首页> 外文期刊>Infection and immunity >Identification of a Novel Two-Component System in Streptococcus gordonii V288 Involved in Biofilm Formation
【24h】

Identification of a Novel Two-Component System in Streptococcus gordonii V288 Involved in Biofilm Formation

机译:戈登链球菌V288中涉及生物膜形成的新型两组分系统的鉴定。

获取原文
获取外文期刊封面目录资料

摘要

Streptococcus gordonii is a pioneer colonizer of the teeth, contributing to the initiation of the oral biofilm called dental plaque. To identify genes that may be important in biofilm formation, a plasmid integration library of S. gordonii V288 was used. After screening for in vitro biofilm formation on polystyrene, a putative biofilm-defective mutant was isolated. In this mutant, pAK36 was inserted into a locus encoding a novel two-component system (bfr [biofilm formation related]) with two cotranscribed genes that form an operon. bfrA encodes a putative response regulator, while bfrB encodes a receptor histidine kinase. The bfr mutant and wild-type strain V288 showed similar growth rates in Todd-Hewitt broth (THB). A bfr-cat fusion strain was constructed. During growth in THB, the reporter activity (chloramphenicol acetyltransferase) was first detected in mid-log phase and reached a maximum in stationary phase, suggesting that transcription of bfr was growth stage dependent. After being harvested from THB, the bfr mutant adhered less effectively than did wild-type strain V288 to saliva-coated hydroxyapatite (sHA). To simulate pioneer colonization of teeth, S. gordonii V288 was incubated with sHA for 4 h in THB with 10% saliva to develop biofilms. RNA was isolated, and expression of bfrAB was estimated. In comparison to that of cells grown in suspension (free-growing cells), bfr mRNA expression by sessile cells on sHA was 1.8-fold greater and that by surrounding planktonic cells was 3.5-fold greater. Therefore, bfrAB is a novel two-component system regulated in association with S. gordonii biofilm formation in vitro.
机译:戈登链球菌(Streptococcus gordonii)是牙齿的先驱定居者,它有助于口腔生物膜的形成(称为牙菌斑)。为了鉴定在生物膜形成中可能重要的基因,请使用 S的质粒整合文库。使用gordonii V288。筛选出在聚苯乙烯上的体外生物膜形成后,分离出一个假定的生物膜缺陷突变体。在该突变体中,将pAK36插入一个编码新型双组分系统( bfr [生物膜形成相关])的基因座,该系统具有形成操纵子的两个共转录基因。 bfrA 编码一个假定的反应调节剂,而 bfrB 编码一个受体组氨酸激酶。 bfr 突变株和野生型V288在Todd-Hewitt肉汤(THB)中显示出相似的生长速率。构建了 bfr - cat 融合菌株。在THB生长期间,首先在对数中期检测到报告基因活性(氯霉素乙酰转移酶),并在稳定期达到最大值,这表明 bfr 的转录与生长期有关。从THB收获后,与野生型菌株V288相比, bfr 突变体对唾液包被的羟基磷灰石(sHA)的粘附效果较差。为了模拟牙齿的先驱定植, S。戈登氏V288与sHA在含10%唾液的THB中孵育4小时,以形成生物膜。分离RNA,并估计 bfrAB 的表达。与悬浮液中生长的细胞(自由生长的细胞)相比,无柄细胞在sHA上的 bfr mRNA表达高1.8倍,周围浮游细胞的表达高3.5倍。因此, bfrAB 是与 S相关的新型两组分系统。戈登氏菌体外生物膜形成

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号