Herzberg M C, Gong K, MacFarlane G D, Erickson P R, Soberay A H, Krebsbach P H, Manjula G, Schilling K, Bowen W H
Department of Preventive Sciences, University of Minnesota, Minneapolis 55455.
Infect Immun. 1990 Feb;58(2):515-22. doi: 10.1128/iai.58.2.515-522.1990.
Certain strains of Streptococcus sanguis adhere (Adh+) selectively to human platelets and, in plasma, induce them to aggregate (Agg+) into in vitro thrombi. In this study, we examined 18 recent endocarditis and dental plaque isolates of microorganisms that were biotyped as S. sanguis for coexpression of platelet interactivity phenotypes with another possible virulence factor in bacterial endocarditis, dextran synthesis. Detectable production of extracellular glucosyltransferase ranged from 0.2 to 66 mU/mg of culture fluid for 10 representative strains tested. Production of extracellular or cell-associated glucosyltransferase, fructosyltransferase, and soluble or insoluble dextrans was not necessarily coexpressed with platelet interactivity phenotypes, since the levels of production of soluble and insoluble dextrans varied among representative Adh+ Agg+ and Adh- Agg- strains. Analysis of a second panel of 38 fresh dental plaque isolates showed that S. sanguis distributes in a reproducible manner into the possible phenotype groups. Strains with different platelet interactivity phenotypes were distinguished with a panel of four murine monoclonal antibodies (MAbs) raised against Adh+ Agg+ strain 133-79 and screened to rule out artifactual reactions with antigenic components in culture media. The MAbs reacted selectively with Adh+ Agg+ strains in a direct-binding, whole-cell, enzyme-linked immunosorbent assay and also inhibited their interactions with platelets. Analysis of minimal tryptic digests of many strains, including variants that failed to bind the MAbs, suggested that some noninteractivity phenotypes possess cryptic surface determinants. Since the ability to adhere to platelets and induce them to aggregate is relatively stable, these traits may be useful in a phenotyping scheme for these Lancefield nontypeable streptococci.
某些血链球菌菌株可选择性地黏附(Adh+)于人类血小板,并在血浆中诱导血小板聚集(Agg+)形成体外血栓。在本研究中,我们检测了18株近期从心内膜炎和牙菌斑中分离出的经生物分型为血链球菌的微生物,以研究血小板相互作用表型与细菌性心内膜炎中另一种可能的毒力因子——葡聚糖合成的共表达情况。对于所检测的10株代表性菌株,细胞外葡糖基转移酶的可检测产量范围为0.2至66 mU/mg培养液。细胞外或细胞相关的葡糖基转移酶、果糖基转移酶以及可溶性或不溶性葡聚糖的产生并不一定与血小板相互作用表型共表达,因为可溶性和不溶性葡聚糖的产生水平在代表性的Adh+ Agg+和Adh- Agg-菌株中有所不同。对另一组38株新鲜牙菌斑分离株的分析表明,血链球菌以可重复的方式分布于可能的表型组中。用针对Adh+ Agg+菌株133 - 79制备的一组四种鼠单克隆抗体(MAb)区分了具有不同血小板相互作用表型的菌株,并进行筛选以排除与培养基中抗原成分的人为反应。这些单克隆抗体在直接结合的全细胞酶联免疫吸附试验中与Adh+ Agg+菌株选择性反应,并且还抑制它们与血小板的相互作用。对许多菌株(包括未能结合单克隆抗体的变体)的最小胰蛋白酶消化产物的分析表明,一些非相互作用表型具有隐蔽的表面决定簇。由于黏附于血小板并诱导其聚集的能力相对稳定,这些特性可能有助于对这些兰斯菲尔德不可分型链球菌进行表型分析。