亚胺培南/西司他汀/瑞巴坦成功治疗1例日本患者由产kpc -2的高致病性肺炎克雷伯菌序列11型引起的腹内脓肿

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES
Kazuhiro Ishikawa , Koko Shibutani , Yumiko Mikami , Sohei Harada , Kohji Komori , Nobuyoshi Mori
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引用次数: 0

摘要

产kpc的肺炎克雷伯菌在日本很少见。在中国,产kpc -2序列型(ST)11肺炎克雷伯菌分离株迅速增加,其中一部分分离株具有高毒力。我们报告一例39岁的日本男性谁发展菌血症和腹腔脓肿引起的高毒力碳青霉烯耐药肺炎克雷伯菌。该患者在新疆维吾尔自治区发生交通事故后腹部受伤,在转至我院前接受了腹部手术。进行脓肿引流,患者最初使用美罗培南(每8小时2 g,延长输注超过3小时)、庆大霉素(5 mg/kg/天)和替加环素(200 mg作为负荷,随后每12小时100 mg)。采用NG- test®CARBA 5 (NG Biotech, France)检测KPC碳青霉烯酶,亚胺培南/西司他汀/瑞巴坦最低抑菌浓度为1 μg/mL,提示药敏。改用亚胺培南/西司他汀/瑞巴坦(每6小时1 g)治疗7周,临床好转。全基因组测序结果显示,病原菌为产kpc -2的高毒力肺炎克雷勃菌(荚膜型K64, ST 11),携带blaKPC-2和blaCTX-M-65,其多复制子质粒(pMTY24772_IncFII-R)是IncFII和IncR的融合体。此外,检测到与高毒力相关的rmpA和iucABCD基因。该菌株携带的抗性质粒和毒力质粒与中国报道的产kpc的ST11-K64菌株携带的毒力质粒相似。亚胺培南/西司他汀/瑞巴坦是治疗由产kpc -2的高毒性K型肺炎引起的感染的潜在选择。必须密切监测多重耐药和高毒性病原体的跨界传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful treatment of an intra-abdominal abscess caused by KPC-2-producing hypervirulent Klebsiella pneumoniae sequence type 11 with imipenem/cilastatin/relebactam in a Japanese patient
KPC-producing K. pneumoniae is rare in Japan. In China, KPC-2-producing sequence type (ST)11 K. pneumoniae isolates have been rapidly increasing, and a subset of these isolates have acquired hypervirulence. We report a case of a 39-year-old Japanese male who developed bacteremia and intra-abdominal abscesses caused by hypervirulent carbapenem-resistant K. pneumoniae. The patient sustained abdominal injuries following a traffic accident in Xinjiang Uygur Autonomous Region and underwent abdominal surgery before being transferred to our hospital. Abscess drainage was performed, and he was initially treated with meropenem (2 g every 8 hours, prolonged infusion over 3 hours), gentamicin (5 mg/kg/day), and tigecycline (200 mg as a loading, followed by 100 mg every 12 hours). KPC carbapenemase was detected using the NG-Test® CARBA 5 (NG Biotech, France), and the minimum inhibitory concentration for imipenem/cilastatin/relebactam was 1 μg/mL, indicating susceptibility. His treatment was switched to imipenem/cilastatin/relebactam (1 g every 6 hours) for 7 weeks, resulting in clinical improvement. Whole-genome sequencing analysis revealed that the causative strain was hypervirulent KPC-2-producing K. pneumoniae (capsular type K64, ST 11) carrying blaKPC-2 and blaCTX-M-65 on a multireplicon plasmid (pMTY24772_IncFII-R), which was a fusion of IncFII and IncR. Additionally, rmpA and iucABCD genes associated with hypervirulence were detected. The strain carried a resistance plasmid and a virulence plasmid similar to those carried by ST11-K64 KPC-producing strains reported from China. Imipenem/cilastatin/relebactam is potentially an option for treating infections caused by KPC-2-producing hypervirulent K, pneumoniae with porin mutations. Cross-border spread of pathogens that are both multidrug-resistant and hyperviirulent must be closely monitored.
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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