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不同底物/生长培养基对唾液源生物膜微生物群落的影响。

Effects of different substrates/growth media on microbial community of saliva-derived biofilm.

作者信息

Li Bolei, Zhou Xinxuan, Zhou Xuedong, Wu Ping, Li Mingyun, Feng Mingye, Peng Xian, Ren Biao, Cheng Lei

机构信息

State Key Laboratory of Oral Diseases, Sichuan University, 610041 Chengdu, China.

Department of Operative Dentistry and Endodontics, West China Hospital of Stomatology, Sichuan University, 610041 Chengdu, China.

出版信息

FEMS Microbiol Lett. 2017 Jul 6;364(13). doi: 10.1093/femsle/fnx123.

Abstract

The aims of this study were to investigate the effects of substrates (glass versus hydroxyapatite [HA]) and growth media (SHI medium versus a modified artificial saliva medium with cysteine) on the microbial community of saliva-derived biofilm in vitro. 16S rRNA gene sequencing technology was used to analyze the microbial community of saliva-derived biofilm cultured for 72 h anaerobically. The metagenomes of biofilms were predicted from the clusters of orthologous groups. No significant difference was found between the saliva-derived biofilms grown on HA and glass in ACE, Chao, Shannon and Simpson indices. The abundances of only a few bacteria on HA were significantly different from those on glass with a low relative abundance (<0.5%). Compared with the biofilms developed in a modified artificial saliva medium with cysteine, biofilms in SHI medium were significantly higher (P < 0.05) in diversity. Linear discriminant analysis coupled with effect size measurement showed that some obligate anaerobic genera (Lactobacillus, Veillonella, Porphyromonas and Leptotrichia) were more abundant in SHI medium biofilms. The biofilms grown in different media were also significantly different in predicted gene categories. In conclusion, the growth media, not the substrates, have significant effects on the microbial community of saliva-derived biofilm in vitro.

摘要

本研究的目的是调查底物(玻璃与羟基磷灰石[HA])和生长培养基(SHI培养基与含半胱氨酸的改良人工唾液培养基)对体外唾液衍生生物膜微生物群落的影响。采用16S rRNA基因测序技术分析厌氧培养72小时的唾液衍生生物膜的微生物群落。从直系同源簇预测生物膜的宏基因组。在ACE、Chao、Shannon和Simpson指数方面,在HA和玻璃上生长的唾液衍生生物膜之间未发现显著差异。HA上只有少数细菌的丰度与玻璃上的细菌丰度存在显著差异,相对丰度较低(<0.5%)。与在含半胱氨酸的改良人工唾液培养基中形成的生物膜相比,SHI培养基中的生物膜多样性显著更高(P<0.05)。线性判别分析结合效应大小测量表明,一些专性厌氧属(乳酸杆菌属、韦荣球菌属、卟啉单胞菌属和纤毛菌属)在SHI培养基生物膜中更为丰富。在不同培养基中生长的生物膜在预测的基因类别上也存在显著差异。总之,生长培养基而非底物对体外唾液衍生生物膜的微生物群落有显著影响。

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