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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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Published in: | Scientific reports 2023-08, Vol.13 (1), p.12983-12983, Article 12983 |
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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. |
doi_str_mv | 10.1038/s41598-023-38954-5 |
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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.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-023-38954-5</identifier><identifier>PMID: 37563252</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/22 ; 631/326/421 ; 631/326/596 ; Ammonium ; Bovine serum albumin ; Disinfectants ; Disinfection & disinfectants ; Ethanol ; Fever ; Green fluorescent protein ; Humanities and Social Sciences ; Hydrogen peroxide ; Inactivation ; Laboratories ; Lassa fever ; Microbicides ; multidisciplinary ; Proteins ; Public health ; R&D ; Research & development ; Science ; Science (multidisciplinary) ; Sodium hypochlorite ; Vero cells ; Viruses</subject><ispartof>Scientific reports, 2023-08, Vol.13 (1), p.12983-12983, Article 12983</ispartof><rights>The Author(s) 2023</rights><rights>2023. Springer Nature Limited.</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Springer Nature Limited 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-31dc86b89a1b4d651ab10bedc941f0d0190ceaa63966b26b2312ccaed8e0b61a3</citedby><cites>FETCH-LOGICAL-c541t-31dc86b89a1b4d651ab10bedc941f0d0190ceaa63966b26b2312ccaed8e0b61a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2848621065/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2848621065?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,74412,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37563252$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cutts, Todd A.</creatorcontrib><creatorcontrib>Nims, Raymond W.</creatorcontrib><creatorcontrib>Rubino, Joseph R.</creatorcontrib><creatorcontrib>McKinney, Julie</creatorcontrib><creatorcontrib>Kuhn, Jens H.</creatorcontrib><creatorcontrib>Ijaz, M. Khalid</creatorcontrib><title>Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><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. 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Khalid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2023-08-10</date><risdate>2023</risdate><volume>13</volume><issue>1</issue><spage>12983</spage><epage>12983</epage><pages>12983-12983</pages><artnum>12983</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>37563252</pmid><doi>10.1038/s41598-023-38954-5</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/326/22 631/326/421 631/326/596 Ammonium Bovine serum albumin Disinfectants Disinfection & disinfectants Ethanol Fever Green fluorescent protein Humanities and Social Sciences Hydrogen peroxide Inactivation Laboratories Lassa fever Microbicides multidisciplinary Proteins Public health R&D Research & development Science Science (multidisciplinary) Sodium hypochlorite Vero cells Viruses |
title | Efficacy of microbicidal actives and formulations for inactivation of Lassa virus in suspension |
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