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多重耐药伊丽莎白菌的临床特征、耐药性分析和基因组特征分析。

Clinical manifestations, antimicrobial resistance and genomic feature analysis of multidrug-resistant Elizabethkingia strains.

机构信息

Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan, 610041, China.

出版信息

Ann Clin Microbiol Antimicrob. 2024 Apr 10;23(1):32. doi: 10.1186/s12941-024-00691-6.

Abstract

BACKGROUND

Elizabethkingia is emerging as an opportunistic pathogen in humans. The aim of this study was to investigate the clinical epidemiology, antimicrobial susceptibility, virulence factors, and genome features of Elizabethkingia spp.

METHODS

Clinical data from 71 patients who were diagnosed with Elizabethkingia-induced pneumonia and bacteremia between August 2019 and September 2021 were analyzed. Whole-genome sequencing was performed on seven isolates, and the results were compared with a dataset of 83 available Elizabethkingia genomes. Genomic features, Kyoto Encyclopedia of Genes and Genomes (KEGG) results and clusters of orthologous groups (COGs) were analyzed.

RESULTS

The mean age of the patients was 56.9 ± 20.7 years, and the in-hospital mortality rate was 29.6% (21/71). Elizabethkingia strains were obtained mainly from intensive care units (36.6%, 26/71) and emergency departments (32.4%, 23/71). The majority of the strains were isolated from respiratory tract specimens (85.9%, 61/71). All patients had a history of broad-spectrum antimicrobial exposure. Hospitalization for invasive mechanical ventilation or catheter insertion was found to be a risk factor for infection. The isolates displayed a high rate of resistance to cephalosporins and carbapenems, but all were susceptible to minocycline and colistin. Genomic analysis identified five β-lactamase genes (bla, bla, bla, bla, and bla) responsible for β-lactam resistance and virulence genes involved in stress adaptation (ureB/G, katA/B, and clpP), adherence (groEL, tufA, and htpB) and immune modulation (gmd, tviB, cps4J, wbtIL, cap8E/D/G, and rfbC). Functional analysis of the COGs revealed that "metabolism" constituted the largest category within the core genome, while "information storage and processing" was predominant in both the accessory and unique genomes. The unique genes in our 7 strains were mostly enriched in KEGG pathways related to microRNAs in cancer, drug resistance (β-lactam and vancomycin), ABC transporters, biological metabolism and biosynthesis, and nucleotide excision repair mechanisms.

CONCLUSION

The Elizabethkingia genus exhibits multidrug resistance and carries carbapenemase genes. This study presents a comparative genomic analysis of Elizabethkingia, providing knowledge that facilitates a better understanding of this microorganism.

摘要

背景

伊丽莎白菌属在人类中作为机会致病菌而出现。本研究旨在调查伊丽莎白菌属的临床流行病学、抗菌药物敏感性、毒力因子和基因组特征。

方法

对 2019 年 8 月至 2021 年 9 月期间被诊断为伊丽莎白菌属引起的肺炎和菌血症的 71 名患者的临床数据进行分析。对 7 个分离株进行全基因组测序,并将结果与 83 个可用的伊丽莎白菌属基因组数据集进行比较。分析基因组特征、京都基因与基因组百科全书(KEGG)结果和直系同源群(COG)。

结果

患者的平均年龄为 56.9±20.7 岁,院内死亡率为 29.6%(21/71)。伊丽莎白菌株主要从重症监护病房(36.6%,26/71)和急诊室(32.4%,23/71)获得。大多数菌株从呼吸道标本中分离(85.9%,61/71)。所有患者均有广谱抗菌药物暴露史。住院期间接受有创机械通气或导管插入术被认为是感染的危险因素。分离株对头孢菌素和碳青霉烯类药物的耐药率较高,但均对米诺环素和黏菌素敏感。基因组分析确定了 5 个β-内酰胺酶基因(blaCTX-M-15、blaDHA-1、blaTEM-1B、blaVEB-1 和 blaOXA-48),这些基因负责β-内酰胺类药物的耐药性,以及与应激适应、黏附、免疫调节相关的毒力基因(ureB/G、katA/B 和 clpP、groEL、tufA 和 htpB、gmd、tviB、cps4J、wbtIL、cap8E/D/G 和 rfbC)。COG 的功能分析表明,“代谢”在核心基因组中占最大类别,而“信息存储和处理”在辅助和独特基因组中占主导地位。我们 7 株的独特基因主要富集在癌症相关的 microRNAs、药物耐药性(β-内酰胺类和万古霉素)、ABC 转运蛋白、生物代谢和生物合成以及核苷酸切除修复机制的 KEGG 途径中。

结论

伊丽莎白菌属表现出多药耐药性,并携带碳青霉烯酶基因。本研究对伊丽莎白菌属进行了比较基因组分析,为更好地了解这种微生物提供了知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2815/11007976/eb61dde75b4a/12941_2024_691_Fig1_HTML.jpg

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