The concentration of airborne bacteria was recorded during a period of 3 years at four localities: (i) in an agricultural district with an average of 99 (range, 2 to 3,400) bacteria per m3; (ii) in a coastal area with an average of 63 (range, 0 to 560) bacteria per m3; (iii) in a city park with an average of 763 (range, 100 to 2,500) bacteria per m3; and (iv) in a city street with an average of 850 (range, 100 to 4,000) bacteria per m3. At all four localities the bacterial concentrations varied within broad limits, but an annual periodicity with high average counts found during summer and autumn could be seen. The influence of certain meteorological factors on the number of airborne bacteria is also reported. Rain or high relative humidity caused a decrease in the bacterial counts, while high temperature or high wind velocities increased the counts. The particle size distribution for the four localities showed that about 50% of the particles carrying bacteria were larger than 8,um.

No abstract

Bacterial spores from a sandstorm area north of the Black Sea were transmitted to Sweden by air, giving increased concentrations of viable bacterial spores at two air sampling stations in Sweden.

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 10(7) or 10(9) bacteria per cell culture (2 X 10(6) 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.

The cation content in commercial media obtained from two manufacturers showed considerable variation. Even different batches of the same make were found to be inconsistent in the content of metal ions. With cultures of Cytophaga sp. and Yersinia pseudotuberculosis in base media, growth stimulation was dependent on additions of certain commercial media. It could be demonstrated that this stimulation was derived solely from increased Mg2+ concentration in the media.