Genomic epidemiology of vancomycin-resistant Enterococcus faecium in Eastern Denmark from 2020 to 2022, and identification of vanB Tn1549 insertion sites.

IF 3.7 3区 医学 Q2 INFECTIOUS DISEASES
Maja Johanne Søndergaard Knudsen, Jose Alfredo Samaniego Castruita, Ingrid Maria Cecilia Rubin, Sarah Mollerup, Helle Krogh Johansen, Rasmus L Marvig, Karen Leth Nielsen, Barbara Juliane Holzknecht, Morten Hoppe, Michael Kemp, Henrik Westh, Mette Pinholt
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引用次数: 0

Abstract

Background: We aimed to describe the genomic epidemiology of vancomycin-resistant Enterococcus faecium (VREfm) in Eastern Denmark from 2020 to 2022, identify and characterise the vanB Transposon 1549 (Tn1549) insertion sites among vanB VREfm clones and identify emerging VREfm clones.

Methods: We analysed all VREfm from our routine diagnostic sequencing during the study period. Using the Seqsphere + v.8.2.0 software (Ridom GmbH, Münster, Germany, ( http://www.ridom.de/seqsphere ), minimum spanning trees were created to visualise clusters. Tn1549 insertion sites were determined by in silico PCR. Nanopore sequencing was performed to assemble the regions surrounding Tn1549, which helped determine the insertion site locations.

Results: We included 2,437 isolates in the study. A total of 463 isolates carried vanA, 1,963 isolates carried vanB, and 11 isolates carried both genes. Of all isolates carrying vanB, 254 isolates had the Tn1549 inserted in the araA2 gene, 1,604 in the sir2 gene, and 116 in neither the araA2 nor sir2 genes. We identified eight chromosomal insertion sites other than in the araA2 and sir2 genes. Three isolates carried the Tn1549 on plasmids. No emerging clones were found.

Results: We have described the genomic epidemiology during the study period and identified ten chromosomal Tn1549 insertion sites.

2020 - 2022年丹麦东部地区万古霉素耐药屎肠球菌基因组流行病学及vanB Tn1549插入位点鉴定
背景:我们旨在描述2020年至2022年丹麦东部万古霉素耐药粪便肠球菌(VREfm)的基因组流行病学,鉴定和表征vanB VREfm克隆中的vanB转座子1549 (Tn1549)插入位点,并鉴定新出现的VREfm克隆。方法:我们对研究期间常规诊断测序的所有VREfm进行分析。使用Seqsphere + v.8.2.0软件(Ridom GmbH, m nster, Germany, (http://www.ridom.de/seqsphere)),创建最小生成树来可视化集群。用PCR法确定Tn1549插入位点。利用纳米孔测序对Tn1549周围的区域进行组装,这有助于确定插入位点的位置。结果:我们纳入了2437株分离株。共有463株携带vanA基因,1963株携带vanB基因,11株同时携带两个基因。在所有携带vanB的分离株中,254株在araA2基因中插入Tn1549, 1604株在sir2基因中插入,116株在araA2和sir2基因中均未插入。我们确定了除araA2和sir2基因外的8个染色体插入位点。三个分离株在质粒上携带Tn1549。没有发现新的克隆。结果:我们描述了研究期间的基因组流行病学,并确定了10个染色体Tn1549插入位点。
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来源期刊
CiteScore
10.40
自引率
2.20%
发文量
138
审稿时长
1 months
期刊介绍: EJCMID is an interdisciplinary journal devoted to the publication of communications on infectious diseases of bacterial, viral and parasitic origin.
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