Stevens D L, Salmi D B, McIndoo E R, Bryant A E
Infectious Disease Section, Veterans Affairs Medical Center, Boise, ID 83702, USA.
J Infect Dis. 2000 Oct;182(4):1117-28. doi: 10.1086/315850. Epub 2000 Sep 8.
Severe invasive group A streptococcal (GAS) infections emerged in the late 1980s, yet no single virulence factor has been common to all isolates from infected patients. A strong association was recently found between isolates of such cases (regardless of M type) and the production of NAD glycohydrolase (NADase). Of interest, all M-1 strains isolated after 1988 were positive for NADase, whereas virtually all M-1 GAS were previously negative for NADase. Genetic analysis demonstrated that GAS isolates were >96% identical in nga and >99% identical in their upstream regulatory sequences. Furthermore, because NADase-negative strains did not produce immunoreactive NADase, we concluded that additional regulatory element(s) control NADase production. NADase purified from GAS altered neutrophil-directed migration and chemiluminescence responses and had potent ADP-ribosyltransferase activity. In summary, the temporal relationship of NADase expression, alone or with other streptococcal virulence factors, may contribute to the pathogenesis of invasive GAS infections.
严重侵袭性A组链球菌(GAS)感染于20世纪80年代末出现,但所有感染患者的分离株中没有单一的毒力因子是共同的。最近发现此类病例的分离株(无论M型如何)与NAD糖水解酶(NADase)的产生之间存在密切关联。有趣的是,1988年后分离的所有M-1菌株NADase呈阳性,而几乎所有以前的M-1 GAS的NADase呈阴性。遗传分析表明,GAS分离株在nga上的同一性>96%,在其上游调控序列上的同一性>99%。此外,由于NADase阴性菌株不产生免疫反应性NADase,我们得出结论,存在其他调控元件控制NADase的产生。从GAS中纯化的NADase改变了中性粒细胞定向迁移和化学发光反应,并具有强大的ADP-核糖基转移酶活性。总之,NADase表达单独或与其他链球菌毒力因子的时间关系可能有助于侵袭性GAS感染的发病机制。