Abstract
Binding of 35[S]- methionine-labeled Helicobacter pylori to tissue culture
was carried out using human colon carcinoma epithelial cells (Caco-2),
and human adenocarcinoma tissue culture cells (AGS). In this research,
clinical isolates (smooth) as well as type culture collection (rough) strains
were used in binding and inhibition of the binding study of H. pylori to
tissue cultures using monoclonal antibodies (MAbs) raised against
bacterial lipopolysaccharides (LPS). The task of the work was to
discriminate and evaluate the role of LPS as bacterial adhesin in the
binding as well as the specificity of the binding of various H. pylori strains
to cell lines. Binding of H. pylori, clinical isolate Hel 305(smooth
strain),to Caco-2 cells was strongly inhibitedby species-specific MAbs
raised against Hel 305-LPS antigen. It was also recognized that inhibition
of binding of Hel 305 strain to Caco-2 cells was high effective when using
species-specific MAbs in comparison with MAbs raised against LPS from
type culture collection CCUG 17874 (rough strain). In the same manner,
binding of rough CCUG 17874 strain to Caco-2 cell line was inhibited by
species-specific LPS MAbs stronger than with MAbs raised against Hel
305 LPS. In both overlay cases, no significant inhibition with other LPS
MAbs of different origins was detected, after bacterial incubation with
MAbs raised against LPSs from other tested H. pylori strains.
was carried out using human colon carcinoma epithelial cells (Caco-2),
and human adenocarcinoma tissue culture cells (AGS). In this research,
clinical isolates (smooth) as well as type culture collection (rough) strains
were used in binding and inhibition of the binding study of H. pylori to
tissue cultures using monoclonal antibodies (MAbs) raised against
bacterial lipopolysaccharides (LPS). The task of the work was to
discriminate and evaluate the role of LPS as bacterial adhesin in the
binding as well as the specificity of the binding of various H. pylori strains
to cell lines. Binding of H. pylori, clinical isolate Hel 305(smooth
strain),to Caco-2 cells was strongly inhibitedby species-specific MAbs
raised against Hel 305-LPS antigen. It was also recognized that inhibition
of binding of Hel 305 strain to Caco-2 cells was high effective when using
species-specific MAbs in comparison with MAbs raised against LPS from
type culture collection CCUG 17874 (rough strain). In the same manner,
binding of rough CCUG 17874 strain to Caco-2 cell line was inhibited by
species-specific LPS MAbs stronger than with MAbs raised against Hel
305 LPS. In both overlay cases, no significant inhibition with other LPS
MAbs of different origins was detected, after bacterial incubation with
MAbs raised against LPSs from other tested H. pylori strains.