中国两家医院耐碳青霉烯类鲍曼不动杆菌临床分离株的全基因组测序和基因组特征分析。

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES
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引用次数: 0

摘要

耐碳青霉烯类鲍曼不动杆菌(CRAB)菌株引起的非医院性疫情在全球范围内迅速出现,令人担忧。在此,我们旨在描述 2023 年从中国两家医院分离的 CRAB 菌株的基因组特征。所分离的鲍曼尼氏菌主要来自重症监护室,从痰中分离(71.43%,15/21),其次是尿液(14.29%,3/21)。21株鲍曼尼杆菌具有多重耐药(MDR)特征,全基因组测序显示它们都携带 blaOXA-23。根据巴斯德多焦点序列分型(MLST)方案,所有菌株都被分型为序列类型 2(ST2)。根据牛津 MLST 方案,6 株菌株属于 ST540 型,其中 3 株属于 ST208 型,4 株属于 ST784 型。Kaptive显示大多数菌株(38.10%,8/21)含有KL93。至于脂寡糖(OC 位点)类型,发现了 OCL1c 和 OCL1d,分别占 33.33%(7/21)和 66.67%(14/21)。根据 BacWGSTdb 服务器,我们发现属于 ST540 和 ST784 的菌株均采集自中国。而 ST938 菌株则分离自马来西亚和泰国。比较基因组学分析表明,AB10菌株与SXAB10-SXAB13菌株有封闭关系,表明传播发生在这两家医院和中国其他医院。此外,从泰国采集的 4300STDY7045869 株与本研究中的分离株具有近似的遗传关系,表明可能在不同国家间传播。此外,在这些菌株中还观察到 3-237 个单核苷酸多态性。总之,本研究对从中国两家医院采集的鲍曼不动杆菌菌株进行了基于基因组的研究,揭示了其流行病学和分子特征。在这两家医院中发生了克隆传播。因此,迫切需要在医院和其他临床环境中加强监测,以预防和控制CRAB的传播。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Whole genome sequencing and genomic characteristics analysis of carbapenem-resistant Acinetobacter baumannii clinical isolates in two hospitals in China

Nosocomial outbreaks caused by carbapenem-resistant Acinetobacter baumannii (CRAB) strains are rapidly emerging worldwide and are cause for concern. Herein, we aimed to describe the genomic characteristics of CRAB strains isolated from two hospitals in China in 2023. The A. baumannii isolates were mainly collected from the ICU and isolated from the sputum (71.43%, 15/21), followed by urine (14.29%, 3/21). Twenty-one A. baumannii strains possessed a multidrug-resistant (MDR) profile, and whole-genome sequencing showed that they all carried blaOXA-23. Based on the Pasteur multilocus sequence typing (MLST) scheme, all strains were typed into a sequence type 2 (ST2). Based on the Oxford MLST scheme, six strains belonged to ST540, three of which were ST208, and four strains were assigned to ST784. Kaptive showed most of the strains (38.10%, 8/21) contained KL93. As for the lipoolygosaccharide (OC locus) type, OCL1c and OCL1d were identified, accounting for 33.33% (7/21) and 66.67% (14/21), respectively. Based on the BacWGSTdb server, we found that the strains belonging to ST540 and ST784 were all collected from China. However, the ST938 strains were isolated from Malaysia and Thailand. Comparative genomics analysis showed that the AB10 strain had a closed relationship with SXAB10-SXAB13 strains, suggesting the transmission happened in these two hospitals and other hospital in China. In addition, the 4300STDY7045869 strain, which was collected from Thailand, possessed near genetic relationship with our isolates in this study, suggesting the possible spread among various countries. Additionally, 3–237 single nucleotide polymorphisms were observed among these strains. In conclusion, this study conducted a genome-based study for A. baumannii strains collected from two hospitals in China and revealed their epidemiological and molecular features. Clone spreading occurred in these two hospitals. Hence, there is an urgent need for increased surveillance in hospitals and other clinical settings to prevent and control CRAB spreading.

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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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