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Biomedical subjects

B Wagner

Publications and source records attributed to B Wagner.

At least 253 records · Page 14Linked to original sources
PubMed1980

Immunoelectron microscopic study of the location of group-specific and protein type-specific antigens of group B streptococci.

The ultrastructural location of the group-specific polysaccharide and the type-specific protein antigens R and X of group B streptococci was studied by means of the direct immunoferritin technique. The group-specific antigen was located on the outer wall layer. The specificity of the reaction was proved by the inhibition of labelling after absorption of the antibody-ferritin conjugate with group B polysaccharide. On the other hand, the demonstration of the polysaccharide was not sterically hindered by protein type antigens. As with group A and C streptococci the group polysaccharide could be localized on both the outer and inner surfaces of isolated walls. The protein antigens R and X were also demonstrated on the wall surface. The specificity of the reaction was ensured by making use of the enzymic sensitivity of these antigens. The location of the R protein on long filaments protruding from the cell surface resembles that of M protein of group A streptococci. In contrast to the group polysaccharide both the R and X protein antigens are localized only on the outer surface of isolated walls.

Antigens, Bacterial↗
PubMed1980

Immunoelectron microscopic study of the location of group-specific and type-specific polysaccharide antigens on isolated walls of group B streptococci.

The ultrastructural locations of the group-specific polysaccharide and the type-specific polysaccharides Ia, Ib, II and III of group B streptococci (Streptococcus agalactiae) were studied on isolated walls by the direct immunoferritin technique. The type polysaccharides were located exclusively on the outer side of the wall on which they formed a distinct capsule. Except for strain 58/59 (type Ia) the thickness of the capsule was characteristic of each strain investigated. In all strains the type-specific ferritin labelling was confined to the outer surface of the capsule. The group-specific polysaccharide could be demonstrated on the inner surface in all strains tested. It could also be demonstrated on the outer surface in strains 59/59 (type Ib) and 8/66 (group B variant) and on most of the walls of strain 58/59 (type Ia). The failure to detect this antigen on the outer side of the walls of strains 60/59 (type II) and 13/63 (type III) and on some walls of strain 58/59 was probably due to the thickness of the type polysaccharide capsule.

Cell Wall↗
PubMed1980

[Immunohistology of the antibody-formation against M-protein of Streptococcus pyogenes in Macaca mulatta (author's transl)].

The immunohistology of the antibody synthesis against M proteins of Streptococcus pyogenes (group A streptococci) was studied in rhesus monkeys (Macaca mulatta). For the immunoelectron microscopic detection of antibody producing cells peroxidase-labelled M protein was used. Cryostat sections of glutaraldehyde-fixed lymphoid organs were incubated with the peroxidase-conjugate followed by 3,3'-diaminobenzidine and H2O2. The labelled tissue sections were further processed for the electron microscopy. Two sites of specific labelling were observed: 1) The cell membrane of lymphocytes and transformed lymphocytes and 2) the endoplasmic reticulum of plasma cells, proplasmocytes and transformed lymphocytes.

Animals↗
PubMed1979

Immunofluorescent and immunoelectron microscopic demonstration of primate heart muscle antigens cross-reactive with Streptococcus pyogenes.

The presence of antigens in heart muscles cross-reactive with antibodies against Streptococcus pyogenes were examined in heart samples of seven primate species (chimpanzee, rhesus macaque, stump-tailed macaque, hamadryas baboon, capuchin monkey, green monkey and patas monkey). Cross-reactive antigens were localized by means of the indirect immunofluorescent technique in nearly all samples tested. The fluorescence pattern was the same as found in the heart muscle of other mammals. Using the indirect immunoferritin technique the substructural distribution of the antigens was investigated in heart muscle of rhesus macaque and hamadryas baboon. Beside the location on the cell surface the antigens were also demonstrated within the cell. Above all there was a strong labelling along the intercalated discs and in the sarcoplasmatic reticulum.

Animals↗
PubMed1979

Immunoelectron microscopic localization of T proteins in the cell wall of Streptococcus pyogenes.

T proteins of Streptococcus pyogenes (group A streptococci) were localized by means of immunochromatographical isolated anti-T-antibodies. For the electron microscopical detection both the direct and the indirect immunoferritin techniques were used. The arrangement of the ferritin particles showed, that the T proteins are evenly distributed on the whole cell surface. They are immediately bound to the outer layer of the cell wall or to only short filaments. On isolated cell walls the T protein was detected only on the outer surface.

Agglutination Tests↗
PubMed1979

Suspension culture of myocardial cells from newborn rats.

Myocardial cells from newborn rats were held in a spinner type culture for 2 days and then explanted into culture flasks. Three main cell types were observed: single multipolar cells of embryonic type, cell aggregates containing 10 to 50 connected cells, and bipolar cells retaining some adult characteristics. Except for the latter, up to 95% of intact cells settled and were beating 6 hours after explantation. The percentage of fibroblast-like cells was drastically reduced when compared with conventional cultures. Cell debris could be removed 2 hours after explantation by changing the culture medium, or more effectively by a density step centrifugation using Lymphoprep or Lymphoprep-Ficoll mixtures.

Animals↗