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解淀粉克雷伯菌是斯德哥尔摩地区血流感染的常见病因,与肺炎克雷伯菌相比,其死亡率更高。

Klebsiella variicola is a frequent cause of bloodstream infection in the stockholm area, and associated with higher mortality compared to K. pneumoniae.

作者信息

Maatallah Makaoui, Vading Malin, Kabir Muhammad Humaun, Bakhrouf Amina, Kalin Mats, Nauclér Pontus, Brisse Sylvain, Giske Christian G

机构信息

Laboratoire d'Analyse, Traitement et Valorisation des Polluants de l'Environnement et des Produits, Faculté de Pharmacie, University of Monastir, Montasir, Tunisia.

Clinical Microbiology, MTC - Karolinska Institutet, Karolinska University, Hospital Solna, Stockholm, Sweden; Department of Infectious Diseases, Karolinska University Hospital Solna, Stockholm, Sweden.

出版信息

PLoS One. 2014 Nov 26;9(11):e113539. doi: 10.1371/journal.pone.0113539. eCollection 2014.

Abstract

Clinical isolates of Klebsiella pneumoniae are divided into three phylogroups and differ in their virulence factor contents. The aim of this study was to determine an association between phylogroup, virulence factors and mortality following bloodstream infection (BSI) caused by Klebsiella pneumoniae. Isolates from all adult patients with BSI caused by K. pneumoniae admitted to Karolinska University Hospital, Solna between 2007 and 2009 (n = 139) were included in the study. Phylogenetic analysis was performed based on multilocus sequence typing (MLST) data. Testing for mucoid phenotype, multiplex PCR determining serotypes K1, K2, K5, K20, K54 and K57, and testing for virulence factors connected to more severe disease in previous studies, was also performed. Data was retrieved from medical records including age, sex, comorbidity, central and urinary catheters, time to adequate treatment, hospital-acquired infection, and mortality, to identify risk factors. The primary end-point was 30- day mortality. The three K. pneumoniae phylogroups were represented: KpI (n = 96), KpII (corresponding to K. quasipneumoniae, n = 9) and KpIII (corresponding to K. variicola, n = 34). Phylogroups were not significantly different in baseline characteristics. Overall, the 30-day mortality was 24/139 (17.3%). Isolates belonging to KpIII were associated with the highest 30-day mortality (10/34 cases, 29.4%), whereas KpI isolates were associated with mortality in 13/96 cases (13.5%). This difference was significant both in univariate statistical analysis (P = 0.037) and in multivariate analysis adjusting for age and comorbidity (OR 3.03 (95% CI: 1.10-8.36). Only three of the isolates causing mortality within 30 days belonged to any of the virulent serotypes (K54, n = 1), had a mucoid phenotype (n = 1) and/or contained virulence genes (wcaG n = 1 and wcaG/allS n = 1). In conclusion, the results indicate higher mortality among patients infected with isolates belonging to K. variicola. The increased mortality could not be related to any known virulence factors, including virulent capsular types or mucoid phenotype.

摘要

肺炎克雷伯菌的临床分离株可分为三个系统发育组,其毒力因子含量有所不同。本研究的目的是确定肺炎克雷伯菌血流感染(BSI)后的系统发育组、毒力因子与死亡率之间的关联。纳入了2007年至2009年间入住索尔纳卡罗林斯卡大学医院的所有由肺炎克雷伯菌引起BSI的成年患者的分离株(n = 139)。基于多位点序列分型(MLST)数据进行系统发育分析。还进行了黏液样表型检测、多重PCR确定血清型K1、K2、K5、K20、K54和K57,以及检测先前研究中与更严重疾病相关的毒力因子。从医疗记录中检索数据,包括年龄、性别、合并症、中心静脉导管和导尿管使用情况、获得充分治疗的时间、医院获得性感染和死亡率,以确定风险因素。主要终点是30天死亡率。肺炎克雷伯菌的三个系统发育组均有代表:KpI(n = 96)、KpII(对应准肺炎克雷伯菌,n = 9)和KpIII(对应类鼻疽克雷伯菌,n = 34)。各系统发育组在基线特征上无显著差异。总体而言,30天死亡率为24/139(17.3%)。属于KpIII的分离株与最高的30天死亡率相关(10/34例,29.4%),而KpI分离株与13/96例(13.5%)的死亡率相关。这种差异在单因素统计分析(P = 0.037)和调整年龄及合并症的多因素分析中均具有统计学意义(OR 3.03(95%CI:1.10 - 8.36))。在30天内导致死亡的分离株中,只有三株属于任何一种强毒株血清型(K54,n = 1)、具有黏液样表型(n = 1)和/或含有毒力基因(wcaG n = 1和wcaG/allS n = 1)。总之,结果表明感染类鼻疽克雷伯菌分离株的患者死亡率更高。死亡率增加与任何已知的毒力因子无关,包括强毒荚膜型或黏液样表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d3fb/4245126/2a9ac22822bb/pone.0113539.g001.jpg

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