Virucidal Effects of Dielectric Barrier Discharge Plasma on Human Norovirus Infectivity in Fresh Oysters (Crassostrea gigas)

This study investigates the effects of dielectric barrier discharge (DBD) plasma treatment (1.1 kV, 43 kHz, N-2 1.5 L/min, 10 similar to 60 min) on human norovirus (HuNoV) GII.4 infectivity in fresh oysters. HuNoV viability in oysters was assessed by using propidium monoazide (PMA) as a nucleic acid...

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Veröffentlicht in:Foods 2020-11, Vol.9 (12), p.1731, Article 1731
Hauptverfasser: Choi, Man-Seok, Jeon, Eun Bi, Kim, Ji Yoon, Choi, Eun Ha, Lim, Jun Sup, Choi, Jinsung, Ha, Kwang Soo, Kwon, Ji Young, Jeong, Sang Hyeon, Park, Shin Young
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container_end_page
container_issue 12
container_start_page 1731
container_title Foods
container_volume 9
creator Choi, Man-Seok
Jeon, Eun Bi
Kim, Ji Yoon
Choi, Eun Ha
Lim, Jun Sup
Choi, Jinsung
Ha, Kwang Soo
Kwon, Ji Young
Jeong, Sang Hyeon
Park, Shin Young
description This study investigates the effects of dielectric barrier discharge (DBD) plasma treatment (1.1 kV, 43 kHz, N-2 1.5 L/min, 10 similar to 60 min) on human norovirus (HuNoV) GII.4 infectivity in fresh oysters. HuNoV viability in oysters was assessed by using propidium monoazide (PMA) as a nucleic acid intercalating dye before performing a real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Additionally, the impact of the DBD plasma treatment on pH and Hunter colors was assessed. When DBD plasma was treated for 60 min, the HuNoV genomic titer reduction without PMA pretreatment was negligible (1 log copy number/mu L in just 30 min. D-1 and D-2-value of HuNoV infectivity were calculated as 36.5 and 73.0 min of the DBD plasma treatment, respectively, using the first-order kinetics model (R-2 = 0.98). The pH and Hunter colors were not significantly different (p > 0.05) between the untreated and DBD-plasma-treated oysters. The results suggest that PMA/RT-qPCR could help distinguish HuNoV infectivity without negatively affecting oyster quality following >30 min treatment with DBD plasma. Moreover, the inactivation kinetics of nonthermal DBD plasma against HuNoV in fresh oysters might provide basic information for oyster processing and distribution.
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HuNoV viability in oysters was assessed by using propidium monoazide (PMA) as a nucleic acid intercalating dye before performing a real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Additionally, the impact of the DBD plasma treatment on pH and Hunter colors was assessed. When DBD plasma was treated for 60 min, the HuNoV genomic titer reduction without PMA pretreatment was negligible (&lt;1 log copy number/mu L), whereas when PMA treatment was used, HuNoV titer was reduced to &gt;1 log copy number/mu L in just 30 min. D-1 and D-2-value of HuNoV infectivity were calculated as 36.5 and 73.0 min of the DBD plasma treatment, respectively, using the first-order kinetics model (R-2 = 0.98). The pH and Hunter colors were not significantly different (p &gt; 0.05) between the untreated and DBD-plasma-treated oysters. The results suggest that PMA/RT-qPCR could help distinguish HuNoV infectivity without negatively affecting oyster quality following &gt;30 min treatment with DBD plasma. Moreover, the inactivation kinetics of nonthermal DBD plasma against HuNoV in fresh oysters might provide basic information for oyster processing and distribution.</description><identifier>ISSN: 2304-8158</identifier><identifier>EISSN: 2304-8158</identifier><identifier>DOI: 10.3390/foods9121731</identifier><identifier>PMID: 33255577</identifier><language>eng</language><publisher>BASEL: Mdpi</publisher><subject>Addition polymerization ; Bacteria ; Copy number ; Deactivation ; Dielectric barrier discharge ; dielectric barrier discharge plasma ; Electrodes ; Experiments ; Food contamination &amp; poisoning ; Food quality ; food safety ; Food science ; Food Science &amp; Technology ; Gastroenteritis ; human norovirus ; Inactivation ; Infections ; Infectivity ; Information processing ; Kinetics ; Life Sciences &amp; Biomedicine ; Nucleic acids ; Oysters ; pH effects ; Plasma ; Polymerase chain reaction ; Pretreatment ; Process controls ; propidium monoazide ; Reverse transcription ; Science &amp; Technology ; Shellfish ; Viruses</subject><ispartof>Foods, 2020-11, Vol.9 (12), p.1731, Article 1731</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 by the authors. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>23</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000602063100001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c478t-81886bdf4514350e8c52d017b438700f5d8d864e45b19fd9de8be864167d70083</citedby><cites>FETCH-LOGICAL-c478t-81886bdf4514350e8c52d017b438700f5d8d864e45b19fd9de8be864167d70083</cites><orcidid>0000-0003-1320-5374 ; 0000-0001-5385-1878 ; 0000-0001-7984-2697</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760321/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7760321/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,886,2103,2115,27929,27930,28253,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33255577$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Man-Seok</creatorcontrib><creatorcontrib>Jeon, Eun Bi</creatorcontrib><creatorcontrib>Kim, Ji Yoon</creatorcontrib><creatorcontrib>Choi, Eun Ha</creatorcontrib><creatorcontrib>Lim, Jun Sup</creatorcontrib><creatorcontrib>Choi, Jinsung</creatorcontrib><creatorcontrib>Ha, Kwang Soo</creatorcontrib><creatorcontrib>Kwon, Ji Young</creatorcontrib><creatorcontrib>Jeong, Sang Hyeon</creatorcontrib><creatorcontrib>Park, Shin Young</creatorcontrib><title>Virucidal Effects of Dielectric Barrier Discharge Plasma on Human Norovirus Infectivity in Fresh Oysters (Crassostrea gigas)</title><title>Foods</title><addtitle>FOODS</addtitle><addtitle>Foods</addtitle><description>This study investigates the effects of dielectric barrier discharge (DBD) plasma treatment (1.1 kV, 43 kHz, N-2 1.5 L/min, 10 similar to 60 min) on human norovirus (HuNoV) GII.4 infectivity in fresh oysters. HuNoV viability in oysters was assessed by using propidium monoazide (PMA) as a nucleic acid intercalating dye before performing a real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Additionally, the impact of the DBD plasma treatment on pH and Hunter colors was assessed. When DBD plasma was treated for 60 min, the HuNoV genomic titer reduction without PMA pretreatment was negligible (&lt;1 log copy number/mu L), whereas when PMA treatment was used, HuNoV titer was reduced to &gt;1 log copy number/mu L in just 30 min. D-1 and D-2-value of HuNoV infectivity were calculated as 36.5 and 73.0 min of the DBD plasma treatment, respectively, using the first-order kinetics model (R-2 = 0.98). The pH and Hunter colors were not significantly different (p &gt; 0.05) between the untreated and DBD-plasma-treated oysters. The results suggest that PMA/RT-qPCR could help distinguish HuNoV infectivity without negatively affecting oyster quality following &gt;30 min treatment with DBD plasma. Moreover, the inactivation kinetics of nonthermal DBD plasma against HuNoV in fresh oysters might provide basic information for oyster processing and distribution.</description><subject>Addition polymerization</subject><subject>Bacteria</subject><subject>Copy number</subject><subject>Deactivation</subject><subject>Dielectric barrier discharge</subject><subject>dielectric barrier discharge plasma</subject><subject>Electrodes</subject><subject>Experiments</subject><subject>Food contamination &amp; poisoning</subject><subject>Food quality</subject><subject>food safety</subject><subject>Food science</subject><subject>Food Science &amp; Technology</subject><subject>Gastroenteritis</subject><subject>human norovirus</subject><subject>Inactivation</subject><subject>Infections</subject><subject>Infectivity</subject><subject>Information processing</subject><subject>Kinetics</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Nucleic acids</subject><subject>Oysters</subject><subject>pH effects</subject><subject>Plasma</subject><subject>Polymerase chain reaction</subject><subject>Pretreatment</subject><subject>Process controls</subject><subject>propidium monoazide</subject><subject>Reverse transcription</subject><subject>Science &amp; 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Biomedicine</topic><topic>Nucleic acids</topic><topic>Oysters</topic><topic>pH effects</topic><topic>Plasma</topic><topic>Polymerase chain reaction</topic><topic>Pretreatment</topic><topic>Process controls</topic><topic>propidium monoazide</topic><topic>Reverse transcription</topic><topic>Science &amp; Technology</topic><topic>Shellfish</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Man-Seok</creatorcontrib><creatorcontrib>Jeon, Eun Bi</creatorcontrib><creatorcontrib>Kim, Ji Yoon</creatorcontrib><creatorcontrib>Choi, Eun Ha</creatorcontrib><creatorcontrib>Lim, Jun Sup</creatorcontrib><creatorcontrib>Choi, Jinsung</creatorcontrib><creatorcontrib>Ha, Kwang Soo</creatorcontrib><creatorcontrib>Kwon, Ji Young</creatorcontrib><creatorcontrib>Jeong, Sang Hyeon</creatorcontrib><creatorcontrib>Park, Shin Young</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Agricultural Science Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural &amp; 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HuNoV viability in oysters was assessed by using propidium monoazide (PMA) as a nucleic acid intercalating dye before performing a real-time reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Additionally, the impact of the DBD plasma treatment on pH and Hunter colors was assessed. When DBD plasma was treated for 60 min, the HuNoV genomic titer reduction without PMA pretreatment was negligible (&lt;1 log copy number/mu L), whereas when PMA treatment was used, HuNoV titer was reduced to &gt;1 log copy number/mu L in just 30 min. D-1 and D-2-value of HuNoV infectivity were calculated as 36.5 and 73.0 min of the DBD plasma treatment, respectively, using the first-order kinetics model (R-2 = 0.98). The pH and Hunter colors were not significantly different (p &gt; 0.05) between the untreated and DBD-plasma-treated oysters. The results suggest that PMA/RT-qPCR could help distinguish HuNoV infectivity without negatively affecting oyster quality following &gt;30 min treatment with DBD plasma. Moreover, the inactivation kinetics of nonthermal DBD plasma against HuNoV in fresh oysters might provide basic information for oyster processing and distribution.</abstract><cop>BASEL</cop><pub>Mdpi</pub><pmid>33255577</pmid><doi>10.3390/foods9121731</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-1320-5374</orcidid><orcidid>https://orcid.org/0000-0001-5385-1878</orcidid><orcidid>https://orcid.org/0000-0001-7984-2697</orcidid><oa>free_for_read</oa></addata></record>
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subjects Addition polymerization
Bacteria
Copy number
Deactivation
Dielectric barrier discharge
dielectric barrier discharge plasma
Electrodes
Experiments
Food contamination & poisoning
Food quality
food safety
Food science
Food Science & Technology
Gastroenteritis
human norovirus
Inactivation
Infections
Infectivity
Information processing
Kinetics
Life Sciences & Biomedicine
Nucleic acids
Oysters
pH effects
Plasma
Polymerase chain reaction
Pretreatment
Process controls
propidium monoazide
Reverse transcription
Science & Technology
Shellfish
Viruses
title Virucidal Effects of Dielectric Barrier Discharge Plasma on Human Norovirus Infectivity in Fresh Oysters (Crassostrea gigas)
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