Xie Panpan, Liu Jie, Feng Yuzhong, Zhao Taiyun, Niu Wenkai, Fang Yun, Zhang Xin, Zhao Xilin, Wang Fusheng, Yuan Xin
Department of Respiratory and Critical Care Medicine, Senior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, Beijing, China.
Senior Department of Infectious Diseases, The Fifth Medical Center of PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China.
Microbiol Spectr. 2025 Jul;13(7):e0339824. doi: 10.1128/spectrum.03398-24. Epub 2025 May 23.
Macrolide resistance in is becoming prevalent. Tetracyclines are an important alternative for patients with macrolide-resistant infections. Tetracycline-resistant has never been reported in clinical isolates or -induced strains. Here, we aimed to explore tetracycline-resistant and the underlying resistance mechanisms. Clinically isolated parental strains were selected for tetracycline resistance by inducing them with increasing concentrations of tetracycline, minocycline, and tigecycline. The whole genomes of the induced resistant and parent strains were both sequenced to identify tetracycline-resistance genes, and their 16S rRNA gene sequences were compared. Ribosome-binding assays were conducted by incubating the 30S ribosomes of the resistant and sensitive strains with various concentrations of H-labeled tetracycline. The effect of efflux pump inhibitor reserpine on the susceptibility of tetracyclines to the resistant mutants was evaluated. Eight resistant mutants were obtained from 12 tetracycline-susceptible strains. Whole-genome sequencing identified point mutations in the 16S rRNA gene of all the resistant mutants. The ribosomes of two induced resistant strains showed lower tetracycline-binding capacities than their parental strains. Reserpine increased the susceptibility of two resistant mutants to tetracyclines by more than fourfold. None of the resistant mutants carried the known tetracycline-resistance genes. strains can develop tetracycline resistance. Mutations in the 16S rRNA gene leading to decreased ribosomal-binding capacity and the presence of efflux pumps may be the mechanisms associated with tetracycline resistance in . This study identifies markers to track the emergence of tetracycline resistance in .IMPORTANCEResistance to anti- antibiotics is a global public health problem. Effective antibiotic treatment strategies are urgently needed. Tetracyclines are among the most commonly used antibiotics for the treatment of drug-resistant infections. Tetracycline-resistant has not been reported; however, treatment with increased concentrations of tetracycline selects hyposensitive mutants. In this study, we successfully induced tetracycline-resistant mutants by 10-month serial passage experiments and found that a 16S rRNA mutation resulting in reduced ribosomal drug binding was the mechanism that led to tetracycline resistance in . In addition, the efflux pump might also be related to decreased tetracycline susceptibility. This study presented the first data on the induction of tetracycline resistance in , providing insights into the development of effective treatment strategies for drug-resistant infections in the future.
[具体细菌名称]对大环内酯类药物的耐药性正变得普遍。四环素是耐大环内酯类[具体细菌名称]感染患者的重要替代药物。临床分离株或诱导菌株中从未报告过耐四环素的[具体细菌名称]。在此,我们旨在探索耐四环素的[具体细菌名称]及其潜在的耐药机制。通过用浓度递增的四环素、米诺环素和替加环素诱导临床分离的亲本[具体细菌名称]菌株,筛选出对四环素耐药的菌株。对诱导产生的耐药菌株和亲本菌株的全基因组进行测序,以鉴定四环素耐药基因,并比较它们的16S rRNA基因序列。通过将耐药菌株和敏感菌株的30S核糖体与不同浓度的H标记四环素孵育,进行核糖体结合试验。评估外排泵抑制剂利血平对四环素对耐药突变体敏感性的影响。从12株四环素敏感的[具体细菌名称]菌株中获得了8个耐药突变体。全基因组测序鉴定出所有耐药突变体的16S rRNA基因存在点突变。两个诱导产生的耐药菌株的核糖体显示出比其亲本菌株更低的四环素结合能力。利血平使两个耐药突变体对四环素的敏感性提高了四倍以上。所有耐药突变体均未携带已知的四环素耐药基因。[具体细菌名称]菌株可产生四环素耐药性。16S rRNA基因中的突变导致核糖体结合能力下降以及外排泵的存在可能是[具体细菌名称]中与四环素耐药性相关的机制。本研究确定了追踪[具体细菌名称]中四环素耐药性出现的标志物。
重要性
对抗[具体细菌名称]抗生素的耐药性是一个全球公共卫生问题。迫切需要有效的抗生素治疗策略。四环素是治疗耐药性[具体细菌名称]感染最常用的抗生素之一。尚未报告耐四环素的[具体细菌名称];然而,用浓度增加的四环素治疗会筛选出低敏突变体。在本研究中,我们通过10个月的连续传代实验成功诱导出耐四环素的[具体细菌名称]突变体,并发现导致核糖体药物结合减少的16S rRNA突变是[具体细菌名称]中产生四环素耐药性的机制。此外,外排泵也可能与四环素敏感性降低有关。本研究提供了关于[具体细菌名称]中四环素耐药性诱导的首批数据,为未来耐药性[具体细菌名称]感染有效治疗策略的开发提供了见解。