Ecology of bacteriophages in mucosa during vertebrate host lifespan (Phaging)
Main funder
Funder's project number: 346772
Funds granted by main funder (€)
- 500 000,00
Funding program
Project timetable
Project start date: 01/09/2022
Project end date: 31/08/2026
Summary
Pathogenic bacteria have a strong affinity towards mucosa. However, the vertebrate mucosal surface is a complex environment including commensal microbiota and host immune mechanisms. An additional factor in mucosal resistance against invading pathogens is the presence of symbiotic bacteriophages. Yet, there are still several fundamental gaps in knowledge regarding the ecology of the phage-bacterium interaction in the mucosal milieu. For example, while interaction with the mucosa directly increases the virulence of many bacterial pathogens, our recent studies suggest that the mucosal environment increases bacterial susceptibility to phage infections, which favours CRISPR-Cas resistance instead of surface resistance. Understanding the ecology of pathogens and their phages in the mucosa is thus central for our health. However, the mucosa of an old individual is drastically different from a younger one, as mucosal barrier and immune responses decline during the senescence, leading to an increased infection susceptibility in the elderly. This change is likely to cause shifts the in the mucosa-phage-bacterium interplay, which may have a major impact on infections and disease resistance in the aging population. Yet, vertebrate host senescence has remained virtually ignored in phage-bacterium interaction and infection ecology studies, biasing our knowledge on host-associated microbiome ecology and health. This project allows us to address these gaps experimentally (in cell cultures and with zebra fish) and broaden our knowledge on the role of the mucosal milieu and its senescence on the ecology of medically relevant phage-bacterium interaction in the vertebrate mucosa. The project is at the core of fundamental and topical questions of host-pathogen interactions, and can open new trajectories in understanding the ecology of host-associated microbial communities and how they shape health and disease during vertebrate lifespan.
Principal Investigator
Primary responsible unit
Follow-up groups
- Cell and Molecular Biology (Department of Biological and Environmental Science BIOENV) SMB
- Nanoscience Center (Department of Physics PHYS, JYFL) (Faculty of Mathematics and Science) (Department of Chemistry CHEM) (Department of Biological and Environmental Science BIOENV) NSC
- School of Resource Wisdom (University of Jyväskylä JYU) JYU.Wisdom
Profiling area: Nanoscience Center (Department of Physics PHYS, JYFL) (Faculty of Mathematics and Science) (Department of Chemistry CHEM) (Department of Biological and Environmental Science BIOENV) NSC; School of Resource Wisdom (University of Jyväskylä JYU) JYU.Wisdom
Related publications and other outputs
- Determinants in the phage life cycle : The dynamic nature of ssDNA phage FLiP and host interactions under varying environmental conditions and growth phases (2024) Mäkelä, Kati; et al.; A1; OA
- Evolutionary trajectories of conjugative resistance plasmids and their interplay in the ecology of clinically relevant bacteria (2024) Jonsdottir, Ilmur; G5; OA; 978-952-86-0224-8
- Heterogeneity of the rearing environment enhances diversity of microbial communities in intensive farming (2024) Ashrafi, Roghaieh; et al.; A1; OA
- Isolation and characterization of Yersinia phage fMtkYen3-01 (2024) Goladze, Sophia; et al.; A1; OA
- Relevance of the bacteriophage adherence to mucus model for Pseudomonas aeruginosa phages (2024) Almeida, Gabriel Magno de Freitas; et al.; A1; OA
- Cryo-EM structure of ssDNA bacteriophage ΦCjT23 provides insight into early virus evolution (2022) Kejzar, Nejc; et al.; A1; OA