染料吸收,在4小时后,有20%的人口用两种染料发出荧光。我们无法将染料吸收与可行数量联系起来。去除两种药物后240分钟,细胞分裂恢复,产生186分钟时的PAE。用氯霉素抑制蛋白质合成可防止环丙沙星诱导的细菌形态,细胞膜电位以及排除核酸结合染料的能力改变。这些变化一直持续到经典定义的PAE结束,并且不是细胞死亡的明确指标,而细胞死亡的定义是菌落形成的丧失,而集落形成的丧失至少部分与丝状化有关。

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