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Adhesion of glucosyltransferase phase variants to Streptococcus gordonii bacterium-glucan substrata may involve lipoteichoic acid.

机译:葡糖基转移酶相变体对戈登链球菌细菌-葡聚糖基质的粘附可能涉及脂磷壁酸。

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摘要

Growing Streptococcus gordonii Spp+ phase variants, which have normal levels of glucosyltransferase (GTF) activity, use sucrose to promote their accumulation on surfaces by forming a cohesive bacterium-insoluble glucan polymer mass (BPM). Spp- phase variants, which have lower levels of GTF activity, do not form BPMs and do not remain in BPMs formed by Spp+ cells when grown in mixed cultures. To test the hypothesis that segregation of attached Spp+ and unattached Spp- cells was due to differences in adhesiveness, adhesion between washed, [3H]thymidine-labeled cells and preformed BPM substrata was measured. Unexpectedly, the results showed that cells of both phenotypes, as well as GTF-negative cells, attached equally well to preformed BPMs, indicating that attachment to BPMs was independent of cell surface GTF activity. Initial characterization of this binding interaction suggested that a protease-sensitive component on the washed cells may be binding to lipoteichoic acids sequestered in the BPM, since exogenous lipoteichoic acid inhibited adhesion. Surprisingly, the adhesion of both Spp+ and Spp- cells was markedly inhibited in the presence of sucrose, which also released lipoteichoic acid from the BPM. These in vitro findings suggest that, in vivo, sucrose and lipoteichoic acid may modify dental plaque development by enhancing or inhibiting the attachment of additional bacteria.
机译:具有正常水平的葡萄糖基转移酶(GTF)活性的不断增长的戈登链球菌Spp +相变体使用蔗糖通过形成粘性细菌不溶性葡聚糖聚合物团块(BPM)来促进其在表面上的积累。在混合培养中生长时,具有较低GTF活性水平的Spp-相变体不会形成BPM,也不会保留在Spp +细胞形成的BPM中。为了检验以下假设:附着的Spp +和未附着的Spp-细胞的分离是由于粘附力的差异所致,测量了洗涤过的[3H]胸苷标记的细胞与预先形成的BPM基质之间的粘附力。出乎意料的是,结果表明,两种表型的细胞以及GTF阴性的细胞均能很好地附着于预先形成的BPM,这表明与BPM的附着与细胞表面GTF活性无关。这种结合相互作用的初步特征表明,洗涤过的细胞上的蛋白酶敏感成分可能与BPM中螯合的脂蛋白结合,因为外源脂蛋白酸抑制了粘附。令人惊讶地,在蔗糖的存在下,Spp +和Spp-细胞的粘附均被显着抑制,这也从BPM中释放了脂磷壁酸。这些体外发现表明,在体内,蔗糖和脂蛋白酸可以通过增强或抑制其他细菌的附着来改变牙菌斑的发育。

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