Bridge recombinase enables versatile rewriting of bacterial genomes

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Authors: Jaymin Patel, Sophia E. Swartz, Agnès Oromí-Bosch, Liana Yong, Zachary W. LaTurner, Jack E. Demaray, Angela Voelker, Ryuichi Ono, Patrick Vu, Preeti Rao, Hannah Luskin, Pia De Andrade
+10 more Michael L. Cui, Givi Mchedlishvili, Madeline M. Hayes, Natalie Aluwihare, Carlos E. Iglesias-Aguirre, Emma C. MacKenzie, Cynthia I. Rodriguez, Suzanne Devkota, Spencer Diamond, Brady F. Cress
Cited by: 2
References: 62

Abstract

Abstract Bacteria drive crucial processes across ecosystems and impact human health, yet tools to rewrite microbiomes remain limited. Here, we show that bridge recombinase enables versatile and programmable genome editing across the bacterial tree of life. In Escherichia coli , we achieved 142 kb insertions at >90% efficiency, megabase-scale inversions (2.3 Mb), and pathway-scale 50 kb excisions. With a single ortholog and bridge RNA (bRNA), we edited bacterial isolates spanning five phyla and diverse members of two human gut communities. We overcame cross-reactivity between co-expressed bRNAs to establish search-and-replace Targetable Recombinase Assisted DNA Exchange (TRADE) editing and demonstrated capture and interphylum transfer of chromosomal pathways, enabling programmable horizontal gene transfer. These advances establish bridge recombinase as a foundation for reprogramming gene flow in complex microbial communities.

Fields of Study & Subjects

CRISPR and Genetic Engineering Bacterial Genetics and Biotechnology Microbial Fuel Cells and Bioremediation

Publication details

Journal / source
bioRxiv (Cold Spring Harbor Laboratory)
Publisher
openRxiv
Publication date
29 April 2026
Document type
Preprint