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一种新型小分子在体外和体内均可抑制变形链球菌生物膜。

A new small molecule inhibits Streptococcus mutans biofilms in vitro and in vivo.

作者信息

Pan W, Fan M, Wu H, Melander C, Liu C

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-Most) & Key Laboratory for Oral Biomedical Engineering of Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China.

Department of Pediatric Dentistry, UAB School of Dentistry, Birmingham, AL, USA.

出版信息

J Appl Microbiol. 2015 Nov;119(5):1403-11. doi: 10.1111/jam.12940. Epub 2015 Sep 24.

Abstract

AIMS

The aim of this study was to identify new small molecules that can inhibit Streptococcus mutans biofilms by in vitro and in vivo model.

METHODS AND RESULTS

We evaluated the effect of a small molecule 2-amino-imidazole/triazole conjugate (2-AI/T) on the formation of Strep. mutans biofilms by culturing in 96-well plates. Toxicity was assessed through cell culture and intragastrically administering to mice. The anti-biofilm and anti-caries effects were investigated in vivo. The inhibitive mechanism was detected by isobaric tag for relative and absolute quantification (itraq) and RT-QPCR. In vitro and in vivo study revealed that 2-AI/T significantly inhibited biofilm formation of Strep. mutans and is more so than inhibiting planktonic cells without toxicity. The ribosome and histidine metabolism pathways of Strep. mutans were significantly regulated by this compound.

CONCLUSIONS

These results suggest that the 2-AI/T conjugate is a potent inhibitor that can be potentially developed into a new drug to treat and prevent dental caries.

SIGNIFICANCE AND IMPACT OF THE STUDY

This is the first study to use small molecule from marine natural products, to protect from dental caries in vivo. It has potential broad range application in clinical caries prevention, or as a bioactive ingredient for food applications.

摘要

目的

本研究旨在通过体外和体内模型鉴定能够抑制变形链球菌生物膜的新型小分子。

方法与结果

我们通过在96孔板中培养来评估小分子2-氨基咪唑/三唑共轭物(2-AI/T)对变形链球菌生物膜形成的影响。通过细胞培养和对小鼠灌胃来评估其毒性。在体内研究其抗生物膜和抗龋效果。通过相对和绝对定量等压标签法(itraq)和RT-QPCR检测其抑制机制。体外和体内研究表明,2-AI/T能显著抑制变形链球菌生物膜的形成,且对浮游细胞的抑制作用更强,且无毒性。该化合物能显著调节变形链球菌的核糖体和组氨酸代谢途径。

结论

这些结果表明,2-AI/T共轭物是一种有效的抑制剂,有可能开发成一种治疗和预防龋齿的新药。

研究的意义和影响

这是第一项使用海洋天然产物小分子在体内预防龋齿的研究。它在临床龋齿预防或作为食品应用的生物活性成分方面具有潜在的广泛应用。

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本文引用的文献

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Regulation of the histidine utilization (hut) system in bacteria.
Microbiol Mol Biol Rev. 2012 Sep;76(3):565-84. doi: 10.1128/MMBR.00014-12.

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