Herzberg M C, Brintzenhofe K L
Infect Immun. 1983 Apr;40(1):120-5. doi: 10.1128/iai.40.1.120-125.1983.
To explore the possibility that Streptococcus sanguis aggregation of platelet-rich plasma (PRP) might be mediated by soluble agents, we tested cell-free S. sanguis supernatant for aggregation activity. The supernatant of untreated S. sanguis was without measurable PRP aggregation activity. In contrast, the cell-free supernatant of ATP-incubated S. sanguis produced an immediate wave of PRP aggregation. The supernatant with PRP aggregating activity contained insufficient protease to produce a response. The response increased with the time of incubation with ATP. Active supernatant was desalted and chromatographed on nucleotide-calibrated columns of Dowex 1-X8. An active ADP function was identified. The activity was insensitive to dicyclohexylcarbodiimide, but was sensitive to both Ca2+ and Ca2+-Mg2+ chelating agents, cold (4 degrees C), heat (80 degrees C), pH (optimum between pH 7 and 8), apyrase, and sodium molybdate. In addition, preincubation of PRP with adenosine inhibited activity. Strains of viridans streptococci were screened for activity. Aggregation-promoting strains showed two times more activity than did other strains. Although it was not vigorously excluded that the ADP was discharged from the microbes, the existence of an exogenous ATPase on S. sanguis was strongly suggested. The expression of the activity was associated with the lag time to onset of PRP aggregation with intact S. sanguis. This activity could, therefore, be a synergistic promoter of PRP aggregation and an additional virulence factor in endocarditis.
为了探究血链球菌对富血小板血浆(PRP)的聚集作用是否可能由可溶性介质介导,我们检测了无细胞的血链球菌上清液的聚集活性。未经处理的血链球菌的上清液没有可测量的PRP聚集活性。相比之下,经ATP孵育的血链球菌的无细胞上清液立即引发了PRP的聚集。具有PRP聚集活性的上清液中蛋白酶含量不足以产生反应。该反应随与ATP孵育时间的延长而增强。将活性上清液脱盐后,在经核苷酸校准的Dowex 1-X8柱上进行色谱分析。鉴定出一种活性ADP功能。该活性对二环己基碳二亚胺不敏感,但对Ca2+和Ca2+-Mg2+螯合剂、低温(4℃)、高温(80℃)、pH(最适pH在7至8之间)、腺苷三磷酸双磷酸酶和钼酸钠敏感。此外,PRP与腺苷预孵育会抑制活性。对草绿色链球菌菌株进行了活性筛选。促进聚集的菌株的活性比其他菌株高两倍。尽管不能完全排除ADP是从微生物中释放出来的,但强烈提示血链球菌存在外源性ATP酶。该活性的表达与完整血链球菌引发PRP聚集的延迟时间有关。因此,这种活性可能是PRP聚集的协同促进因子,也是心内膜炎中的一种额外毒力因子。