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The effect of erythromycin (10 micrograms/ml) on the morphology and developmental cycle of Chlamydia trachomatis HAR-13 was examined by electron microscopy. When the antibiotic was added later than 24 h post infection, the HAR-13 morphology or developmental cycle was not altered. Addition at 18 or 24 h post infection inhibited glycogen production, blocked the transformation of the reticulate body to elementary body, and produced ghost bodies and reticulate bodies twice the diameter of untreated reticulate bodies. When erythromycin was added within 12 h post infection, the conversion of the elementary body to reticulate body was inhibited. Erythromycin (10 micrograms/ml) was bactericidal to strain HAR-13 throughout the developmental cycle.

The effect of cycloheximide and penicillin on the ultrastructural morphology of C. trachomatis strain HAR-13 was examined by electron microscopy. HAR-13 infected McCoy cells were either treated with cycloheximide (1 microgram/ml) or cycloheximide (1 microgram/ml) plus penicillin G (100 U/ml). The studies revealed that cycloheximide alone induced no morphological alterations into the ultrastructure of HAR-13. Both HAR-13 developmental forms, the elementary body and reticulate body, were present inside the treated McCoy cells. The elementary bodies contained the central dense nucleoid and were about 0.3 microns in diameter, while the reticulate bodies were of typical gram negative bacterial morphology and were from 0.5-1.0 microns in diameter. Cycloheximide in combined treatment with pencillin produced giant, swollen reticulate bodies that were 2-4 microns in diameter and in some cases vacuolated. Elementary bodies were noticeably absent. These results indicate that cycloheximide does not alter the morphology of HAR-13. This system is a useful model for studying the ultrastructural morphology of C. trachomatis strain HAR-13.

Lanthanum nitrate solution adjusted to pH 7.4 and pH 7.7 was subjected to column chromatography, ultrafiltration and conductivity measurements. Lanthanum concentration was measured by a colorimetric method employing eriochrome cyanine RC. Under these conditions, lanthanum was not excluded from the column by a packing with an exclusion limit of 1800 daltons. Ultrafiltration through a membrane with a filter limit of 500 daltons allowed approximately 75% of the lanthanum to pass. Conductivity measurements showed a decrease of charge of about 20% on adding sodium hydroxide to a solution of lanthanum nitrate up to a pH of 7.7. It is concluded that approximately 80% of the lanthanum exists as a charged particle of less than 500 daltons at pH 7.7; the other 20% consists of larger, possibly colloidal particles. Nonfiltered and ultrafiltered lanthanum have equally good staining and tracer properties in the electron microscope, suggesting that staining depends largely on the ultrafiltrable noncolloidal lanthanum ion.

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