dc.contributor.author | Myllynen, Mira | |
dc.contributor.author | Kazmertsuk, Artur | |
dc.contributor.author | Marjomäki, Varpu | |
dc.date.accessioned | 2016-07-22T07:06:21Z | |
dc.date.available | 2016-07-22T07:06:21Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Myllynen, M., Kazmertsuk, A., & Marjomäki, V. (2016). A Novel Open and Infectious Form of Echovirus 1. <i>Journal of Virology</i>, <i>90</i>(15), 6759-6770. <a href="https://doi.org/10.1128/JVI.00342-16" target="_blank">https://doi.org/10.1128/JVI.00342-16</a> | |
dc.identifier.other | CONVID_26123065 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/50878 | |
dc.description.abstract | One of the hallmarks of enterovirus genome delivery is the formation of an uncoating intermediate particle. Based on previous studies of mostly heated picornavirus particles, intermediate particles were shown to have externalized the innermost capsid protein (VP4) and exposed the N terminus of VP1 and to have reduced infectivity. Here, in addition to the native and intact particle type, we have identified another type of infectious echovirus 1 (E1) particle population during infection. Our results show that E1 is slightly altered during entry, which leads to the broadening of the major virion peak in the sucrose gradient. In contrast, CsCl gradient separation revealed that in addition to the light intact and empty particles, a dense particle peak appeared during infection in cells. When the broad peak from the sucrose gradient was subjected to a CsCl gradient, it revealed light and dense particles, further suggesting that the shoulder represents the dense particle. The dense particle was permeable to SYBR green II, it still contained most of its VP4, and it was able to bind to its receptor 21 integrin and showed high infectivity. A thermal assay further showed that the 21 integrin binding domain (I-domain) stabilized the virus particle. Finally, heating E1 particles to superphysiological temperatures produced more fragile particles with aberrant ultrastructural appearances, suggesting that they are distinct from the dense E1 particles. These results describe a more open and highly infectious E1 particle that is naturally produced during infection and may represent a novel form of an uncoating intermediate. | |
dc.language.iso | eng | |
dc.publisher | American Society for Microbiology | |
dc.relation.ispartofseries | Journal of Virology | |
dc.subject.other | Echovirus 1 | |
dc.subject.other | genome delivery | |
dc.subject.other | intermediate particles | |
dc.title | A Novel Open and Infectious Form of Echovirus 1 | |
dc.type | research article | |
dc.identifier.urn | URN:NBN:fi:jyu-201607203642 | |
dc.contributor.laitos | Bio- ja ympäristötieteiden laitos | fi |
dc.contributor.laitos | Department of Biological and Environmental Science | en |
dc.contributor.oppiaine | Solu- ja molekyylibiologia | fi |
dc.contributor.oppiaine | Nanoscience Center | fi |
dc.contributor.oppiaine | Cell and Molecular Biology | en |
dc.contributor.oppiaine | Nanoscience Center | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.date.updated | 2016-07-20T06:15:09Z | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 6759-6770 | |
dc.relation.issn | 0022-538X | |
dc.relation.numberinseries | 15 | |
dc.relation.volume | 90 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | Copyright © 2016, American Society for Microbiology | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.subject.yso | enterovirukset | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p20689 | |
dc.relation.doi | 10.1128/JVI.00342-16 | |
dc.type.okm | A1 | |