头孢唑烷/他唑巴坦及其比较物对革兰氏阴性杆菌的活性:来自抗生素耐药性趋势监测研究的结果(SMART - Brazil), 2018-2021。

IF 3 4区 医学 Q2 INFECTIOUS DISEASES
Amanda Azevedo Bittencourt , Vinicius Lima Faustino , Paula de Mendonça Batista , Lays Paulino Leonel , Marina Della Negra de Paula , Thales José Polis
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引用次数: 0

摘要

革兰氏阴性杆菌(GNB)抗菌素耐药性传播加剧构成全球挑战,大流行后负担加重。本研究的目的是研究头孢唑烷/他唑巴坦及其比较物对2018-2019年和2020-2021年期间巴西医疗机构入院患者中分离的常见GNB的体外活性。还评估了大流行对抗菌素耐药性和β-内酰胺酶基因存在的影响。采用聚合酶链反应(PCR)和DNA测序对主要来自腹腔、呼吸道和尿路感染的GNB进行了抗菌药敏试验和ß-内酰胺酶编码基因的分子鉴定,并按照BrCAST/EUCAST指南进行了解释。共鉴定出3994株GNB,主要包括大肠杆菌、肺炎克雷伯菌和铜绿假单胞菌。Ceftolozane/tazobactam在2018-2019年(96.0%)和2020-2021年(98.5%)对大肠杆菌分离株均保持高活性。在肺炎克雷伯菌中,头孢唑烷/他唑巴坦(2018-2019年和2020-2021年易感率分别为47.6%和43.0%)由于blaKPC-2而表现出较差的活性。粘菌素和头孢氧唑烷/他唑巴坦是2018-2019年和2020-2021年对铜绿假单胞菌(P. aeruginosa)最具活性的β-内酰胺类药物(分别为99.3%和88.8%),包括头孢他啶和美罗培南耐药菌株(分别为100%和92.8%)。对β-内酰胺酶编码基因进行了鉴定,发现大肠杆菌、肺炎克雷伯菌和铜绿假单胞菌中均存在碳青霉烯酶和广谱β-内酰胺酶(ESBL)产生物。头孢唑烷/他唑巴坦在巴西对大肠杆菌和铜绿假单胞菌分离株在大流行前和大流行后都有显著的体外活性,可能成为治疗尿路感染、腹腔感染和呼吸道感染的有效治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activity of ceftolozane/tazobactam and comparators against gram-negative bacilli: Results from the Study for Monitoring Antimicrobial Resistance Trends (SMART – Brazil), 2018‒2021
Increased spread of antimicrobial resistance by Gram-Negative Bacilli (GNB) poses a global challenge, with exacerbated burden post-pandemic. The aim of this study was to investigate the in vitro activity of ceftolozane/tazobactam and its comparators against the frequently identified GNB isolated from patients admitted to Brazilian medical sites between the year 2018‒2019 and 2020‒2021. The impact of pandemic on antimicrobial resistance and presence of β-lactamase genes were also evaluated. Antimicrobial susceptibility testing and molecular characterization of ß-lactamase encoding genes using Polymerase Chain Reaction (PCR) and DNA sequencing were carried out from GNB isolated mostly from intra-abdominal, respiratory, and urinary tract infections and interpreted following BrCAST/EUCAST guidelines. A total of 3994 GNB isolates were evaluated which mostly included E. coli, K. pneumoniae and P. aeruginosa. Ceftolozane/tazobactam remained highly active against E. coli isolates during both 2018‒2019 (96.0 %) and 2020‒2021 (98.5 %). Among K. pneumoniae, ceftolozane/tazobactam (47.6 % and 43.0 % susceptible during 2018‒2019 and 2020‒2021, respectively) showed poor activity due to blaKPC-2. Colistin and ceftolozane/tazobactam were the most active β-lactam agents tested against P. aeruginosa in 2018‒2019 (99.3 % and 88.8 %) and 2020‒2021 (100 % and 92.8 %), including ceftazidime and meropenem resistant isolates. β-lactamase encoding gene characterization was carried out and both carbapenemases and Extended-Spectrum β-Lactamase (ESBL) producers were found in E. coli, K. pneumoniae and P. aeruginosa isolates. Ceftolozane/tazobactam documented remarkable in vitro activity against E. coli and P. aeruginosa isolates in Brazil, both pre- and post-pandemic periods and could constitute an effective therapeutic option for the treatment of urinary tract infections, intra-abdominal infections, and respiratory tract infections.
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来源期刊
CiteScore
5.50
自引率
0.00%
发文量
925
审稿时长
41 days
期刊介绍: The Brazilian Journal of Infectious Diseases is the official publication of the Brazilian Society of Infectious Diseases (SBI). It aims to publish relevant articles in the broadest sense on all aspects of microbiology, infectious diseases and immune response to infectious agents. The BJID is a bimonthly publication and one of the most influential journals in its field in Brazil and Latin America with a high impact factor, since its inception it has garnered a growing share of the publishing market.
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