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与印度北部一家教学医院常规使用的其他氨基糖苷类药物相比,异帕米星对革兰氏阴性菌的体外活性

In-vitro Activity of Isepamicin against Gram-negative Bacteria in Comparison to Other Aminoglycosides Routinely used at a Teaching Hospital in Northern India.

作者信息

Siddiqui Tasneem, Kar Mitra, Dubey Akanksha, Patel Sangram Singh, Sahu Chinmoy

机构信息

Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.

出版信息

J Lab Physicians. 2023 Mar 22;15(3):419-424. doi: 10.1055/s-0043-1761928. eCollection 2023 Sep.

Abstract

Isepamicin is a 1-N-S-a-hydroxy-b-aminopropionyl derivative of gentamicin B and the spectrum of pathogenic microorganisms covered by it and its effectiveness is similar to that of amikacin except the action of aminoglycoside inhibitor enzymes is ineffectual on it.  We performed a prospective study in the Bacteriology section of the Department of Microbiology at a 1,600-bedded hospital in Northern India from Jan 2022 to March 2022. Isepamicin was tested for susceptibility against gram-negative bacteria, identified by routine biochemicals and matrix-assisted-desorption/ionization -time of flight-mass spectrometry (MALDI-TOF-MS) assay. The antibiotic susceptibility testing for each of the isolates was performed by Kirby Bauer's disc diffusion method, according to the CLSI 2019 guidelines.  The majority of isolates were obtained from blood samples (50, 39.1%). Among the non-inducible , was least susceptible to amikacin (8/27, 29.63%) and most susceptible to isepamicin (18/27, 66.67%). followed the same pattern of susceptibility as and was least susceptible to Amikacin (20/46, 43.48%) and most susceptible to isepamicin (24/46, 52.17%). (6/7, 85.71%) was most susceptible to both amikacin and isepamicin, followed by 71.43% (5/7, 71.43%) susceptibility to gentamicin and tobramycin each. was equally 53.33% (8/15) susceptible to all antibiotics. was the most susceptible isolate to all antibiotics (18/21, 85.71%).  Isepamicin is a potential antimicrobial agent for treating an array of gram-negative bacteria-associated infections and shows better in vitro activity than older aminoglycoside agents.

摘要

异帕米星是庆大霉素B的1-N-S-α-羟基-β-氨基丙酰衍生物,其覆盖的致病微生物谱及其有效性与阿米卡星相似,只是氨基糖苷类抑制剂酶对其不起作用。2022年1月至2022年3月,我们在印度北部一家拥有1600张床位的医院的微生物学系细菌学部门进行了一项前瞻性研究。对异帕米星针对革兰氏阴性菌的敏感性进行了检测,这些细菌通过常规生化方法和基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF-MS)分析进行鉴定。根据CLSI 2019指南,采用 Kirby Bauer 纸片扩散法对每种分离株进行抗生素敏感性测试。大多数分离株来自血液样本(50株,39.1%)。在非诱导型中,对阿米卡星最不敏感(8/27,29.63%),对异帕米星最敏感(18/27,66.67%)。与情况相同,对阿米卡星最不敏感(20/46,43.48%),对异帕米星最敏感(24/46,52.17%)。(6/7,85.71%)对阿米卡星和异帕米星均最敏感,其次对庆大霉素和妥布霉素的敏感性均为71.43%(5/7,71.43%)。对所有抗生素的敏感性均为53.33%(8/15)。是对所有抗生素最敏感的分离株(18/21,85.71%)。异帕米星是一种治疗一系列革兰氏阴性菌相关感染的潜在抗菌剂,并且比旧的氨基糖苷类药物显示出更好的体外活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae64/10411113/b2f057a41c94/10-1055-s-0043-1761928-i2281377-1.jpg

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