Pathogenesis of bacterial infections and immunity

@article{pmid34853303,

title = {Cross-species analysis of viral nucleic acid interacting proteins identifies TAOKs as innate immune regulators},

author = {Friederike L Pennemann and Assel Mussabekova and Christian Urban and Alexey Stukalov and Line Lykke Andersen and Vincent Grass and Teresa Maria Lavacca and Cathleen Holze and Lila Oubraham and Yasmine Benamrouche and Enrico Girardi and Rasha E Boulos and Rune Hartmann and Giulio Superti-Furga and Matthias Habjan and Jean-Luc Imler and Carine Meignin and Andreas Pichlmair},

doi = {10.1038/s41467-021-27192-w},

issn = {2041-1723},

year  = {2021},

date = {2021-12-01},

urldate = {2021-12-01},

journal = {Nat Commun},

volume = {12},

number = {1},

pages = {7009},

abstract = {The cell intrinsic antiviral response of multicellular organisms developed over millions of years and critically relies on the ability to sense and eliminate viral nucleic acids. Here we use an affinity proteomics approach in evolutionary distant species (human, mouse and fly) to identify proteins that are conserved in their ability to associate with diverse viral nucleic acids. This approach shows a core of orthologous proteins targeting viral genetic material and species-specific interactions. Functional characterization of the influence of 181 candidates on replication of 6 distinct viruses in human cells and flies identifies 128 nucleic acid binding proteins with an impact on virus growth. We identify the family of TAO kinases (TAOK1, -2 and -3) as dsRNA-interacting antiviral proteins and show their requirement for type-I interferon induction. Depletion of TAO kinases in mammals or flies leads to an impaired response to virus infection characterized by a reduced induction of interferon stimulated genes in mammals and impaired expression of srg1 and diedel in flies. Overall, our study shows a larger set of proteins able to mediate the interaction between viral genetic material and host factors than anticipated so far, attesting to the ancestral roots of innate immunity and to the lineage-specific pressures exerted by viruses.},

keywords = {antiviral innate immunity, imler, M3i, meignin},

pubstate = {published},

tppubtype = {article}

}

@article{pmid33441291,

title = {[Viral sensing by RNA helicases]},

author = {C Rousseau and C Meignin},

url = {https://pubmed.ncbi.nlm.nih.gov/33441291/},

doi = {10.1684/vir.2020.0871 },

isbn = {1267-8694},

year  = {2020},

date = {2020-12-01},

journal = {Virologie (Montrouge)},

volume = {24},

number = {6},

pages = {419-436},

keywords = {antiviral innate immunity, M3i, meignin},

pubstate = {published},

tppubtype = {article}

}

@article{pmid33441288,

title = {Viral sensing by RNA helicases},

author = {C Rousseau and C Meignin},

url = {https://pubmed.ncbi.nlm.nih.gov/33441288/},

doi = {10.1684/vir.2020.0872},

issn = {1267-8694},

year  = {2020},

date = {2020-12-01},

journal = {Virologie (Montrouge)},

volume = {24},

number = {6},

pages = {36-52},

keywords = {antiviral innate immunity, M3i, meignin},

pubstate = {published},

tppubtype = {article}

}

@article{pmid32843367,

title = {In vitro studies provide insight into effects of Đicer-2 helicase mutations in Đrosophila melanogaster},

author = {H M Donelick and L Talide and M Bellet and P J Aruscavage and E Lauret and E R G R Aguiar and J T Marques and C Meignin and B L Bass},

year  = {2020},

date = {2020-01-01},

journal = {RNA},

volume = {26},

number = {12},

pages = {1847--1861},

note = {[PubMed Central:hrefhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7668257PMC7668257] [DOI:hrefhttps://dx.doi.org/10.1261/rna.077289.12010.1261/rna.077289.120] [PubMed:hrefhttps://www.ncbi.nlm.nih.gov/pubmed/2136255421362554]},

keywords = {antiviral innate immunity, Dicer-2, Drosophila melanogaster, M3i, meignin},

pubstate = {published},

tppubtype = {article}

}