对巴西出现的明尼苏达沙门氏菌系进行基因组鉴定,发现了一种新型抗性和毒力巨型质粒。

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Applied and Environmental Microbiology Pub Date : 2024-11-20 Epub Date: 2024-10-30 DOI:10.1128/aem.01579-24
Anamaria M P Dos Santos, Pedro Panzenhagen, Rafaela G Ferrari, Ana Beatriz Portes, Ana Carolina de Jesus, Alan Ochioni, Dália Rodrigues, Magaly Toro, Jianghong Meng, Marc Allard, Carlos A Conte-Junior
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引用次数: 0

摘要

在巴西,明尼苏达沙门氏菌与海德堡沙门氏菌已成为家禽和家禽产品中的主要血清型。为了了解明尼苏达沙门氏菌过去几年在巴西的出现情况,我们对病原体检测数据库中选出的 69 个明尼苏达沙门氏菌基因组和从巴西分离的 65 个克隆新基因组进行了比较分析。我们发现,在新出现的基因组中存在对四环素[tet(A)]、磺胺(sul2)和AmpC β-内酰胺酶(blaCMY-2)的多药抗性基因,同时还携带有抗性和毒力巨型质粒(约 210 kb),命名为 pESM(新出现的明尼苏达沙门氏菌质粒)。pESM 是一个 IncC/A2 质粒,据预测可提高明尼苏达沙门氏菌对汞的环境耐受性(mer 操作子),并由于 tet(A) 和 blaCMY-2 的存在而分别提供对四环素和氨苄西林的抗性。此外,pESM 还携带与铁吸收有关的耶尔森氏菌嗜铁素(耶尔森氏菌的高致病性岛)。时间推断表明,最近的共同祖先是1978年左右,携带pESM的克隆出现的基因组属于明尼苏达鼠疫的一个完全不同的系。我们的研究结果表明,pESM 的存在很可能促成了明尼苏达沙门氏菌的出现,并与这一特定克隆系在巴西的成功传播密切相关。重要意义明尼苏达沙门氏菌已在巴西成为与人类和动物感染有关的主要血清型之一,具有高毒力和抗生素耐药性,被列为人类临床治疗的最优先药物。本研究通过全基因组测序、时间分析和系统发生学来了解明尼苏达沙门氏菌在巴西出现的相关基因知识。通过长读测序,确定并描述了携带毒力、抗生素耐药性和重金属耐受性基因的独特巨型质粒,这可能是明尼苏达沙门氏菌在巴西乃至全球成功出现的关键因素。这种质粒可能在克隆和血清型之间高度传播,对公共卫生构成风险,因为获得这种质粒可能会提高沙门氏菌的适应性、毒力、抗药性和持久性。了解与血清型出现有关的遗传学方面的知识有助于制定措施,减少危险的耐多药菌株的传播。
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Genomic characterization of a clonal emergent Salmonella Minnesota lineage in Brazil reveals the presence of a novel megaplasmid of resistance and virulence.

Salmonella Minnesota has emerged in Brazil as the predominant serovar in poultry and poultry products, along with Salmonella Heidelberg. To understand the emergence of Salmonella Minnesota over the last few years in Brazil, we performed a comparative analysis between 69 selected S. Minnesota genomes from Pathogen Detection database and 65 clonal emergent genomes isolated from Brazil. We demonstrate the presence of multidrug resistance genes against tetracycline [tet(A)], sulfonamide (sul2), and AmpC beta-lactamase (blaCMY-2) in emergent genomes, along with the carriage of a megaplasmid of resistance and virulence (~210 kb), designated pESM (plasmid for emergent Salmonella Minnesota). pESM is an IncC/A2 plasmid predicted to increase S. Minnesota environmental tolerance to mercury (mer operon) and provide resistance to tetracycline and ampicillin due to the presence of tet(A) and blaCMY-2, respectively. Moreover, pESM carries the yersiniabactin siderophore (high-pathogenicity island of Yersinia) related to the iron uptake. The temporal inference demonstrated that the most recent common ancestor dated from ~1978 and that the clonal emergent genomes carrying the pESM belong to a completely different lineage of S. Minnesota. Our results indicate that the presence of pESM likely contributes to the emergence of S. Minnesota and is precisely related to the successful spread of this particular clonal lineage in Brazil.IMPORTANCESalmonella Minnesota has emerged in Brazil as one of the leading serovars related to human and animal infection, presenting high virulence and antibiotic resistance to drugs classified as the highest priority for clinical treatment in humans. This study performed whole-genome sequencing, temporal analysis, and phylogenetics to understand the genetic insights related to the emergence of Salmonella Minnesota in Brazil. Long-read sequencing has led to the identification and characterization of a unique megaplasmid carrying virulence, antibiotic resistance, and heavy-metal tolerance genes, which may play a central role in S. Minnesota's successful emergence in Brazil and possibly worldwide. The potentially high transmissibility of this plasmid between clones and serovars represents a risk to public health since its acquisition may increase Salmonella's fitness, virulence, resistance, and persistence. Understanding the genetic aspects related to the emergence of serovars can help devise measures to mitigate the spread of hazardous multidrug-resistant strains.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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