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泛耐药奇异变形杆菌分离株的基因组分析揭示了抗菌药物耐药性和毒力基因景观。

Genomic profiling of pan-drug resistant proteus mirabilis Isolates reveals antimicrobial resistance and virulence gene landscape.

机构信息

Trauma Intensive Care Unit, Zagazig University Hospitals, Zagazig, Egypt.

Department of Microbiology and Immunology, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt.

出版信息

Funct Integr Genomics. 2024 Sep 3;24(5):154. doi: 10.1007/s10142-024-01419-7.

Abstract

Proteus mirabilis is a gram-negative pathogen that caused significant opportunistic infections. In this study we aimed to identify antimicrobial resistance (AMR) genes and virulence determinants in two pan-drug resistant isolate "Bacteria_11" and "Bacteria_27" using whole genome sequencing. Proteus mirabilis "Bacteria_11" and "Bacteria_27" were isolated from two different hospitalized patients in Egypt. Antimicrobial susceptibility determined using Vitek 2 system, then whole genome sequencing (WGS) using MinION nanopore sequencing was done. Antimicrobial resistant genes and virulence determinants were identified using ResFinder, CADR AMR database, Abricate tool and VF analyzer were used respectively. Multiple sequence alignment was performed using MAFFT and FastTree, respectively. All genes were present within bacterial chromosome and no plasmid was detected. "Bacteria_11" and "Bacteria_27" had sizes of approximately 4,128,657 bp and 4,120,646 bp respectively, with GC content of 39.15% and 39.09%. "Bacteria_11" and "Bacteria_27" harbored 43 and 42 antimicrobial resistance genes respectively with different resistance mechanisms, and up to 55 and 59 virulence genes respectively. Different resistance mechanisms were identified: antibiotic inactivation, antibiotic efflux, antibiotic target replacement, and antibiotic target change. We identified several genes associated with aminoglycoside resistance, sulfonamide resistance. trimethoprim resistance tetracycline resistance proteins. Also, those responsible for chloramphenicol resistance. For beta-lactam resistance, only blaVEB and blaCMY-2 genes were detected. Genome analysis revealed several virulence factors contribution in isolates pathogenicity and bacterial adaptation. As well as numerous typical secretion systems (TSSs) were present in the two isolates, including T6SS and T3SS. Whole genome sequencing of both isolates identify their genetic context of antimicrobial resistant genes and virulence determinants. This genomic analysis offers detailed representation of resistant mechanisms. Also, it clarifies P. mirabilis ability to acquire resistance and highlights the emergence of extensive drug resistant (XDR) and pan-drug resistant (PDR) strains. This may help in choosing the most appropriate antibiotic treatment and limiting broad spectrum antibiotic use.

摘要

奇异变形杆菌是一种革兰氏阴性病原体,可导致严重的机会性感染。在这项研究中,我们使用全基因组测序的方法,旨在从埃及的两位住院患者中分离出的两种泛耐药株“Bacteria_11”和“Bacteria_27”中鉴定出抗生素耐药(AMR)基因和毒力决定因素。奇异变形杆菌“Bacteria_11”和“Bacteria_27”是从埃及的两位不同住院患者中分离出来的。使用 Vitek 2 系统测定了抗生素敏感性,然后使用 MinION 纳米孔测序进行了全基因组测序(WGS)。使用 ResFinder、CADR AMR 数据库、Abricate 工具和 VF 分析器分别鉴定了抗生素耐药基因和毒力决定因素。使用 MAFFT 和 FastTree 分别进行了多重序列比对。所有基因都存在于细菌染色体中,没有检测到质粒。“Bacteria_11”和“Bacteria_27”的大小分别约为 4,128,657 bp 和 4,120,646 bp,GC 含量分别为 39.15%和 39.09%。“Bacteria_11”和“Bacteria_27”分别携带 43 种和 42 种抗生素耐药基因,具有不同的耐药机制,分别携带多达 55 种和 59 种毒力基因。不同的耐药机制被鉴定为:抗生素失活、抗生素外排、抗生素靶标替换和抗生素靶标改变。我们鉴定了一些与氨基糖苷类耐药、磺胺类耐药、甲氧苄啶耐药、四环素耐药蛋白相关的基因。同时,那些负责氯霉素耐药的基因。对于β-内酰胺类耐药,仅检测到 blaVEB 和 blaCMY-2 基因。基因组分析揭示了几种毒力因子对分离株致病性和细菌适应性的贡献。此外,在两个分离株中还存在许多典型的分泌系统(TSSs),包括 T6SS 和 T3SS。对两个分离株的全基因组测序确定了其抗生素耐药基因和毒力决定因素的遗传背景。这种基因组分析提供了耐药机制的详细描述。此外,它还阐明了奇异变形杆菌获得耐药性的能力,并强调了广泛耐药(XDR)和泛耐药(PDR)菌株的出现。这有助于选择最合适的抗生素治疗,并限制广谱抗生素的使用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/062e/11369002/ae50ffabf836/10142_2024_1419_Fig1_HTML.jpg

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