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Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension
The World Health Organization’s R&D Blueprint list of priority diseases for 2022 includes Lassa fever, signifying the need for research and development in emergency contexts. This disease is caused by the arenavirus Lassa virus (LASV). Being an enveloped virus, LASV should be susceptible to a va...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415271/ https://www.ncbi.nlm.nih.gov/pubmed/37563252 http://dx.doi.org/10.1038/s41598-023-38954-5 |
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author | Cutts, Todd A. Nims, Raymond W. Rubino, Joseph R. McKinney, Julie Kuhn, Jens H. Ijaz, M. Khalid |
author_facet | Cutts, Todd A. Nims, Raymond W. Rubino, Joseph R. McKinney, Julie Kuhn, Jens H. Ijaz, M. Khalid |
author_sort | Cutts, Todd A. |
collection | PubMed |
description | The World Health Organization’s R&D Blueprint list of priority diseases for 2022 includes Lassa fever, signifying the need for research and development in emergency contexts. This disease is caused by the arenavirus Lassa virus (LASV). Being an enveloped virus, LASV should be susceptible to a variety of microbicidal actives, although empirical data to support this expectation are needed. We evaluated the virucidal efficacy of sodium hypochlorite, ethanol, a formulated dual quaternary ammonium compound, an accelerated hydrogen peroxide formulation, and a p-chloro-m-xylenol formulation, per ASTM E1052-20, against LASV engineered to express green fluorescent protein (GFP). A 10-μL volume of virus in tripartite soil (bovine serum albumin, tryptone, and mucin) was combined with 50 μL of disinfectant in suspension for 0.5, 1, 5, or 10 min at 20–25 °C. Neutralized test mixtures were quantified by GFP expression to determine log(10) reduction. Remaining material was passaged on Vero cells to confirm absence of residual infectious virus. Input virus titers of 6.6–8.0 log(10) per assay were completely inactivated by each disinfectant within 1–5 min contact time. The rapid and substantial inactivation of LASV suggests the utility of these microbicides for mitigating spread of infectious virus during Lassa fever outbreaks. |
format | Online Article Text |
id | pubmed-10415271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104152712023-08-12 Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension Cutts, Todd A. Nims, Raymond W. Rubino, Joseph R. McKinney, Julie Kuhn, Jens H. Ijaz, M. Khalid Sci Rep Article The World Health Organization’s R&D Blueprint list of priority diseases for 2022 includes Lassa fever, signifying the need for research and development in emergency contexts. This disease is caused by the arenavirus Lassa virus (LASV). Being an enveloped virus, LASV should be susceptible to a variety of microbicidal actives, although empirical data to support this expectation are needed. We evaluated the virucidal efficacy of sodium hypochlorite, ethanol, a formulated dual quaternary ammonium compound, an accelerated hydrogen peroxide formulation, and a p-chloro-m-xylenol formulation, per ASTM E1052-20, against LASV engineered to express green fluorescent protein (GFP). A 10-μL volume of virus in tripartite soil (bovine serum albumin, tryptone, and mucin) was combined with 50 μL of disinfectant in suspension for 0.5, 1, 5, or 10 min at 20–25 °C. Neutralized test mixtures were quantified by GFP expression to determine log(10) reduction. Remaining material was passaged on Vero cells to confirm absence of residual infectious virus. Input virus titers of 6.6–8.0 log(10) per assay were completely inactivated by each disinfectant within 1–5 min contact time. The rapid and substantial inactivation of LASV suggests the utility of these microbicides for mitigating spread of infectious virus during Lassa fever outbreaks. Nature Publishing Group UK 2023-08-10 /pmc/articles/PMC10415271/ /pubmed/37563252 http://dx.doi.org/10.1038/s41598-023-38954-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Cutts, Todd A. Nims, Raymond W. Rubino, Joseph R. McKinney, Julie Kuhn, Jens H. Ijaz, M. Khalid Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title_full | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title_fullStr | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title_full_unstemmed | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title_short | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
title_sort | efficacy of microbicidal actives and formulations for inactivation of lassa virus in suspension |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415271/ https://www.ncbi.nlm.nih.gov/pubmed/37563252 http://dx.doi.org/10.1038/s41598-023-38954-5 |
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