Strateva Tanya V, Hristova Preslava, Stoeva Temenuga J, Hitkova Hristina, Peykov Slavil
Department of Medical Microbiology "Corr. Mem. Prof. Ivan Mitov, MD, DMSc", Faculty of Medicine, Medical University of Sofia, 2 Zdrave Str., 1431 Sofia, Bulgaria.
Department of Microbiology and Virology, Faculty of Pharmacy, Medical University of Pleven, 1 St. Kliment Ohridski Str., 5800 Pleven, Bulgaria.
Microorganisms. 2025 Jan 17;13(1):195. doi: 10.3390/microorganisms13010195.
Linezolid is an oxazolidinone antibiotic and is considered a last-resort treatment option for serious infections caused by problematic Gram-positive pathogens, including vancomycin-resistant enterococci. The present study aimed to explore the linezolid resistance mechanisms and genomic characteristics of two vancomycin-susceptible isolates from Bulgaria. The strains designated Efs2503-bg (inpatient from Pleven) and Efs966-bg (outpatient from Varna) were recovered from wounds in 2018 and 2023, respectively. Antimicrobial susceptibility testing, whole-genome sequencing, multilocus sequence typing, and phylogenomic analysis based on 332 linezolid-resistant genomes were performed. Efs2503-bg was high-level resistant to linezolid (MIC > 256 mg/L) and displayed the G2576T mutation affecting three of the four 23S rDNA loci. Efs966-bg (MIC = 8 mg/L) carried a plasmid-located determinant surrounded by and . No mutations in the genes encoding for ribosomal proteins L3, L4, and L22 were detected. The isolates belonged to the sequence types ST6 (Efs2503-bg) and ST1102 (Efs966-bg). Phylogenomic analysis revealed that Efs2503-bg and Efs966-bg are genetically distinct, with a difference of 12,051 single-nucleotide polymorphisms. To our knowledge, this is the first report of linezolid-resistant enterococci in Bulgaria. Although the global incidence of linezolid-resistant enterococci is still low, their emergence is alarming and poses a growing clinical threat to public health.
利奈唑胺是一种恶唑烷酮类抗生素,被认为是治疗由难对付的革兰氏阳性病原体引起的严重感染的最后手段,这些病原体包括耐万古霉素肠球菌。本研究旨在探索来自保加利亚的两株万古霉素敏感分离株的利奈唑胺耐药机制和基因组特征。分别命名为Efs2503-bg(来自普列文的住院患者)和Efs966-bg(来自瓦尔纳的门诊患者)的菌株于2018年和2023年从伤口中分离得到。进行了抗菌药物敏感性测试、全基因组测序、多位点序列分型以及基于332个耐利奈唑胺基因组的系统基因组分析。Efs2503-bg对利奈唑胺高度耐药(最低抑菌浓度>256mg/L),并显示出影响四个23S rDNA位点中三个位点的G2576T突变。Efs966-bg(最低抑菌浓度=8mg/L)携带一个位于质粒上的决定簇,其周围有 和 。未检测到核糖体蛋白L3、L4和L22编码基因的突变。这些分离株分别属于序列类型ST6(Efs2503-bg)和ST1102(Efs966-bg)。系统基因组分析表明,Efs2503-bg和Efs966-bg在基因上是不同的,单核苷酸多态性差异为12,051个。据我们所知,这是保加利亚耐利奈唑胺肠球菌的首次报道。尽管全球耐利奈唑胺肠球菌的发病率仍然很低,但其出现令人担忧,并对公共卫生构成日益严重的临床威胁。