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对菌血症分离株的基因组分析揭示了与新冠疫情相关的遗传特征。

Genomic analysis of isolates from bacteremia reveals genetic features associated with the COVID-19 pandemic.

作者信息

Sánchez-Osuna Miquel, Pedrosa Marc, Bierge Paula, Gómez-Sánchez Inmaculada, Alguacil-Guillén Marina, Espasa Mateu, Erill Ivan, Gasch Oriol, Pich Oscar Q

机构信息

Laboratori de Recerca en Microbiologia i Malalties Infeccioses, Hospital Universitari Parc Taulí, Institut d'Investigació i Innovació Parc Taulí (I3PT-CERCA), Universitat Autònoma de Barcelona, Sabadell, Spain.

Institut de Biotecnologia i Biomedicina, Universitat Autònoma de Barcelona, Cerdanyola del Vallès, Spain.

出版信息

iScience. 2024 Jun 28;27(8):110402. doi: 10.1016/j.isci.2024.110402. eCollection 2024 Aug 16.

Abstract

Genomic analyses of bacterial isolates are effective to compare the prevalence of antibiotic resistance genes and virulence determinants in different contexts. This study provides a comprehensive genomic description of 339 strains isolated from patients with bacteremia (2014-2022). Nosocomial acquisition accounted for 56.6% of cases, with vascular catheters being the main infection source (31.8%). Fatality (27.4%), persistent bacteremia (19.5%), and septic emboli (24.2%) were documented. During the COVID-19 pandemic, bacteremia episodes increased by 140%. Genetic features in pandemic isolates revealed higher prevalence of methicillin () and macrolide ( and ) resistance genes. Additionally, genes encoding clumping factors A and B, involved in fibrinogen binding, were more prevalent. This was linked to extensive macrolide use in COVID-19 accessory therapy and elevated fibrinogen levels in SARS-CoV-2 infection. These findings highlight adaptation to COVID-19 selective pressures and the value of whole-genome sequencing in molecular epidemiology studies.

摘要

对细菌分离株进行基因组分析,有助于比较不同情况下抗生素耐药基因和毒力决定因素的流行情况。本研究全面描述了2014年至2022年间从菌血症患者中分离出的339株菌株的基因组情况。医院获得性感染占病例的56.6%,血管导管是主要感染源(31.8%)。记录了死亡率(27.4%)、持续性菌血症(19.5%)和脓毒性栓子(24.2%)情况。在新冠疫情期间,菌血症发作增加了140%。疫情期间分离株的基因特征显示,耐甲氧西林()和大环内酯类(和)耐药基因的流行率更高。此外,编码参与纤维蛋白原结合的凝聚因子A和B的基因更为普遍。这与新冠辅助治疗中大量使用大环内酯类药物以及新冠病毒感染中纤维蛋白原水平升高有关。这些发现凸显了对新冠选择性压力的适应性以及全基因组测序在分子流行病学研究中的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6dd6/11301081/f102a52d1865/fx1.jpg

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