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基质辅助激光解吸电离飞行时间质谱技术对生物膜产生嗜麦芽窄食单胞菌临床株的鉴别。

Discrimination of biofilm-producing Stenotrophomonas maltophilia clinical strains by matrix-assisted laser desorption ionization-time of flight.

机构信息

Facultad de Ciencias Biológicas, Universidad Autónoma de Nuevo León, NL, México.

Hospital Universitario Dr. José Eleuterio González, Universidad Autónoma de Nuevo León, NL, México.

出版信息

PLoS One. 2020 Dec 31;15(12):e0244751. doi: 10.1371/journal.pone.0244751. eCollection 2020.

Abstract

Stenotrophomonas maltophilia is a Gram-negative drug-resistant pathogen responsible for healthcare-associated infections. The aim was to search for biomarker peaks that could rapidly detect biofilm production in S. maltophilia clinical isolates obtained from two tertiary care hospitals in Mexico. Isolates were screened for the presence of biofilm-associated genes, in which the fsnR gene was associated with biofilm production (p = 0.047), whereas the rmlA+ genotype was associated with the rpfF- genotype (p = 0.017). Matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectra comparison yielded three potential biomarker peaks (4661, 6074, and 6102 m/z) of biofilm-producing rmlA+ and rpfF- genotypes with >90% sensitivity (p<0.001). MALDI-TOF MS analyses showed a correlation between the relative abundance of 50S ribosomal proteins (L30 and L33) and the presence of the fnsR, rmlA and rpfF-2 genes, suggested to play a role in biofilm formation. Isolates obtained in the intensive care unit showed low clonality, suggesting no transmission within the hospital ward. The detection of biomarkers peaks by MALDI-TOF MS could potentially be used to early recognize and discriminate biofilm-producing S. maltophilia strains and aid in establishing appropriate antibiotic therapy.

摘要

嗜麦芽寡养单胞菌是一种革兰氏阴性耐药病原体,可导致与医疗保健相关的感染。本研究旨在寻找生物标志物峰,以便快速检测从墨西哥两家三级医院获得的嗜麦芽寡养单胞菌临床分离株中的生物膜产生情况。筛选分离物中与生物膜相关的基因,其中 fsnR 基因与生物膜产生有关(p=0.047),而 rmlA+基因型与 rpfF-基因型有关(p=0.017)。基质辅助激光解吸电离飞行时间(MALDI-TOF)质谱比较得到三个潜在的生物膜产生 rmlA+和 rpfF-基因型的生物标志物峰(4661、6074 和 6102 m/z),具有>90%的敏感性(p<0.001)。MALDI-TOF MS 分析表明,50S 核糖体蛋白(L30 和 L33)的相对丰度与 fnsR、rmlA 和 rpfF-2 基因的存在之间存在相关性,这些基因可能在生物膜形成中发挥作用。从重症监护病房获得的分离物显示出较低的克隆性,表明在医院病房内没有传播。MALDI-TOF MS 检测生物标志物峰可能有助于早期识别和区分产生生物膜的嗜麦芽寡养单胞菌菌株,并有助于建立适当的抗生素治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29d6/7775041/502872e3923b/pone.0244751.g001.jpg

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