Nobbs Angela H, Lamont Richard J, Jenkinson Howard F
Oral Microbiology Unit, Department of Oral and Dental Science, University of Bristol, Bristol BS1 2LY, United Kingdom.
Microbiol Mol Biol Rev. 2009 Sep;73(3):407-50, Table of Contents. doi: 10.1128/MMBR.00014-09.
Streptococci readily colonize mucosal tissues in the nasopharynx; the respiratory, gastrointestinal, and genitourinary tracts; and the skin. Each ecological niche presents a series of challenges to successful colonization with which streptococci have to contend. Some species exist in equilibrium with their host, neither stimulating nor submitting to immune defenses mounted against them. Most are either opportunistic or true pathogens responsible for diseases such as pharyngitis, tooth decay, necrotizing fasciitis, infective endocarditis, and meningitis. Part of the success of streptococci as colonizers is attributable to the spectrum of proteins expressed on their surfaces. Adhesins enable interactions with salivary, serum, and extracellular matrix components; host cells; and other microbes. This is the essential first step to colonization, the development of complex communities, and possible invasion of host tissues. The majority of streptococcal adhesins are anchored to the cell wall via a C-terminal LPxTz motif. Other proteins may be surface anchored through N-terminal lipid modifications, while the mechanism of cell wall associations for others remains unclear. Collectively, these surface-bound proteins provide Streptococcus species with a "coat of many colors," enabling multiple intimate contacts and interplays between the bacterial cell and the host. In vitro and in vivo studies have demonstrated direct roles for many streptococcal adhesins as colonization or virulence factors, making them attractive targets for therapeutic and preventive strategies against streptococcal infections. There is, therefore, much focus on applying increasingly advanced molecular techniques to determine the precise structures and functions of these proteins, and their regulatory pathways, so that more targeted approaches can be developed.
链球菌易于在鼻咽部的黏膜组织、呼吸道、胃肠道、泌尿生殖道以及皮肤中定殖。每个生态位都对成功定殖提出了一系列挑战,链球菌必须应对这些挑战。一些菌种与宿主处于平衡状态,既不刺激针对它们的免疫防御,也不被免疫防御所抑制。大多数是机会致病菌或真正的病原体,可引发咽炎、龋齿、坏死性筋膜炎、感染性心内膜炎和脑膜炎等疾病。链球菌作为定殖菌成功的部分原因在于其表面表达的一系列蛋白质。黏附素能够与唾液、血清和细胞外基质成分、宿主细胞以及其他微生物相互作用。这是定殖、形成复杂群落以及可能侵入宿主组织的关键第一步。大多数链球菌黏附素通过C末端的LPxTz基序锚定在细胞壁上。其他蛋白质可能通过N末端的脂质修饰锚定在表面,而其他蛋白质与细胞壁结合的机制尚不清楚。总的来说,这些表面结合蛋白为链球菌提供了一层“多彩的外衣”,使细菌细胞与宿主之间能够进行多种密切接触和相互作用。体外和体内研究已经证明许多链球菌黏附素作为定殖或毒力因子具有直接作用,这使得它们成为抗链球菌感染治疗和预防策略的有吸引力的靶点。因此,人们非常关注应用日益先进的分子技术来确定这些蛋白质的精确结构和功能及其调控途径,以便开发出更具针对性的方法。