CBASS is a cyclic nucleotide-based antiviral system in bacteria that is related to cGAS-STING signaling in animals. One of the big questions is how CBASS is activated during phage infection? We made some progress on this during my final year in the Kranzusch lab.
www.biorxiv.org/content/10.6...
06.03.2026 05:27
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Out today: We discovered new viral proteins that target immune signaling molecules, solely based on their AlphaFold-predicted shapes
www.science.org/doi/10.1126/...
Congrats Nitzan Tal and coauthors! Thank you Kranzusch lab for the fun collaboration!
Linking below previous thread on our findings
05.03.2026 19:28
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@nitzantal.bsky.social @romihadary.bsky.social @soreklab.bsky.social use structure prediction and in silico binding site analysis to discover viral immune evasion proteins! Exciting for our lab @reneechang.bsky.social @riveralopz.bsky.social to help with this project.
www.science.org/doi/10.1126/...
05.03.2026 20:23
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"Remarkably, dCas12fโRNAโฯE complexes drove potent gene expression in the absence of any requisite promoter motifs, with de novo transcription start sites defined exclusively by the relative distance from the dCas12f-mediated R-loop." ๐คฏ
05.03.2026 08:28
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Ground-breaking studies reveal the mechanism of "natural CRISPRa" ๐คฉ
Looking forward to seeing all the technological applications !
05.03.2026 08:27
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Out now! In collaboration with Leifu Chang, we uncover the molecular and structural underpinnings of CRISPR-Cas12f-like RNA-guided transcription systems!
Links to the published articles:
tinyurl.com/55kpavet
tinyurl.com/sk6djwx3
Previous thread for the preprint:
bsky.app/profile/did:...
04.03.2026 20:28
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New post-doctoral research position in my phage-host interactions (Phi) laboratory in @otagomicroimmuno.bsky.social at @universityofotago.bsky.social New Zealand. The project is focused on defences against jumbo phages. Please share and if interested apply using the link in the comments.
04.03.2026 00:20
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In our latest work, we characterise the Tmn defence system. We reveal plasmolysis as a new way to block phage infection, dramatically reducing secondary infections.
03.03.2026 19:55
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๐ We are thrilled to share our latest study revealing a new mechanism by which Legionella pneumophila evades antibiotic killing via reversible genetic variation mediated by integrative and conjugative elements (ICEs).
๐ Here for the full story:
www.biorxiv.org/content/10.6...
02.03.2026 08:44
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A while back, we showed that P2-like phages and their P4-like satellites encode hotspots of defense systems.
Great work from @jmouradesousa.bsky.social et al. majorly expands the diversity of these systems and explores gene flows with other MGEs ๐คฉ Striking that P2s and P4s never exchange systems !
02.03.2026 10:14
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Congratulations to Sonomi Yamaguchi for her paper at @nature.com. Sonomi discovered Clover defense and explained how nucleotide signals control each step of viral sensing, immune regulation, and viral restriction โ named for her beautiful "four-leaf" structures ๐
www.nature.com/articles/s41...
18.02.2026 17:11
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Chemical inhibition of a bacterial immune system
Bacteriophages are promising alternatives to antibiotics for treating bacterial infections.
However, bacteria possess immune systems that neutralize bacteriophages. Zang et al.
discover small molecule...
Chemical inhibition of a bacterial immune system
Small molecules inhibit type II Thoeris anti-phage systems from diverse bacteria. One compound, IP6C, improves phage-therapy against P. aeruginosa & is effective against Thoeris in polymicrobial communities
www.cell.com/cell-host-mi...
30.01.2026 17:20
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New layers to the NAD+ immune arms race - itโs a never ending fight!๐ฆ ๐งช
I was very happy to contribute to this story. Congratulations Ilya for an amazing discovery!!๐
29.01.2026 11:35
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Bacterial defense via RES-mediated NAD+ depletion is countered by phage phosphatases
Many bacterial defense systems restrict phage infection by breaking the molecule NAD+ to its constituents, adenosine diphosphate ribose (ADPR) and nicotinamide (Nam). To counter NAD+ depletion-mediated defense, phages evolved NAD+ reconstitution pathway 1 (NARP1), which uses ADPR and Nam to rebuild NAD+. Here we report a bacterial defense system called aRES, involving RES-domain proteins that degrade NAD+ into Nam and ADPR-1โณ-phosphate (ADPR-1P). This molecule cannot serve as a substrate for NARP1, so that NAD+ depletion by aRES defends against phages even if they encode NARP1. We further discover that some phages evolved an extended NARP1 pathway capable of overcoming aRES defense. In these phages, the NARP1 operon also includes a specialized phosphatase, which dephosphorylates ADPR-1P to form ADPR, a substrate from which NARP1 then reconstitutes NAD+. Other phages encode inhibitors that directly bind aRES proteins and physically block their active sites. Our study describes new layers in the NAD+-centric arms race between bacteria and phages and highlights the centrality of the NAD+ pool in cellular battles between viruses and their hosts. ### Competing Interest Statement The authors have declared no competing interest. European Research Council, ERC-AdG GA 101018520 Israel Science Foundation, MAPATS grant 2720/22 Deutsche Forschungsgemeinschaft, SPP 2330, grant 464312965 Minerva Foundation with funding from the Federal German Ministry for Education and Research research grant from Magnus Konow in honor of his mother Olga Konow Rappaport Ministry of Aliyah and Immigrant Absorption, https://ror.org/05aycsg86 Clore Scholars Program
๐งฌ Metabolic arms race continues!
We discovered a new NADโบ-depleting bacterial immune system aRES and phage enzymes that overcome it.
Our preprint is out: www.biorxiv.org/content/10.6...
29.01.2026 11:20
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Great new story from Sophie Helaine and Molly Sargen!
www.helainelab.com
28.01.2026 23:01
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Wow ๐ฎ Phage-mediated degradation of the bacterial genome generates di-nucleotides that are sensed by the ApeA defense system ! Beautiful structures and elegant mechanism !
28.01.2026 08:44
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Hello world! I am excited to announce my lab is open at the University of Utah in the Department of Biochemistry. We are looking for scientists at all levels interested in studying host-virus interactions in both bacteria and animals. Come join us in beautiful Utah! (photo is 10 steps from lab)
22.01.2026 22:06
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Congrats Philip !! A very well deserved recognition of the pioneering science done in your lab ๐
22.01.2026 18:21
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Poste de MCU en Bacteriologie - Dรฉpartement de Biologie ENS de Lyon / CIRI :
ciri.ens-lyon.fr/teams/I2BA/n...
21.01.2026 07:28
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A methylome-derived m6-dAMP trigger assembles a PUA-Cal-HAD immune filament that depletes dNTPs to abort phage infection
Bacteria must distinguish phage attack from normal homeostatic processes, yet the danger signals that trigger many defence systems remain unknown. Here, we show that a PUA-Calcineurin-CE-HAD module from Escherichia coli ECOR28 confers broad anti-phage protection by binding Dam-methylated deoxyadenosine monophosphate (m6-dAMP) generated during phage-induced chromosome degradation. Ligand binding converts a preassembled PUA-Calcineurin-CE hexamer loaded with six HAD phosphatases into a polymerising filament. The filament acts as a high-flux dNTP sink through a two-enzyme cascade: HAD first dephosphorylates dATP to dADP, and Calcineurin-CE then converts dADP to dAMP. dNTP collapse halts phage replication and enforces abortive infection. Multiple mobile-element DNA mimic proteins block filament assembly, revealing a direct phage counter-defence. More broadly, our findings extend a conserved, cross-kingdom paradigm of immune filament assembly to nucleotide-depletion antiviral defence and suggest modified-nucleotide sensing by related PUA-Calcineurin-CE modules as a widespread, underappreciated bacterial strategy. ### Competing Interest Statement The authors have declared no competing interest. NIHR Southampton Biomedical Research Centre, https://ror.org/01qqpzg67, Postdoctoral Bridging Fellowship F.L.N. is supported by a Wessex Health Partners (WHP) and National Institute for Health and Care Research Wessex Experimental Medicine Network (NIHR WEMN), Seed fund National Institutes of Health, GM145888, U24 GM129539) Maloris Foundation Memorial Sloan Kettering Cancer Center, P30-CA008748 Simons Foundation, SF349247 New York State Assembly
Preprint out: We characterise PUA-Cal-HAD, a widespread bacterial antiphage defence family. An infection cue switches a preassembled complex into an immune filament that drains dNTPs via a coupled two-enzyme cascade, and phage DNA mimics can block filament assembly (anti-polymerisation).
17.01.2026 14:52
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Bien รฉvidemment, il me semblait que "maรฎtre de confรฉrence" couvrait tous les genres mais je me trompe peut-รชtre !
15.01.2026 08:16
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๐จL'ENS de Lyon recrute un.e maรฎtre de confรฉrence qui rejoindra le CIRI pour dรฉvelopper ses recherches sur l'immunitรฉ bactรฉrienne, les transferts horizontaux et les MGE.
๐ Une trรจs belle opportunitรฉ d'enseigner ร des รฉtudiants brillants tout en menant des recherches excitantes !
14.01.2026 17:02
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Une opportunitรฉ unique de former des รฉtudiants talentueux ร la biologie des bactรฉries ร l'ENS Lyon et mener des recherches sur les phages, l'immunitรฉ bactรฉrienne, le transfert gรฉnรฉtique horizontal (HGT) et/ou les รฉlรฉments gรฉnรฉtiques mobiles au sein du dรฉpartement de bactรฉriologie du CIRI.
13.01.2026 14:01
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Happy to share our recent preprint:
"DNA-intercalating antiphage molecules trigger abortive infection through mutual destruction and synergize with bacterial immunity"
www.biorxiv.org/content/10.6...
@spp2330.bsky.social, @mibinet.bsky.social, @dfg.de @hhu.de @fzj.bsky.social
14.01.2026 08:57
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Here, we find that many Genomic islands have origins of transfer (oriT) mobilisable by conjugation, incl. known Pathogenicity & defense islands. iOriT use only an oriT for transfer by hitching on conjugative elements: they make abundant, diverse, ancient families of mobile genetic elements. See๐งต
14.01.2026 11:26
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I'm humbled to receive the Paoletti Prize awarded by @cnrsbiologie.bsky.social ๐ and very grateful to present and past mentors !
08.01.2026 21:12
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Fullfabric :: AITHYRA-CeMM PhD
I'm recruiting 1-2 grad students through the AITHYRA-CeMM PhD program! Applications are due January 30th. This is a fully-funded PhD program, combining AI and biology to advance biological discovery. Please forward to anyone who may be interested! You can apply here: apply.cemm.at
08.01.2026 10:48
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