EVAg

The end-user provided virus (e.g. as a tick homogenate) will be used to experimentally infect castor bean tick nymphs (Ixodes ricinus). The nymphs will be infected by micro-capillary inoculation into the coxal plate of the second pair of legs (transcoxal infection) using a digital microinjector system. First, 100 nymphs will be used for evaluation of the virus replication dynamics. Based on the obtained results, tick-derived virus stock will be generated from an additional 100 nymphs and provided to the end-user.

The end-user provided virus (e.g. as a tick homogenate) will be used to experimentally infect adult castor bean ticks (Ixodes ricinus). The ticks will be infected by micro-capillary inoculation into the coxal plate of the second pair of legs (transcoxal infection) using a digital microinjector system. First, 100 ticks will be used for evaluation of the virus replication dynamics. Based on the obtained results, tick-derived virus stock will be generated from an additional 100 ticks and provided to the end-user.

Virus production of viruses available on the EVAg catalogue from BMC-SAS in a single batch upon request containing 30 cryotubes containing 0.5mL.

We offer a 5 day training session to colleagues from endemic regions. Participants will visit the Viroscience clinical virology lab, where they will perform all required laboratory and analysis procedures for the quantification rabies virus and neutralizing antibodies.

Institut Pasteur Paris - Access to BSL 3 containment facility. The access will comprise a detailed theoretical and subject to availability practical application of the biosafety and biosecurity management at Institut Pasteur. Among others, establishment and validation of suitable decontamination methods for waist, rooms and material, as well as documentation and information management will be addressed.

In this 2-day course the basic principles of routine virus neutralization and ELISA assays will be addressed by a combination of lectures, demonstration and hands-on training. Special attention will be given to quality control and assay validation. Topics include: cell culture, biosafety procedures, preparation of sera and virus stocks, ELISA and microarray formats, different virus neutralization tests using pseudotyped viruses and wildtype viruses, immunofluorescence staining of cells, calculation of titers, assay validation and quality control.

Access to the BSL-3 facility including equipment and personal protective equipment, theoretical and practical training; preparation and evaluation of the BSL-3 work; BSL-3 virus collection as predefined within the project of the end user; personal support for performing specifically designed experiments; expert supervision.

Institut Pasteur Paris - Access to BSL 3 containment facility. The access will comprise a detailed theoretical and practical application of different methods to grow lyssaviruses: strain isolation from clinical sample, virus adaptation to cell culture and Virus titration Access to BSL 3 containment facility. The access will comprise a detailed theoretical and practical application of different methods to grow lyssaviruses: strain isolation from clinical sample, virus adaptation to cell culture and Virus titration

Institut Pasteur Paris - General description of the RFFIT and required skills and equipment. Preparation of cells, sera and titrated virus. Read-out of the results and interpretation.

Institut Pasteur Paris - General description of fluorecent antibody tets (FAT), virus isolation, lateral flow device in the context of rabies diagnosis and surveillance. Practical training in these technique in BSL3.

Institut Pasteur Paris - In this 2 weeks course the basic principles of routine virus typing will be addressed by a combination of lectures, demonstration and hands-on training. Participants will perform all required laboratory and analysis procedures for routine typing of lyssaviruses: Special attention will be given to quality control and assay validation.

Institut Pasteur Paris - In this 2 days course the principles of QMS and its implementation for routine lyssavirus and rabies virus diagnosis will be addressed by a combination of lectures and demonstration

Access to UL infrastructure for learning/training on techniques related to virus isolation and characterization.