Lab Microbiologia Molecolare e Biotecnologia, Dip Biologia Molecolare, Università di Siena, Siena, Italy.
PLoS One. 2012;7(3):e33320. doi: 10.1371/journal.pone.0033320. Epub 2012 Mar 13.
The aerotolerant anaerobe Streptococcus pneumoniae is part of the normal nasopharyngeal microbiota of humans and one of the most important invasive pathogens. A genomic survey allowed establishing the occurrence of twenty-one phosphotransferase systems, seven carbohydrate uptake ABC transporters, one sodium:solute symporter and a permease, underlining an exceptionally high capacity for uptake of carbohydrate substrates. Despite high genomic variability, combined phenotypic and genomic analysis of twenty sequenced strains did assign the substrate specificity only to two uptake systems. Systematic analysis of mutants for most carbohydrate transporters enabled us to assign a phenotype and substrate specificity to twenty-three transport systems. For five putative transporters for galactose, pentoses, ribonucleosides and sulphated glycans activity was inferred, but not experimentally confirmed and only one transport system remains with an unknown substrate and lack of any functional annotation. Using a metabolic approach, 80% of the thirty-two fermentable carbon substrates were assigned to the corresponding transporter. The complexity and robustness of sugar uptake is underlined by the finding that many transporters have multiple substrates, and many sugars are transported by more than one system. The present work permits to draw a functional map of the complete arsenal of carbohydrate utilisation proteins of pneumococci, allows re-annotation of genomic data and might serve as a reference for related species. These data provide tools for specific investigation of the roles of the different carbon substrates on pneumococcal physiology in the host during carriage and invasive infection.
耐氧厌氧链球菌肺炎链球菌是人类鼻咽部正常菌群的一部分,也是最重要的侵袭性病原体之一。基因组调查确定了 21 个磷酸转移酶系统、7 个碳水化合物摄取 ABC 转运蛋白、1 个钠:溶质协同转运蛋白和 1 个渗透酶的存在,这突显了其对碳水化合物底物摄取的极高能力。尽管基因组高度变异,但对 20 株测序菌株进行的表型和基因组综合分析仅将底物特异性分配给两个摄取系统。对大多数碳水化合物转运蛋白的突变体进行系统分析使我们能够为 23 个转运系统分配表型和底物特异性。对于五个假定的半乳糖、戊糖、核糖核苷和硫酸化糖的转运蛋白,推断出了它们的活性,但没有经过实验证实,只有一个转运系统的底物仍然未知,并且缺乏任何功能注释。使用代谢方法,将 32 种可发酵碳底物中的 80%分配给相应的转运蛋白。许多转运蛋白具有多种底物,许多糖由不止一种系统运输,这突出了糖摄取的复杂性和稳健性。本工作允许绘制肺炎球菌完整的碳水化合物利用蛋白武器库的功能图谱,允许对基因组数据进行重新注释,并可能作为相关物种的参考。这些数据为特定研究不同碳底物在携带和侵袭性感染期间对肺炎链球菌生理的作用提供了工具。