Infectious Diseases Unit, 3rd Department of Pediatrics, Medical Faculty, School of Health Sciences, Hippokration General Hospital, Konstantinoupoleos 49, GR-546 42, Thessaloniki, Greece.
Microbiology Department, National and Kapodistrian University School of Medicine, Athens, Greece.
Eur J Clin Microbiol Infect Dis. 2018 Jul;37(7):1211-1220. doi: 10.1007/s10096-018-3244-4. Epub 2018 Apr 11.
Carbapenem-resistant Pseudomonas aeruginosa (CRPA) is an endemic problem in certain countries including Greece. CRPA and multidrug-resistant P. aeruginosa (MDRPA) firstly emerged in our region during the 80s, right after the launch of imipenem and meropenem as therapeutic agents against P. aeruginosa infections. The role of outer membrane protein (Opr) inactivation has been known to contribute to imipenem resistance since many years, while efflux overexpression systems have been mainly associated with meropenem resistance. Among carbapenemases, metallo-β-lactamases (MBL) and mostly Verona integron-mediated (VIM) MBL's have played the most crucial role in CRPA emergence. VIM-2 and VIM-4 producing CRPA, usually belonging to clonal complexes (CC) 111 and 235 respectively, have most frequently been isolated. Bla and bla are usually associated with a class 1 integron. VIM-17 also has appeared in Greece. On the other hand, other VIM subtypes detected in a global level, such as VIM-3, VIM-5, VIM-6, VIM-7, VIM-11, VIM-14, VIM-15, VIM-16 and VIM-18 have not yet emerged in Greece. However, new VIM subtypes will probably emerge in the future. In addition, MBL carbapenemases other than VIM, detected worldwide have not yet appeared. A single CRPA isolate producing KPC has emerged in our region several years ago. The study of the molecular basis of Opr deficiency and efflux overexpression remains a challenge for the future. In this article, we review the molecular epidemiology of CRPA in an endemic area, compared to global data.
耐碳青霉烯铜绿假单胞菌(CRPA)是包括希腊在内的某些国家的地方病问题。80 年代,当碳青霉烯类药物(如亚胺培南和美罗培南)被用于治疗铜绿假单胞菌感染时,CRPA 和多药耐药铜绿假单胞菌(MDRPA)首次在本地区出现。多年来,人们已经知道外膜蛋白(Opr)失活有助于亚胺培南耐药,而外排泵过表达系统主要与美罗培南耐药相关。在碳青霉烯酶中,金属β-内酰胺酶(MBL)和主要由 Verona 整合子介导(VIM)MBL 对 CRPA 的出现起了最重要的作用。产生 CRPA 的 VIM-2 和 VIM-4 通常分别属于克隆群(CC)111 和 235,是最常分离到的。bla 和 bla 通常与 1 类整合子有关。VIM-17 也已在希腊出现。另一方面,在全球范围内检测到的其他 VIM 亚型,如 VIM-3、VIM-5、VIM-6、VIM-7、VIM-11、VIM-14、VIM-15、VIM-16 和 VIM-18,尚未在希腊出现。然而,未来可能会出现新的 VIM 亚型。此外,尚未在全球范围内发现除 VIM 以外的其他 MBL 碳青霉烯酶。几年前,我们地区出现了一株单独的产 KPC 的 CRPA 分离株。Opr 缺乏和外排泵过表达的分子基础研究仍是未来的挑战。本文综述了地方病地区耐碳青霉烯铜绿假单胞菌的分子流行病学,并与全球数据进行了比较。