Séminaires à l’IRIM
Les séminaires à l’IRIM ont lieu tous les vendredis à 11h00 dans la salle « Marcel Dorée ». Il y a une alternance entre séminaires internes faits par les équipes et les séminaires externes sur invitation (voir liste ci-dessous).
Début 2019, l’IRIM a également lancé une nouvelle série séminaire ‘career outside academia seminars’ visant à présenter aux doctorants et postdoctorants du campus les parcours professionnels possibles en dehors de la recherche académique, après un doctorat et post-doctorat. Ces séminaires ont lieu dans un contexte informal et détendu, laissant libre cours aux questions et discussions. Plus d’information ici.
Séminaires à venir :
- Dr. Silke Stertz, (University of Zurich) « MHC class II as novel entry receptor of influenza A viruses »- 1er Mars 2024 à 11h00, Salle Marcel dorée.
Silke Stertz studied biology in Freiburg, Germany, where she stayed on to obtain her PhD in the lab of Prof. Otto Haller. She then trained as postdoctoral fellow in the lab of Prof. Peter Palese at Icahn School of Medicine at Mount Sinai in New York, U.S.. Since 2011 she leads her own research group at the Institute of Medical Virology (University of Zurich), where she was promoted to Associate Professor in 2019. Her work focuses on influenza virus-host cell interactions, particularly at the stage of viral entry.
- Dr. Alexander Francis Palazzo, (Harvard Medical School) « How mRNA nuclear export allows you to live with a genome filled with junk DNA » 7 Juin 2024 à 11h00, Salle Marcel dorée.
Alexander Francis Palazzo was born and raised in Montreal, Canada. As a graduate student in Gregg Gundersen’s laboratory at Columbia University, he discovered two major pathways that regulate cell polarity in migrating fibroblasts. After receiving his PhD in 2003, he moved to Tom Rapoport’s laboratory at Harvard Medical School where he was a Jane Coffin Childs Postdoctoral Fellow. There, he investigated how newly synthesized mRNA is exported from the nucleus and then targeted to specific sites in the cytoplasm of mammalian cells, such as the surface of the endoplasmic reticulum. In 2009 he started his lab in the Biochemistry Department. Besides his work on mRNA export and localization, Dr. Palazzo is interested in how biological information is extracted from the mammalian genome. He has published several well-regarded reviews on how mRNA processing and nuclear export is used to sort useful information from a genome that is mostly filled with junk DNA.
Séminaires passés :
- Dr. William Bakhache (NIH-Bethesda) « Uncovering Structural Plasticity of Enterovirus A through Deep Insertional and Deletional Scanning« . Lundi 19 Février 2024 à 11h00. Salle Marcel Dorée.
William Bakhache, Ph.D., is a postdoctoral fellow at the Quantitative Virology and Evolution Unit led by Patrick Dolan, Ph.D., at the National Institutes of Health. His research is focused on studying the evolutionary constraints of RNA virus evolution. He has adapted deep mutational scanning methods to scan for fitness effects of all possible mutations in viral genomes. In his talk, William will share his work on uncovering Enterovirus A’s structural plasticity through deep insertion and deletion scanning.
- Dr. Michele Trabucchi (INSERM – Nice) « Decoding the mode of microRNA binding to mRNA« . Lundi 23 Février 2024 (11h en Salle Marcel Dorée)
Michele Trabucchi is Directeur de Recherche at the Inserm and Group Leader at the Mediterranean Center for Molecular Medicine in Nice (Inserm U1065). Michele heads the team « Control of Gene Expression ». After an European PhD on Molecular Biology at the University of Rouen, he moved to the University of California at San Diego in 2004 to perform a post-doctoral training in Michael Rosenfeld’s laboratory on gene expression regulation in human cells. During the post-doctoral training he made important discoveries on new biochemical mechanisms of miRNA biogenesis, pointing out the biological relevance of the terminal loop sequence of microRNA precursors as an important CIS regulator of miRNA processing in normal and pathological events of cell physiology (Trabucchi et al, Nature 2009). Thanks to the ATIP/Avenir and the European Curie Integration Grant programs, Michele Trabucchi started his own team in Nice in 2011. His research interests are focused on miRNA biology and other small RNA species in cellular models that pertain to pathophysiology of human cells, including macrophages and stem cells, using biochemical, molecular biology and computational approaches.
- Dr. Yonatan Ganor (Institut Cochin) « Neuro-immune-epithelial interplay in mucosal viral infections » Mercredi 6 Mars 2024 à 11h00 (Salle Marcel Dorée).
After a successful PhD on neuroimmunology at the Weizmann Institute in Rehovot / Israel (2002-2006), Yonatan moved to the Cochin Institute in Paris / France as a postdoctoral fellow (2006-2013) to investigate HIV-1 mucosal entry and persistence. During this period, he pioneered the use of human tissues derived from the male genitals of healthy or HIV-1 infected patients and he developed unique experimental tissue explants and reconstruction models which allowed him to unveil host immune cells critically involved in the very first events of HIV-1 transmission of infection (Ganor et al., Mucosal. Immunol 2010, 2013) or identified as HIV-1 reservoirs (Ganor et al., Nat Microbiol 2019). Yonatan was then recruited as Research Associate to the CNRS in 2013 and became group leader in 2017. He was recently promoted to Research Director (2022) and he will co-direct the “Mucosal entry, persistence and neuro-immune control of HIV-1 and other viruses” from 2025. The current scientific interests of his team are in neuroimmune interactions that control transmission of human mucosal viruses, especially focusing on the neuropeptide calcitonin gene-related peptide (CGRP) for which he described an unexpected anti-viral role against HIV-1 (Ganor et al., JEM 2013, Ganor et al., Acta Physiol 2015, Bomsel et l., J Virol 2017, Mariotton Front Immunol 2021) as well as HSV-2 (Cohen et al., Mucosal Immunol 2022) and SARS-CoV-2 (Bomfim et al., Submitted 2024).
- Dr. Yoshiho Ikeuchi (IIS – University of Tokyo) »Building circuits by connecting neural organoids » Vendredi 15 Décembre 2023 à 11h00 (Salle Marcel Dorée).
Yoshiho Ikeuchi is a researcher in IIS, The University of Tokyo. He is also affiliated with Institute for AI and Beyond, and Department of Chemistry and Biotechnology, School of Engineering in the University. He received PhD degree in 2007 at Department of Chemistry and Biotechnology in The University of Tokyo. He did his post-doctoral neuroscience research at Harvard Medical School from 2007 to 2013, and at Washington University in St. Louis from 2013 to 2014. He was appointed as Lecturer in 2014, and then Associate Professor in 2018 at Institute of Industrial Science, The University of Tokyo. His goal of research is to construct nervous tissues from human multipotent stem cells (iPS cells) and to functionalize them to better understand the mechanisms of the brain. The group develops a technology to connect neural organoids via an axon bundle to model neuronal circuits, and to analyze network activity of the neural tissues using multielectrode arrays. The groups also use the tissues to analyze local and activity-dependent protein synthesis regulations in the neurons.
- Dr. Cyrille Mathieu, CRCN CNRS, HDR, Group Leader NITROVIRE Lab (CIRI Lyon). « Measles virus NeuroInvasion can rely on a single mutation » Vendredi 8 Décembre 2023 à 11h00 (Salle Marcel Dorée).
After a thesis on the pathogenesis of the Nipah virus at the human virology laboratory (Lyon, France), He left for a postdoc at Weil Medical College of Cornell University (NYC, USA) to study the fusion machinery of Mononegavirales and develop fusion inhibitors. He returned with an ANR Retour Post doc to the CIRI to develop an Axis of study of neuroInvasion by Paramyxoviruses. He obtained then in 2017 a full academic position of research associate at Columbia University (NY) to co-lead a group on viral evolution and neuroinvasion. He entered the CRCN position at CNRS in 2018 in Lyon, before founding in 2021 the emerging group NITROVIRE at the CIRI focusing on neuroinvasion and the development of encephalitis following infection with biosafety level 2 to 4 pathogens.
- Fabio Romerio (Johns Hopkins University, Baltimore) « The HIV-1 antisense gene asp: the eclectic lifestyle of a contrarian » Lundi 27 Novembre 2023 à 14h00 (Salle Marcel Dorée)
HIV-1 antisense gene asp was discovered more than 30 years ago, but its role in the virus lifecycle remains largely a mystery. This seminar will discuss recent advances in our understanding on the creation and function of this neglected HIV-1 gene ». Dr. Romerio obtained his doctoral degree in Biomedical Sciences with a specialization in Molecular Genetics in 1992 from the University of Pavia (Italy). After completing a first postdoctoral fellowship at the Institute of Biochemical and Evolutionary Genetics in Pavia (Italy), Dr. Romerio took a second postdoctoral fellowship in 1995 with Dr. David Margolis at the University of Maryland, Baltimore, where he began his work on transcriptional regulation of HIV-1. When Dr. Robert Gallo established the Institute of Human Virology at the University of Maryland, Dr. Romerio started a third postdoctoral fellowship with Dr. Gallo working on mechanisms of HIV-1 immunopathogenesis focusing on the role of type I interferons. In 2004, Dr. Romerio was promoted to the position of Assistant Professor in the Division of Basic Science at the Institute of Human Virology and he began his studies on HIV-1 latency and epigenetic regulation of HIV-1 transcription. This led to his interest in the HIV-1 antisense transcript AST and subsequently on the antisense protein ASP. In 2020, Dr. Romerio was recruited to the Johns Hopkins School of Medicine as an Associate Professor where he continues his studies on the HIV-1 antisense gene asp.
- Dr. Maximiliano Gutierrez (The Francis Crick Institute – London) « Mycobacterium tuberculosis infection of host cells in time and space” Vendredi 24 Novembre 2023 à 11h00 (Salle Marcel Dorée).
Max is a cell biologist originally from Mendoza, Argentina. In 2005, he obtained a PhD in cell biology from the University of San Luis, Argentina. During his PhD work, he discovered a novel innate immune pathway, later named “Xenophagy”. In 2006, he moved to EMBL in Heidelberg, Germany as a postdoc in Gareth Griffiths Laboratory, first as a fellow of the Alexander von Humboldt Foundation and then as an EMBO fellow. His work in Heidelberg focused on the cell biology and imaging of macrophages; it was also in Heidelberg that he felt in love with Electron Microscopy. In 2009, he started his independent research group at the Helmholtz Centre for Infection Research in Braunschweig, Germany as head of the Junior Research Group ‘Phagosome Biology’. In 2012, he was recruited as a Program Leader Track at the Medical Research Council’s National Institute for Medical Research, which became part of the Francis Crick Institute in 2015. Since 2018, he is a Senior Group Leader at the Francis Crick Institute.
- Dr. Laurence Abrami (EPFL – Lausanne) « How S-acylation affects all major cellular process: focus on SARS-CoV-2 Spike » Vendredi 27 Octobre 2023 à 11h (Salle Marcel Dorée)
Protein S-acylation, often referred to as S-palmitoylation, has emerged as a critical regulator of many signaling pathways. S-acylation is a reversible post-translational lipid modification that confers significant hydrophobicity, and thereby the association with membranes. It can concern up to 10-20% of the human proteome. Understanding of the function of acyltransferases and de-acylating enzymes, the impact of these enzymes on protein function, cellular processes, and physiological pathways, as well as their spatiotemporal regulation will be presented in the seminar. During SARS-CoV-2 infection, we and others have shown that S-acylation of Spike is mediated predominantly by the ZDHHC20 acyltransferase. In the presentation, we will focus on how SARS-CoV-2 infection, whether in human cells or in mice, triggers the use of an upstream transcriptional start site of the zdhhc20 gene, leading to the production of a N-terminally extended enzyme, ZDHHC20-Long. ZDHHC20-Long drastically enhances Spike acylation, leading to the enhanced fatty acid decoration of the Spike trimers. As a consequence, the fusogenic capacity of Spike is augmented, and viral infectivity is optimized.
- Mini-symposium on Viruses and Immunity – Wednesday the 8th of November from 10 to 11 am, Philippe Jeanteur Room (IGMM).
Prof. Volker Thiel (University of Bern, Switzerland): “Lost in translation – generation of live-attenuated SARS-CoV-2 vaccine by genome recoding”
Prof. Sam Wilson (University of Cambridge, UK): “Innate immune barriers to viral emergence and pathogenesis”.
Prof. Volker Thiel (University of Bern, Switzerland) obtained his PhD from the University of Würzburg, Germany, in 1998. He did a postdoc (1998-2001) and started his own group in the same university (2001-2003). He then moved his group to the Institute of Immunobiology, Kantonal Hospital St.Gallen, in Switzerland, where he stayed until 2013. Since 2014, he has been Professor of Virology at the University of Bern and Head of Division of Virology, at Federal Food Safety and Veterinary Office FSV, Institute of Virology and Immunology, Bern and Mittelhäusern, Switzerland.
Prof. Volker Thiel is a world leading expert on coronaviruses (CoV), which he has studied for more than 20 years. His current research focuses on various aspects of the CoV replication cycle, including the regulation of genome expression or the host factors required, and on the innate immune responses induced by CoV, using cellular and in vivo models. His team has generated reverse genetic systems for many CoVs, including for instance human seasonal HCoV-229E, Mouse Hepatitis Virus, or SARS-CoV-1. His team was notably the very first to develop a molecular clone of SARS-CoV-2, as early as February 2020, and has shared it with >100 laboratories over the world. His team has published an impressive amount of studies on SARS-CoV-2 and other coronaviruses (Nature 2020, Nature 2021, Science 2021, Nature 2022, Nat Comm 2022, Autophagy 2023…).
Prof. Sam Wilson (University of Cambridge, UK) obtained his PhD from University College London (UCL), UK, in 2006. After a first postdoc at UCL (2006-2008), he did a second postdoc at Rockefeller University (USA) (2008-2012). He started his own lab at MRC University of Glasgow CVR in 2012. This year, he has moved his lab to the Institute of Therapeutic Immunology and Infectious Disease, at the University of Cambridge (UK) and he is Professor of Microbial Pathogenesis there.
Prof. Sam Wilson is a molecular virologist whose research focuses on genome-encoded antiviral defences (AKA restriction factors) and how these factors influence the replication, emergence and pathogenesis of viruses. He’s notably recently made highly significant contributions to the understanding of avian influenza A virus species barrier in humans (Nature 2023) or to natural protection against severe Covid-19 (Science 2022).
- Dr. Jomon Joseph (National Center for Cell Science, University of Pune, India) « Cell biology of Annulate Lamellae – an underexplored organelle » Mercredi 11 Octobre 2023 (Salle Marcel Dorée)
Dr. Jomon Joseph obtained his PhD from the Indian Institute of Science, Bangalore, India on plant virology. He then carried out a post-doc with Prof. Mary Dasso at the NIH, Bethesda, USA on role of RanGTPase and SUMO in mitosis. Dr. Joseph moved to the National Centre for Cell Science, Pune, India in 2005 and started his lab. His team focuses on non-traditional roles of nucleoporins and annulate lamellae.
- Prof. Patricia Beltão-Braga (University of São Paulo ) « Modelling the interplay between genetics and environmental risk factors for neurodevelopmental disorders » Mardi 26 Septembre 2023 (Salle Marcel Dorée)
Patricia Beltrão-Braga is a Biologist, with a Master’s in Virology, and a Ph.D. in Molecular Biology, both from the Federal University of São Paulo (UNIFESP). She did two postdocs in Brazil, one at the School of Medicine (Cellular Biology) and the other at the School of Veterinary Medicine (Cellular Biology and Cell Therapy), both at the University of São Paulo, and a sabbatical postdoc in neuroscience at the University of California San Diego (UCSD). She is currently an Associate Professor at the Department of Microbiology at the Institute of Biomedical Sciences (ICB), University of São Paulo (USP), and Principal Investigator at Institut Pasteur de São Paulo. Using human iPSC, Dr. Beltrão-Braga’s lab explores the mechanisms involved in genetic and infectious diseases that affect the CNS. Among her projects, Dr. Beltrão-Braga is responsible for the « Tooth Fairy Project, » a Brazilian initiative that uses the stem cells of autistic children’s milk teeth to study the mechanisms involved in Autism. Her group was responsible for proving the causal relationship of the Zika virus to microcephaly using brain organoids and animal models.
- Dr Romain Volmer (Ecole Nationale Vétérinaire de Toulouse) « Viral and host factors modulating the emergence of highly pathogenic avian influenza viruses » Vendredi 17 Mars 2023 (Salle Marcel Dorée)
Romain Volmer holds a DVM (Doctorate of Veterinary Medicine) from the Ecole nationale vétérinaire d’Alfort and a PhD in Virology from the Institut Pasteur, Paris. Following a post-doc at the University of Cambridge, he joined the Ecole nationale vétérinaire de Toulouse, where he teaches infectious diseases and leads a research program on influenza virus evolution in the joint research unit UMR IHAP INRAE- Ecole nationale vétérinaire de Toulouse.
- Prof. Jan Rehwinkel (MRC Human Immunology Unit, Univ. Oxford) « Nucleic Acids Sensing by Innate Immune Receptors » Mercredi 12 Avril 2023 (Salle Marcel Dorée)
The innate immune response is critical for host defence against viruses. Cell-intrinsic mechanisms detect virus presence and restrict virus replication. Nucleic acids are often a molecular signature of infection and are recognised by receptors including Toll-like receptors, RIG-I-like receptors and cytosolic DNA sensors. These receptors signal for the induction of innate response genes such as those encoding type I interferons. These then induce the expression of restriction factors, host proteins that limit virus replication. Our work focuses on cytosolic nucleic acid sensors, in particular RIG-I, MDA5 and cGAS. We use in vitro and in vivo models of virus infections and are interested in rare genetic diseases linked to chronic anti-viral innate immune responses. In this presentation, I will discuss our recent work on MDA5, cGAS and other nucleic acid sensors.
- Dr. Chiara Zurzolo (Institut Pasteur) « Tunneling nanotubes: structure/function and role in the spreading of SARS-CoV-2 » Mardi 31 Janvier 2023, 15h00 (Salle Marcel Dorée)
Chiara Zurzolo, MD PhD, is head of the Membrane Trafficking and Pathogenesis Unit and head of the Department of Cell Biology and Infection. In 1995, started her lab as professor of Cell Biology at Naples University Federico II, where she graduated, focusing on protein trafficking and specifically on the mechanisms of apical sorting of GPI-proteins (GPI-AP) in polarized epithelia. In 2003 she moved to the Pasteur Institute where she pioneered studies on the role of protein trafficking in prion diseases. She has made seminal discoveries in both protein trafficking and neurodegeneration. Her group has shown that the mechanism of sorting of GPI-APs (cholesterol dependent oligomerization) in the Golgi of polarized cells controls the protein function at the apical plasma membrane (2008, 2014). They uncovered the intracellular site of prion conversion and showed that prion dissemination occurs by Tunneling Nanotubes (TNTs), a new mechanism of direct intercellular communication (2009). She proposes that TNTs are involved in the spreading of different amylogenic proteins in the brain (2013) and therefore represent a suitable target to halt incurable neurodegenerative diseases. She recently showed that TNTs provide a route for SARS-CoV-2 spreading (2022).
- Dr. Sarah Gallois-Montbrun (Institut Cochin) « From HIV-1 to SARS-CoV-2 infection: viral RNAs in all their states!« Vendredi 3 Février 2023, 11h00 (Salle Marcel Dorée)
Sarah Gallois-Montbrun was trained in biochemistry, molecular biology and virology at Institut Pasteur and received her PhD from the University Pierre et Marie Curie in 2004. In 2005, she was granted an EMBO fellowship and moved to the Department of Infectious Diseases in the laboratory of Michael Malim at King’s College, London. Her post-doctoral research focused on the cellular roles of APOBEC3G and APOBEC3F, two restriction factors of HIV. Her work revealed that both proteins belong to large ribonucleoprotein complexes and localize to cytoplasmic structures induced by phase separation called P-bodies and Stress granules. In 2009, she was recruited as Chargée de Recherche (CR) by Inserm and joined the laboratory of Host-Pathogen Interactions co-directed by Clarisse Berlioz-Torrent and Stéphane Emiliani at Institut Cochin, France. Through a panel of techniques in cell biology (CRISPR-CAS9 KO, siRNA KD), molecular biology (HITS-CLIP, Long-read sequencing) and virology, her group focused on the role of cellular and viral factors in the fate of cellular and viral RNAs during infection by HIV-1, the causing agent of AIDS and more recently SARS-CoV-2, the causing agent of Covid-19.
- Dr. Nolwenn Jouvenet (Institut Pasteur) « Clash of the titans: RNA viruses and interferons » Vendredi 25 Novembre 2022, 11h00 (Salle Marcel Dorée)
Dr. Nolwenn Jouvenet is the head of the ‘Virus sensing and signaling’ team based in the Institut Pasteur, Paris. The interaction between viruses and their hosts has been the driving force behind her research since she completed her Ph.D. at the Pirbright Institute, Surrey, UK. Her post-doctoral work at the Rockefeller University, New York, USA, focused on the mechanisms of assembly and budding of retroviruses. In 2012, she was granted a permanent position by the French state research organization CNRS. In 2015, she was awarded the prestigious EMBO Young Investigator Prize. She was promoted to Research Director by the CNRS and was granted her own laboratory by the directorship of the Institut Pasteur in 2021. Her team focuses on mechanisms underlying virus-induced innate immunity, particularly on emerging and re-emerging RNA viruses that threaten human health, such as dengue virus, Zika virus and coronaviruses.
- Dr. Arinjay Banerjee (Université de Saskatchewan) « Lessons learnt from coronavirus – host interactions in wildlife reservoirs and spill over hosts » Vendredi 9 Décembre 2022, 11h00 (Salle Marcel Dorée)
Short abstract: Bats perform important ecological roles in our ecosystem. However, bats are also reservoirs of emerging viruses that have spilled over into humans and agricultural animals to cause severe disease. These viruses include Hendra and Nipah paramyxoviruses, Ebola and Marburg filoviruses, and coronaviruses that are closely related to severe acute respiratory syndrome coronavirus (SARS-CoV), Middle East respiratory syndrome coronavirus (MERS-CoV), and the recently emerged SARS-CoV-2. Intriguingly, bats that are naturally or experimentally infected with these viruses do not show clinical signs of disease. Highly pathogenic zoonotic coronaviruses have evolved proteins that can effectively block innate and intrinsic responses in human cells. In this talk, we shall explore how coronaviruses interact with innate and intrinsic responses in their wildlife (bat) and spill over (human) hosts. We will discuss lessons learnt from our studies on bat antiviral responses and translational outcomes that will enable us to design better countermeasures for coronavirus infections in humans.
Dr. Arinjay Banerjee (PhD) is the Principal Investigator of the Laboratory of Zoonotic Viruses and Comparative Immunology at the Vaccine and Infectious Disease Organization, University of Saskatchewan, and adjunct faculty member at the Universities of Saskatchewan, Waterloo, British Columbia, and Toronto. Dr. Banerjee is the co-lead for One Health at the University of Saskatchewan. Research within Dr. Banerjee’s laboratory focuses on three main themes that are inspired by the One Health ideology, (1) virus-host interactions in wildlife reservoir species, such as bats, (2) virus-host interactions in spillover species, such as humans, and (3) viral vaccine development. Dr. Banerjee’s laboratory is a member of Canada’s Coronavirus Variants Rapid Response Network (CoVaRR-Net), and as part of this network, his laboratory investigates emerging SARS-CoV-2 variants. Dr. Banerjee completed his Master of Science degree in virology from the National Institute of Virology in India where his Master’s thesis was awarded the university gold medal. Next, Dr. Banerjee completed his PhD from the University of Saskatchewan where his doctoral thesis on coronavirus-host interactions was awarded Canada’s Governor General’s Gold medal. Dr. Banerjee’s postdoctoral research at McMaster University was awarded the Gerard Wright postdoctoral award in Infection Research and the postdoctoral fellow impact award. More recently, Dr. Banerjee was selected as CBC Saskatchewan’s Top 40 under 40.
- Dr. Esther Nolte-‘t Hoen (Utrecht University) « Egress of picornaviruses from infected cells via enclosure in Extracellular Vesicles: the ultimate package deal? » Vendredi 30 Septembre 2022, 11h00 (Salle Marcel Dorée)
Esther Nolte-‘t Hoen is associate professor at the Department of Biomolecular Health Sciences of the Faculty of Veterinary Medicine Utrecht University, the Netherlands. Nolte-‘t Hoen has been active in research on extracellular vesicles (EV) for more than 15 years and has longstanding experience in studying the formation, composition, and function of extracellular vesicles in various (patho)physiological processes, including immune responses and virus/microbial infections. She received a European Research Council Starting Grant in 2013, after which she started her own independent research group. She has developed a high-resolution flow cytometry methodology to perform high-throughput analysis of individual EV and to sort-isolate EV subpopulations for downstream analysis. Being the first to have sequenced the small RNA transcriptome of extracellular vesicles, Dr Nolte-‘t Hoen has also puts strong emphasis on analyzing EV-contained RNA types as important players in the biological effects induced by EV and as biomarkers. More recently, her research group has focused on the role of EVs in host-pathogen communication. Within this area, the team aims to unravel how naked RNA viruses escape infected cells by enclosure in EVs, and how this affects virus spreading and antiviral responses.
Nolte-‘t Hoen strongly supports the idea that collaborative efforts, transparency in reporting, effective knowledge sharing during scientific meetings, and training of newcomers to the field are key to bringing the young EV research field to the next level. To reach these goals, she has organized workshops and meetings, and gave scientific, educational, and ‘meet the expert’ lectures for the International Society for Extracellular Vesicles. Moreover, she is associate editor for the main journal in the EV field (Journal of Extracellular Vesicles), she co-founded and is the current president of the Netherlands Society for Extracellular Vesicles, organizes EMBL (Heidelberg) hands-on training courses on EV research, and coordinated position papers.
- Dr. Jérémy DUFOURT (IGMM – Montpellier) « Lighting up the central dogma of molecular biology in living embryos: Lights, Camera, Action on translation » Vendredi 16 Septembre 2022, 11h00 (Salle Marcel Dorée)
Jeremy Dufourt did his PhD in the laboratory of Chantal Vaury (GReD Clermont Ferrand) where he studied the regulation of transposable elements (TE) by small RNAs. Then he moved to the laboratory of Martine Simonelig (IGH Montpellier) for his first post-doc continuing his study on small RNAs but on the regulation of coding (non TE) mRNAs. Finally he moved to IGMM for a second post-doc in Mounia Lagha laboratory where he first worked on transcription factor dynamics and transcriptional memory during the genome awakening in Drosophila embryos. He then obtained a CNRS CRCN permanent position in 2019, and recently implemented the live imaging of translation in Drosophila, allowing for the first time to analyse spatio-temporal dynamics of translation in a living organism.
- Dr. Stacey Gilk (Associate Professor at the University of Nebraska Medical Center) « Fine tuning cholesterol in the intracellular niche » Mardi 30 août 2022, 11h (Salle Marcel Dorée)
- Prof. Dan V. Nicolau (Université McGill, Montréal). « Something has to give: Computation with motile biological agents« . Mardi 28 Juin 2022, 14h00 (Salle Marcel Dorée)
Dan, who is a Professor at, and the Head of the Department of Bioengineering at McGill University, has a PhD in Chemical Engineering, a MS in Cybernetics, Informatics & Statistics and a MEng in Polymer Science & Engineering. He has published ~130 papers in peer-reviewed scientific journals, a similar number of full papers in conference proceedings and 6 book chapters. He has edited one book (with U. Muller; on microarray technology and applications), and edited or co-edited the proceedings of 30+ conferences. Dan is a Fellow of the International Society of Optical Engineering (SPIE) and the Editor-in-Chief of IEEE NanoBioScience. His present research aggregates around three themes: (i) technologies for both largely-parallel, and rapid-sequential high throughput screening; (ii) information storage and processing in biomolecular and/or nano-systems; and (iii) intelligent-like behaviour of microorganisms in confined spaces.
- Dr. Nathalie Sauvonnet (Institut Pasteur – Paris). « Impact of tissue microenvironment and mechanical forces of the gut on pathogens invasion« . Vendredi 8 Juillet 2022
As a cell biologist and microbiologist Nathalie Sauvonnet major interest focused on protein trafficking in different cellular compartments. In bacteria, during her PhD and postdoc she studied secretion mechanisms (Type 1,2,3 secretion system, TnSS) and type IV pili, often involved in pathogenic processes. Using microbiology methods, genetics screens, scanning electron microscopy and biochemistry approaches, she uncovered characteristic features of secreted cargos, revealed the close relation between type IV pili and T2SS and analysed the impact of T3SS on host cell transcriptome. As a permanent researcher, she turned her interest to eukaryotes having multi-compartmentalized cells and studied endocytosis and the dynamics of the endomembrane system. Since 2006, she leads a small team aiming to determine the interplay between intracellular trafficking, tissue mechanics, tissue homeostasis and host-pathogen interactions. On endocytosis, her team used RNAi screen, CrispR-Cas9 gene edition, live TIRF microscopy, robust image analysis and single particle tracking, to characterize the molecular and dynamical aspect of clathrin-independent endocytosis. In parallel, she also studied the consequence of pathogens invasion on the host cell intracellular trafficking. More recently she developed organ-on-chip technology to investigate host-pathogen interactions at the tissue scale using several examples of pathogens (ex: Shigella and SARS-CoV-2) in the aim to decipher the impact of tissue microenvironment and mechanical forces on pathogen invasion.
- Dr. Christel Vérollet (IPBS – Toulouse). « Understanding cell-to-cell transfer of HIV-1 towards macrophages: a perspective for HIV/Tuberculosis co-infection« . Vendredi 25 Mars 2022
Notre équipe à l’IPBS, Toulouse (dirigée par C. Vérollet et R. Poincloux, https://www.ipbs.fr/phagocyte-architecture-and-dynamics) étudie les mécanismes cellulaires et moléculaires utilisés par les macrophages pour interagir avec leur environnement dans différents contextes physiologiques et pathologiques, y compris la co-infection VIH-1 et VIH/Mtb. En particulier, je suis une biologiste cellulaire qui travaille sur la façon dont le VIH-1 détourne le cytosquelette des macrophages (podosomes et nanotubes à effet tunnel) pour se propager et se disséminer.
Dufrancais O, Mascarau R et al. . CMLS, 2021; Mascarau R, et al. . IJMS, 2020; Dupont M, et al. Elife, 2020; Xie M, et al. MBio, 2019; Souriant S, et al. Cell Reports, 2019; Raynaud-Messina B, et al. Proc Natl Acad Sci U S A. 2018; Vérollet C, et al. Blood, 2015
- Dr. Félix Rey (Institut Pasteur, Paris). « Structure and evolution of class II enveloped viruses« . Vendredi 11 Mars 2022 (Visio Zoom disponible)
Felix Rey est un biologiste structural (doctorat en 1988 à l’Université de Paris-Sud), avec une formation postdoctorale à l’Université de Harvard (1988- 1995), où il s’est spécialisé dans la structure des virus. En 2004 il rejoint l’Institut Pasteur en tant que chef du département de virologie et création en même temps de l’Unité de Virologie Structurale (UMR 3569 CNRS/Pasteur), qu’il dirige toujours aujourd’hui. Ses recherches ont porté sur les structures 3D des polymérases virales et sur la matrice nucléoprotéique de réplication des virus à ARN à brin négatif. Il s’est surtout concentré sur l’étude des protéines d’enveloppe virale, sur la manière dont elles induisent la fusion de membranes avec des implications dans la « vaccinologie inversée » (« reverse vaccinology »), ouvrant la voie à la conception de vaccins axés sur certains épitopes spécifiques pour des virus tels que la dengue et le Zika, et plus récemment aussi sur des bunyavirus. Les travaux de Felix Rey ont notamment conduit à identification d’une classe à part de protéines de fusion membranaire (appelée « classe II ») présente dans des virus tels que les flavivirus (Zika), les alphavirus (Chikungunya), les bunyavirus (virus de la fièvre de la vallée du Rift), les rubivirus (virus de la rubéole).
- Dr. Roy Matkovic (Institut Cochin, Paris). « A dual repressive effect employed by HUSH to keep HIV silent« . Vendredi 4 Février 2022 (Visio Zoom disponible)
If on a long time scale the mobile DNA elements and retroviruses constitute positive drivers of the evolution of species, on a short time scale they can disrupt the integrity of our genome by integrating/spreading into it. One of the complexes that allows them to be epigenetically repressed, by deposition of H3K9me3 marks and heterochromatinization, is HUSH. We have previously shown that this complex can inhibit the expression of an HIV-1 minigenome in the J-Lat A1 latency model and that its antagonism by HIV-2 Vpx is able to increase the expression of HIV-1 LTR-derived RNAs. How HUSH is able to repress the HIV provirus remains enigmatic. Together, we will discuss the mechanism used by HUSH to keep HIV silent. We will show that the HUSH member TASOR is actually at the RNA/epigenetic repression interface and that it associates with epigenetic/transcriptional and RNA degradation factors to repress HIV at two steps. Finally, we will build a model of its mechanism that appears to be globally conserved during evolution when it comes to silence exogenous DNA in order to preserve the genome integrity.
- Dr. Delphine Judith (Institut Cochin, Paris). « ATG5 drives an LC3-associated pathway to counter BST2/Tetherin antiviral functions« . Vendredi 28 Janvier 2022 en visio (lien zoom)
Delphine performed her PhD at the Pasteur Institute in the laboratory of Pr. Lecuit (Inserm U1117). During her PhD research, she focused her work on the study of the impact of the autophagy machinery on CHIKV replication. Her major achievement was the discovery of the critical species specificity of the virus, which sheds light on the differential behavior of mouse vs. human cells in response to CHIKV.
After her PhD, she moved to London for a post-doctoral position in the laboratory of Dr. Tooze at The Francis Crick institute. The aims of her project were to dissect the intracellular trafficking route through which mammalian ATG9A travels and determine the role of this protein in autophagy by an in-depth analysis of the ATG9A compartment. First, she established an immuno-isolation approach to purify endogenous ATG9A compartments from mammalian cells. Then, she revealed that ATG9A-positive membranes containing activated PI4KIIIb catalyze the production of PI4P at the formation site and thus initiating and driving autophagosome biogenesis and subsequently autophagy. This study opens up a whole new perspective on this process as it has been assumed PI3P is the only lipid required in the autophagy pathway.
After this work she joined, for a postdoctoral work, the laboratory of Dr. Clarisse Berlioz-Torrent in Paris, at the Cochin Institute, where she studied the impact of LC3-associated pathway on HIV-1 infection. The focus of her work is to dissect the LC3-associated process subverted by Vpu to counteract BST2 restriction, and more precisely the initial step occurring at the plasma membrane and required to initiate the process.
- Dr. Coralie Daussy (MFP – Bordeaux). « Viral control by Adenovirus of the cellular membrane damage response« . Vendredi 18 Juin 2021 à 11h en visio (lien Zoom:)
Equipe : « Spatial and temporal control of virus-host interactions » / Laboratoire Microbiologie Fondamentale et Pathogénicité (MFP) – UMR 5234 – Bordeaux
- Dr. Elizabeth Bik. « The Dark Side of Science: Misconduct in Biomedical Research ». Mercredi 8 Septembre à 13h via Zoom. Elisabeth Bik is a Dutch microbiologist living in California, who has worked for 15 years at Stanford University and 2 years in industry. Since 2019, she is a science integrity volunteer and occasional consultant, who scans the biomedical literature for images or other data of concern and has reported over 4,000 scientific papers.
Abstract: Science builds upon science. Even after peer-review and publication, science papers could still contain images or other data of concern. If not addressed post-publication, papers containing incorrect or even falsified data could lead to wasted time and money spent by other researchers trying to reproduce those results. Several high-profile science misconduct cases have been described, but many cases are yet undetected. Elisabeth Bik is an image forensics detective who left her paid job in industry to search for and report biomedical articles that contain errors or data of concern. She has done a systematic scan of 20,000 papers in 40 journals and found that about 4% of these contained inappropriately duplicated images. In her talk she will present her work and show several types of inappropriately duplicated images and other examples of research misconduct. In addition, she will show how to report scientific papers of concern, and how journals and institutions handle such allegations.
Elisabeth Bik’s minibio: E. Bik is a science integrity consultant who specializes in finding image duplications in scientific papers. After receiving her PhD in Microbiology at Utrecht University in The Netherlands, she worked 15 years at the Stanford University School of Medicine on the microbiomes of humans and marine mammals. From 2016-2019, she worked at two microbiome startup companies. In March 2019, she left her job to become a science integrity volunteer and occasional consultant. She can often be found discussing science papers on Twitter at @MicrobiomDigest, writing for her blog ScienceIntegrityDigest or searching the biomedical literature for inappropriately duplicated or manipulated photographic images and plagiarized text. She has reported over 4,000 papers for issues with image duplication or other concerns. Her work has been featured in Nature, Science, Wall Street Journal, New York Times, Washington Post, Le Monde, and The Times (UK). In April 2021 she was awarded the Peter Wildy Prize by the UK Microbiology Society for her contributions in science communication.
Séminaires reportés (pandémie Covid-19)
- Pr Alessia Zamborlini (Paris Saclay University). « SUMOylation of Lysine 595 cooperates with phosphorylation of Threonine 592 to regulate SAMHD1 antiviral activity »
Summary of the talk: SAMHD1 is a cellular triphosphohydrolase that inhibits the replication of HIV-1 in non-cycling immune cells by reducing the concentration of dNTP below a threshold required for efficient reverse transcription of the viral genome. Phosphorylation of residue T592 suppresses the antiviral activity of SAMHD1 in cycling cells. However, phosphomimetic mutants efficiently deplete the cellular dNTP pools, indicating that additional functions and/or post-translational modifications play a role in the regulation of SAMHD1 restriction activity.
A. Zamborlini’s team found that SAMHD1 is SUMOylated on residue K595, a modification that relies on the integrity of a SUMO-interacting motif. Furthermore, their data provide compelling evidence that, in non-cycling cells where most of the protein harbors an unphosphorylated T592 residue, SUMOylation of K595 defines the fraction of restriction competent SAMHD1.
Minibio du Pr. Alessandra Zamborlini : A. Zamborlini a obtenu un diplôme M2 en Chimie et Technologies Pharmaceutiques (Faculté de Pharmacie) puis un PhD en Virologie (Faculté de Médecine) à l’Université de Padoue (Italie). Au cours de sa formation doctorale, elle a étudié le rôle des composants cellulaires de la machinerie ESCRT dans le bourgeonnement du VIH-1 dans le laboratoire de Heinrich Gottlinger (Harvard Medical School, Boston, USA). Elle a ensuite rejoint le laboratoire d’Ali Saïb en tant que post-doctorante où elle a développé plusieurs projets visant à mieux comprendre la persistance du virus dans les cellules T quiescentes et la régulation de l’étape d’intégration par des modifications post-traductionnelles. En 2010 elle a obtenu un poste de Maître de conférences au Cnam (Conservatoire national des arts et métiers, Paris), puis en 2019 un poste de Professeur de Virologie à l’Université Paris Saclay. Ses projets de recherche visent à déchiffrer les bases moléculaires sous-jacentes à la coordination des multiples activités de SAMHD1 ainsi que la contribution de SUMOylation à la réponse antivirale dans les cellules immunitaires au repos ou post-mitotiques.
- Dr Christophe Mueller (Strasbourg university). « Host immune evasion by Pseudomonas aeruginosa? A study of the impact of its lectin LecB on the murine immune system. » POSTPONED DUE TO COVID19 PANDEMIC
Dr. Christopher Mueller is CNRS director of research at the University of Strasbourg, France, and the CNRS research team Immunology and Immunopathology. He has obtained his PhD in Heidelberg / the University of London on c-fos transcription factors and spent two years as a postdoctoral fellow in UC-Berkeley working on transcriptional regulation in the yeast S. cerevisiae. He became an immunologists at Schering-Plough, Inc., France, and integrated the French national research system CNRS to continue his research on the immunobiology of the myeloid cell lineage in the skin and lymphoid tissue. He now heads a research team in Strasbourg to study the impact of the cellular microenvironment on immune cell differentiation and activation in the context of infection and autoimmunity. He has recently shown that mesenchymal cells instruct lymphatic endothelial cells via TNFSF11 (RANKL) – TNFRSF11a (RANK) to create the niche for sinusoidal macrophage differentiation.
He is a member of the Labex Medalis, former director of the International PhD programme of the University of Strasbourg, and co-founder of the Upper Rhine Immunology group, comprising the Universities of Strasbourg, Freiburg and Basel.
- Dr. Sarah Gallois-Montbrun (Institut Cochin, Paris) « Non-canonical Roles of Argonaute proteins in HIV-1 viral RNA expression« – initialement planifié le 13 Décembre 2019 mais reporté à une date ultérieure
Summary of the talk: During its replication, HIV-1 produces more than 50 different transcripts coding for all the proteins necessary for viral particles assembly. Balanced production of viral isoforms is highly regulated both temporally and spatially. Current research in my group aims at characterizing the role of viral and cellular factors involved in HIV-1 RNA production. In particular, we investigated the role of the miRNA pathway and demonstrated that key proteins of these pathway, Argonaute 1 and Argonaute 2, participate at different levels of viral RNA production independently of the presence of miRNA. In parallel, we recently developed a long-read sequencing assay to quantify production of HIV-1 isoforms and to decipher the cascade of splicing events taking place at early time points after infection.
Dr Gallois-Montbrun’s minibiography: After completing her PhD studies at Pasteur Institute Paris in 2004 on cellular metabolism of anti-HIV-1 drugs, she undertook post-doctoral training with Prof Michael Malim at King’s College London. There she focused on characterizing cellular protein and RNA partners of APOBEC3G and APOBEC3F, two HIV-1 restriction factors. She was recruited as Inserm research scientist at Cochin Institute in 2009. Since then, her group has aimed at dissecting mechanisms regulating HIV-1 RNA fate and how these impact on viral replication.
- Prof. Jack Stapleton (Iowa university, USA) « A flavivirus genome-derived noncoding RNA regulates T cell function and restricts virus replication » Friday the 21st of February 11 am
Jack Stapleton’s minibio: Jack is a Professor of Internal Medicine, Infectious Diseases and Microbiology at the University of Iowa. Over the last 3 decades, his laboratory has focused on positive strand RNA viruses (HIV, HCV, GBV-C/HPgv) and how members of the Flaviviridae interact with HIV and immune function. Most recently, the lab studies how HCV and yellow fever virus genomic RNA is processed into short, noncoding RNAs that regulate T cell function and enhance viral replication. He also has conducted numerous translational studies on how human pegivirus (GBV-C) prolongs survival in HIV infected people, and characterized mechanisms involved in this beneficial co-infection.
- Dr. Philippe Benaroch « Host-HIV interplay in human primary myeloid cells » – 22 Novembre 2019
Philippe Benaroch is research director at the CNRS and heads the team “Myeloid cells and immunity” within the Department of Immunology at the Institut Curie in Paris. He will present recent work and unpublished data regarding a recently identified blood dendritic cell subset, its unique relationship with HIV and some of its shared properties with infected macrophages.
Philippe Benaroch is particularly interested by myeloid cells that represent a very ancient form of cellular immunity against pathogens and tumor cells. Myeloid cells are very plastic, endowed with an ever-growing list of functions in innate and adaptive immunity. How myeloid cells crosstalk with HIV and tumor cells and how this interplay is regulated remains to be established at the molecular level and represent the focus of his lab.
- Dr. Lise Chauveau (Oxford university, UK) « The immune system’s Trojan horse: Using cGAMP-loaded VLPs for vaccination » – 11 Octobre 2019
Dr Lise Chauveau is interested in how viruses induce an immune response, the type of response induced and how viruses may counteract it. She studied Biology at the Ecole Normal Superieure de Lyon where she obtained a Master degree in 2012. She then moved to the Pasteur Institute in Paris to complete a PhD in the laboratory of Prof Olivier Schwartz in 2016. There, she studied factors influencing the ability of HIV-1 and HIV-2 to infect cells of the immune system, CD4 T cells and dendritic cells. This is where her interest in antiviral immunity and how viruses might modulate it sparked. She is now a postdoctoral researcher with Dr Jan Rehwinkel at the Weatherall Institute of Molecular Medicine, University of Oxford, UK. She currently works on an original vaccination strategy using HIV-derived virus-like particles that incorporate an innate immune messenger (cGAMP) to induce potent and protective immune response against viruses.
- Prof. Ricardo Soto-Rifo (Universidad de Chile) « The complex life of HIV-1 full-length RNA » – Mardi 1er octobre 2019
Dr. Soto-Rifo has been always interested in the molecular and cellular mechanisms controlling gene expression in Eukaryotes with a special emphasis in RNA viruses as study models. Dr. Soto-Rifo studied biochemistry at Universidad de Santiago de Chile and then moved to France where he obtained a Master in Sciences degree from Université Claude Bernard Lyon-1 in 2006 and then a Ph.D in Life Sciences from Ecole Normale Supérieure de Lyon in 2010. He worked at the Human Virology Department (currently the International Center for Infectiology Research, CIRI) under the supervision of Dr. Théophile Ohlmann on the translational control of the HIV-1 and HIV-2 genomic RNA. During his post-doctoral training at Dr. Ohlmann’s lab, Dr. Soto-Rifo worked on the remodeling and localization of the messenger ribonucleoprotein complexes (mRNPs) containing the HIV-1 genomic RNA by analyzing the role of the DEAD-box RNA helicase DDX3 in these processes. In 2013, he moved to Biomedical Sciences Institute at Universidad de Chile Faculty of Medicine to start his own laboratory at the Virology Program. Since then, Dr. Soto-Rifo’s reasearch has been mainly focused in understanding the mechanisms involved in RNA metabolism during HIV-1, HIV-2, respiratory syncytial virus and Zika virus replication.
The presentation will be focused on the role of the RNA modification N6-methyladenosine (m6A) and its associated cellular machinery in defining the cytoplasmic destiny of the HIV-1 genomic RNA during the late steps of the viral replication cycle.
- Dr. Pierre-Olivier Vidalain (CIRI) « Searching for chemical activators of the interferon response : surprises from a chemobiological approach » – 13 Septembre 2019
Pierre-Olivier Vidalain, Directeur de Recherche, CNRS. Après avoir soutenu une thèse en immunologie à l’Ecole Normale Supérieure de Lyon, Pierre-Olivier s’est familiarisé avec les techniques de criblage à haut débit et l’étude des interactions protéine-protéine dans l’équipe de Marc Vidal (Harvard Medical School, Boston). Recruté en 2005 au CNRS, il a travaillé successivement à l’Institut Pasteur puis à l’Université Paris Descartes où il a étudié les interactions entre protéines virales et cellulaires et à mis au point différents systèmes pour l’identification de molécules antivirales ciblant l’hôte. Il s’intéresse plus particulièrement aux effets immunomodulateurs de composés inhibant la voie de biosynthèse des pyrimidines. En janvier 2019, il a rejoint le Centre International de Recherche en Infectiologie à Lyon pour poursuivre ses travaux à l’interface entre immunité innée, métabolisme et approches chémobiologiques.
- Dr. Jost Enninga (Institut Pasteur, Paris) « Subversion of infection associated macropinosomes drives the intracellular niche formation of bacterial pathogens » – 5 Juillet 2019
Jost Enninga heads the research unit « Dynamics of host-pathogen interactions » within the Department of Cell Biology and Infection at the Institut Pasteur in Paris. He performed his Ph.D. studies in the Laboratory of Cell Biology at the Rockefeller University, New York, under the supervision of Dr. Guenter Blobel. There, he focused on how viruses subvert host cellular trafficking processes. Afterwards, Jost moved to the Institut Pasteur in Paris in 2004 to study the early events of bacterial host cellular invasion with Dr. Philippe Sansonetti and Dr. Guy Tran Van Nhieu. Between 2008 and 2012, Jost built up his own junior team at the Institut Pasteur, and he heads his current research unit since 2013. His team investigates the intracellular niche formation of different bacterial pathogens, including Shigella and Salmonella. Main questions are membrane trafficking subversion by the pathogens, and how specific intracellular localizations trigger distinct immune responses. His research unit develops imaging-based technologies that allow the analysis of host-pathogen interaction dynamics with unprecedented spatiotemporal resolution.
- Dr. F. Perez (Institut Curie, Paris) « Exploring the Secretory Pathway : from Basic to Translational Research » – 28 Juin 2019
- Dr. Sylvie Lecollinet (Virology department at ANSES/Veterinary school, Maisons-Alfort) “From basic to applied research on zoonotic West Nile and Usutu flaviviruses” – 14 Juin 2019
- Dr. Niedergang Florence (Institut Cochin – Paris) « Macrophages upon viral infection, emergence of opportunistic diseases » – 9 Mai 2019
- Dr. Mauffret Olivier (LBPA – ENS Cachan) « Structures-functions relationships of the zinc fingers domains of HIV-1 nuclecocapsid protein » – 15 Février 2019
- Dr. Manel Nicolas (Institut Curie) – « Activation of innate immune sensors by viruses and self » –1er Février 2019
- Dr. Carocci Margot (INSERM UMR-949, Université de Strasbourg) « Development of novel strategies to fight flaviviruses: from targeted screen to in vivo antiviral validation » – 7 Décembre 2018
- Dr. Cimarelli Andrea (Inserm U1111 – CNRS UMR 5308 – Université / ENS de Lyon) « Interferon-stimulated transmembrane proteins (ifitms) as a novel paradigm of restriction factors targeting the in and out of a viral life cycle » – 14 Novembre 2018
- Dr. Margottin-Goguet Florence (Institut Cochin – Paris) « HIV Latency as an intrinsic host defense antagonized by lentiviral proteins » – 21 Septembre 2018
- Dr. Oehlers Stefan (Centenary Institute – University of Sidney) « Vascular control of mycobacterial immunity » – 6 Juillet 2018
- Dr. Shu Sin Chng (Department of Chemistry, National University of Singapore) « Bacterial lipid trafficking and outer membrane homeostasis »
- Prof. Slupphaug Geir (Department of Clinical and Molecular Medicine, Trondheim, Norway) « Are endogenous and chemically induced base methylations in human mRNA processed differentially? »
- Dr. Chojnacki Jakub (IrsiCaixa AIDS research institut – Barcelona) « STED microscopy studies of HIV-1 dynamic structure and virus-cell interactions. »
- Dr. Gaudin Raphaël (Inserm U1110 – Strasbourg) « Zika virus induces monocyte transmigration, spreading the infection to the brain »
- Dr. Muriaux D. (CEMIPAI) « Présentation de la plateforme CEMIPAI et ses technologies innovantes »
- Prof. Yegutgin G. (University of Turku – Finland) « Emerging roles of purine-converting ectoenzymes in inflammation and tumorigenesis »
- Dr. Smyth R. (IBMC, Strasbourg)
- Dr. Lyonnais S. (IBMB-CSIC, Barcelone)
- Dr. Long J. (Imperial College of London)
- Dr. Meunier E. (IPBS, Toulouse)
- Dr. Herbeuval J.P. (UMR 8601, Paris)
- Dr. Wodrich G. (UMR 5234, Bordeaux)
- Dr. Henriet S. (University of Bergen, Norway)
- Dr. Janvier K. (Institut Cochin, Paris)