key: cord-0861131-uilejxmi authors: van den Hoogen, Bernadette; Santoni, Angela; Sciumé, Giuseppe; Bowie, Andrew; O’Farrelly, Cliona; O’Neill, Luke; Anthonsen, Marit; Pardalli, Katerina; Young, Simon; Bergthaler, Andreas; Manel, Nicolas; Zahn, Ronald; Kikkert, Marjolein; Snijder, Eric; van Kuppeveld, Frank; Fouchier, Ron; Hiscott, John title: Immunometabolism pathways as the basis for innovative anti-viral strategies (INITIATE): A Marie Sklodowska-Curie innovative training network date: 2020-07-28 journal: Virus Res DOI: 10.1016/j.virusres.2020.198094 sha: 31c708faa4ac0533bb3a27eb1b9f14912ecd1fa9 doc_id: 861131 cord_uid: uilejxmi The past century has witnessed major advances in the control of many infectious diseases, yet outbreaks and epidemics caused by (re-) emerging RNA viruses continue to pose a global threat to human health. As illustrated by the global COVID19 pandemic, high healthcare costs, economic disruption and loss of productivity reinforce the unmet medical need to develop new antiviral strategies to combat not only the current pandemic but also future viral outbreaks. Pivotal for effective anti-viral defense is the innate immune system, a first line host response that senses and responds to virus infection. While molecular details of the innate immune response are well characterized, this research field is now being revolutionized with the recognition that cell metabolism has a major impact on the antiviral and inflammatory responses to virus infections. A detailed understanding of the role of metabolic regulation with respect to antiviral and inflammatory responses, together with knowledge of the strategies used by viruses to exploit immunometabolic pathways, will ultimately change our understanding and treatment of pathogenic viral diseases. INITIATE is a Marie Sklodowska-Curie Actions Innovative Training Network (MSCA-ITN), with the goal to train 15 early stage PhD researchers (ESRs) to become experts in antiviral immunometabolism (https://initiate-itn.eu/). To this end, INITIATE brings together a highly complementary international team of academic and corporate leaders from 7 European countries, with outstanding track records in the historically distinct research fields of virology, immunology and metabolism. The ESRs of INITIATE are trained in these interdisciplinary research fields through individual investigator-driven research projects, specialized scientific training events, workshops on academia-industry interactions, outreach & communication. INITIATE will deliver a new generation of creative and entrepreneurial researchers who will be able to face the inevitable future challenges in combating viral diseases. Pivotal for effective anti-viral defense is the innate immune system, a first line host response that senses and responds to virus infection. While molecular details of the innate immune response are well characterized, this research field is now being revolutionized with the recognition that cell metabolism has a major impact on the antiviral and inflammatory responses to virus infections. A detailed understanding of the role of metabolic regulation with respect to antiviral and inflammatory responses, together with knowledge of the strategies used by viruses to exploit immunometabolic pathways, will ultimately change our understanding and treatment of pathogenic viral diseases. INITIATE is a Marie Sklodowska-Curie Actions Innovative Training Network (MSCA-ITN), with the goal to train 15 early stage PhD researchers (ESRs) to become experts in antiviral immunometabolism (https://initiate-itn.eu/). To this end, INITIATE brings together a highly complementary international team of academic and corporate leaders from 7 European countries, with outstanding track records in the historically distinct research fields of virology, immunology and metabolism. The ESRs of INITIATE are trained in these interdisciplinary research fields through individual investigator-driven research projects, specialized scientific training events, workshops on academia-industry interactions, outreach & communication. INITIATE will deliver a new generation of creative and entrepreneurial researchers who will be able to face the inevitable future challenges in combating viral diseases. Key words: virology, innate immunity, immunometabolism, coronavirus, influenza virus, pneumovirus, innovative training network The past century has witnessed major advances in the control of many infectious diseases, as well as the mechanistic basis of the immune responses that limit virus replication and pathogenesis. Nevertheless, viral outbreaks and epidemics caused by (re-) emerging RNA viruses continue to pose an imminent global threat to human and animal health. During the early years of the 21 st century, prominent examples of such viral outbreaks included the H1N1 influenza pandemic of 2009, SARS-and MERS-coronavirus outbreaks in 2003 and 2012 respectively, ebola virus in 2014, 2018 and 2019, zika virus in 2016 and annual outbreaks of dengue viruses in tropical regions -each of which resulted in a dramatic strain on health care infrastructure and major societal disruptions. But since the start of 2020, the global community has been engulfed by the current pandemic of coronavirus induced disease (COVID-19) caused by the novel SARS-CoV-2. At the time of writing, the pandemic rages on, and in the absence of effective therapeutics or a vaccine, as well as a strong international political strategy, the only defence available to humankind is the use of masks, social distancing and personal hygiene. Despite an unparalleled effort by the global biomedical community, knowledge of the mechanisms of pathogenesis remains limited [1, 2] . Such outbreaks are expected to continue because the environmental, demographic and behavioural drivers of infectious disease emergence are likely to remain intact for the foreseeable future. As illustrated by the current COVID-19 pandemic, high healthcare costs, economic disruption and loss of productivity are additional pandemic consequences that reinforce the urgent medical need to develop new antiviral strategies and therapeutics to combat, not only the current pandemic, but also future viral outbreaks [3] . The innate immune system is pivotal in host defense against virus infection and this field is now being revolutionized by the recognition that cell metabolism is also critical to host defense against several diseases [4, 5] . Immunometabolism is defined as "the changes in intracellular metabolic pathways in immune cells that alter their function" or "the interface of immune and metabolic responses in disease" [6] . It is now clear that immunometabolism pathways also have a major impact on the host antiviral and inflammatory response to virus infections. To drive the emerging field of antiviral immunometabolism, a new generation of scientists is needed with expertise in the interrelationships between viral pathogenesis, host metabolism and immune defences. INITIATE MSCA-ITN addresses this unmet need by bringing together multidisciplinary European academics and private sector partners with a passion to understand interrelationships between antiviral innate immunity and host metabolism. INITIATE includes researchers from 7 academic institutions and 3 industrial partners from 7 European countries ( Figure 1 ); 15 PhD students -Early Stage Researchers (ESRs) have been recruited to INITIATE and each ESR is pursuing an individual research project at one of the partner institutions ( Table 1 ). The research components of INITIATE are complemented with specialized scientific training events, workshops on academia-industry interactions, outreach, communication and public engagement activities. These components of the network are organized by outstanding partners -Agilent, Biocrates, Elsevier and Sovalaccwho will provide essential training to the ESRs. The INITIATE training program will deliver a new generation of creative biomedical entrepreneurial researchers at the forefront of antiviral immunometabolism. To meet the ESRs and the research projects, visit: https://initiateitn.eu/early-stage-researchers/. Antiviral immunity is initiated with the sensing and recognition by a set of patternrecognition receptors (PRRs) of pathogen-associated molecular patterns (PAMPs). Beststudied are the Toll-like (TLRs), RIG-I-like (RLRs), and NOD-like (NLRs) receptors, cGAS-STING and the PYHIN proteins. Activation of PRRs triggers downstream signaling through a myriad of adapters (MyD88, STING and MAVS), protein kinases (Jaks, TBK1, IKKs) and transcriptional regulators (STAT, IRF and NF-B) to trigger the induction of type-I and III interferons (IFN), and hundreds of IFN stimulated genes (ISGs) that culminate in the generation of the so-called antiviral state; inflammatory signaling converges on the assembly and activation of the inflammasome (NLRP3, Asc, Pyhin). However, what has emerged more recently, is that cells activated by PAMPs also undergo profound metabolic changes. These changes are required for biosynthesis and energy production, but also drive key changes in immune signaling processes [7, 8] . The innate immune response also relies on a wide range of innate lymphocytes (ILCs), which are now considered as critical players of the immune response. Natural killer (NK) cells are the founding member of this family and have been studied for decades and their role in providing early protection against viral infections. The ILC family comprises other four prototypical subsets including ILC1, ILC2, ILC3, and lymphoid tissue-inducer (LTi) cells. Independence from antigen recognition, tissue residency, and poised nature of key genomic loci (e.g. those encoding cytokines and other effector molecules) are the main features that make ILCs unique in regulating the early events of viral infection [9] . Increased glycolysis is the hallmark metabolic switch in most immune cells undergoing rapid activation in response to detection of viruses and stimulation of PRRs, cytokine receptors or antigen receptors [10] , [11] . In addition, viruses are likewise dependent on host metabolism for energy production and macromolecular synthesis, in order to complete efficient replication. While many mammalian viruses have evolved ingenious strategies to reprogram immune pathways to secure their maintenance in the infected host [12, 13] , few studies have investigated the crosstalk between virus infection, innate antiviral activity and metabolic pathways [14] . In addition, by-products from the Krebs cycle such as succinate and itaconate act to stimulate or repress the antiviral and inflammatory response to infection [15] . The research program is divided into 3 work packages (Figure 2 The objective of WP1 is to obtain in-depth knowledge of the roles of different organelles and signaling complexes (such as mitochondria, signalosomes, stress granules, replication organelles) in modulation of immune-and metabolic pathways in response to RNA virus infections, including influenza virus, pneumoviruses and coronaviruses. pathways. The objective of WP2 is to obtain in-depth knowledge of the interaction of viruses, viral products and viral mechanisms that modulate the immune-and metabolism pathways and the interaction between these pathways. Viral interaction with these pathways will elucidate new functions of viral proteins and modulatory interactions. In WP3, innate lymphoid cells, natural killer cells, hepatocytes, dendritic cells and in vivo animal models relevant for RNA virus infection will be used to investigate the regulatory interface between immune and metabolic pathways on antiviral immunity. To unravel the innate and metabolic signature of mucosal vaccination by adenoviral vectors Immunology of COVID-19: Current State of the Science Imbalanced Host Response to SARS-CoV-2 Drives Development of COVID-19 The global impact of the coronavirus pandemic Coupling Krebs cycle metabolites to signalling in immunity and cancer Cytokine-like Roles for Metabolites in Immunity A guide to immunometabolism for immunologists Crosstalk between Cytoplasmic RIG-I and STING Sensing Pathways Self-RNA sentinels signal viral invasion Innate Lymphoid Cells: 10 Years On Control strategies in systemic metabolism Immunometabolism of infections Innate Immune Evasion by Human Respiratory RNA Viruses Ten Strategies of Interferon Evasion by Viruses Flavivirus modulation of cellular metabolism Itaconate is an anti-inflammatory metabolite that activates Nrf2 via alkylation of KEAP1