Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies

No cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transfusion-transmitted infections (TTI) have been reported. The detection of viral RNA in peripheral blood from infected patients and blood components from infected asymptomatic blood donors is, however, concerning. This study...

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Main Authors: Felicia Santa Maria, Yan-Jang S. Huang, Dana L. Vanlandingham, Peter Bringmann
Format: Article
Language:English
Published: MDPI AG 2022-04-01
Series:Pathogens
Subjects:
Online Access:https://www.mdpi.com/2076-0817/11/5/521
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author Felicia Santa Maria
Yan-Jang S. Huang
Dana L. Vanlandingham
Peter Bringmann
author_facet Felicia Santa Maria
Yan-Jang S. Huang
Dana L. Vanlandingham
Peter Bringmann
author_sort Felicia Santa Maria
collection DOAJ
description No cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transfusion-transmitted infections (TTI) have been reported. The detection of viral RNA in peripheral blood from infected patients and blood components from infected asymptomatic blood donors is, however, concerning. This study investigated the efficacy of the amotosalen/UVA light (A/UVA) and amustaline (S-303)/glutathione (GSH) pathogen reduction technologies (PRT) to inactivate SARS-CoV-2 in plasma and platelet concentrates (PC), or red blood cells (RBC), respectively. Plasma, PC prepared in platelet additive solution (PC-PAS) or 100% plasma (PC-100), and RBC prepared in AS-1 additive solution were spiked with SARS-CoV-2 and PR treated. Infectious viral titers were determined by plaque assay and log reduction factors (LRF) were determined by comparing titers before and after treatment. PR treatment of SARS-CoV-2-contaminated blood components resulted in inactivation of the infectious virus to the limit of detection with A/UVA LRF of >3.3 for plasma, >3.2 for PC-PAS-plasma, and >3.5 for PC-plasma and S-303/GSH LRF > 4.2 for RBC. These data confirm the susceptibility of coronaviruses, including SARS-CoV-2 to A/UVA treatment. This study demonstrates the effectiveness of the S-303/GSH treatment to inactivate SARS-CoV-2, and that PRT can reduce the risk of SARS-CoV-2 TTI in all blood components.
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spelling doaj.art-26a6ad0d46914ddda28aa516d89e169a2023-11-23T12:31:57ZengMDPI AGPathogens2076-08172022-04-0111552110.3390/pathogens11050521Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction TechnologiesFelicia Santa Maria0Yan-Jang S. Huang1Dana L. Vanlandingham2Peter Bringmann3Cerus Corporation, Concord, CA 94520, USADepartment of Diagnostic Medicine/Pathobiology, Biosecurity Research Institute, Kansas State University, Manhattan, KS 66506, USADepartment of Diagnostic Medicine/Pathobiology, Biosecurity Research Institute, Kansas State University, Manhattan, KS 66506, USACerus Corporation, Concord, CA 94520, USANo cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) transfusion-transmitted infections (TTI) have been reported. The detection of viral RNA in peripheral blood from infected patients and blood components from infected asymptomatic blood donors is, however, concerning. This study investigated the efficacy of the amotosalen/UVA light (A/UVA) and amustaline (S-303)/glutathione (GSH) pathogen reduction technologies (PRT) to inactivate SARS-CoV-2 in plasma and platelet concentrates (PC), or red blood cells (RBC), respectively. Plasma, PC prepared in platelet additive solution (PC-PAS) or 100% plasma (PC-100), and RBC prepared in AS-1 additive solution were spiked with SARS-CoV-2 and PR treated. Infectious viral titers were determined by plaque assay and log reduction factors (LRF) were determined by comparing titers before and after treatment. PR treatment of SARS-CoV-2-contaminated blood components resulted in inactivation of the infectious virus to the limit of detection with A/UVA LRF of >3.3 for plasma, >3.2 for PC-PAS-plasma, and >3.5 for PC-plasma and S-303/GSH LRF > 4.2 for RBC. These data confirm the susceptibility of coronaviruses, including SARS-CoV-2 to A/UVA treatment. This study demonstrates the effectiveness of the S-303/GSH treatment to inactivate SARS-CoV-2, and that PRT can reduce the risk of SARS-CoV-2 TTI in all blood components.https://www.mdpi.com/2076-0817/11/5/521SARS-CoV-2pathogen reduction technologyamotosalenamustaline
spellingShingle Felicia Santa Maria
Yan-Jang S. Huang
Dana L. Vanlandingham
Peter Bringmann
Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
Pathogens
SARS-CoV-2
pathogen reduction technology
amotosalen
amustaline
title Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
title_full Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
title_fullStr Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
title_full_unstemmed Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
title_short Inactivation of SARS-CoV-2 in All Blood Components Using Amotosalen/Ultraviolet A Light and Amustaline/Glutathione Pathogen Reduction Technologies
title_sort inactivation of sars cov 2 in all blood components using amotosalen ultraviolet a light and amustaline glutathione pathogen reduction technologies
topic SARS-CoV-2
pathogen reduction technology
amotosalen
amustaline
url https://www.mdpi.com/2076-0817/11/5/521
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AT danalvanlandingham inactivationofsarscov2inallbloodcomponentsusingamotosalenultravioletalightandamustalineglutathionepathogenreductiontechnologies
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