Minimum inhibitory concentrations of aztreonam–avibactam, ceftazidime–avibactam and meropenem in clinical isolates of Klebsiella pneumoniae harboring carbapenemase genes

IF 2.1 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Antibiotics Pub Date : 2024-07-01 DOI:10.1038/s41429-024-00758-8
Vladimir Ageevets, Ofelia Sulian, Alisa Avdeeva, Polina Chulkova, Irina Ageevets, Vladimir Gostev, Kamilla Alieva, Maria Golikova, Sergey Sidorenko
{"title":"Minimum inhibitory concentrations of aztreonam–avibactam, ceftazidime–avibactam and meropenem in clinical isolates of Klebsiella pneumoniae harboring carbapenemase genes","authors":"Vladimir Ageevets, Ofelia Sulian, Alisa Avdeeva, Polina Chulkova, Irina Ageevets, Vladimir Gostev, Kamilla Alieva, Maria Golikova, Sergey Sidorenko","doi":"10.1038/s41429-024-00758-8","DOIUrl":null,"url":null,"abstract":"This study was aimed at understanding the distributions of the MICs (minimum inhibitory concentrations) of aztreonam–avibactam, ceftazidime–avibactam and meropenem with respect to Klebsiella pneumoniae isolates producing different types of carbapenemases and their combinations. K. pneumoniae isolates were collected between 2019 and 2022 from 37 hospitals. PCR was used to screen for blaKPC-, blaNDM- and blaOXA-48-like genes. MICs were determined by the broth microdilution method for meropenem, aztreonam–avibactam and ceftazidime–avibactam at a constant avibactam concentration of 4 mg l−1. MIC distributions were analyzed for groups of isolates based on the identified carbapenemases including their combinations. The AZT/AVI MIC50 and MIC90 for all NDM-positive isolates were 0.25 and 0.5, respectively, and for serine-carbapenemase-only producers, they were 0.25 and 1 mg l−1, respectively. The CZD/AVI MIC50 and MIC90 values for serine-carbapenemase-only producers were 1 and 4 mg l−1, respectively. The AZT/AVI MIC50 and MIC90 values for co-producers and single carbapenemase producers were the same (i.e., 0.25 and 1 mg l−1, respectively). The total proportion of meropenem-susceptible isolates (≤8 mg l−1) among all the carbapenemase producers was 25.1% (31.1% among single-carbapenemase producers and 9.2% among co-producers). The results support the use of aztreonam–avibactam for the empirical treatment of infections caused by any carbapenemase producers.","PeriodicalId":54884,"journal":{"name":"Journal of Antibiotics","volume":"77 10","pages":"706-710"},"PeriodicalIF":2.1000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Antibiotics","FirstCategoryId":"3","ListUrlMain":"https://www.nature.com/articles/s41429-024-00758-8","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This study was aimed at understanding the distributions of the MICs (minimum inhibitory concentrations) of aztreonam–avibactam, ceftazidime–avibactam and meropenem with respect to Klebsiella pneumoniae isolates producing different types of carbapenemases and their combinations. K. pneumoniae isolates were collected between 2019 and 2022 from 37 hospitals. PCR was used to screen for blaKPC-, blaNDM- and blaOXA-48-like genes. MICs were determined by the broth microdilution method for meropenem, aztreonam–avibactam and ceftazidime–avibactam at a constant avibactam concentration of 4 mg l−1. MIC distributions were analyzed for groups of isolates based on the identified carbapenemases including their combinations. The AZT/AVI MIC50 and MIC90 for all NDM-positive isolates were 0.25 and 0.5, respectively, and for serine-carbapenemase-only producers, they were 0.25 and 1 mg l−1, respectively. The CZD/AVI MIC50 and MIC90 values for serine-carbapenemase-only producers were 1 and 4 mg l−1, respectively. The AZT/AVI MIC50 and MIC90 values for co-producers and single carbapenemase producers were the same (i.e., 0.25 and 1 mg l−1, respectively). The total proportion of meropenem-susceptible isolates (≤8 mg l−1) among all the carbapenemase producers was 25.1% (31.1% among single-carbapenemase producers and 9.2% among co-producers). The results support the use of aztreonam–avibactam for the empirical treatment of infections caused by any carbapenemase producers.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
携带碳青霉烯酶基因的肺炎克雷伯菌临床分离物中阿曲南类-阿维菌素、头孢唑肟类-阿维菌素和美罗培南的最小抑菌浓度。
本研究旨在了解产生不同类型碳青霉烯酶的肺炎克雷伯菌分离株与阿曲南-阿维菌素、头孢唑肟-阿维菌素和美罗培南及其组合的MICs(最低抑菌浓度)的分布情况。肺炎克雷伯菌分离株是在 2019 年至 2022 年期间从 37 家医院采集的。利用 PCR 筛选 blaKPC、blaNDM 和 blaOXA-48 类基因。在阿维菌素浓度为 4 毫克/升的恒定条件下,采用肉汤微量稀释法测定美罗培南、阿曲南-阿维菌素和头孢唑肟-阿维菌素的 MIC。根据已确定的碳青霉烯酶(包括其组合)分析了各组分离菌的 MIC 分布。所有 NDM 阳性分离菌株的 AZT/AVI MIC50 和 MIC90 分别为 0.25 和 0.5,仅产生丝氨酸碳青霉烯酶的分离菌株的 MIC50 和 MIC90 分别为 0.25 和 1 mg l-1。仅产生丝氨酸碳青霉烯酶的菌株的 CZD/AVI MIC50 和 MIC90 值分别为 1 和 4 毫克升-1。共同生产者和单一碳青霉烯酶生产者的 AZT/AVI MIC50 和 MIC90 值相同(即分别为 0.25 和 1 毫克升-1)。在所有碳青霉烯酶生产者中,对美罗培南敏感的分离物(≤8 毫克升-1)的总比例为 25.1%(单碳青霉烯酶生产者为 31.1%,联合生产者为 9.2%)。研究结果支持将阿曲南胺-阿维巴坦用于任何碳青霉烯酶生产者引起的感染的经验性治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Antibiotics
Journal of Antibiotics 医学-免疫学
CiteScore
6.60
自引率
3.00%
发文量
87
审稿时长
1 months
期刊介绍: The Journal of Antibiotics seeks to promote research on antibiotics and related types of biologically active substances and publishes Articles, Review Articles, Brief Communication, Correspondence and other specially commissioned reports. The Journal of Antibiotics accepts papers on biochemical, chemical, microbiological and pharmacological studies. However, studies regarding human therapy do not fall under the journal’s scope. Contributions regarding recently discovered antibiotics and biologically active microbial products are particularly encouraged. Topics of particular interest within the journal''s scope include, but are not limited to, those listed below: Discovery of new antibiotics and related types of biologically active substances Production, isolation, characterization, structural elucidation, chemical synthesis and derivatization, biological activities, mechanisms of action, and structure-activity relationships of antibiotics and related types of biologically active substances Biosynthesis, bioconversion, taxonomy and genetic studies on producing microorganisms, as well as improvement of production of antibiotics and related types of biologically active substances Novel physical, chemical, biochemical, microbiological or pharmacological methods for detection, assay, determination, structural elucidation and evaluation of antibiotics and related types of biologically active substances Newly found properties, mechanisms of action and resistance-development of antibiotics and related types of biologically active substances.
期刊最新文献
The secondary metabolites of the alga-derived fungus Aspergillus niveoglaucus КММ 4176 and their antimicrobial and antibiofilm activities. Blue benzoquinone from scorpion venom shows bactericidal activity against drug-resistant strains of the priority pathogen Acinetobacter baumannii. Streptomyces tabacisoli sp. nov, isolated from the rhizosphere soil of Nicotiana tabacum. Evaluation of tirandamycins with selective activity against Enterococci in the silkworm infection model. KRN7000 analogues as biofilm disrupting agents against Streptococcus pyogenes and Proteus mirabilis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1