Author:
Bovallius Åke,Nilsson Gustaf
Abstract
HeLa cells were infected with Yersinia pseudotuberculosis for 0.5–3 h. Intracellular bacteria could then be demonstrated by three different techniques: viable count, fluorescent-antibody staining, and electron microscopy. Most of the bacteria seemed to be viable, since there was a good positive correlation (0.94) between viable and fluorescent bacteria. The bacterial uptake seemed to be mediated by a phagocytic-like procedure. The intracellular bacteria seemed to reside in vacuoles some of which increased in size as a function of time. The kinetics of infection was studied after addition of 107 or 109 bacteria per cell culture (2 × 106 cells). After a lag period of about 30 min there was a linear increase of intracellular bacteria, and this uptake proceeded for 1–2 h until most of the bacteria were ingested or an upper limit of ingested bacteria was reached. The upper limit was calculated to be a mean of 60 per infected cell in the cell culture. More than 90% of the cells could be infected and a reasonable number of the bacteria survive in the cells for at least 3 days, as demonstrated by the viable-count technique.The bacteria–cell system may be used to study, for example, the effect of antibiotics or antibodies on intracellular bacteria and pathogenicity of intracellular diseases.
Publisher
Canadian Science Publishing
Subject
Genetics,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Immunology,Microbiology
Cited by
59 articles.
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