A single-center retrospective study of the molecular epidemiological characteristics of different Klebsiella pneumoniae infections in northern China.

IF 2.1 3区 医学 Q3 RESPIRATORY SYSTEM
Journal of thoracic disease Pub Date : 2024-11-30 Epub Date: 2024-11-29 DOI:10.21037/jtd-24-1148
Wei Chen, Zhao Cai, Shuangqing Liu, Giovanni Sotgiu, Ignacio Martin-Loeches, Yang Cao
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引用次数: 0

Abstract

Background: Klebsiella pneumoniae (K. pneumoniae) is an opportunistic pathogen that can cause multiple life-threatening infections. Recently, there has been an upward trend in carbapenem-resistant K. pneumoniae infections in China. This epidemiological trend needs to be examined to enable better disease control. We sought to analyze the genomic characteristics, including the prevalent sequence type (ST), resistance, virulence, and evolutionary relationship, of K. pneumoniae strains isolated from patients with different types of infections in northern China to provide theoretical support for the effective prevention and control of the evolution and transmission of K. pneumoniae.

Methods: The STs were analyzed using multi-locus sequence typing (MLST). Drug susceptibility tests were used to examine the resistance of these STs to various antibiotics. A phylogenetic tree of these isolates was constructed using the National Center for Biotechnology Information genome as the reference. Antibiotic resistance genes were identified by comparing the genomic sequences against those in the Comprehensive Antibiotic Resistance Database. Virulence genes were identified using the Virulence Factor database, while the pathogenicity of the isolates was predicted using PathogenFinder.

Results: In total, 38 clinical isolates of K. pneumoniae were identified and sequenced by high-throughput sequencing. Multidrug-resistant ST11 and hypervirulent ST23 were found to be the prevalent K. pneumoniae strains. The distribution of the ST11 strains was strongly correlated with stays in the neurosurgery department (chi square test, P=0.02), while the ST23 strains were more frequently isolated from patients with liver abscesses and gallbladder infections. The ST23 strains were significantly more pathogenic than the other STs (Wilcox test, P<0.001). The resistance analysis showed that the rmtB genes were significantly correlated with amikacin resistance (P<2.2e-16, R2=1). The ST11 strains were also found to co-harbor the KPC-2, rmtB, and TEM-1 genes. To the best of our knowledge, this is the first study to report on the dissemination of such multidrug-resistant K. pneumoniae ST11 strains in Tianjin.

Conclusions: The carbapenem-resistant K. pneumoniae (CRKP) ST11 may become highly virulent K. pneumoniae (CR-hvKP) due to the acquisition of virulence plasmids. Attention should be paid to the evolutionary pressure of a caused by the overuse of antibiotics, which may trigger the further development of multidrug-resistant K. pneumoniae infections.

关于中国北方不同肺炎克雷伯菌感染分子流行病学特征的单中心回顾性研究。
背景:肺炎克雷伯菌(K. pneumoniae)是一种机会性病原体,可引起多种危及生命的感染。最近,中国耐碳青霉烯类的肺炎克雷伯菌感染呈上升趋势。为了更好地控制疾病,需要对这一流行病学趋势进行研究。我们试图分析从中国北方不同类型感染患者中分离出的肺炎克雷伯菌株的基因组特征,包括流行序列类型(ST)、耐药性、毒力和进化关系,为有效预防和控制肺炎克雷伯菌的进化和传播提供理论支持:方法:采用多焦点序列分型(MLST)对 STs 进行分析。方法:采用多焦点序列分型法(MLST)对STs进行分析,并通过药敏试验检测STs对各种抗生素的耐药性。以美国国家生物技术信息中心基因组为参考,构建了这些分离物的系统发生树。通过将基因组序列与抗生素耐药性综合数据库(Comprehensive Antibiotic Resistance Database)中的序列进行比较,确定了抗生素耐药性基因。利用病毒因子数据库鉴定了病毒性基因,并利用 PathogenFinder 预测了分离物的致病性:结果:通过高通量测序,共鉴定并测序了 38 株肺炎克雷伯菌临床分离株。发现耐多药 ST11 和高病毒性 ST23 是肺炎克雷伯菌的主要菌株。ST11菌株的分布与神经外科的住院时间密切相关(卡方检验,P=0.02),而ST23菌株则更多地从肝脓肿和胆囊感染患者中分离出来。ST23 菌株的致病性明显高于其他 STs(Wilcox 检验,PrmtB 基因与阿米卡星耐药性显著相关(P2=1)。此外,还发现 ST11 菌株共同携带 KPC-2、rmtB 和 TEM-1 基因。据我们所知,这是第一份关于耐多药肺炎克菌 ST11 菌株在天津传播的研究报告:结论:耐碳青霉烯类药物的肺炎克雷伯菌(CRKP)ST11可能因获得毒力质粒而成为高毒力肺炎克雷伯菌(CR-hvKP)。应注意过度使用抗生素造成的进化压力,这可能会引发耐多药肺炎克菌感染的进一步发展。
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来源期刊
Journal of thoracic disease
Journal of thoracic disease RESPIRATORY SYSTEM-
CiteScore
4.60
自引率
4.00%
发文量
254
期刊介绍: The Journal of Thoracic Disease (JTD, J Thorac Dis, pISSN: 2072-1439; eISSN: 2077-6624) was founded in Dec 2009, and indexed in PubMed in Dec 2011 and Science Citation Index SCI in Feb 2013. It is published quarterly (Dec 2009- Dec 2011), bimonthly (Jan 2012 - Dec 2013), monthly (Jan. 2014-) and openly distributed worldwide. JTD received its impact factor of 2.365 for the year 2016. JTD publishes manuscripts that describe new findings and provide current, practical information on the diagnosis and treatment of conditions related to thoracic disease. All the submission and reviewing are conducted electronically so that rapid review is assured.
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