Rafal Mostowy

@rafalmostowy.bsky.social

Group leader at Jagiellonian University in Krakow, cofounder of Polonium Foundation. Working on evolution of sex in bugs.

Polish phage science meets Polish visual storytelling 🇵🇱🦠 To celebrate our last paper, we collaborated with an artist who previously worked on The Witcher 3 — to create a comic about phages and why understanding them matters in the fight against antibiotic-resistant bacteria. Comic below 👇

Bild
Rafal Mostowy@rafalmostowy.bsky.social · 3mo ago

🎉 New in @plosbiology.org: Temperate phages of Klebsiella pneumoniae show capsule-driven host tropism — but how? The working assumption was depolymerases: enzymes that chew through the bacterial sugar capsule. Turns out that's not the whole story. 🧵 journals.plos.org/plosbiology/...

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...

With Eugene Koonin, we propose a concept of “the selfish ribosome”, under which evolution of life is viewed as a ribosomal takeover, where the ribosome evolved to consume most of the cell’s resources, while other cellular componentry ensures the propagation of the ribosome. arxiv.org/abs/2602.23268

Bild

📢 Hiring a Postdoc in Computational Phage Biology (Kraków, Poland) We study the evolution & structural modularity of prophage-encoded glycan-degrading enzymes in Klebsiella pneumoniae — combining genomics and AlphaFold-based analyses. Details in attached PDF 👇

Postdoc Ad

Postdoctoral Position in Computational Phage Biology Microbial Genomics Group, Malopolska Centre of Biotechnology (MCB), Jagiellonian University, Kraków PL Summary We are seeking a postdoctoral rese...

docs.google.com

🌟 Exciting news! We’re launching three fully-funded postdoc positions for "New Horizons for Synthetic Phages” Join us in tackling antimicrobial resistance with cutting-edge synthetic biology + AI bioinformatics. Based at Flinders Uni in vibrant Adelaide. 👇 Read on for details! #Phage

What determines who a phage can infect? We tackled this question for temperate phages of Klebsiella — a bacterial pathogen — using a genome-wide association study (GWAS) and a massive protein testing effort. 👇 A thread!

Bild

🚀 Follow-up on my recent MANIAC tweet: our new MMseqs2-blased tool is optimised for ANI and alignment fraction (AF) calculation in viral genomes. Unlike many other tools, it excels at ANI ~70%, an important range for viral taxonomy & evolution. Here’s why that matters ➡️ a thread! 🧵

Bild