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携带OXA-48样碳青霉烯酶快速传播。

Rapidly spreading with OXA-48-like carbapenemases.

作者信息

Peirano Gisele, Pitout Johann D D

机构信息

Division of Microbiology, Alberta Precision Laboratories, Calgary, Alberta, Canada.

Department of Pathology & Laboratory Medicine, Cummings School of Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

J Clin Microbiol. 2025 Feb 19;63(2):e0151524. doi: 10.1128/jcm.01515-24. Epub 2025 Jan 6.

DOI:10.1128/jcm.01515-24
PMID:39760498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11837536/
Abstract

(mostly , ) with OXA-48-like carbapenemases (e.g., OXA-48, -181, -232, -244) are undermining the global efficiency of carbapenem therapy. In the Middle East, North Africa, and some European countries, OXA-48-like carbapenemases are the most common types of carbapenemases among . Currently, OXA-48 is endemic in the Middle East, North Africa, Spain, France, and Belgium; OXA-181 is endemic in Sub-Saharan Africa and the Indian Subcontinent, while OXA-232 has been increasing in the Indian Subcontinent. European countries (e.g., Germany, Denmark, Switzerland, France) are experiencing community outbreaks with ST38 that produce OXA-244, and these strains have been introduced into Norwegian, Polish, and Czech hospitals. The global ascendancy of OXA-48-like genes is due to the combination of carbapenemases with horizontal spread through promiscuous plasmids (e.g., IncL, IncX3, ColE2) and vertical spread with certain high-risk multidrug-resistant clones (e.g., ST14, ST15, ST147, ST307; ST38, ST410). This is a powerful "gene survival strategy" that has assisted with the survival of OXA-48-like genes in different environments including the community setting. The laboratory diagnosis is complex; therefore, bacteria with "difficult to detect" variants (e.g., OXA-244, OXA-484) are likely underreported and are spreading silently "beneath the radar" in hospital and community settings. and with OXA-48-like carbapenemases are forces to be reckoned with.

摘要

(主要是)携带OXA - 48样碳青霉烯酶(如OXA - 48、- 181、- 232、- 244)正在破坏碳青霉烯类疗法的全球有效性。在中东、北非和一些欧洲国家,OXA - 48样碳青霉烯酶是碳青霉烯酶中最常见的类型。目前,OXA - 48在中东、北非、西班牙、法国和比利时呈地方性流行;OXA - 181在撒哈拉以南非洲和印度次大陆呈地方性流行,而OXA - 232在印度次大陆呈上升趋势。欧洲国家(如德国、丹麦、瑞士、法国)正经历产OXA - 244的ST38社区暴发,并且这些菌株已被引入挪威、波兰和捷克的医院。OXA - 48样基因的全球优势归因于碳青霉烯酶通过混杂质粒(如IncL、IncX3、ColE2)的水平传播以及与某些高风险多重耐药克隆(如ST14、ST15、ST147、ST307;ST38、ST410)的垂直传播。这是一种强大的“基因生存策略”,有助于OXA - 48样基因在包括社区环境在内的不同环境中生存。实验室诊断复杂;因此,携带“难以检测”变体(如OXA - 244、OXA - 484)的细菌可能报告不足,并在医院和社区环境中“在雷达之下”悄然传播。携带OXA - 48样碳青霉烯酶的细菌是不可忽视的力量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/11837536/ad6a57f2cc94/jcm.01515-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/11837536/b82c73b48b94/jcm.01515-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/11837536/ad6a57f2cc94/jcm.01515-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/11837536/b82c73b48b94/jcm.01515-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d74b/11837536/ad6a57f2cc94/jcm.01515-24.f002.jpg

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