Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
1991-10-17
|
pubmed:abstractText |
The isolation and purification of a neutral glycolipid fraction from Taenia crassiceps metacestodes (KBS strain), harvested from both male and female NMRI mice at 70-80 days following intraperitoneal infection, revealed 24 thin-layer chromatography-designated glycolipid bands. The glycolipids were defined as ceramide mono- (n = 3), di- (n = 3), tri- (n = 4), tetra- (n = 5), and greater than tetrasaccharides (n = 9) according to their running properties as defined by thin-layer chromatography against standards of known structure. The defined glycolipids were tested for immunoreactivity with sera from noninfected and T. crassiceps-infected NMRI mice (intraperitoneal injection or implantation of 15 larvae/animal) using the enzyme-linked immunosorbent assay (ELISA) until day 33 p.i. (IgM and IgG reaction) and high-performance thin-layer chromatography (HPTLC) combined with immunostaining (IgG reaction) until day 7 p.i. ELISA-determined IgM and IgG titres were significantly elevated from day 5 p.i. Immunostaining revealed early reactivity for certain ceramide tetra- and greater than tetrasaccharides (n = 6) on day 3 p.i. From day 5 p.i. onwards, nearly all glycolipids, including ceramide mono- and disaccharides, were recognized by the sera from metacestode-challenged mice. On day 7 p.i., a total of 22 bands were serologically active; of these, a considerable number (n = 10) showed increased staining intensity. Remarkably, in many cases (10 of 20), 3 glycolipids (tetra- and greater than tetrasaccharides) were weakly recognized by mouse sera taken before infection.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Helminth,
http://linkedlifedata.com/resource/pubmed/chemical/Glycolipids,
http://linkedlifedata.com/resource/pubmed/chemical/Immune Sera,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0932-0113
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
77
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
443-7
|
pubmed:dateRevised |
2003-11-14
|
pubmed:meshHeading |
pubmed-meshheading:1891452-Animals,
pubmed-meshheading:1891452-Antibodies, Helminth,
pubmed-meshheading:1891452-Chromatography, High Pressure Liquid,
pubmed-meshheading:1891452-Chromatography, Ion Exchange,
pubmed-meshheading:1891452-Chromatography, Thin Layer,
pubmed-meshheading:1891452-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:1891452-Female,
pubmed-meshheading:1891452-Glycolipids,
pubmed-meshheading:1891452-Immune Sera,
pubmed-meshheading:1891452-Immunoglobulin G,
pubmed-meshheading:1891452-Immunoglobulin M,
pubmed-meshheading:1891452-Male,
pubmed-meshheading:1891452-Mice,
pubmed-meshheading:1891452-Taenia,
pubmed-meshheading:1891452-Taeniasis
|
pubmed:year |
1991
|
pubmed:articleTitle |
Immunological recognition of larval Taenia crassiceps glycolipids by sera from parasite-infected mice.
|
pubmed:affiliation |
Fachbereich Biologie, Philipps-Universität Marburg, Federal Republic of Germany.
|
pubmed:publicationType |
Journal Article
|