Chatterjee S N, Maiti M
J Virol. 1973 Jun;11(6):872-8. doi: 10.1128/JVI.11.6.872-878.1973.
Furazolidone in concentrations which had little effect on the growth of host organisms greatly reduced the yield of phage phi149 from the host Vibrio cholerae OGAWA 154. This phage was resistant to the in vitro action of the drug. The phage yield of infected bacteria depended significantly on the time of addition or withdrawal of the drug. The average burst size of the drug-treated and infected bacteria decreased exponentially with increase in drug concentration. The latent period of phage multiplication and also the eclipse period did not change significantly from the control values. A concentration of 0.05 mug of furazolidone per ml inhibited DNA synthesis by about 50% in phage-infected cells and only by about 18% in noninfected ones, relative to the respective controls. RNA and protein synthesis were affected by a much smaller degree both in infected and noninfected cells. Quantitative deduction of the length of furazolidone-treated cells from their phage adsorption characteristics and its agreement with previous electron microscopy data indicated that furazolidone did not affect the phage receptors.
呋喃唑酮在对宿主生物体生长影响很小的浓度下,极大地降低了噬菌体phi149从宿主霍乱弧菌小川154中的产量。这种噬菌体对该药物的体外作用具有抗性。受感染细菌的噬菌体产量显著取决于药物添加或去除的时间。药物处理过的受感染细菌的平均裂解量随着药物浓度的增加呈指数下降。噬菌体增殖的潜伏期以及隐蔽期与对照值相比没有显著变化。相对于各自的对照,每毫升0.05微克的呋喃唑酮浓度在噬菌体感染的细胞中抑制DNA合成约50%,而在未感染的细胞中仅抑制约18%。RNA和蛋白质合成在感染和未感染的细胞中受到的影响程度要小得多。根据呋喃唑酮处理过的细胞的噬菌体吸附特性对其长度进行定量推断,并与先前的电子显微镜数据相符,这表明呋喃唑酮不会影响噬菌体受体。