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耐甲氧西林金黄色葡萄球菌中第84位突变在对德拉氟沙星高水平耐药中的作用

Role of Mutations at Position 84 on High-Level Delafloxacin Resistance in Methicillin-Resistant .

作者信息

Bolaños Silvia, Acebes Cesar, Martínez-Expósito Óscar, Boga José Antonio, Fernández Javier, Rodríguez-Lucas Carlos

机构信息

Servicio de Microbiología, Hospital Universitario Central de Asturias (HUCA), Avenida de Roma s/n, 33011 Oviedo, Spain.

Grupo de Microbiología y Patología Infecciosa, Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Spain.

出版信息

Antibiotics (Basel). 2024 Jul 11;13(7):641. doi: 10.3390/antibiotics13070641.

Abstract

High-level delafloxacin-resistant (H-L DLX-R) isolates (minimum inhibitory concentration ≥1 mg/L) associated with mutations affecting position 84 of ParC have emerged. We aimed to elucidate the role of these mutations as a mechanism of H-L DLX resistance in methicillin-resistant (MRSA) isolates recovered from blood cultures. Susceptibility to DLX was determined in 75 MRSA isolates by E-test, and an rt-PCR was developed to detect mutations affecting position 84 of ParC to screen a further 185 MRSA isolates. The genomes of 48 isolates, including all DLX-R isolates or with alterations at position 84, and also a subset of DLX-susceptible isolates were analyzed. Among the 75 isolates studied, 77.34% were DLX-susceptible and only 4 H-L DLX-R isolates were found. Seven (3.8%) isolates with alterations at position 84 of ParC were detected by rt-PCR. Genomic analysis showed that 89.9% (8/9) of isolates with the substitution E84K/G in ParC, together with other mutations in and , were H-L DLX-R. However, the E84K substitution in ParC alone or with other alterations was found in two isolates without H-L DLX-R. Alterations at position 84 of ParC are rare but play a key role in H-L DLX resistance in MRSA but only when other alterations in GyrA are present.

摘要

已出现与影响ParC第84位的突变相关的高水平德拉氟沙星耐药(H-L DLX-R)菌株(最低抑菌浓度≥1mg/L)。我们旨在阐明这些突变在从血培养物中分离出的耐甲氧西林金黄色葡萄球菌(MRSA)菌株中作为H-L DLX耐药机制的作用。通过E试验测定了75株MRSA菌株对DLX的敏感性,并开发了逆转录聚合酶链反应(rt-PCR)来检测影响ParC第84位的突变,以筛选另外185株MRSA菌株。分析了48株菌株的基因组,包括所有DLX-R菌株或在第84位有改变的菌株,以及一部分DLX敏感菌株。在所研究的75株菌株中,77.34%对DLX敏感,仅发现4株H-L DLX-R菌株。通过rt-PCR检测到7株(3.8%)在ParC第84位有改变的菌株。基因组分析表明,ParC中发生E84K/G替代且在gyrA和其他区域有其他突变的菌株中有89.9%(8/9)为H-L DLX-R。然而,仅在ParC中发生E84K替代或与其他改变同时存在的情况在2株非H-L DLX-R菌株中被发现。ParC第84位的改变很少见,但在MRSA的H-L DLX耐药中起关键作用,但仅当gyrA中有其他改变时才会如此。

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