Emergence of population heterogeneity in Klebsiella pneumoniae with a blaOXA-232-harboring plasmid: carbapenem resistance, virulence, and fitness.

IF 9 2区 医学 Q1 CELL BIOLOGY
Yun Young Cho, Sun Ju Kim, Kwan Soo Ko
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引用次数: 0

Abstract

Background: This study aimed to investigate the population heterogeneity on carbapenem susceptibility in Klebsiella pneumoniae strains that acquired a blaOXA-232-bearing ColE-type plasmid.

Methods: A blaOXA-232-bearing plasmid was electroporated into two carbapenem-susceptible K. pneumoniae strains. High- and low-carbapenem-resistant subpopulations were identified and isolated using patch plating. The strains were subsequently subcultured in antibiotic-free media, yielding two distinct populations: a stable, high-level carbapenem-resistant strains and a heterogeneous strains. Antibiotic susceptibility tests, time-killing assays, and population profiles were conducted, along with a competition assay was performed and the growth curve analysis. To assess virulence, we performed human serum resistance and Galleria mellonella infection assays, and measured the expression of virulence genes using qRT-PCR. Additionally, whole genome sequencing was carried out for further anaysis.

Results: Introduction of pOXA-232 into carbapenem-susceptible K. pneumoniae strains resulted in two isogenic transformants with distinct resistance profiles: an unstable, high-level carbapenem-resistant (HCR), and highly virulent subpopulation; and a stable, low-level carbapenem-resistant (LCR), and low-virulence subpopulation. Whole genome and expression analyses revealed dysfunctionality of ompK36 in HCR subpopulations. Subculturing of HCR led to the re-emergence of heterogeneous populations with variations in carbapenem resistance and an additional compensatory mutation of 9,000 bp deletion in the genome. Thus, stable HCR strains featuring both mutations in ompK36 and compensatory mutations developed.

Conclusion: This study demonstrated that underlying heterogeneity can promote the emergence of stable, high-level antibiotic resistance, even with the introduction of a plasmid carrying a low-level antibiotic resistance gene, such as blaOXA-232. This highlights the critical need to closely monitor bacterial population dynamics.

携带blaoxa -232的质粒的肺炎克雷伯菌群体异质性的出现:碳青霉烯耐药性、毒力和适应性。
背景:本研究旨在调查获得含 blaOXA-232 ColE 型质粒的肺炎克雷伯菌株对碳青霉烯类药物敏感性的群体异质性:本研究旨在调查获得含 blaOXA-232 ColE 型质粒的肺炎克雷伯菌株对碳青霉烯类药物敏感性的群体异质性:方法:将含 blaOXA-232 质粒电穿孔到两株对碳青霉烯类药物敏感的肺炎克雷伯菌株中。使用贴片培养法鉴定并分离出高碳青霉烯类耐药亚群和低碳青霉烯类耐药亚群。随后在无抗生素培养基中对菌株进行亚培养,结果发现了两个不同的群体:一个是稳定的高碳青霉烯类耐药菌株,另一个是异质性菌株。我们进行了抗生素敏感性试验、时间杀伤试验和种群谱分析,还进行了竞争试验和生长曲线分析。为了评估毒力,我们进行了人类血清抗性和沙门氏菌感染试验,并使用 qRT-PCR 技术测量了毒力基因的表达。此外,我们还进行了全基因组测序以进一步分析:结果:将 pOXA-232 导入易感碳青霉烯类的肺炎双球菌菌株后,产生了两个具有不同抗性特征的同源转化子:一个不稳定、高水平碳青霉烯类抗性(HCR)和高致病性亚群;一个稳定、低水平碳青霉烯类抗性(LCR)和低致病性亚群。全基因组和表达分析表明,HCR 亚群中的 ompK36 功能失调。对 HCR 进行亚培养后,再次出现了具有碳青霉烯耐药性差异的异质性种群,基因组中还出现了 9,000 bp 缺失的补偿性突变。因此,形成了具有 ompK36 突变和补偿突变的稳定 HCR 菌株:本研究表明,即使引入了携带低水平抗生素耐药基因(如 blaOXA-232)的质粒,潜在的异质性也能促进稳定的高水平抗生素耐药性的出现。这凸显了密切监控细菌种群动态的迫切需要。
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来源期刊
Journal of Biomedical Science
Journal of Biomedical Science 医学-医学:研究与实验
CiteScore
18.50
自引率
0.90%
发文量
95
审稿时长
1 months
期刊介绍: The Journal of Biomedical Science is an open access, peer-reviewed journal that focuses on fundamental and molecular aspects of basic medical sciences. It emphasizes molecular studies of biomedical problems and mechanisms. The National Science and Technology Council (NSTC), Taiwan supports the journal and covers the publication costs for accepted articles. The journal aims to provide an international platform for interdisciplinary discussions and contribute to the advancement of medicine. It benefits both readers and authors by accelerating the dissemination of research information and providing maximum access to scholarly communication. All articles published in the Journal of Biomedical Science are included in various databases such as Biological Abstracts, BIOSIS, CABI, CAS, Citebase, Current contents, DOAJ, Embase, EmBiology, and Global Health, among others.
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