Peter Fineran

@peterfineran.bsky.social

Prof. and Head of Phage-host interactions (Phi) lab. Phage defences, counter-defences, CRISPR-Cas, toxin-antitoxin. FRSNZ / James Cook Fellow

Our paper is out in Nature Microbiology: functional analysis of 80 phage sponges, revealing new sponges that inhibit bac immunity by binding the immune signals cCMP, cUMP and N7-cADPR Thanks to all coauthors and our collaborators at the Kranzusch Lab. Congrats Romi! www.nature.com/articles/s41...

Functional diversity of phage sponge proteins that sequester host immune signals - Nature Microbiology

A functional screen reveals phage sponge proteins that bind Pycsar, Thoeris and CBASS signalling molecules to inhibit bacterial immunity.

nature.com

Romi Hadary@romihadary.bsky.social · 2mo ago

Excited to see our work out in @natmicrobiol.nature.com! We uncovered broad functional diversity within phage sponge families🧽. Huge thanks to all coauthors and brilliant collaborators @kranzuschlab.bsky.social @reneechang.bsky.social ! www.nature.com/articles/s41...

Out now–our work on bacterial cGAS-like enzymes making 2′,3′-cGAMP! Read Uday's thread for updates since the preprint including determining our lab's first protein structure and developing a new system to study bacterial STING homologs in phage defense👇

Uday Tak@snowkaryote.bsky.social · 4mo ago

Happy to share the final version of my postdoc work on bacterial CBASS immunity with @aaronwhiteley.bsky.social published in @cp-cellhostmicrobe.bsky.social www.cell.com/cell-host-mi...

How do you kill a MRSA superbug armed with 15 different anti-phage defense systems? You make a smarter phage. Check out our latest preprint on overcoming bacterial immunity using defense-guided engineering to build durable therapeutic phage cocktails! Led by Sarah Voss. doi.org/10.64898/202...

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Great fun presenting some of our research @otagomicroimmuno.bsky.social @universityofotago.bsky.social Including transposon mutagenesis of phages. www.biorxiv.org/content/10.6...

High-throughput transposon mutagenesis defines the essential genome of diverse phages

Phages are important drivers of bacterial evolution with therapeutic potential as antimicrobials. However, gaps in our understanding of phages and our inability to rapidly engineer them with new genetic cargo hinders progress towards phage-based therapies. To address the lack of unbiased, genome-wide mutational tools for phages, we developed transposon mutagenesis employing CRISPR-anti-CRISPR (Acr)-based selection and deep-sequencing (Phage Tn-seq). Transposon mutagenesis was effective for phages with unmodified or hypermodified genomes and a jumbo phage that protects its DNA within a nucleus. Phage Tn-seq enabled phage gene essentiality assignment consistent with structural proteomics and core gene conservation. Insertion biases allowed prediction of transcriptional direction and early injected phage DNA regions. We exploited the method to rapidly deliver new cargo to phage genomes in just a few days and used an AI-designed Acr to expand the phage transposon toolbox. Phage Tn-seq is a versatile tool to advance our understanding and applications of phages. ### Competing Interest Statement The authors have declared no competing interest. Royal Society Te Apārangi, https://ror.org/04tajb587 Alexander von Humboldt Foundation, https://ror.org/012kf4317 The L’Oréal Groupe Australia University of Otago, https://ror.org/01jmxt844

biorxiv.org

Asaf Levy@asaflevylab.bsky.social · 5mo ago

Arabinose isn't only an inducer! @peterfineran.bsky.social gave a talk in our Hebrew Univ. microbiology journal club and mentioned his recent amazing finding that some phages add up to 3 arabinoses (!!) to their DNA to evade bacterial defense. Mahler et al. CHM 2025 www.cell.com/cell-host-mi...

Join us for the first Rangahau Rising of 2026 with Dr Nils Birkholz (University of Otago). Nils will talk about his research on the plant pathogen Pectobacterium, highlighting new solutions for targeting problematic bacterial pathogens. 📍 Online, Register via Zoom: zurl.co/FLQvS

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🚨Preprint alert - this is a big one! We transfer the revolutionary power of TnSeq to bacteriophages. Our HIDEN-SEQ links the "dark matter" genes of your favorite phage to any selectable phenotype, guiding the path from fun observations to molecular mechanisms. A thread 1/8

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Hot off the press! Our latest paper led by @fernpizza.bsky.social, understanding how plasmids evolve inside cells. These small, self-replicating DNA circles live inside bacteria and carry antibiotic resistance genes, but also compete with one another to replicate. 1/ www.science.org/doi/10.1126/...

Intracellular competition shapes plasmid population dynamics

From populations of multicellular organisms to selfish genetic elements, conflicts between levels of biological organization are central to evolution. Plasmids are extrachromosomal, self-replicating g...

science.org