Goodwin M S, Weiss A A
Department of Microbiology and Immunology, Medical College of Virginia, Richmond 23298.
Infect Immun. 1990 Oct;58(10):3445-7. doi: 10.1128/iai.58.10.3445-3447.1990.
Proliferation of Bordetella pertussis in the lungs of infant mice challenged by the intranasal route was examined. The bacteria rapidly proliferated in the lungs of mice challenged with a sublethal dose of a wild-type strain (BP338) or a filamentous hemagglutinin mutant (BPM409) from 500 at day 0 to 10(7) at day 15. The infection cleared in about 40 days. Pertussis toxin-deficient mutant BP357 gave a similar profile; however, the number of bacteria recovered was slightly reduced, suggesting that pertussis toxin is not essential for bacterial growth in the lungs. In contrast, adenylate cyclase toxin mutant BP348 was rapidly cleared from the lungs, with no viable bacteria remaining 10 days postchallenge, suggesting that the adenylate cyclase toxin is a colonization factor required for the bacteria to initiate infection.
对经鼻途径感染的幼鼠肺部中百日咳博德特氏菌的增殖情况进行了研究。用亚致死剂量的野生型菌株(BP338)或丝状血凝素突变体(BPM409)攻击小鼠后,细菌在小鼠肺部迅速增殖,从第0天的500个增至第15天的10⁷个。感染在约40天内清除。百日咳毒素缺陷突变体BP357呈现出类似的情况;然而,回收的细菌数量略有减少,这表明百日咳毒素对于细菌在肺部的生长并非必不可少。相比之下,腺苷酸环化酶毒素突变体BP348在肺部迅速清除,攻击后10天无存活细菌残留,这表明腺苷酸环化酶毒素是细菌引发感染所需的定植因子。