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首页> 外文期刊>American journal of transplantation: official journal of the American Society of Transplantation and the American Society of Transplant Surgeons >Epidemiology and molecular characterization of bacteremia due to carbapenem-resistant klebsiella pneumoniae in transplant recipients
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Epidemiology and molecular characterization of bacteremia due to carbapenem-resistant klebsiella pneumoniae in transplant recipients

机译:耐碳青霉烯类肺炎克雷伯菌引起的菌血症的流行病学和分子特征

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摘要

We conducted a retrospective study of 17 transplant recipients with carbapenem-resistant Klebsiella pneumoniae bacteremia, and described epidemiology, clinical characteristics and strain genotypes. Eighty-eight percent (15/17) of patients were liver or intestinal transplant recipients. Outcomes were death due to septic shock (18%), cure (24%) and persistent (>7 days) or recurrent bacteremia (29% each). Thirty- and 90-day mortality was 18% and 47%, respectively. Patients who were cured received at least one active antimicrobial agent and underwent source control interventions. Forty-one percent (7/17) of patients had intra-abdominal infections; all except one developed persistent/recurrent bacteremia despite drainage. Two patients tolerated persistent bacteremia for >300 days. All patients except one were infected with sequence type 258 (ST258), K. pneumoniae carbapenemase (KPC)-2-producing strains harboring a mutant ompK35 porin gene; the exception was infected with an ST37, KPC-3-producing strain. Seventy-one percent (12/17) of patients were infected with ST258 ompK36 mutant strains. In two patients, persistent bacteremia was caused by two strains with different ompK36 genotypes. Three ompK36 mutations were associated with significantly higher carbapenem minimum inhibitory concentrations than wild-type ompK36. Pulse-field gel electrophoresis identified a single ST258 lineage; serial strains from individual patients were indistinguishable. In conclusion, KPC-K. pneumoniae bacteremia exhibited highly diverse clinical courses following transplantation, and was caused by clonal ST258 strains with different ompK36 genotypes. This study describes long-term outcomes of organ transplant recipients with bacteremia due to carbapenem-resistant Klebsiella pneumoniae and evaluates the genetic profiles of infecting strains.
机译:我们对17位接受碳青霉烯耐药的肺炎克雷伯菌的移植受者进行了回顾性研究,并描述了流行病学,临床特征和菌株基因型。 88%(15/17)的患者为肝或肠移植受者。结果是败血性休克导致的死亡(18%),治愈(24%)和持续性(> 7天)或复发性菌血症(各占29%)。 30天和90天死亡率分别为18%和47%。治愈的患者至少接受了一种活性抗菌剂并接受了源控制干预。 41%(7/17)的患者患有腹腔内感染;尽管有引流,但除一名患者外,其他所有患者均出现持续性/复发性菌血症。两名患者耐受持续的菌血症超过300天。除一名患者外,所有患者均感染了具有突变型ompK35孔蛋白基因的258型序列(ST258),肺炎克雷伯菌碳青霉烯酶(KPC)-2生产菌株。唯一的例外是感染了生产KPC-3的ST37菌株。百分之七十一(12/17)的患者感染了ST258 ompK36突变株。在两名患者中,持久性菌血症是由两种具有不同ompK36基因型的菌株引起的。与野生型ompK36相比,三个ompK36突变与碳青霉烯最低抑制浓度显着相关。脉冲场凝胶电泳鉴定出单个ST258谱系;来自个别患者的系列菌株难以区分。最后,KPC-K。肺炎菌血症在移植后表现出非常多样的临床过程,并且是由具有不同ompK36基因型的ST258克隆菌株引起的。这项研究描述了由于对碳青霉烯类耐药的肺炎克雷伯菌引起的菌血症的器官移植接受者的长期结果,并评估了感染菌株的遗传特征。

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