Periodic Reporting for period 1 - MOBILISE (MOBILISE: A novel and green mobile One Health laboratory for (re-)emerging infectious disease outbreaks)
Berichtszeitraum: 2022-10-01 bis 2024-03-31
MOBILISE aims to develop a novel, quality-assured, mobile One Health laboratory solution. It will receive human/animal/environmental samples for diagnostics and host a whole genome sequencing platform for pathogen discovery and epidemiological analysis. We will further develop novel rapid diagnostic tests for BSL-3/4 pathogens. A novel AI-based "Emergency Operating Centre and Decision Support System" software will assist end-users in coordinating MOBILISE fleets across Europe and manage outbreaks in real-time. Hosted on an electric/hybrid truck platform, and using solar and wind-energy, it will also reduce CO2 emissions in compliance with the European Green Deal. The lab will be field-tested to TRL-7 by National agencies and first-responders in Austria, Romania, Greece and Africa.
To efficiently coordinate mobile laboratory activities, a centralised repository European mobile laboratory capacities was already available at the proposal writing stage. But to drive internalisation, and because risk group 4 pathogens often emerge in Africa, we extended our review and dataset.This database was further curated and mobile laboratory initiatives from both continents were contacted to assess whether the projects are still operational and a total of 13 active mobile laboratory projects from Greece, Italy, Germany, Albania, Ukraine, Tanzania, UK, Hungary and Czech Republic were so far identified. Future mobile laboratory initiatives can register through the MOBILISE homepage (https://mobilise-lab.eu(öffnet in neuem Fenster)) in which the survey can still be accessed. Our inventory can serve as a novel resource for first responders, national agencies, international health organisations and other stakeholders commissioned with epidemic and pandemic preparedness to orchestrate joint mobile laboratory activities in Europe and Africa. In the second half of the project, we will discuss the hand-over of the database to stakeholders.
Trial development to field validate the MOBILISE laboratory to TRL-7 was divided into two main sections; (1) Development of trial guidance methodology for each of the planned field trials and (2) planning of the field trials in each of the countries. As a first step, the outbreak reporting algorithms for WNV and CCHF in the Human and Veterinary sectors were identified to be evaluated in a tabletop exercise, identifying any challenges of system integration before the actual field deployment. In the second stage, the field missions in Austria, Greece, Romania and East Africa are being planned to re-evaluate MOBILISE's integration into national reporting systems as well as the actual laboratory SOPs.
Within WP3 AIT is developing novel nucleic-acid based rapid diagnostic kits (RDTs) which, as opposed to conventional RDTs that detect antigens produced by a pathogen, directly detect genetic material of CCHFV and WNV. If successful, we are aiming for a low tech, rapid test with a sensitivity comparable to PCR, which can be utilized in low resource settings as well. A particularly interesting feature is that these RDTs are machine-readable and can be automatically analyzed from within the glovebox, thus significantly reducing the turn-around time to diagnosis for risk group 4 pathogens such as CCHFV.