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A phylogenetic tree of insects is shown annotating the presence or absence of a an antimicrobial peptide gene across winged insects

A phylogenetic tree of insects is shown annotating the presence or absence of a an antimicrobial peptide gene across winged insects

Various phylogenetic secondary loss events are mapped to a tree of insects to explain the parsimony calculations necessary to explain the diversity of insect Drosomycin antimicrobial peptide genes

Various phylogenetic secondary loss events are mapped to a tree of insects to explain the parsimony calculations necessary to explain the diversity of insect Drosomycin antimicrobial peptide genes

Antimicrobial peptides (AMPs) are key defence molecules of the innate immune system of plants and animals. Understanding the evolutionary origins of AMPs can help to explain how immune systems acquire novelty and vary in their defensive capabilities. However, AMPs evolve rapidly, and so the origins of similar AMPs across organisms is often unclear. Furthermore, false negatives due to low search sensitivity are common and can hinder confident annotations about true absences. Due to these difficulties, understanding whether similar AMP genes found in diverse organisms represent ancestral molecules or evolutionary novelties has been challenging. In this report, we present evidence of
horizontal gene transfer (HGT) of the antifungal peptide gene Drosomycin across insects. We show that in Diptera, the presence of Drosomycin is restricted to the Melanogaster group and additionally the
distant relative Drosophila busckii. We go on to recover Drosomycin genes in cockroaches (Blattodea), mantises (Mantodea), one katydid (Orthoptera), various beetles (Coleoptera), and a recently acquired
pseudogenized Drosomycin locus in Liposcelis booklice (Psocodea), but no other insects. Explaining this diversity through shared ancestry requires at least 50 independent loss events, or just seven HGT
events. Previous studies have suggested that similar AMPs found across divergent species reflect conservation from a common ancestor, or due to their small size, that they arose via convergent evolution resulting from pathogen-imposed selection. Our findings suggest horizontal gene transfer can be responsible for the presence of some AMP genes found scattered across the tree of life. By presenting a mechanism through which immune systems can acquire novelty, our study also suggests a possible explanation for certain lineage-specific competencies for defence against infectious disease. While loss of AMP genes is common in certain lineages, here we suggest gain of AMPs can occur just as suddenly.

Antimicrobial peptides (AMPs) are key defence molecules of the innate immune system of plants and animals. Understanding the evolutionary origins of AMPs can help to explain how immune systems acquire novelty and vary in their defensive capabilities. However, AMPs evolve rapidly, and so the origins of similar AMPs across organisms is often unclear. Furthermore, false negatives due to low search sensitivity are common and can hinder confident annotations about true absences. Due to these difficulties, understanding whether similar AMP genes found in diverse organisms represent ancestral molecules or evolutionary novelties has been challenging. In this report, we present evidence of horizontal gene transfer (HGT) of the antifungal peptide gene Drosomycin across insects. We show that in Diptera, the presence of Drosomycin is restricted to the Melanogaster group and additionally the distant relative Drosophila busckii. We go on to recover Drosomycin genes in cockroaches (Blattodea), mantises (Mantodea), one katydid (Orthoptera), various beetles (Coleoptera), and a recently acquired pseudogenized Drosomycin locus in Liposcelis booklice (Psocodea), but no other insects. Explaining this diversity through shared ancestry requires at least 50 independent loss events, or just seven HGT events. Previous studies have suggested that similar AMPs found across divergent species reflect conservation from a common ancestor, or due to their small size, that they arose via convergent evolution resulting from pathogen-imposed selection. Our findings suggest horizontal gene transfer can be responsible for the presence of some AMP genes found scattered across the tree of life. By presenting a mechanism through which immune systems can acquire novelty, our study also suggests a possible explanation for certain lineage-specific competencies for defence against infectious disease. While loss of AMP genes is common in certain lineages, here we suggest gain of AMPs can occur just as suddenly.

Pleased to finally share this fun collab that began at #Ento23

@cedricaumont.bsky.social presented & I had seen NCBI annotated some cockroach genomes as "contaminated." Turns out NCBI & I were wrong (much more fun).

Horizontal transfer of an #AntimicrobialPeptide across insects
bit.ly/DrsHGT

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📖 Thank you to all students and speakers for their participation in the MaxImmun project Training School at Abbaye de Royaumont, France, March 2-4, 2026. 🇪🇺
#EUeic #Europe #MaxImmun #Innovation #Healthcare #AMR #Antimicrobialpeptide #Royaumont

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🧬 Sarah Khazaal from École Normale Supérieure deciphering the action mechanisms of AMP-inducer molecules in the antimicrobial defense of human epithelial cells.
Paris, France, February, 2026.
#Europe #EUeic #MaxImmun #Innovation #Healthcare #AMR #Antimicrobialpeptide

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🧪 Vivek K. Mishra from Helmholtz Centre for Infection Research working on the chemical optimization of natural marine compounds identified by screening of AMP-inducer molecules.
Braunschweig, Germany, November, 2025.
#EUeic #Europe #MaxImmun #Innovation #Healthcare #AMR #Antimicrobialpeptide

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Antimicrobial peptide class that forms discrete β-barrel stable pores anchored by transmembrane helices Nature Communications - Bacteriocins include antimicrobial peptides (AMPs) that often disrupt the cytoplasmic membrane. Here, the authors describe TMcin (transmembrane helix-containing...

We found a new #bacteriocin family that forms large pores using transmembrane helices!

#MicroSky #antimicrobialpeptide #RiPP

rdcu.be/ezuY1

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Disentangling the impact of obesity, diet, host factors, and microbiota on small intestinal antimicrobial peptide expression The small intestinal mucosa has the delicate task of allowing absorption of nutrients and limiting microbial colonization at the mucosal surface through production of antimicrobial peptides and pro...

Our study on disentangling the impact of #obesity, #diet, host factors, and #microbiota on small intestinal #antimicrobialpeptide expression is now published in Gut Microbes!
Fantastic work by Fabiola Puértolas-Balint et al!
#microbiomesky #microsky #GastroSky
www.tandfonline.com/doi/full/10....

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🔬 Elisa Bouvier from École Normale Supérieure working on the identification and characterization of new molecules inducing expression of human antimicrobial peptides. Paris, France, June 2025.
#EUeic #Europe #MaxImmun #Innovation #AMR #AntimicrobialPeptide

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📎 Thank you to all European partners, senior and young scientists, of the MaxImmun project for their participation to the 1st General Assembly held in Bordeaux, France, June 5, 2025. 🇪🇺🇫🇷🇸🇪🇩🇪+🇱🇧🇮🇳🇵🇱
#EUeic #Europe #Healthcare #Innovation #AMR #AntimicrobialPeptide

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Paillotin mutants are not sensitive to fungal toxins. Interestingly, in our hands, spz mutants also were not susceptible, differing from a previous study. However fungal toxin injection resulted in a high mortality in all lines, suggesting the preparations were virulent enough to reveal a differential sensitivity.

Paillotin mutants are not sensitive to fungal toxins. Interestingly, in our hands, spz mutants also were not susceptible, differing from a previous study. However fungal toxin injection resulted in a high mortality in all lines, suggesting the preparations were virulent enough to reveal a differential sensitivity.

No in vitro activity of Paillotin was found alone or in combination with another AMP, Cecropin.

No in vitro activity of Paillotin was found alone or in combination with another AMP, Cecropin.

Many features of Pai suggest an #antimicrobialpeptide activity, incl. a net +ve charge, higher bacterial load in flies lacking Pai, and its upregulation by the Imd pathway.

But we found no any activity in vitro, nor evidence of another function. We refer to Pai only as a #HostDefensePeptide

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Great work! Definitely adding to our journal club. Adding some tags #MicroSky #ImmunoSky #antimicrobialpeptide #IDsky

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Really neat work on #antimicrobialpeptide kinetics by @alessiofragasso.bsky.social who had a 🎆 poster at #GRC2025 on AMP*bacteria populations. A dissection of pore formers vs ribosome inhibitors in their uptake - both eventually attack ribosomes it seems? Plus dynamics per cell density. Cool stuff!

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How inspiring was it attending the Gordon Research Conferences Symposium on „Antimicrobial Peptides“ in Ventura!

I presented the #microfluidics based project on #liposomes as model systems for #antimicrobialPeptide efficacy and mode of action, done by fantastic PhD student Janina Nandy…

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I've also now made a Starter Pack for the #AntimicrobialPeptide field here:

go.bsky.app/JLHHzt1

Please let me know who I am missing! This is a very incomplete list so far. I also expect many will join Bluesky later. I will happily keep populating this list! 📣🧬🦠

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Full list of Antimicrobial Peptide #Feed hashtags:

#AMPs
#HDPs
#AntimicrobialPeptides
#AntimicrobialPeptide
#HostDefensePeptide
#HostDefencePeptide
#HostDefensePeptides
#HostDefencePeptides
#GRCAMP2025

(last updated Feb 27th 2025)

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The evolutionary novelty of insect defensins: from bacterial killing to toxin neutralization - PubMed Insect host defense comprises two complementary dimensions, microbial killing-mediated resistance and microbial toxin neutralization-mediated resilience, both jointly providing protection against path...

pubmed.ncbi.nlm.nih.gov/38780625/
Looks like a very cool #Drosophila virilis study where a #Defensin #antimicrobialpeptide duplication was modified into a very different peptide product that may have a role in tolerance/resilience by helping keep the host alive after toxin exposure.

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