日本南茨城地区由产碳青霉烯酶肠杆菌引起的菌血症的临床和微生物学特征。

Michie Uchida, Norihiko Terada, Kazuhito Saito, Hiroichi Ishikawa, Yasunori Funayama, Tsuyoshi Oishi, Hiroyuki Shinohara, Tsugio Ebihara, Yoko Kurihara, Shigemi Hitomi
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摘要

尽管近年来产碳青霉烯酶肠杆菌(CPE)的传播已成为全球范围内的一个问题,但日本的 CPE 感染情况尚未完全阐明。在这项研究中,我们考察了2001年7月至2017年6月期间南茨城地区8家医院发生的侵袭性CPE感染的临床和微生物学特征。在从独立菌血症和/或脑膜炎病例中分离出的 7294 株肠杆菌中,有 10 株(0.14%)是 CPE(8 株泄殖腔肠杆菌、1 株大肠埃希菌和 1 株达氏爱德华氏菌),这些菌株均带有 blaIMP-1 基因,对庆大霉素和三甲双胍/磺胺甲噁唑敏感。这些菌株是从 2007 年后的 7 例成人和 2 例婴儿菌血症中分离出来的(其中 1 例婴儿患者两次出现 CPE 菌血症)。最常见的侵入途径是静脉导管。所有成人患者均已康复,而婴儿患者最终死亡。基因组分析表明,8 株泄殖腔大肠杆菌复合菌株可分为 5 组,每组菌株在间隔长达 3 年的时间内只在特定设施中被检测到,这表明这些设施中存在持续的菌落。这项研究表明,该地区的侵袭性CPE感染非常罕见,由对各种抗生素敏感的IMP-1型CPE引起,而且在成年患者中并不致命。
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Clinical and Microbiological Characteristics of Bacteremia Caused by Carbapenemase-producing Enterobacterales in Minami Ibaraki Area, Japan.

Although recent propagation of carbapenemase-producing Enterobacterales (CPE) has become a problem worldwide, the picture of CPE infection in Japan has not fully been elucidated. In this study, we examined clinical and microbiological characteristics of invasive CPE infection occurring at 8 hospitals in Minami Ibaraki Area between July 2001 to June 2017. Of 7294 Enterobacterales strains isolated from independent cases of bacteremia and/or meningitis, 10 (0.14%) were CPE (8 Enterobacter cloacae-complex, 1 Escherichia coli, and 1 Edwardsiella tarda), all of which had the blaIMP-1 gene and susceptible to gentamicin and trimethoprim/sulfamethoxazole. These strains were isolated from 7 adult and 2 infant bacteremia (1 infant patient developed CPE bacteremia twice) after 2007. The most common portal of entry was intravenous catheters. All of the adult patients were recovered, while the infant patients eventually died. Genomic analyses showed that the 8 E. cloacae-complex strains were classified into 5 groups, each of which was exclusively detected in specific facilities at intervals of up to 3 years, suggesting persistent colonization in the facilities. This study showed that invasive CPE infection in the area was rare, caused by IMP-1-type CPE having susceptibility to various antibiotics, and nonfatal among adult patients.

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