Pipeline for Antimicrobial Resistance Gene Quantification from Host Tissue

Levi M. Svaren, Wenli Li
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引用次数: 0

Abstract

Antibiotics are frequently used in food production animals to control disease and improve productivity, but this promotes the development of antimicrobial resistance (AMR) and subsequent broader spread of AMR bacteria throughout food chain, endangering the well-being and health of both animals and humans. In humans, the gut microbiome harbors a diverse range of AMR bacteria, known as the resistome. To effectively mitigate AMR in food animals requires first determining the expression and abundance of AMR-related genes in the gut resistome. Currently, such knowledge in regard to food animals is largely lacking. Gut tissue RNA sequencing (GTRS) can capture metabolically active transcripts from both the host and the microbes attached to the gut epithelium. Ideally, AMR genes can be quantified using GTRS data, making it possible to study the relationship between host and microbe. For the majority of these GTRS studies, only host transcriptome changes have been reported, while the microbial AMR remains largely unexamined, mainly due to the lack of easily implementable bioinformatics tools. Here we present a straightforward workflow to accomplish that using common command-line bioinformatics tools. With this pipeline, the host is considered noise, and host data are filtered out from the microbial reads. Transcript quantification of the AMR genes is then performed. The pipeline then continues through AMR transcript quantification, differential gene expression, and SNP analysis. Using open-source tools, we made this analytical pipeline easy to implement and able to generate results ready to be incorporated into publishable reports. Published 2025. This article is a U.S. Government work and is in the public domain in the USA.

Basic Protocol: Running the gene quantification pipeline

Support Protocol 1: Downloading FASTQ files from the NCBI database

Support Protocol 2: Building a genome reference index of the host

Support Protocol 3: Differential gene expression analysis

Support Protocol 4: Single-nucleotide polymorphism (SNP) analysis

宿主组织中抗菌素耐药基因定量的管道
为了控制疾病和提高生产力,经常在食品生产动物中使用抗生素,但这促进了抗菌素耐药性(AMR)的发展,并随后在整个食物链中更广泛地传播AMR细菌,危及动物和人类的福祉和健康。在人类的肠道微生物群中,有各种各样的抗菌素耐药性细菌,被称为抵抗组。为了有效减轻食用动物的抗菌素耐药性,首先需要确定肠道抵抗组中抗菌素耐药性相关基因的表达和丰度。目前,这种关于食用动物的知识在很大程度上是缺乏的。肠道组织RNA测序(GTRS)可以捕获宿主和附着在肠道上皮上的微生物的代谢活性转录物。理想情况下,可以使用GTRS数据对AMR基因进行量化,从而使研究宿主与微生物之间的关系成为可能。在大多数GTRS研究中,仅报道了宿主转录组的变化,而微生物AMR在很大程度上仍未得到检验,这主要是由于缺乏易于实现的生物信息学工具。在这里,我们提出了一个简单的工作流程来完成使用常见的命令行生物信息学工具。在这个管道中,宿主被认为是噪声,宿主数据从微生物读取中过滤出来。然后进行AMR基因的转录物定量。然后继续进行AMR转录物量化、差异基因表达和SNP分析。使用开源工具,我们使这个分析管道易于实现,并且能够生成准备合并到可发布报告中的结果。2025年出版。这篇文章是美国政府的作品,在美国属于公有领域。基本协议:运行基因定量管道支持协议1:从NCBI数据库下载FASTQ文件支持协议2:建立宿主基因组参考索引支持协议3:差异基因表达分析支持协议4:单核苷酸多态性(SNP)分析
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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