Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH, Ionic Strength, and Temperature and Implications for Adhesion to Surfaces
Loss of ordered molecular structure in proteins is known to increase their adhesion to surfaces. The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and te...
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description | Loss of ordered molecular structure in proteins is known to increase their adhesion to surfaces. The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and temperature conditions studied correspond to those prevalent in the principal vehicles of viral transmission (vomit and feces) and in the food processing and handling environment (pasteurization and refrigeration). The structures of virus-like particles representing GI.1, GII.4, and feline calicivirus (FCV) were studied using circular dichroism and intrinsic UV fluorescence. The particles were remarkably stable under most of the conditions. However, heating to 65°C caused losses of β-strand structure, notably in GI.1 and FCV, while at 75°C the α-helix content of GII.4 and FCV decreased and tertiary structures unfolded in all three cases. Combining temperature with pH or ionic strength caused variable losses of structure depending on the particle type. Regardless of pH, heating to pasteurization temperatures or higher would be required to increase GII.4 and FCV adhesion, while either low or high temperatures would favor GI.1 adhesion. Regardless of temperature, increased ionic strength would increase GII.4 adhesion but would decrease GI.1 adhesion. FCV adsorption would be greater at refrigeration, pasteurization, or high temperature combined with a low salt concentration or at a higher NaCl concentration regardless of temperature. Norovirus adhesion mediated by hydrophobic interaction may depend on hydrophobic residues normally exposed on the capsid surface at pH 3, pH 8, physiological ionic strength, and low temperature, while at pasteurization temperatures it may rely more on buried hydrophobic residues exposed upon structural rearrangement. |
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The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and temperature conditions studied correspond to those prevalent in the principal vehicles of viral transmission (vomit and feces) and in the food processing and handling environment (pasteurization and refrigeration). The structures of virus-like particles representing GI.1, GII.4, and feline calicivirus (FCV) were studied using circular dichroism and intrinsic UV fluorescence. The particles were remarkably stable under most of the conditions. However, heating to 65°C caused losses of β-strand structure, notably in GI.1 and FCV, while at 75°C the α-helix content of GII.4 and FCV decreased and tertiary structures unfolded in all three cases. Combining temperature with pH or ionic strength caused variable losses of structure depending on the particle type. Regardless of pH, heating to pasteurization temperatures or higher would be required to increase GII.4 and FCV adhesion, while either low or high temperatures would favor GI.1 adhesion. Regardless of temperature, increased ionic strength would increase GII.4 adhesion but would decrease GI.1 adhesion. FCV adsorption would be greater at refrigeration, pasteurization, or high temperature combined with a low salt concentration or at a higher NaCl concentration regardless of temperature. Norovirus adhesion mediated by hydrophobic interaction may depend on hydrophobic residues normally exposed on the capsid surface at pH 3, pH 8, physiological ionic strength, and low temperature, while at pasteurization temperatures it may rely more on buried hydrophobic residues exposed upon structural rearrangement.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.01278-15</identifier><identifier>PMID: 26296729</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Adsorption ; Biophysical Phenomena ; Calicivirus, Feline - chemistry ; Calicivirus, Feline - ultrastructure ; Feline calicivirus ; Food - virology ; Food Microbiology ; Food Services ; High temperature ; Hydrogen-Ion Concentration ; Molecular structure ; Norovirus ; Norovirus - chemistry ; Norovirus - ultrastructure ; Osmolar Concentration ; Pasteurization ; Proteins ; Surface Properties ; Temperature ; Ultraviolet radiation ; Virion</subject><ispartof>Applied and Environmental Microbiology, 2015-11, Vol.81 (22), p.7680-7686</ispartof><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved.</rights><rights>Copyright American Society for Microbiology Nov 2015</rights><rights>Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c511t-892b187378b6f3cb07ff98b213a30453f36a384a67251bd50e786e8ea85a9e53</citedby><cites>FETCH-LOGICAL-c511t-892b187378b6f3cb07ff98b213a30453f36a384a67251bd50e786e8ea85a9e53</cites><orcidid>0000-0003-2553-4204</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/PMC4616957/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616957/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26296729$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Samandoulgou, Idrissa</creatorcontrib><creatorcontrib>Hammami, Riadh</creatorcontrib><creatorcontrib>Morales Rayas, Rocio</creatorcontrib><creatorcontrib>Fliss, Ismail</creatorcontrib><creatorcontrib>Jean, Julie</creatorcontrib><title>Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH, Ionic Strength, and Temperature and Implications for Adhesion to Surfaces</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Loss of ordered molecular structure in proteins is known to increase their adhesion to surfaces. The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and temperature conditions studied correspond to those prevalent in the principal vehicles of viral transmission (vomit and feces) and in the food processing and handling environment (pasteurization and refrigeration). The structures of virus-like particles representing GI.1, GII.4, and feline calicivirus (FCV) were studied using circular dichroism and intrinsic UV fluorescence. The particles were remarkably stable under most of the conditions. However, heating to 65°C caused losses of β-strand structure, notably in GI.1 and FCV, while at 75°C the α-helix content of GII.4 and FCV decreased and tertiary structures unfolded in all three cases. Combining temperature with pH or ionic strength caused variable losses of structure depending on the particle type. Regardless of pH, heating to pasteurization temperatures or higher would be required to increase GII.4 and FCV adhesion, while either low or high temperatures would favor GI.1 adhesion. Regardless of temperature, increased ionic strength would increase GII.4 adhesion but would decrease GI.1 adhesion. FCV adsorption would be greater at refrigeration, pasteurization, or high temperature combined with a low salt concentration or at a higher NaCl concentration regardless of temperature. Norovirus adhesion mediated by hydrophobic interaction may depend on hydrophobic residues normally exposed on the capsid surface at pH 3, pH 8, physiological ionic strength, and low temperature, while at pasteurization temperatures it may rely more on buried hydrophobic residues exposed upon structural rearrangement.</description><subject>Adsorption</subject><subject>Biophysical Phenomena</subject><subject>Calicivirus, Feline - chemistry</subject><subject>Calicivirus, Feline - ultrastructure</subject><subject>Feline calicivirus</subject><subject>Food - virology</subject><subject>Food Microbiology</subject><subject>Food Services</subject><subject>High temperature</subject><subject>Hydrogen-Ion Concentration</subject><subject>Molecular structure</subject><subject>Norovirus</subject><subject>Norovirus - chemistry</subject><subject>Norovirus - ultrastructure</subject><subject>Osmolar Concentration</subject><subject>Pasteurization</subject><subject>Proteins</subject><subject>Surface Properties</subject><subject>Temperature</subject><subject>Ultraviolet radiation</subject><subject>Virion</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkkuP0zAUhSMEYsrAjjWyxIZFM_gRJw6LkapRYSqVh2jF1nKc69ZDGgfbGWl-Gv8Op1NGwIqVdX0_n-tzdbLsJcEXhFDxdrH8eIEJrURO-KNsRnAtcs5Y-TibYVzXOaUFPsuehXCDMS5wKZ5mZ7SkdVnRepb93ETV2M7GO-QM2oB2fav8HVJ9i7bgo52KTfSjjqOHMEHfrB9DvrbfAX1RidBduv8KQ2pDH22_Q5-cd7cTBeEdWhoDOh5fDtdztHK91ZMi9Lu4n58GHQbwappwrFeHobNaRev6gIzzaNHuIaQKRYc2ozdKQ3iePTGqC_DidJ5n2_fL7dV1vv78YXW1WOeaExJzUdOGiIpVoikN0w2ujKlFQwlTDBecGVYqJgqV1sFJ03IMlShBgBJc1cDZeXZ5LzuMzQFanSx61cnB20NajXTKyr87vd3LnbuVRUnKmldJ4M1JwLsfI4QoDzZo6DrVgxuDJFVRipoVhPwHSjmnlBUsoa__QW_c6Pu0iImqCpIwnKj5PaW9C8GDefg3wXJKj0zpkcf0SDJ5ffWn1wf4d1zYL4mqwqI</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Samandoulgou, Idrissa</creator><creator>Hammami, Riadh</creator><creator>Morales Rayas, Rocio</creator><creator>Fliss, Ismail</creator><creator>Jean, Julie</creator><general>American Society for Microbiology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2553-4204</orcidid></search><sort><creationdate>20151101</creationdate><title>Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH, Ionic Strength, and Temperature and Implications for Adhesion to Surfaces</title><author>Samandoulgou, Idrissa ; Hammami, Riadh ; Morales Rayas, Rocio ; Fliss, Ismail ; Jean, Julie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c511t-892b187378b6f3cb07ff98b213a30453f36a384a67251bd50e786e8ea85a9e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adsorption</topic><topic>Biophysical Phenomena</topic><topic>Calicivirus, Feline - chemistry</topic><topic>Calicivirus, Feline - ultrastructure</topic><topic>Feline calicivirus</topic><topic>Food - virology</topic><topic>Food Microbiology</topic><topic>Food Services</topic><topic>High temperature</topic><topic>Hydrogen-Ion Concentration</topic><topic>Molecular structure</topic><topic>Norovirus</topic><topic>Norovirus - chemistry</topic><topic>Norovirus - ultrastructure</topic><topic>Osmolar Concentration</topic><topic>Pasteurization</topic><topic>Proteins</topic><topic>Surface Properties</topic><topic>Temperature</topic><topic>Ultraviolet radiation</topic><topic>Virion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Samandoulgou, Idrissa</creatorcontrib><creatorcontrib>Hammami, Riadh</creatorcontrib><creatorcontrib>Morales Rayas, Rocio</creatorcontrib><creatorcontrib>Fliss, Ismail</creatorcontrib><creatorcontrib>Jean, Julie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Samandoulgou, Idrissa</au><au>Hammami, Riadh</au><au>Morales Rayas, Rocio</au><au>Fliss, Ismail</au><au>Jean, Julie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH, Ionic Strength, and Temperature and Implications for Adhesion to Surfaces</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2015-11-01</date><risdate>2015</risdate><volume>81</volume><issue>22</issue><spage>7680</spage><epage>7686</epage><pages>7680-7686</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>Loss of ordered molecular structure in proteins is known to increase their adhesion to surfaces. The aim of this work was to study the stability of norovirus secondary and tertiary structures and its implications for viral adhesion to fresh foods and agrifood surfaces. The pH, ionic strength, and temperature conditions studied correspond to those prevalent in the principal vehicles of viral transmission (vomit and feces) and in the food processing and handling environment (pasteurization and refrigeration). The structures of virus-like particles representing GI.1, GII.4, and feline calicivirus (FCV) were studied using circular dichroism and intrinsic UV fluorescence. The particles were remarkably stable under most of the conditions. However, heating to 65°C caused losses of β-strand structure, notably in GI.1 and FCV, while at 75°C the α-helix content of GII.4 and FCV decreased and tertiary structures unfolded in all three cases. Combining temperature with pH or ionic strength caused variable losses of structure depending on the particle type. Regardless of pH, heating to pasteurization temperatures or higher would be required to increase GII.4 and FCV adhesion, while either low or high temperatures would favor GI.1 adhesion. Regardless of temperature, increased ionic strength would increase GII.4 adhesion but would decrease GI.1 adhesion. FCV adsorption would be greater at refrigeration, pasteurization, or high temperature combined with a low salt concentration or at a higher NaCl concentration regardless of temperature. Norovirus adhesion mediated by hydrophobic interaction may depend on hydrophobic residues normally exposed on the capsid surface at pH 3, pH 8, physiological ionic strength, and low temperature, while at pasteurization temperatures it may rely more on buried hydrophobic residues exposed upon structural rearrangement.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>26296729</pmid><doi>10.1128/AEM.01278-15</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-2553-4204</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adsorption Biophysical Phenomena Calicivirus, Feline - chemistry Calicivirus, Feline - ultrastructure Feline calicivirus Food - virology Food Microbiology Food Services High temperature Hydrogen-Ion Concentration Molecular structure Norovirus Norovirus - chemistry Norovirus - ultrastructure Osmolar Concentration Pasteurization Proteins Surface Properties Temperature Ultraviolet radiation Virion |
title | Stability of Secondary and Tertiary Structures of Virus-Like Particles Representing Noroviruses: Effects of pH, Ionic Strength, and Temperature and Implications for Adhesion to Surfaces |
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