台湾对头孢他啶/阿维菌素耐药的肺炎克雷伯菌临床菌株的机制和适应性。

IF 4.9 2区 医学 Q1 INFECTIOUS DISEASES International Journal of Antimicrobial Agents Pub Date : 2024-08-01 DOI:10.1016/j.ijantimicag.2024.107244
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引用次数: 0

摘要

背景:耐碳酸培南肺炎克雷伯菌(CRKP)感染是一个全球性的公共卫生问题,头孢他啶/阿维菌素被国际指南推荐为治疗产KPC和OXA-48的CRKP的首选药物。自2019年头孢他啶/阿维巴坦引入台湾以来,出现了耐头孢他啶/阿维巴坦的菌株。我们的目的是调查台湾CRKP对头孢他啶/阿维菌素耐药的机制,并研究其相关的健康成本:方法:2020 年,我们在台北荣民总医院连续收集了从临床标本中分离出的头孢他啶/阿维巴坦耐药 CRKP 菌株。使用全基因组测序(WGS)对从同一患者分离的头孢他啶/阿维菌素敏感和头孢他啶/阿维菌素耐药表型的连续菌株进行鉴定,并检测其生长速度和竞争能力:结果:共鉴定出35株头孢他啶/阿维菌素耐药的CRKP菌株,其中20株是金属-β-内酰胺酶生产者。10 株菌株含有 KPC 变异株,对头孢他啶/阿维菌素的 MIC 为 64 至 ≥256 mg/L。对头孢他啶/阿维菌素具有高度耐药性的 10 株菌株拥有变异的 KPC 变体:KPC-33(n=3)、KPC-31(n=1)、KPC-39(n=1)、KPC-44(n=1)、KPC-58(n=1)、KPC-90(n=1)和两个新型 KPC 变体。与亲本菌株相比,耐头孢唑肟/阿维菌素的 KPC-33 和 KPC-39 菌株表现出显著的适应性代价和较低的生长率。相比之下,KPC-58和KPC-58加D179Y的头孢他啶/阿维菌素耐药菌株的生长率和竞争能力与其亲本菌株相似:在台湾,KPC变异株产生了高水平的头孢他啶/阿维菌素耐药性。对头孢他啶/阿维菌素耐药的 KPC-33 和 KPC-39 株系中都观察到了显著的适应成本。尽管对头孢他啶/阿维菌素的耐药性水平相似,但不同的 KPC 变种可能会带来不同程度的适应性成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mechanisms and fitness of ceftazidime/avibactam-resistant Klebsiella pneumoniae clinical strains in Taiwan

Background

Carbapenem-resistant Klebsiella pneumoniae (CRKP) infection is a global public health issue, and ceftazidime/avibactam is recommended by international guidelines as the preferred treatment for KPC- and OXA-48-producing CRKP. Since its introduction in Taiwan in 2019, ceftazidime/avibactam-resistant strains have emerged. Our aim is to investigate the mechanisms of ceftazidime/avibactam resistance in CRKP in Taiwan and study their associated fitness costs.

Methods

Ceftazidime/avibactam-resistant CRKP strains with exposure to ceftazidime/avibactam isolated from clinical specimens were consecutively collected at Taipei Veterans General Hospital in 2020. The serial strains exhibiting ceftazidime/avibactam-susceptible and ceftazidime/avibactam-resistant phenotypes isolated from the same patient were characterized using whole-genome sequencing and tested for their growth rates and competitive abilities.

Results

A total of 35 ceftazidime/avibactam-resistant CRKP strains were identified, with 20 being metallo-β-lactamase producers. Ten strains harboured KPC variants, exhibiting MIC for ceftazidime/avibactam ranging from 64 to ≥256 mg/L. The 10 strains demonstrating high-level ceftazidime/avibactam resistance possessed mutated KPC variants: KPC-33 (n = 3), KPC-31 (n = 1), KPC-39 (n = 1), KPC-44 (n = 1), KPC-58 (n = 1), KPC-90 (n = 1), and two novel KPC variants. Ceftazidime/avibactam-resistant strains with KPC-33 and KPC-39 showed a significant fitness cost and lower growth rate compared to their parental strains. In contrast, ceftazidime/avibactam-resistant strains with KPC-58 and KPC-58 plus D179Y showed similar growth rates and competitive abilities compared to their parental strains.

Conclusions

Mutated KPC variants conferred high-level ceftazidime/avibactam resistance in Taiwan. Significant fitness costs were observed in both the ceftazidime/avibactam-resistant KPC-33 and KPC-39 strains. Despite conferring a similar level of ceftazidime/avibactam resistance, different KPC variants could entail varying degrees of fitness costs.

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来源期刊
CiteScore
21.60
自引率
0.90%
发文量
176
审稿时长
36 days
期刊介绍: The International Journal of Antimicrobial Agents is a peer-reviewed publication offering comprehensive and current reference information on the physical, pharmacological, in vitro, and clinical properties of individual antimicrobial agents, covering antiviral, antiparasitic, antibacterial, and antifungal agents. The journal not only communicates new trends and developments through authoritative review articles but also addresses the critical issue of antimicrobial resistance, both in hospital and community settings. Published content includes solicited reviews by leading experts and high-quality original research papers in the specified fields.
期刊最新文献
International Society of Antimicrobial Chemotherapy (ISAC) News and Information Page Ceftazidime-avibactam (CAZ-AVI) pharmacokinetics in critically ill patients undergoing continuous venovenous hemodiafiltration (CVVHDF). Response regulator protein CiaR regulates the transcription of ccn-microRNAs and β-lactam antibiotic resistance conversion of Streptococcus pneumoniae. Model-Informed Drug Development (MIDD) for Antimicrobials An isogenic E. coli population gives rise to multiple persister phenotypes.
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