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在变形链球菌GS-5菌株中检测到的gbpC和pac基因突变。

gbpC and pac gene mutations detected in Streptococcus mutans strain GS-5.

作者信息

Sato Y, Okamoto K, Kizaki H

机构信息

Department of Biochemistry, Tokyo Dental College, 2-2, Masago 1-chome, Mihama-ku, Chiba City, 261-8502 Japan.

出版信息

Oral Microbiol Immunol. 2002 Aug;17(4):263-6. doi: 10.1034/j.1399-302x.2002.170410.x.

Abstract

The Streptococcus mutans gbpC gene encoding cell wall-anchoring glucan-binding protein C is involved in the dextran(alpha-1,6 glucan)-dependent aggregation (ddag) of this organism. Unlike cells of other strains of S. mutans, strain GS-5 cells did not exhibit dextran(alpha-1,6 glucan)-dependent aggregation under any conditions. We therefore hypothesized that the gbpC gene may be mutated in strain GS-5. Sequencing analysis of the 1752-nucleotide GS-5 gbpC gene revealed a point mutation that switched codon 65 to a TAA termination codon. Strain GS-5 was previously reported also to have a mutation in the pac gene encoding the cell wall-anchored major protein antigen. The laboratory-maintained strain GS-5 is regarded as having lower cariogenicity than the original isolate. The decreased cariogenicity developed during the laboratory culture of strain GS-5 may have been caused by mutations in an environment lacking appropriate selective pressures.

摘要

编码细胞壁锚定葡聚糖结合蛋白C的变形链球菌gbpC基因参与该生物体的葡聚糖(α-1,6-葡聚糖)依赖性聚集(ddag)。与其他变形链球菌菌株的细胞不同,GS-5菌株的细胞在任何条件下均未表现出葡聚糖(α-1,6-葡聚糖)依赖性聚集。因此,我们推测gbpC基因可能在GS-5菌株中发生了突变。对1752个核苷酸的GS-5 gbpC基因进行测序分析,发现一个点突变,该突变将第65位密码子转换为TAA终止密码子。先前也有报道称,GS-5菌株在编码细胞壁锚定主要蛋白抗原的pac基因中存在突变。实验室保存的GS-5菌株被认为比原始分离株的致龋性更低。GS-5菌株在实验室培养过程中致龋性降低可能是由于在缺乏适当选择压力的环境中发生了突变。

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