Cope L D, Pelzel S E, Latimer J L, Hansen E J
Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235.
Infect Immun. 1990 Oct;58(10):3312-8. doi: 10.1128/iai.58.10.3312-3318.1990.
An isogenic mutant of Haemophilus influenzae type b (Hib) lacking the ability to express the P2 major outer membrane (porin) protein was constructed and characterized in various model systems. Linker insertion mutagenesis of a cloned Hib DNA insert containing the P2 structural gene was used in conjunction with a genetic transformation system to obtain a transformant unreactive with a P2-specific monoclonal antibody. This transformant was shown to lack detectable P2 protein by both protein staining and immunoblot methods. The P2 mutant exhibited a generation time in complex broth medium that was significantly longer than that of the wild-type parent strain. The P2 mutant was also unable to produce detectable bacteremia in infant rats after intraperitoneal challenge, while the wild-type parent strain produced bacteremia in all animals challenged with this strain. Reintroduction of a wild-type copy of the P2 gene into this mutant yielded a transformant strain that had a generation time in vitro identical to that of the wild-type parent strain and that was also fully virulent in the infant rat model. These findings suggest that the ability to synthesize the P2 protein may be necessary but not sufficient for full expression of virulence by this pathogen.
构建了缺乏表达b型流感嗜血杆菌(Hib)P2主要外膜(孔蛋白)蛋白能力的同基因突变体,并在各种模型系统中对其进行了表征。使用含有P2结构基因的克隆Hib DNA插入片段的接头插入诱变技术,结合遗传转化系统,获得了与P2特异性单克隆抗体无反应的转化体。通过蛋白质染色和免疫印迹方法均显示该转化体缺乏可检测到的P2蛋白。P2突变体在复合肉汤培养基中的代时明显长于野生型亲本菌株。在腹腔注射后,P2突变体也无法在幼鼠中产生可检测到的菌血症,而野生型亲本菌株在用该菌株攻击的所有动物中均产生了菌血症。将P2基因的野生型拷贝重新引入该突变体后,得到了一个转化菌株,其体外代时与野生型亲本菌株相同,并且在幼鼠模型中也具有完全的毒力。这些发现表明,合成P2蛋白的能力对于该病原体充分表达毒力可能是必要的,但不是充分的。