生物
屎肠球菌
基因组
遗传学
质粒
微生物学
水平基因转移
细菌基因组大小
鲍曼不动杆菌
流动遗传元素
分枝杆菌
肺炎克雷伯菌
DNA测序
纳米孔测序
基因组岛
基因
计算生物学
铜绿假单胞菌
细菌
大肠杆菌
作者
Masato Suzuki,Yusuke Hashimoto,Aki Hirabayashi,Koji Yahara,Mitsunori Yoshida,Hanako Fukano,Yoshihiko Hoshino,Keigo Shibayama,Haruyoshi Tomita
标识
DOI:10.1007/978-1-0716-2996-3_16
摘要
Antimicrobial-resistant (AMR) bacterial infections caused by clinically important bacteria, including ESKAPE pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species) and mycobacteria (Mycobacterium tuberculosis and nontuberculous mycobacteria), have become a global public health threat. Their epidemic and pandemic clones often accumulate useful accessory genes in their genomes, such as AMR genes (ARGs) and virulence factor genes (VFGs). This process is facilitated by horizontal gene transfer among microbial communities via mobile genetic elements (MGEs), such as plasmids and phages. Nanopore long-read sequencing allows easy and inexpensive analysis of complex bacterial genome structures, although some aspects of sequencing data calculation and genome analysis methods are not systematically understood. Here we describe the latest and most recommended experimental and bioinformatics methods available for the construction of complete bacterial genomes from nanopore sequencing data and the detection and classification of genotypes of bacterial chromosomes, ARGs, VFGs, plasmids, and other MGEs based on their genomic sequences for genomic epidemiological analysis of AMR bacteria.
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