INHIBITORY EFFECT OF FORMYCIN ON INTRACELLULAR CHLAMYDIA PSITTACI
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Inhibitory effect of formycin and formycin B on the intracellular multiplication of goat pneumonitis agent (GP), a member of Chlamydia psittaci, was investigated. Drug was added to the nutrient fluid at two hours after inoculation to monolayers of either Earle's L or Yasumura's VERO cell lines. Infective units produced in cells cultivated in media which containd the antibiotic at varying dosage were assayed after an incubation period for 48 hours at 37°C. The "inclusion forming units" were assayed by the "infected cell count method".The inhibitory action of both formycin and formycin B on GP-agent was far more effective in VERO cells than in L cells. The growth of the psittacosis agent in VERO cells was completely inhibited by formycin at a level of 1.4mcg per ml, whereas the drug did not inhibit the multiplication of the agent at the same concentration when L cells were chosen. The result may indicate that the psittacosis agent itself is resistant to these drugs, and that the inhibitory action is a result of some inhibitory effects of the host cell metabolism.The inhibitory effect of formycin and formycin B on the psittacosis agent can be reversed to some extent by an addition of excessive purine or purine nucleoside to the nutrient media. Inosine, Na-inosinate, adenine or adenosine reversed the inhibitory effect of the two antibiotics. However, guanine and guanosine did not reverse the inhibitory effect. This may suggest that these drugs act as purine analogues, inhibiting certain essential metabolic pathway where adenosine may act an important role.
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