Del Rio C, Stephens D S, Knapp J S, Rice R J, Schalla W O
Veterans Administration Medical Center, Atlanta, Georgia 30033.
J Clin Microbiol. 1989 May;27(5):1045-9. doi: 10.1128/jcm.27.5.1045-1049.1989.
We studied a previously healthy 20-year-old woman who presented with gonococcal meningitis. The gonococcal isolate, HT-1, was prototrophic by auxotyping, was protein I serovar IB-1, and agglutinated with wheat germ lectin. This isolate differed from the proline-requiring, serovar IA-1 and IB-4, wheat germ-agglutination-negative gonococcal isolates recovered from three patients during a recent outbreak of gonococcal meningitis in Philadelphia. HT-1 was killed by normal pooled human sera (greater than or equal to 98% at 30 min) but not effectively killed by the convalescent-phase sera of the patient (greater than 30% survival at 30 min). Similar results were obtained when mucosal and cerebrospinal fluid isolates from a Philadelphia patient were exposed to these sera, but mucosal and blood isolates from another Philadelphia case showed increased resistance to killing by normal pooled human sera. Further characterization revealed multiple differences in outer membrane and cellular proteins and lipopolysaccharide between case isolates. Absence of the L8 lipopolysaccharide epitope was noted for all isolates. Sera of our patient were found to have low total hemolytic complement (CH100 = 21 U/ml; normal = 55 to 100 U/ml) due to deficiency of C8 (C8 less than 1,000 CH50 U/ml; normal = greater than or equal to 16,000 CH50 U/ml). This is the first reported case of gonococcal meningitis occurring in a patient with a terminal-complement deficiency. Gonococcal meningitis is a rare complication of gonococcal bacteremia. Both defects in host defenses (e.g., terminal-complement deficiency) and organisms with unusual virulence appear to contribute to the pathogenesis of this complication of gonococcal bacteremia.
我们研究了一名既往健康的20岁女性,她患有淋菌性脑膜炎。分离出的淋球菌HT-1通过营养型分类为原养型,蛋白I血清型为IB-1,能与麦胚凝集素发生凝集反应。该分离株与近期费城淋菌性脑膜炎暴发期间从3例患者中分离出的需要脯氨酸、血清型为IA-1和IB-4、麦胚凝集反应阴性的淋球菌分离株不同。HT-1被正常人混合血清杀死(30分钟时大于或等于98%),但未被该患者的恢复期血清有效杀死(30分钟时存活率大于30%)。当将费城一名患者的黏膜和脑脊液分离株暴露于这些血清时,也得到了类似结果,但另一名费城患者的黏膜和血液分离株对正常人混合血清杀伤的抵抗力增强。进一步的特性分析显示病例分离株在外膜、细胞蛋白和脂多糖方面存在多种差异。所有分离株均未检测到L8脂多糖表位。我们发现该患者的血清总溶血补体水平较低(CH100 = 21 U/ml;正常范围为55至100 U/ml),原因是C8缺乏(C8小于1000 CH50 U/ml;正常范围为大于或等于16000 CH50 U/ml)。这是首次报道的一例在终末补体缺乏患者中发生的淋菌性脑膜炎病例。淋菌性脑膜炎是淋菌血症的一种罕见并发症。宿主防御缺陷(如终末补体缺乏)和具有异常毒力的病原体似乎都与这种淋菌血症并发症的发病机制有关。