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The Lab, mapped

Tools and models for microbiome research.

The Ronda Lab connects microbial genome editing with the study of host–microbe interactions. Explore the tools, experimental models, and collaborations behind this work.

Microbiome editing tools

Developing tools to edit resident microbes directly within their communities.

An illustration of two microbes exchanging DNA, the in situ delivery the editing tools build on.

Novel delivery systems

  • Extracellular contractile systems (eCIS)

    Metagenomic mining of new systems, protein engineering for targeted protein and DNA delivery.

    With Rubin, Sachdeva

  • Mobilome engineering

    Mining and domesticating novel mobile genetic elements, and high-throughput capture of their hosts.

    With Diamond, Sachdeva, Cress

  • Targeted, more efficient conjugation

    Programming donor synthetic binding to target cells, and new materials to extend donor-recipient contact.

    With Murthy

Novel editors

  • Generative AI editors

    Compact, reprogrammable RNA-guided transposases, recombinases, and integrases.

    With Yun Song

  • Metagenomic mining

    Reprogramming Y recombinases, plus a machine-learning approach that compacts large multi-gene payloads by nesting genes.

    With Sandia

Localization and engraftment

  • Synthetic binders

    Programming bacterial attachment to epithelial cells.

  • Novel PUL and CAZymes

    Tuning which microbes take hold and persist.

Modulation of community structure

  • Rumen editing

    Editing rumen communities in vitro, testing antimicrobial peptides against methanogens, and exploring bromoform production in rumen commensals.

    With Diamond, Hess, Cress

  • Airways editing

    Novel editing systems and AMPs for Moraxella catarrhalis.

    With Lynch

  • Infants microbiome editing

    Extending in situ editing to the developing infant gut.

    With Banfield

Host–microbiome interactome

Studying host–microbe interactions using human tissue models and an anaerobic co-culture platform that preserves the spatial structure of microbial communities.

An illustration of microbes wired into a host interactome network.

Anaerobic co-culture with gut geography

  • Gut-geography co-culture

    An anaerobic co-culturing system that keeps the spatial structure of the community intact while it is studied.

Human stem cells and organoids

  • Asthma sample co-culture

    Cultivating patient samples in the anaerobic co-culture organoid system.

    With Lynch, Diamond

  • Bifido colonization

    Tnseq libraries to test how commensals colonize human gut organoids.

    With Huang (Stanford)

  • Inflammation reporters

    Reporter systems in human gut organoids and macrophages to read the tissue response.

    With Braverman

Reprogramming host physiology

  • Engineering commensals for tolerance

    Developing commensals designed to deliver tolerance-promoting signals in host-relevant and preclinical models.

    With Brown Lab (MSK)

Expanded BIOME group

Automated microbial culturing and next-generation sequencing.

An illustration of a diverse field of cultured microbial species.

Automation

  • AI-automated culturomics

    High-throughput, automated culturing guided by machine learning.

  • Automated NGS

    Automated next-generation sequencing to keep pace with the culturing.

From discovery to mechanism

From an unknown signal to immune tolerance.

A candidate molecule is not yet a mechanism. Follow the evidence from metagenomic sequence to a receiving immune cell, a causal test, and an engineered microbial function.

This work is preclinical. It is not a demonstrated treatment.

A signal is hidden in the community

Metagenomic sequence contains clues to microbial molecules that standard annotation can miss. The search begins among billions of letters, and thousands of possible signals.

From metagenomic sequence to a receiving immune cell.