Department of Cariology and Comprehensive Care, New York University College of Dentistry, New York, New York, United States of America.
PLoS One. 2013;8(2):e56305. doi: 10.1371/journal.pone.0056305. Epub 2013 Feb 14.
Glucosyltransferases (Gtfs) catalyze the synthesis of glucans from sucrose and are produced by several species of lactic-acid bacteria. The oral bacterium Streptococcus mutans produces large amounts of glucans through the action of three Gtfs. GtfD produces water-soluble glucan (WSG), GtfB synthesizes water-insoluble glucans (WIG) and GtfC produces mainly WIG but also WSG. These enzymes, especially those synthesizing WIG, are of particular interest because of their role in the formation of dental plaque, an environment where S. mutans can thrive and produce lactic acid, promoting the formation of dental caries. We sequenced the gtfB, gtfC and gtfD genes from several mutans streptococcal strains isolated from the oral cavity of humans and searched for their homologues in strains isolated from chimpanzees and macaque monkeys. The sequence data were analyzed in conjunction with the available Gtf sequences from other bacteria in the genera Streptococcus, Lactobacillus and Leuconostoc to gain insights into the evolutionary history of this family of enzymes, with a particular emphasis on S. mutans Gtfs. Our analyses indicate that streptococcal Gtfs arose from a common ancestral progenitor gene, and that they expanded to form two clades according to the type of glucan they synthesize. We also show that the clade of streptococcal Gtfs synthesizing WIG appeared shortly after the divergence of viviparous, dentate mammals, which potentially contributed to the formation of dental plaque and the establishment of several streptococci in the oral cavity. The two S. mutans Gtfs capable of WIG synthesis, GtfB and GtfC, are likely the product of a gene duplication event. We dated this event to coincide with the divergence of the genomes of ancestral early primates. Thus, the acquisition and diversification of S. mutans Gtfs predates modern humans and is unrelated to the increase in dietary sucrose consumption.
葡糖基转移酶(Gtfs)催化蔗糖合成葡聚糖,由几种乳杆菌产生。口腔细菌变异链球菌通过三种 Gtfs 产生大量葡聚糖。GtfD 产生水溶性葡聚糖(WSG),GtfB 合成水不溶性葡聚糖(WIG),GtfC 主要产生 WIG,但也产生 WSG。这些酶,特别是那些合成 WIG 的酶,因其在牙菌斑形成中的作用而受到特别关注,牙菌斑是变异链球菌能够茁壮成长并产生乳酸的环境,促进龋齿的形成。我们从人类口腔分离的变异链球菌株中测序了 gtfB、gtfC 和 gtfD 基因,并在从黑猩猩和猕猴分离的菌株中搜索它们的同源物。将序列数据与其他细菌属中的链球菌、乳杆菌和肠膜明串珠菌中的可用 Gtf 序列一起进行分析,以深入了解该酶家族的进化历史,特别关注变异链球菌 Gtfs。我们的分析表明,链球菌 Gtfs 起源于一个共同的祖先基因,并根据它们合成的葡聚糖类型扩展形成两个分支。我们还表明,合成 WIG 的链球菌 Gtfs 分支出现在胎生、有齿哺乳动物分化后不久,这可能有助于牙菌斑的形成和口腔中几种链球菌的定植。能够合成 WIG 的两种变异链球菌 Gtfs,GtfB 和 GtfC,可能是基因复制事件的产物。我们将这一事件的发生时间追溯到早期灵长类动物基因组分化的时候。因此,变异链球菌 Gtfs 的获得和多样化发生在现代人类之前,与饮食中蔗糖消耗的增加无关。