Dengue serotypes 1-4 exhibit unique host specificity in vitro
Background: Over 3000 cell lines from over 150 species are commercially available today from the American Type Culture Collection. These cell lines offer alternative approaches to investigating the interactions between arboviruses and other vertebrates at the cellular level. The various cell origins...
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description | Background: Over 3000 cell lines from over 150 species are commercially available today from the American Type Culture Collection. These cell lines offer alternative approaches to investigating the interactions between arboviruses and other vertebrates at the cellular level. The various cell origins, types, and morphologies can be valuable resources for studying viral ecology and examining hypotheses regarding viral reservoirs. Dengue viruses (DENV) are major re-emerging pathogens that have been studied classically in only a few cell lines. Methods: We evaluated the susceptibility of 19 distinct mammalian, avian, and reptilian cell lines to DENV infection. Cell lines were infected with DENV serotypes 1-4 and evaluated for susceptibility via focus-forming unit assays and quantitative reverse-transcription polymerase chain reaction. Results: Both methods demonstrated the ability of DENV to replicate in 14 cell lines derived from various vertebrates with viral titers ranging from 1 x [10.sup.3] to 1 x [10.sup.7] infectious units per milliliter. Cell line susceptibility to DENV infection was serotype specific, with DENV-1 and DENV-4 infecting more cell lines than either DENV-2 or DENV-3. Cellular type also seemed to affect the infectivity of DENV. Human endothelial cells were only susceptible to DENV-4. Of six fibroblast lines, 100% were susceptible to at least one DENV serotype whereas only 62% of 13 epithelial lines were susceptible to DENV serotypes 1-4. Conclusion: These data indicate that a variety of cell lines from human and animal species can be used to culture DENV. The serotype-specific susceptibility for certain cell lines may provide a tool to help characterize specific DENV serotypes as well as an in vitro platform for the study of host-pathogen interactions and the co-circulation of DENV serotypes in a specific region or individual. Keywords: dengue virus, cell culture, host |
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These cell lines offer alternative approaches to investigating the interactions between arboviruses and other vertebrates at the cellular level. The various cell origins, types, and morphologies can be valuable resources for studying viral ecology and examining hypotheses regarding viral reservoirs. Dengue viruses (DENV) are major re-emerging pathogens that have been studied classically in only a few cell lines. Methods: We evaluated the susceptibility of 19 distinct mammalian, avian, and reptilian cell lines to DENV infection. Cell lines were infected with DENV serotypes 1-4 and evaluated for susceptibility via focus-forming unit assays and quantitative reverse-transcription polymerase chain reaction. Results: Both methods demonstrated the ability of DENV to replicate in 14 cell lines derived from various vertebrates with viral titers ranging from 1 x [10.sup.3] to 1 x [10.sup.7] infectious units per milliliter. Cell line susceptibility to DENV infection was serotype specific, with DENV-1 and DENV-4 infecting more cell lines than either DENV-2 or DENV-3. Cellular type also seemed to affect the infectivity of DENV. Human endothelial cells were only susceptible to DENV-4. Of six fibroblast lines, 100% were susceptible to at least one DENV serotype whereas only 62% of 13 epithelial lines were susceptible to DENV serotypes 1-4. Conclusion: These data indicate that a variety of cell lines from human and animal species can be used to culture DENV. The serotype-specific susceptibility for certain cell lines may provide a tool to help characterize specific DENV serotypes as well as an in vitro platform for the study of host-pathogen interactions and the co-circulation of DENV serotypes in a specific region or individual. Keywords: dengue virus, cell culture, host</description><identifier>ISSN: 1179-1624</identifier><identifier>EISSN: 1179-1624</identifier><identifier>DOI: 10.2147/VAAT.S36856</identifier><language>eng</language><publisher>Abingdon: Dove Medical Press Limited</publisher><subject>Adaptation ; American Type Culture Collection ; Amino acids ; Antibodies ; Cell culture ; Cell lines ; Cellular control mechanisms ; Dengue fever ; Dengue viruses ; Disease susceptibility ; Ecology ; Endothelial cells ; Fibroblasts ; Host specificity ; Host-parasite relationships ; Host-pathogen interactions ; Infections ; Infectivity ; Observations ; Pathogens ; Penicillin ; Physiological aspects ; Polymerase chain reaction ; Public health ; Serotypes ; Susceptibility ; Vertebrates ; Viruses</subject><ispartof>Virus adaptation and treatment, 2012-01, Vol.4, p.65</ispartof><rights>COPYRIGHT 2012 Dove Medical Press Limited</rights><rights>2012. This work is licensed under https://creativecommons.org/licenses/by-nc/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c274t-5877357f04375b74730240c3e97c849bd2de099049dd986234b51e95957523123</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,3863,27928,27929</link.rule.ids></links><search><creatorcontrib>Barr, Kelli L</creatorcontrib><creatorcontrib>Anderson, Benjamin D</creatorcontrib><creatorcontrib>Heil, Gary L</creatorcontrib><creatorcontrib>Friary, John A</creatorcontrib><creatorcontrib>Gray, Gregory C</creatorcontrib><creatorcontrib>Focks, Dana A</creatorcontrib><title>Dengue serotypes 1-4 exhibit unique host specificity in vitro</title><title>Virus adaptation and treatment</title><description>Background: Over 3000 cell lines from over 150 species are commercially available today from the American Type Culture Collection. These cell lines offer alternative approaches to investigating the interactions between arboviruses and other vertebrates at the cellular level. The various cell origins, types, and morphologies can be valuable resources for studying viral ecology and examining hypotheses regarding viral reservoirs. Dengue viruses (DENV) are major re-emerging pathogens that have been studied classically in only a few cell lines. Methods: We evaluated the susceptibility of 19 distinct mammalian, avian, and reptilian cell lines to DENV infection. Cell lines were infected with DENV serotypes 1-4 and evaluated for susceptibility via focus-forming unit assays and quantitative reverse-transcription polymerase chain reaction. Results: Both methods demonstrated the ability of DENV to replicate in 14 cell lines derived from various vertebrates with viral titers ranging from 1 x [10.sup.3] to 1 x [10.sup.7] infectious units per milliliter. Cell line susceptibility to DENV infection was serotype specific, with DENV-1 and DENV-4 infecting more cell lines than either DENV-2 or DENV-3. Cellular type also seemed to affect the infectivity of DENV. Human endothelial cells were only susceptible to DENV-4. Of six fibroblast lines, 100% were susceptible to at least one DENV serotype whereas only 62% of 13 epithelial lines were susceptible to DENV serotypes 1-4. Conclusion: These data indicate that a variety of cell lines from human and animal species can be used to culture DENV. The serotype-specific susceptibility for certain cell lines may provide a tool to help characterize specific DENV serotypes as well as an in vitro platform for the study of host-pathogen interactions and the co-circulation of DENV serotypes in a specific region or individual. Keywords: dengue virus, cell culture, host</description><subject>Adaptation</subject><subject>American Type Culture Collection</subject><subject>Amino acids</subject><subject>Antibodies</subject><subject>Cell culture</subject><subject>Cell lines</subject><subject>Cellular control mechanisms</subject><subject>Dengue fever</subject><subject>Dengue viruses</subject><subject>Disease susceptibility</subject><subject>Ecology</subject><subject>Endothelial cells</subject><subject>Fibroblasts</subject><subject>Host specificity</subject><subject>Host-parasite relationships</subject><subject>Host-pathogen interactions</subject><subject>Infections</subject><subject>Infectivity</subject><subject>Observations</subject><subject>Pathogens</subject><subject>Penicillin</subject><subject>Physiological aspects</subject><subject>Polymerase chain reaction</subject><subject>Public health</subject><subject>Serotypes</subject><subject>Susceptibility</subject><subject>Vertebrates</subject><subject>Viruses</subject><issn>1179-1624</issn><issn>1179-1624</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkUtLw0AQxxdRsNSe_AIBwYuk7jObPXgI9QkFD1avS7LZNFvSbNzdiPn2plSwBWcOM8z85gF_AC4RnGNE-e1Hlq3mbyRJWXICJghxEaME09OD_BzMvN_A0VIIGeMTcHev23WvI6-dDUOnfYRiGunv2hQmRH1rPsdmbX2IfKeVqYwyYYhMG32Z4OwFOKvyxuvZb5yC98eH1eI5Xr4-vSyyZawwpyFmKeeE8QpSwlnBKScQU6iIFlylVBQlLjUUAlJRliJNMKEFQ1owwTjDBGEyBVf7vZ2z40M-yI3tXTuelBhjJCjDOP2j1nmjpWkrG1yutsYrmRHKRCogQiM1_4cavdRbo2yrKzPWjwauDwZqnTeh9rbpg7GtPwZv9qBy1nunK9k5s83dIBGUO4nkTiK5l4j8AIZVfes</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Barr, Kelli L</creator><creator>Anderson, Benjamin D</creator><creator>Heil, Gary L</creator><creator>Friary, John A</creator><creator>Gray, Gregory C</creator><creator>Focks, Dana A</creator><general>Dove Medical Press Limited</general><general>Taylor & Francis Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>20120101</creationdate><title>Dengue serotypes 1-4 exhibit unique host specificity in vitro</title><author>Barr, Kelli L ; Anderson, Benjamin D ; Heil, Gary L ; Friary, John A ; Gray, Gregory C ; Focks, Dana A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-5877357f04375b74730240c3e97c849bd2de099049dd986234b51e95957523123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adaptation</topic><topic>American Type Culture Collection</topic><topic>Amino acids</topic><topic>Antibodies</topic><topic>Cell culture</topic><topic>Cell lines</topic><topic>Cellular control mechanisms</topic><topic>Dengue fever</topic><topic>Dengue viruses</topic><topic>Disease susceptibility</topic><topic>Ecology</topic><topic>Endothelial cells</topic><topic>Fibroblasts</topic><topic>Host specificity</topic><topic>Host-parasite relationships</topic><topic>Host-pathogen interactions</topic><topic>Infections</topic><topic>Infectivity</topic><topic>Observations</topic><topic>Pathogens</topic><topic>Penicillin</topic><topic>Physiological aspects</topic><topic>Polymerase chain reaction</topic><topic>Public health</topic><topic>Serotypes</topic><topic>Susceptibility</topic><topic>Vertebrates</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Barr, Kelli L</creatorcontrib><creatorcontrib>Anderson, Benjamin D</creatorcontrib><creatorcontrib>Heil, Gary L</creatorcontrib><creatorcontrib>Friary, John A</creatorcontrib><creatorcontrib>Gray, Gregory C</creatorcontrib><creatorcontrib>Focks, Dana A</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Virus adaptation and treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Barr, Kelli L</au><au>Anderson, Benjamin D</au><au>Heil, Gary L</au><au>Friary, John A</au><au>Gray, Gregory C</au><au>Focks, Dana A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dengue serotypes 1-4 exhibit unique host specificity in vitro</atitle><jtitle>Virus adaptation and treatment</jtitle><date>2012-01-01</date><risdate>2012</risdate><volume>4</volume><spage>65</spage><pages>65-</pages><issn>1179-1624</issn><eissn>1179-1624</eissn><abstract>Background: Over 3000 cell lines from over 150 species are commercially available today from the American Type Culture Collection. These cell lines offer alternative approaches to investigating the interactions between arboviruses and other vertebrates at the cellular level. The various cell origins, types, and morphologies can be valuable resources for studying viral ecology and examining hypotheses regarding viral reservoirs. Dengue viruses (DENV) are major re-emerging pathogens that have been studied classically in only a few cell lines. Methods: We evaluated the susceptibility of 19 distinct mammalian, avian, and reptilian cell lines to DENV infection. Cell lines were infected with DENV serotypes 1-4 and evaluated for susceptibility via focus-forming unit assays and quantitative reverse-transcription polymerase chain reaction. Results: Both methods demonstrated the ability of DENV to replicate in 14 cell lines derived from various vertebrates with viral titers ranging from 1 x [10.sup.3] to 1 x [10.sup.7] infectious units per milliliter. Cell line susceptibility to DENV infection was serotype specific, with DENV-1 and DENV-4 infecting more cell lines than either DENV-2 or DENV-3. Cellular type also seemed to affect the infectivity of DENV. Human endothelial cells were only susceptible to DENV-4. Of six fibroblast lines, 100% were susceptible to at least one DENV serotype whereas only 62% of 13 epithelial lines were susceptible to DENV serotypes 1-4. Conclusion: These data indicate that a variety of cell lines from human and animal species can be used to culture DENV. The serotype-specific susceptibility for certain cell lines may provide a tool to help characterize specific DENV serotypes as well as an in vitro platform for the study of host-pathogen interactions and the co-circulation of DENV serotypes in a specific region or individual. Keywords: dengue virus, cell culture, host</abstract><cop>Abingdon</cop><pub>Dove Medical Press Limited</pub><doi>10.2147/VAAT.S36856</doi><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation American Type Culture Collection Amino acids Antibodies Cell culture Cell lines Cellular control mechanisms Dengue fever Dengue viruses Disease susceptibility Ecology Endothelial cells Fibroblasts Host specificity Host-parasite relationships Host-pathogen interactions Infections Infectivity Observations Pathogens Penicillin Physiological aspects Polymerase chain reaction Public health Serotypes Susceptibility Vertebrates Viruses |
title | Dengue serotypes 1-4 exhibit unique host specificity in vitro |
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