Cress Lab

Cress Lab

@cresslab.bsky.social

The Cress Lab | Innovative Genomics Institute @ UC Berkeley | Microbiome Editing | Microbiome Delivery Technologies | Phage and MGE Functional Genomics | Hiring! https://www.cresslab.bio/

1.1K followers1.4K following81 posts

Pinned

Our lab is proud to present our latest work harnessing Bridge Recombinase for genome-scale editing in diverse bacteria, microbiome editing, and programmable horizontal gene transfer.

bioRxiv Synthetic Biology@biorxiv-synthbio.bsky.social

Bridge recombinase enables versatile rewriting of bacterial genomes https://www.biorxiv.org/content/10.64898/2026.04.29.721476v1

Cress Lab reposted

🚨 New preprint 🚨 We’ve discovered millions of viruses from sequencing data but we don’t always know who they infect. Our new tool, VHAMSTeR generates broad virus host predictions across the tree of life (prokaryote, plant, animal, fungi and protist hosts) A thread 🧵👇 www.biorxiv.org/content/10.6...

biorxiv.orgViral host assignment across the tree of life with VHAMSTeRViruses infect organisms across the tree of life, but many are not associated with a specific host. Here we present VHAMSTeR (Virus Host Assignment Model using Sequence Transformers and Reading-frames...

Cress Lab reposted

Cress Lab reposted

Forgot to tag #phage #phagesky #AMR

Vivek Mutalik@vivekmutalik.bsky.social

A new preprint 🎉 from phagefoundry.org Mycobacteriophages are candidate therapies for drug-resistant mycobacterial infections, but we still don't know how most of them get into their hosts. Our new preprint tackles this challenge 👉🏽 www.biorxiv.org/content/10.6...

Cress Lab reposted

#plasmidbiology #plasmid Just out! 🚀 Thrilled by our discovery: the function of the C-terminal domain of MOBH1 relaxases! We uncovered this thanks to a fertility inhibitor encoded by a parasitic mobile genetic element. Congrats to Florence on a great piece of work! 👏 academic.oup.com/nar/article/...

academic.oup.comConjugative transfer inhibition of IncA and IncC plasmids by SGI1-like elements via relaxosome assembly interferenceAbstract. Broad-host-range IncA and IncC (A/C) conjugative plasmids propagate multidrug resistance in bacteria and mobilize chromosomal resistance islands,

Cress Lab reposted

Excited to share our work on bacterial immune signaling! Our preprint reveals how RNA-guided Cas13 cleaves host tRNAs to generate small-molecule messengers that activate 2TMβ, linking RNA recognition to membrane damage and phage defense. 1/11

Cress Lab reposted

Pleased to share my first preprint from my postdoc, where I ask what drives mobile DNA movement between bacterial cells in complex communities like the gut microbiome. To answer this, we built a way to capture mobile DNA in the act of moving between cells, using short-read metagenomics. 🧵

doi.orgdoi.org

Cress Lab reposted

Reminder🎗️: MCB is hiring Assistant Professors across 3 divisions! 🗓️ Application Deadline: October 19, 2026

UC Berkeley MCB@berkeleymcb.bsky.social

MCB is hiring Assistant Professors across 3 divisions!: 🧪BBS: aprecruit.berkeley.edu/JPF05483 🧬GGED: aprecruit.berkeley.edu/JPF05481 🦠IMM: aprecruit.berkeley.edu/JPF05486 🗓️ Application Deadline: October 19, 2026 🔗 Click the links or scan the QR codes to learn more and apply

Cress Lab reposted

Cress Lab reposted

Our story with @hobbslabutah.bsky.social discovering CBASS sensing of phage proteases out now in @science.org New data include CBASS recognition of diverse proteases beyond T4, and verifying CD-NTase activation loop cleavage as the trigger for defense in vivo www.science.org/doi/10.1126/...

science.orgPhage proteases activate CBASS antiphage immunityCyclic oligonucleotide–based antiphage signaling systems (CBASS) are bacterial immune pathways evolutionarily related to cGAS-STING (cyclic GMP-AMP synthase–stimulator of interferon genes) in humans. ...
Kranzusch Lab@kranzuschlab.bsky.social

After >10 years of our lab studying bacterial cGAS-like enzymes, @hobbslabutah.bsky.social finally reconstitutes viral sensing in vitro and discovers how these ancient receptors sense phage protease enzymes to detect virion assembly and activate antiviral immunity www.biorxiv.org/content/10.6...

Cress Lab reposted

The final version of our manuscript on TnSeq in bacteriophages (“HIDEN-SEQ”) is out today – if you have an interesting phage phenotype and want to know the underlying genetic basis, this one is for you! 1/4

Cress Lab reposted

*PLEASE RE-POST* Applications for the trainee-focussed GRS immediately preceding this meeting are also now open! We will begin accepting applicants on *January 15th, 2027*. We will expedite our review for applicants requiring Visas, so please submit ASAP. www.grc.org/microbial-po...

grc.org2027 Microbial Population Biology (GRS) Seminar GRCThe 2027 Gordon Research Seminar on Microbial Population Biology (GRS) will be held in Andover, New Hampshire. Apply today to reserve your spot.
Will Ratcliff@wcratcliff.bsky.social

1/17 Submissions are now open for the 2027 Microbial Population Biology GRC! We expect this meeting to be extraordinarily oversubscribed. If you want to come, time is of the essence--apply ASAP! June 27–July 2 • Andover, NH www.grc.org/microbial-po...

Cress Lab reposted

Happy to share the core work of my PhD! Our CRISPRi screens revealed key genes for E. coli survival in a gut environment shaped by diet and inflammation. Many thanks to my co-supervisors @dbikard.bsky.social and @nathalierolhion.bsky.social, and to all co-authors! Details in David's thread👇

David Bikard@dbikard.bsky.social

New paper from the lab, out in Nature Microbiology. We ran CRISPRi screens to ask what genes E. coli needs in order to live in a gut and what this can tell us about the gut environment itself. https://doi.org/10.1038/s41564-026-02471-8

Cress Lab reposted

Using recombinases to build robust cross-kingdom genetic circuits? 🧬 Need to know what they are *actually* doing? We got you covered! In the latest from the lab, we show the power of nanopore sequencing for unraveling the inner workings of these circuits. doi.org/10.1038/s414...

Cress Lab reposted

We built this tool and resource to share. These systematic gene functional annotations have been critical for our own work and we hope that they are widely useful for everyone. Enjoy!

Alexis Verger 🧬🧫🧪@alexis-verger.cpesr.fr

Affinage: Genome-Scale Mechanistic Gene Annotation from the Published Literature arxiv.org/html/2607.02... affinage.wi.mit.edu this tool looks fantastic @iaincheeseman.bsky.social ! 🤯

Cress Lab reposted

Cress Lab reposted

Cress Lab reposted

Proud and excited to share our first preprint 🚀 in which we • create a high-fitness firewalled organism, • that stably colonizes the mouse gut for >100 days, • resists all tested phages in the gut, • and blocks horizontal gene transfer. + A new method: Chimera genomes to tailor existing synthetic

Cress Lab reposted

VIPR is now out in Science! What started with a mysterious RNA led us to an unexpected way of recognizing DNA, as well as some clues to CRISPR’s origins. So happy to share these two papers with an incredible team. Links below; original discovery thread here ↓

Kenneth Loi@kenjmloi.bsky.social

Excited to share our discovery of a new programmable RNA-guided DNA-targeting system hiding inside bacteriophages that predates CRISPR. We call it VIPR (Viral Interference Programmable Repeat), and it uses an entirely new logic to find its targets. Thread + link below.

Cress Lab reposted

Cress Lab reposted

Microbial intergenic regions encode much of the regulatory and functional logic of the genome, but they remain systematically difficult to discover and annotate. We trained a sparse autoencoder on gLM2 to identify recurring patterns across hundreds of millions of microbial intergenic regions... 🧵

Cress Lab reposted

Microbial genomes have been extensively mined for new proteins, but the noncoding sequences between genes remain largely unexplored despite encoding important regulatory and functional information. In our new work, we asked whether gLM2 could help systematically discover these intergenic features.

Tatta Bio@tattabio.bsky.social

Microbial intergenic regions encode much of the regulatory and functional logic of the genome, but they remain systematically difficult to discover and annotate. We trained a sparse autoencoder on gLM2 to identify recurring patterns across hundreds of millions of microbial intergenic regions... 🧵

Cress Lab reposted