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沙门氏菌亚种伤寒血清型 Typhi 菌株在二十年期间的耐药模式,特别针对环丙沙星和头孢曲松。

Drug resistance patterns in Salmonella enterica subspecies enterica serotype Typhi strains isolated over a period of two decades, with special reference to ciprofloxacin and ceftriaxone.

机构信息

Department of Microbiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, India.

出版信息

Int J Antimicrob Agents. 2010 May;35(5):482-5. doi: 10.1016/j.ijantimicag.2009.12.020. Epub 2010 Feb 25.

Abstract

Fluoroquinolone-resistant Salmonella enterica subspecies enterica serotype Typhi are being increasingly reported from the Asian subcontinent. This has been hypothesised to be due to a double mutation in the gyrA gene. A total of 113 S. Typhi strains isolated during 1987-2006 in a tertiary-level hospital of North India were monitored for their antibiotic susceptibility by the disk diffusion and minimum inhibitory concentration (MIC) methods. The study period was arbitrarily divided into four equal parts, each comprising 5 years. The antibiotics tested showed an extremely wide range of MICs during all four periods except for ceftriaxone, which showed no resistance during the study period. However, a gradual increase in the MIC of this drug was observed, i.e. 0.047 mg/L, 0.098 mg/L, 0.211 mg/L and 0.3652 mg/L during the four study periods. Ninety-one percent of the strains isolated in the final study period were observed to have MIC levels > or = 0.125 mg/L to ciprofloxacin. Furthermore, gyrA restriction analysis showed no mutation at the two reported sites of the gene, suggesting that the double mutation theory in the development of ciprofloxacin resistance may not be the only mechanism responsible for fluoroquinolone resistance.

摘要

从亚洲次大陆不断有氟喹诺酮耐药伤寒沙门氏菌亚种血清型 Typhi 的报告。这被假设是由于 gyrA 基因的双重突变。在印度北部的一家三级医院,对 1987-2006 年间分离的 113 株伤寒沙门氏菌 Typhi 菌株进行了抗生素敏感性监测,采用纸片扩散法和最低抑菌浓度(MIC)法。研究期间被任意分为四个相等的部分,每个部分包括 5 年。除头孢曲松外,所有四个时期测试的抗生素均显示出极其广泛的 MIC,头孢曲松在研究期间未显示出耐药性。然而,观察到该药物的 MIC 逐渐增加,即在四个研究期间分别为 0.047mg/L、0.098mg/L、0.211mg/L 和 0.3652mg/L。在最后一个研究期间分离的 91%的菌株对环丙沙星的 MIC 水平≥0.125mg/L。此外,gyrA 限制分析显示该基因的两个报告位点没有突变,这表明氟喹诺酮耐药性发展中的双重突变理论可能不是导致氟喹诺酮耐药的唯一机制。

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