pubmed-article:20023636 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0020094 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0205466 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0521119 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0039062 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C1521797 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0282629 | lld:lifeskim |
pubmed-article:20023636 | lifeskim:mentions | umls-concept:C0086597 | lld:lifeskim |
pubmed-article:20023636 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:20023636 | pubmed:dateCreated | 2010-1-8 | lld:pubmed |
pubmed-article:20023636 | pubmed:abstractText | Human T cell leukemia virus type 1 (HTLV-1) is a lymphotropic retrovirus whose cell-to-cell transmission requires cell contacts. HTLV-1-infected T lymphocytes form 'virological synapses', but the mechanism of HTLV-1 transmission remains poorly understood. We show here that HTLV-1-infected T lymphocytes transiently store viral particles as carbohydrate-rich extracellular assemblies that are held together and attached to the cell surface by virally-induced extracellular matrix components, including collagen and agrin, and cellular linker proteins, such as tetherin and galectin-3. Extracellular viral assemblies rapidly adhere to other cells upon cell contact, allowing virus spread and infection of target cells. Their removal strongly reduces the ability of HTLV-1-producing cells to infect target cells. Our findings unveil a novel virus transmission mechanism based on the generation of extracellular viral particle assemblies whose structure, composition and function resemble those of bacterial biofilms. HTLV-1 biofilm-like structures represent a major route for virus transmission from cell to cell. | lld:pubmed |
pubmed-article:20023636 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20023636 | pubmed:language | eng | lld:pubmed |
pubmed-article:20023636 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20023636 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:20023636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20023636 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:20023636 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:20023636 | pubmed:month | Jan | lld:pubmed |
pubmed-article:20023636 | pubmed:issn | 1546-170X | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:GessainAntoin... | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:AlcoverAndrés... | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:GoutOlivierO | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:SachseMartinM | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:LasserreRémiR | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:ThoulouzeMari... | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:GuadagniniSté... | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:Pais-CorreiaA... | lld:pubmed |
pubmed-article:20023636 | pubmed:author | pubmed-author:RobbiatiValen... | lld:pubmed |
pubmed-article:20023636 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:20023636 | pubmed:volume | 16 | lld:pubmed |
pubmed-article:20023636 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:20023636 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:20023636 | pubmed:pagination | 83-9 | lld:pubmed |
pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
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pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
pubmed-article:20023636 | pubmed:meshHeading | pubmed-meshheading:20023636... | lld:pubmed |
pubmed-article:20023636 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:20023636 | pubmed:articleTitle | Biofilm-like extracellular viral assemblies mediate HTLV-1 cell-to-cell transmission at virological synapses. | lld:pubmed |
pubmed-article:20023636 | pubmed:affiliation | Institut Pasteur, Unité de Biologie Cellulaire des Lymphocytes, Centre National de Recherche Scientifique (CNRS), Unité de Recherche Associée 1961, Paris, France. | lld:pubmed |
pubmed-article:20023636 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:20023636 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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