West Nile and Usutu viruses are efficiently inactivated in platelet concentrates by UVC light using the THERAFLEX UV‐Platelets system

Author:

Gravemann Ute1,Boelke Mathias23,Könenkamp Laura34,Söder Lars5,Maurer Maurice23,Ziegler Ute6,Schulze Torsten J.17,Seltsam Axel8ORCID,Becker Stefanie C.23ORCID,Steffen Imke34

Affiliation:

1. German Red Cross Blood Service NSTOB Springe Germany

2. Institute for Parasitology University of Veterinary Medicine Hannover Germany

3. Research Center for Emerging Infections and Zoonoses University of Veterinary Medicine Hannover Germany

4. Department of Biochemistry University of Veterinary Medicine Hannover Germany

5. Institute of Virology University of Veterinary Medicine Hannover Germany

6. Institute of Novel and Emerging Infectious Diseases Friedrich‐Loeffler‐Institut Greifswald‐Island of Riems Germany

7. Institute of Clinical Chemistry and Laboratory Medicine University Medicine Oldenburg Oldenburg Germany

8. Bavarian Red Cross Blood Service Institute Nuremberg Nuremberg Germany

Abstract

AbstractBackground and ObjectivesWest Nile virus (WNV) and Usutu virus (USUV) are mosquito‐borne flaviviruses (Flaviviridae) that originated in Africa, have expanded their geographical range during the last decades and caused documented infections in Europe in the last years. Acute WNV and USUV infections have been detected in asymptomatic blood donors by nucleic acid testing. Thus, inactivation of both viral pathogens before blood transfusion is necessary to ensure blood product safety. This study aimed to investigate the efficacy of the THERAFLEX UV‐Platelets system to inactivate WNV and USUV in platelet concentrates (PCs).Materials and MethodsPlasma‐reduced PCs were spiked with the virus suspension. Spiked PC samples were taken after spiking (load and hold sample) and after UVC illumination on the Macotronic UV illumination machine with different light doses (0.05, 0.1, 0.15 and 0.2 (standard) J/cm2). Virus loads of WNV and USUV before and after illumination were measured by titration.ResultsInfectivity assays showed that UVC illumination inactivated WNV and USUV in a dose‐dependent manner. At a UVC dose of 0.2 J/cm2, the WNV titre was reduced by a log10 factor of 3.59 ± 0.43 for NY99 (lineage 1) and 4.40 ± 0.29 for strain ED‐I‐33/18 (lineage 2). USUV titres were reduced at the same UVC dose by a log10 factor of 5.20 ± 0.70.ConclusionsOur results demonstrate that the THERAFLEX UV‐Platelets procedure is an effective technology to inactivate WNV and USUV in contaminated PCs.

Funder

Deutsche Forschungsgemeinschaft

Bundesministerium für Bildung und Forschung

Publisher

Wiley

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