scholarly journals Sixth European Seminar in Virology on Virus–Host Interaction at Single Cell and Organism Level

Viruses ◽  
2018 ◽  
Vol 10 (8) ◽  
pp. 400
Author(s):  
Elisa Saccon ◽  
Adriana Vitiello ◽  
Marta Trevisan ◽  
Cristiano Salata ◽  
Giorgio Palù

The 6th European Seminar in Virology (EuSeV) was held in Bertinoro, Italy, 22–24 June 2018, and brought together international scientists and young researchers working in the field of Virology. Sessions of the meeting included: virus–host-interactions at organism and cell level; virus evolution and dynamics; regulation; immunity/immune response; and disease and therapy. This report summarizes lectures by the invited speakers and highlights advances in the field.

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Julia Badstöber ◽  
Claire M. M. Gachon ◽  
Jutta Ludwig-Müller ◽  
Adolf M. Sandbichler ◽  
Sigrid Neuhauser

Blood ◽  
2009 ◽  
Vol 114 (22) ◽  
pp. 2673-2673
Author(s):  
Shlomit Reich-Zeliger ◽  
Yaron Emanuel Antebi ◽  
Jacob Rimer ◽  
Nir Friedmann

Abstract Abstract 2673 Poster Board II-649 Cytokines provide a main regulatory mechanism of a developing immune response, which allows for intercellular communication. This sharing of information enables cells to make collective decisions based on the state of the system rather than that of a single cell. In our research we focus on several examples of cytokine mediated regulatory mechanisms that function in helper T-cells (Th), whose role is to direct the immune response in the desired course by affecting responses of other cells. To analyze the relative importance of the different components affecting the behavior of the cells we employ mathematical modeling and numerical simulations of specific experimental settings. Quantitative experiments are performed to evaluate unknown parameters and to verify model predictions. We focus on two examples of cytokine mediated regulatory mechanisms that function in the helper T-cell (Th) differentiation. IL-12 and IL-4 direct differentiation into the main fates of Th cells, Th1 and Th2, respectively. By exposing cells to varied combinations of the two cytokines we experimentally map the “decision space” of the differentiation process. We measured, at the single cell level, eight key parameters relating to the state of the cells, from which we can deduce properties of the network describing the system. Our data indicate that under certain mixed conditions, with cells exposed to both IL-12 and IL-4, a new class of Th cells is observed, which secret both IL-4 and IFN-γ upon restimulation. This is preceded by co-expression of the two lineage specific transcription factors T-bet and GATA3 at earlier time points. We incorporate our experimental results and other known data into a cellular automata based simulation. Each cell is simulated as a node on a dynamic network, whose links describe the propagation of intercellular cytokine signals. The intracellular protein network for each node is realized as an automaton with cytokines levels as inputs and their secretion rates as output. By varying model parameters and comparing to experimental results we can gain insight into the significance of the various components driving the differentiation process. We also analyze the roles of heterogeneity in expression levels of cytokine receptors in the differentiation decision. To that end, naïve mice CD4 cells were sorted into separate groups according to their expression level of the IL-4 receptor. The different groups of cells were cultured separately, under “controlled milieu” conditions, at different IL-4 or IL-12 concentrations. Expression levels of key proteins involved in the differentiation process were measured at the single cell level every 24h. This was compared to expression levels of those proteins in a whole population of cells growing together. Our results reveal differences in the differentiation abilities between the sorted, controlled milieu, groups. Additionally, the weighted average of expression levels of the controlled milieu populations is different than that of the full heterogeneous population of cells growing together. These differences are caused by intercellular interactions, as cells secrete cytokines which are involved in and drive the differentiation process (e.g. IL-4, IFN-γ). Thus, these experiments provide an opportunity to evaluate the importance and roles played by intercellular communication in this process, and to asses what are the effects of stochastic levels of a protein (IL-4R in this case) on the following differentiation process. Disclosures: No relevant conflicts of interest to declare.


2018 ◽  
Author(s):  
Meng Wang ◽  
Shaoqing Wang ◽  
Jianan Sun ◽  
Yaqian Li ◽  
Kai Dou ◽  
...  

AbstractCochliobolus heterostrophusis a crucial pathogenic fungus that causes southern corn leaf blight (SCLB) in maize worldwide, however, the virulence mechanism of the dominant race O remains unclear. In this report, the single-cell level of pathogen tissue at three infection stages were collected from the host interaction-situ, and were performed next-generation sequencing from the perspectives of mRNA, circular RNA(circRNA) and long noncoding RNA(lncRNA). In the mRNA section, signal transduction, kinase, oxidoreductase, and hydrolase, et al. were significantly related in both differential expression and co-expression between virulence differential race O strains. The expression pattern of the traditional virulence factors nonribosomal peptide synthetases (NPSs), polyketide synthases (PKSs) and small secreted proteins (SSPs) were multifarious. In the noncoding RNA section, a total of 2279 circRNAs and 169 lncRNAs were acquired. Noncoding RNAs exhibited differential expression at three stages. The high virulence strain DY transcribed 450 more circRNAs than low virulence strain WF. Informatics analysis revealed numbers of circRNAs which positively correlate with race O virulence, and a cross-kingdom interaction between the pathogenic circRNA and host miRNA was predicted. An important exon-intron circRNA Che-cirC2410 combines informatics characteristics above, and highly expressed in the DY strain. Che-cirC2410 initiate from the pseudogenechhtt, which doesn’t translate genetic code into protein. In-situ hybridization tells the sub-cellular localization of Che-cirC2410 include pathogen`s mycelium, periplasm, and the diseased host tissues. The target of Che-cirC2410 was predicted to be zma-miR399e-5P, and the interaction between noncoding RNAs was proved. More, the expression of zma-miR399e-5P exhibited a negative correlation to Che-cirC2410 in vivo. The deficiency of Che-circ2410 decreased the race O virulence. The host resistance to SCLB was weakened when zma-miR399e-5P was silenced. Thus, a novel circRNA-type effector and its resistance related miRNA target are proposed cautiously in this report. These findings enriched the pathogen-host dialogue by using noncoding RNAs as language, and revealed a new perspective for understanding the virulence of race O, which may provide valuable strategy of maize breeding for disease resistance.Author SummaryThe southern corn leaf blight (caused byCochliobolus heterostrophus) is not optimistic in Asia, however we have limit knowledge about the infection mechanism of the dominantC.heterostrophusrace O. We take full advantage of the idealC.heterostrophusgenome database, laser capture microdissection and single-cell level RNA sequencing. Hence, we could avert the artificial influence such as medium, and profile the real gene mobilization strategy in the infection. The results of coding RNA section were accessible, virulence related genes (such as the signal transduction, PKS, SSP) were detected in RNA-seq,which accord with previous reports. However, the results of noncoding RNA was astonished, 2279 circular RNAs (circRNA) and 169 long noncoding RNAs (lncRNA) were revealed in our results. Generally, the function of noncoding RNA was hypothesized in single species, but we boldly guess that the function of circRNA is rather complicated in the pathogen-host interaction. Finally, the circRNA in-situ hybridization (ISH) demonstrate the secretion of pathogen circRNA into the host tissue. By bioinformatic prediction, we found a sole microRNA target, and proved the interaction between circRNA and microRNA. These findings are likely to reveal a novel pathogen effector type: secreted circRNA.


2019 ◽  
Author(s):  
Francesca Pia Caruso ◽  
Luciano Garofano ◽  
Fulvio D’Angelo ◽  
Kai Yu ◽  
Fuchou Tang ◽  
...  

ABSTRACTSingle-cell RNA sequencing is the reference technique to characterize the heterogeneity of tumor microenvironment and can be efficiently used to discover cross-talk mechanisms between immune cells and cancer cells. We present a novel method, single cell Tumor-Host Interaction tool (scTHI), to identify significantly activated ligand-receptor interactions across clusters of cells from single-cell RNA sequencing data. We apply our approach to uncover the ligand-receptor interactions in glioma using six publicly available human glioma datasets encompassing 71 patients. We provide a comprehensive map of the signalling mechanisms between malignant cells and non-malignant cells in glioma uncovering potential novel therapeutic targets.


1997 ◽  
Vol 9 (4) ◽  
pp. 219-227 ◽  
Author(s):  
Michael G. McHeyzer-Williams

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