van Belkum Alex
Erasmus MC, Department of Medical Microbiology and Infectious Diseases, Unit Research and Development, Rotterdam, The Netherlands.
Curr Opin Infect Dis. 2006 Aug;19(4):339-44. doi: 10.1097/01.qco.0000235159.40184.61.
This review identifies trends in the study of interactions between Staphylococcus aureus and humans. When nasal colonization is in the neutral state, infection clearly represents a state of host-pathogen disbalance. The features leading from apparent homeostatic colonization to pathogenesis are identified at an increasing rate.
Persistent carriage of S. aureus predisposes to infection but limits bacteraemia-associated mortality. Intermittent carriage is usually imposed and of lesser clinical relevance. The nature and function of several staphylococcal virulence factors have been elucidated and near complete gene catalogues have been established. There does not seem to be a difference in virulence, however, between methicillin-susceptible and resistant S. aureus. Biological selection takes place in the nose and innate immune features relevant to colonization have been discovered. Acquired immunity remains underexposed, but the host factors involved in the host-pathogen interaction have been identified.
Virulence assessment of S. aureus has been facilitated by novel technology: genome-wide inventories of virulence potential can be made and new pathogenic mechanisms have been presumptively identified. These involve invasion procedures but also (innate) immune evasion strategies. These cross-fertilizing developments shed light on the feasibility of novel prophylactic or therapeutic strategies for combating staphylococcal carriage and disease.
本综述确定了金黄色葡萄球菌与人类相互作用研究的趋势。当鼻腔定植处于中性状态时,感染显然代表了宿主 - 病原体失衡的一种状态。从明显的稳态定植到发病机制的特征正以越来越快的速度被确定。
金黄色葡萄球菌的持续携带易引发感染,但可降低菌血症相关的死亡率。间歇性携带通常是被动的,临床相关性较小。几种葡萄球菌毒力因子的性质和功能已得到阐明,并且已建立了近乎完整的基因目录。然而,甲氧西林敏感和耐药的金黄色葡萄球菌在毒力方面似乎没有差异。在鼻腔中会发生生物选择,并且已发现与定植相关的固有免疫特征。获得性免疫仍未得到充分研究,但已确定了参与宿主 - 病原体相互作用的宿主因素。
新技术促进了金黄色葡萄球菌的毒力评估:可以进行全基因组毒力潜力清单分析,并初步确定了新的致病机制。这些机制不仅涉及侵袭过程,还包括(固有)免疫逃避策略。这些相互促进的进展为对抗葡萄球菌携带和疾病的新型预防或治疗策略的可行性提供了线索。