National Multicenter Study on the Prevalence of Carbapenemase-Producing Enterobacteriaceae in the Post-COVID-19 Era in Argentina: The RECAPT-AR Study.

IF 4.3 2区 医学 Q1 INFECTIOUS DISEASES Antibiotics-Basel Pub Date : 2024-11-27 DOI:10.3390/antibiotics13121139
Mariano Echegorry, Paulina Marchetti, Cristian Sanchez, Laura Olivieri, Diego Faccone, Florencia Martino, Tomas Sarkis Badola, Paola Ceriana, Melina Rapoport, Celeste Lucero, Ezequiel Albornoz, Recapt-Ar Group, Alejandra Corso, Fernando Pasteran
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Abstract

The COVID-19 pandemic has exacerbated the global antimicrobial resistance (AMR) crisis. Consequently, it is more urgent than ever to prioritize AMR containment and support countries in improving the detection, characterization, and rapid response to emerging AMR threats. We conducted a prospective, multicenter study to assess the prevalence of carbapenemase-producing Enterobacterales in infectious processes in Argentina during the post-COVID-19 pandemic period and explore therapeutic alternatives for their treatment (RECAPT-AR study).

Methods: A total of 182 hospitals participated by submitting Enterobacterales clinical isolates to the National Reference Laboratory (NRL) during the first three weeks of November 2021. Inclusion criteria were defined as an ertapenem MIC ≥ 0.5 mg/L, a zone diameter ≤ 22 mm. Carbapenemase genes and those coding for major extended-spectrum β-lactamases were molecularly characterized using multiplex PCR at the NRL. Antibiotic susceptibility testing followed international standards (CLSI and EUCAST).

Results: The NRL analyzed 821 Enterobacterales isolates. Metallo-β-lactamase (MBL, 42.0%) and KPC (39.8%) accounted for 81.8% of carbapenemases, followed by OXA-163 (7.4%), a variant of OXA-48 with additional activity against extended-spectrum cephalosporins, and enzyme combinations (8.3%). These combinations included NDM plus KPC (3.4%), OXA-163 plus KPC (2.4%), and OXA-163 plus NDM (2.1%). Klebsiella pneumoniae was the main species recovered, representing 76% of the isolates. According to the carbapenemase classes or combinations, tigecycline exhibited a susceptibility range of 33-83%, fosfomycin 59-81%, colistin 27-78%, and amikacin 17-81%. Ceftazidime-avibactam (CZA) and imipenem-relebactam (IMR) showed 92% and 98% susceptibility against serine carbapenemases, respectively. Meanwhile, aztreonam-avibactam (AZA) exhibited 96-98% susceptibility against all carbapenemase classes.

Conclusions: A new epidemiological landscape has emerged, characterized by the equivalent circulation of NDM and KPC. K. pneumoniae remains the primary species responsible for their dissemination. The co-production of carbapenemase combinations, particularly KPC plus NDM, was confirmed, mainly in K. pneumoniae. High activity was observed for AZA against MBLs and for CZA and IMR against KPC and OXA-163 carbapenemases.

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阿根廷后covid -19时代产碳青霉烯酶肠杆菌科流行的国家多中心研究:RECAPT-AR研究
2019冠状病毒病大流行加剧了全球抗微生物药物耐药性(AMR)危机。因此,比以往任何时候都更迫切需要优先考虑遏制抗菌素耐药性,并支持各国改进对新出现的抗菌素耐药性威胁的检测、定性和快速反应。我们开展了一项前瞻性、多中心研究,以评估2019冠状病毒病大流行后阿根廷感染过程中产碳青霉烯酶肠杆菌的流行情况,并探索其治疗方案(RECAPT-AR研究)。方法:共有182家医院于2021年11月前三周向国家参考实验室(NRL)提交肠杆菌临床分离株。纳入标准定义为厄他培南MIC≥0.5 mg/L,带直径≤22 mm。碳青霉烯酶基因和主要扩展谱β-内酰胺酶编码基因在NRL采用多重PCR进行了分子表征。药敏试验按国际标准(CLSI和EUCAST)进行。结果:NRL共分离出821株肠杆菌。金属β-内酰胺酶(MBL, 42.0%)和KPC(39.8%)占碳青霉烯酶的81.8%,其次是OXA-163 (7.4%), OXA-48的一个变体,对广谱头孢菌素具有额外的活性,以及酶组合(8.3%)。这些组合包括NDM + KPC(3.4%)、OXA-163 + KPC(2.4%)和OXA-163 + NDM(2.1%)。肺炎克雷伯菌是回收的主要菌种,占分离株的76%。根据碳青霉烯酶的类别或组合,替加环素的敏感性范围为33-83%,磷霉素为59-81%,粘菌素为27-78%,阿米卡星为17-81%。头孢他啶-阿维巴坦(CZA)和亚胺培南-勒巴坦(IMR)对丝氨酸碳青霉烯酶的敏感性分别为92%和98%。aztreonam-avibactam (AZA)对碳青霉烯酶的敏感性为96% ~ 98%。结论:一种新的流行病学格局已经出现,其特征是NDM和KPC的等效循环。肺炎克雷伯菌仍然是导致其传播的主要物种。碳青霉烯酶组合,特别是KPC加NDM,主要在肺炎克雷伯菌中被证实共同产生。观察到AZA对MBLs的高活性,CZA和IMR对KPC和OXA-163碳青霉烯酶的高活性。
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来源期刊
Antibiotics-Basel
Antibiotics-Basel Pharmacology, Toxicology and Pharmaceutics-General Pharmacology, Toxicology and Pharmaceutics
CiteScore
7.30
自引率
14.60%
发文量
1547
审稿时长
11 weeks
期刊介绍: Antibiotics (ISSN 2079-6382) is an open access, peer reviewed journal on all aspects of antibiotics. Antibiotics is a multi-disciplinary journal encompassing the general fields of biochemistry, chemistry, genetics, microbiology and pharmacology. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers.
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