pubmed-article:2470679 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:2470679 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
pubmed-article:2470679 | lifeskim:mentions | umls-concept:C0008148 | lld:lifeskim |
pubmed-article:2470679 | lifeskim:mentions | umls-concept:C0007603 | lld:lifeskim |
pubmed-article:2470679 | lifeskim:mentions | umls-concept:C0003320 | lld:lifeskim |
pubmed-article:2470679 | lifeskim:mentions | umls-concept:C0023810 | lld:lifeskim |
pubmed-article:2470679 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:2470679 | pubmed:dateCreated | 1989-6-23 | lld:pubmed |
pubmed-article:2470679 | pubmed:abstractText | The presence of a chlamydia-specified antigen associated with the plasma membrane of infected cell lines was demonstrated by indirect immunofluorescence staining with a monoclonal antibody, designated 47A2, specific for the chlamydial genus-specific lipopolysaccharide (LPS) antigen. Staining of HeLa, L-929, and McCoy cells infected with the L2 or F serovar of Chlamydia trachomatis was observed either without fixation or following aldehyde fixation and brief drying. The 47A2-reactive antigen appeared to be present on the plasma membrane, on bleb-like structures on the host cell surface, and on proximal processes of neighboring uninfected cells. Antibodies to chlamydial protein antigens such as the major outer membrane protein produced no surface staining under similar conditions. Membrane vesicles elaborated from infected cells were enriched for the 47A2-reactive antigen. Superinfection of chlamydia-infected cells with vesicular stomatitis virus, an enveloped virus which buds from the plasma membrane, allowed purification of progeny virions that were enriched with chlamydial LPS. These results are consistent with the presence of chlamydial LPS in the plasma membranes of infected host cells. | lld:pubmed |
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pubmed-article:2470679 | pubmed:language | eng | lld:pubmed |
pubmed-article:2470679 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:2470679 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:2470679 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:2470679 | pubmed:month | Jun | lld:pubmed |
pubmed-article:2470679 | pubmed:issn | 0019-9567 | lld:pubmed |
pubmed-article:2470679 | pubmed:author | pubmed-author:WildeC ECE3rd | lld:pubmed |
pubmed-article:2470679 | pubmed:author | pubmed-author:SchloemerR... | lld:pubmed |
pubmed-article:2470679 | pubmed:author | pubmed-author:KarimiS TST | lld:pubmed |
pubmed-article:2470679 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:2470679 | pubmed:volume | 57 | lld:pubmed |
pubmed-article:2470679 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:2470679 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:2470679 | pubmed:pagination | 1780-5 | lld:pubmed |
pubmed-article:2470679 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:2470679 | pubmed:year | 1989 | lld:pubmed |
pubmed-article:2470679 | pubmed:articleTitle | Accumulation of chlamydial lipopolysaccharide antigen in the plasma membranes of infected cells. | lld:pubmed |
pubmed-article:2470679 | pubmed:affiliation | Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis 46223. | lld:pubmed |
pubmed-article:2470679 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:2470679 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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