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用于结核分枝杆菌基因型贝达喹啉耐药性检测的环化

Circularization of for Genotypic Bedaquiline Resistance Testing of Mycobacterium tuberculosis.

作者信息

Limberis Jason D, Nalyvayko Alina, Ernst Joel D, Metcalfe John Z

机构信息

Division of Experimental Medicine, University of California, San Francisco, California, USA.

Division of Pulmonary and Critical Care Medicine, Zuckerberg San Francisco General Hospital and Trauma Centre, University of California, San Francisco, California, USA.

出版信息

Microbiol Spectr. 2023 Mar 6;11(2):e0412722. doi: 10.1128/spectrum.04127-22.

Abstract

Circular DNA offers benefits over linear DNA in diagnostic and field assays, but currently, circular DNA generation is lengthy, inefficient, highly dependent on the length and sequence of DNA, and can result in unwanted chimeras. We present streamlined methods for generating PCR-targeted circular DNA from a 700 bp amplicon of , the high GC content (65%) gene implicated in Mycobacterium tuberculosis bedaquiline resistance, and demonstrate that these methods work as desired. We employ self-circularization with and without splints, a Gibson cloning-based approach, and novel 2 novel methods for generating pseudocircular DNA. The circular DNA can be used as a template for rolling circle PCR followed by long-read sequencing, allowing for the error correction of sequence data, and improving the confidence in the drug resistance determination and strain identification; and, ultimately, improving patient treatment. Antimicrobial resistance is a global health threat, and drug resistant tuberculosis is a principal cause of antimicrobial resistance-related fatality. The long turnaround time and the need for high containment biological laboratories of phenotypic growth-based Mycobacterium tuberculosis drug susceptibility testing often commit patients to months of ineffective treatment, and there is a groundswell of effort in shifting from phenotypic to sequencing-based genotypic assays. Bedaquiline is a key component to newer, all oral, drug resistant, tuberculosis regimens. Thus, we focus our study on demonstrating the circularization of , the gene that underlies most M. tuberculosis bedaquiline resistance. We present 2 novel methods for generating pseudocircular DNA. These methods greatly reduce the complexity and time needed to generate circular DNA templates for rolling circle amplification and long-read sequencing, allowing for error correction of sequence data, and improving confidence in the drug resistance determination and strain identification.

摘要

环状DNA在诊断和现场检测方面比线性DNA更具优势,但目前环状DNA的生成过程冗长、效率低下,高度依赖DNA的长度和序列,并且可能产生不需要的嵌合体。我们提出了从结核分枝杆菌贝达喹啉耐药相关的高GC含量(65%)的700 bp扩增子生成PCR靶向环状DNA的简化方法,并证明这些方法按预期发挥作用。我们采用了有或没有夹板的自环化、基于吉布森克隆的方法以及两种生成假环状DNA的新方法。环状DNA可作为滚环PCR的模板,随后进行长读长测序,从而实现序列数据的错误校正,提高耐药性测定和菌株鉴定的可信度;并最终改善患者治疗。抗菌药物耐药性是全球健康威胁,耐药结核病是抗菌药物耐药性相关死亡的主要原因。基于表型生长的结核分枝杆菌药物敏感性测试周转时间长且需要高防护生物实验室,这常常使患者接受数月的无效治疗,因此,从表型检测转向基于测序的基因型检测的努力正在兴起。贝达喹啉是更新的全口服耐药结核病治疗方案的关键组成部分。因此,我们将研究重点放在证明结核分枝杆菌大多数贝达喹啉耐药性所基于的基因的环化上。我们提出了两种生成假环状DNA的新方法。这些方法大大降低了生成用于滚环扩增和长读长测序的环状DNA模板所需的复杂性和时间,实现了序列数据的错误校正,提高了耐药性测定和菌株鉴定的可信度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc22/10100719/371d85698620/spectrum.04127-22-f001.jpg

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