학술논문

Species- and site-specific genome editing in complex bacterial communities
Document Type
article
Source
Nature Microbiology. 7(1)
Subject
Microbiology
Biological Sciences
Ecology
Genetics
Biotechnology
Human Genome
Prevention
Aetiology
2.2 Factors relating to the physical environment
Infection
Archaea
Bacteria
CRISPR-Cas Systems
Gastrointestinal Microbiome
Gene Editing
Genome
Bacterial
Humans
Infant
Microbial Consortia
RNA
Guide
Kinetoplastida
Soil Microbiology
Medical Microbiology
Language
Abstract
Understanding microbial gene functions relies on the application of experimental genetics in cultured microorganisms. However, the vast majority of bacteria and archaea remain uncultured, precluding the application of traditional genetic methods to these organisms and their interactions. Here, we characterize and validate a generalizable strategy for editing the genomes of specific organisms in microbial communities. We apply environmental transformation sequencing (ET-seq), in which nontargeted transposon insertions are mapped and quantified following delivery to a microbial community, to identify genetically tractable constituents. Next, DNA-editing all-in-one RNA-guided CRISPR-Cas transposase (DART) systems for targeted DNA insertion into organisms identified as tractable by ET-seq are used to enable organism- and locus-specific genetic manipulation in a community context. Using a combination of ET-seq and DART in soil and infant gut microbiota, we conduct species- and site-specific edits in several bacteria, measure gene fitness in a nonmodel bacterium and enrich targeted species. These tools enable editing of microbial communities for understanding and control.