Department of Medicine, Institute for Therapeutic Innovation, University of Florida, School of Medicine, Lake Nona, Florida, USA.
Antimicrob Agents Chemother. 2013 May;57(5):2010-5. doi: 10.1128/AAC.02504-12. Epub 2013 Feb 12.
After a relatively short untreated interval, pneumonic plague has a mortality approaching 100%. We employed a murine model of aerosol challenge with Yersinia pestis to investigate the early course of pneumonic plague in the lung, blood, and spleen. We fit a mathematical model to all data simultaneously. The model fit to the data was acceptable. The number of organisms in the lung at baseline was estimated to be 135 (median) or 1,184 (mean) CFU/g. The doubling time was estimated as 1.5 to 1.7 h. Between 1 and 12 h postexposure, counts declined, but they then increased by 24 h, a finding hypothesized to be due to innate immunity. The model predicted that innate immunity declined with a half-time of 3 to 3.8 h. The threshold for bacteremia was 6.4 × 10(4) to 1.52 × 10(6) CFU/g. By 42 to 48 h, stationary phase was obtained. Lung bacterial burdens exceeded 10 log CFU/g. Obviating early defenses allows for rapid amplification of Y. pestis in bacteremia, making the rapid course with high mortality understandable.
未经治疗的潜伏期相对较短,肺鼠疫的死亡率接近 100%。我们使用鼠疫耶尔森菌气溶胶感染的小鼠模型,研究了肺部、血液和脾脏中肺鼠疫的早期发病过程。我们对所有数据同时拟合了一个数学模型。模型对数据的拟合是可以接受的。肺脏中细菌数量在基线时估计为 135(中位数)或 1184(平均值)CFU/g。倍增时间估计为 1.5 至 1.7 小时。暴露后 1 至 12 小时,细菌数量减少,但在 24 小时后增加,这一发现假设是由于先天免疫。该模型预测先天免疫的半衰期为 3 至 3.8 小时。菌血症的阈值为 6.4×10(4)至 1.52×10(6)CFU/g。42 至 48 小时时,达到稳定期。肺部细菌负荷超过 10 log CFU/g。先天防御的消除使鼠疫耶尔森菌在菌血症中迅速扩增成为可能,从而使病情迅速发展和高死亡率变得可以理解。