Emergence of plasmid-borne tet(X4) resistance gene in clinical isolate of eravacycline- and omadacycline-resistant Klebsiella pneumoniae ST485.

IF 3.7 2区 生物学 Q2 MICROBIOLOGY Microbiology spectrum Pub Date : 2024-09-03 Epub Date: 2024-07-23 DOI:10.1128/spectrum.00496-24
Xiaojing Liu, Yi Liu, Xiaohan Ma, Ruyan Chen, Chenyu Li, Hongxin Fu, Yu Yang, Kexin Guo, Xiaoping Zhang, Ruishan Liu, Hao Xu, Junfei Zhu, Beiwen Zheng
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Abstract

Omadacycline and eravacycline are gradually being used as new tetracycline antibiotics for the clinical treatment of Gram-negative pathogens. Affected by various tetracycline-inactivating enzymes, there have been reports of resistance to eravacycline and omadacycline in recent years. We isolated a strain carrying the mobile tigecycline resistance gene tet(X4) from the feces of a patient in Zhejiang Province, China. The strain belongs to the rare ST485 sequence type. The isolate was identified as Klebsiella pneumoniae by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The MICs of antimicrobial agents were determined using either the agar dilution method or the micro broth dilution method. The result showed that the isolate was resistant to eravacycline (MIC = 32 mg/L), omadacycline (MIC > 64 mg/L), and tigecycline (MIC > 32 mg/L). Whole-genome sequencing revealed that the tet(X4) resistance gene is located on the IncFII(pCRY) conjugative plasmid. tet(X4) is flanked by ISVsa3, and we hypothesize that this association contributes to the spread of the resistance gene. Plasmids were analyzed by S1-nuclease pulsed-field gel electrophoresis (S1-PFGE), Southern blotting, and electrotransformation experiment. We successfully transferred the plasmid carrying tet(X4) to the recipient bacteria by electrotransformation experiment. Compared with the DH-5α, the MICs of the transformant L3995-DH5α were increased by eight-fold for eravacycline and two-fold higher for omadacycline. Overall, the emergence of plasmid-borne tet(X4) resistance gene in a clinical isolate of K. pneumoniae ST485 underscores the essential requirement for the ongoing monitoring of tet(X4) to prevent and control its further dissemination in China.IMPORTANCEThere are still limited reports on Klebsiella pneumoniae strains harboring tetracycline-resistant genes in China, and K. pneumoniae L3995hy adds a new example to those positive for the tet(X4) gene. Importantly, our study raises concerns that plasmid-mediated resistance to omadacycline and eravacycline may spread further to a variety of ecological and clinical pathogens, limiting the choice of medication for extensively drug-resistant bacterial infections. Therefore, it is important to continue to monitor the prevalence and spread of tet(X4) and other tetracyclines resistance genes in K. pneumoniae and diverse bacterial populations.

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耐阿维菌素和奥美拉唑类药物的肺炎克雷伯菌 ST485 临床分离株中出现质粒携带的 tet(X4) 耐药基因。
奥马他环素和麦拉伐环素正逐渐作为新的四环素类抗生素用于临床治疗革兰氏阴性病原体。受多种四环素失活酶的影响,近年来出现了对埃拉伐环素和奥美拉唑环素产生抗药性的报道。我们从中国浙江省一名患者的粪便中分离出了一株携带有移动的替加环素耐药基因 tet(X4) 的菌株。该菌株属于罕见的 ST485 序列类型。通过基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)鉴定,该分离菌株为肺炎克雷伯氏菌。采用琼脂稀释法或微肉汤稀释法测定了抗菌药物的 MIC 值。结果显示,该分离株对依拉维辛(MIC = 32 mg/L)、奥美拉唑(MIC > 64 mg/L)和替加环素(MIC > 32 mg/L)具有耐药性。全基因组测序显示,tet(X4)抗性基因位于 IncFII(pCRY) 共轭质粒上。tet(X4)的侧翼是 ISVsa3,我们推测这种关联有助于抗性基因的扩散。我们通过 S1 核酸酶脉冲场凝胶电泳(S1-PFGE)、Southern 印迹和电转化实验对质粒进行了分析。通过电转化实验,我们成功地将携带 tet(X4) 的质粒转移到了受体细菌中。与 DH-5α 相比,转化株 L3995-DH5α 对依拉维辛的 MICs 提高了 8 倍,对奥美拉唑的 MICs 提高了 2 倍。总之,在肺炎克雷伯菌 ST485 临床分离株中出现质粒携带的 tet(X4) 耐药基因突出表明,必须对 tet(X4) 进行持续监测,以防止和控制其在中国的进一步传播。重要的是,我们的研究引起了人们的关注,即质粒介导的对奥马他环素和阿拉伐环素的耐药性可能会进一步扩散到各种生态和临床病原体中,从而限制了广泛耐药细菌感染的药物选择。因此,必须继续监测 tet(X4) 和其他四环素耐药基因在肺炎克雷伯菌和各种细菌群体中的流行和传播情况。
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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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