ENDOCYTOSIS OF SALMONELLA TYPHIMURIUM 395 MS AND MR10 BY HELA CELLS

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Abstract
Monolayers of HeLa cells were examined for their ability to endocytose S. typhimurium 395 MS (wild) and MR10 (chemotype Rd). Monolayers treated with the glycolytic inhibitors iodoacetic acid (IAA) or N-ethylmaleimide (NEM) or the respiratory inhibitor sodium azide (NaN3) or cytochalasin B (CB) were incubated with S. typhimurium. The numbers of cell-associated (intracellular plus cell-membrane attached extracellular) and intracellular bacteria were determined by viable counts, together with the HeLa cell ATP levels. IAA and NEM at concentrations 10-4 M and 10-3 M decreased significantly the number of intracellular MR10 and the cellular ATP levels, but did not influence significantly the total number of cell-associated bacteria except for 10-3 M IAA which slightly increased the association. NaN3 at concentrations 10-4 M and 10-3 M did not affect the number of associated or intracellular bacteria or the cellular ATP levels. CB at concentrations of 5, 10 and 20 .mu.g/ml increased the number of associated bacteria, decreased the number of intracellular bacteria and caused a small decrease in cellular ATP levels. Thus, HeLa cells may internalize S. typhimurium by an energy-requiring, glycolysis-dependent process. CB had a dose-dependent inhibitory effect on the internalization without influencing significantly the HeLa cell ATP levels. This indicates that CB might affect the internalization process by some means other than decreasing the ATP content.