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基于功能宏基因组学的口腔菌斑微生物组耐酸基因

Acid-resistant genes of oral plaque microbiome from the functional metagenomics.

作者信息

Zhang Meng, Zheng Yuqiao, Li Yuhong, Jiang Han, Huang Yuping, Du Minquan

机构信息

MOST KLOS & KLOBM, School & Hospital of Stomatology, Wuhan University, Wuhan, China.

Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Wuhan University, Wuhan, China.

出版信息

J Oral Microbiol. 2018 Jan 30;10(1):1424455. doi: 10.1080/20002297.2018.1424455. eCollection 2018.

Abstract

Acid resistance is one of key properties assisting the survival of cariogenic bacteria in a dental caries environment, but only a few genes conferring acid resistance have been identified to data. Functional metagenomics provides a systematic method for investigating commensal DNA to identify genes that encode target functions. Here, the host strain Escherichia coli DH10B and a constructed bidirectional transcription vector pSKII-lacZ contributed to the construction of a metagenomic library, and 46.6 Mb of metagenomic DNA was cloned from carious supragingival plaque of 8children along with screening for lethal functionality. The screen identified 2 positive clones that exhibited a similar aciduric phenotype to that of the positive controls. Bioinformatic analysis revealed that these two genes encoded an ATP/GTP-binding protein and a malate dehydrogenase. Moreover, we also performed functional screening of Streptococcus mutans, since it is one of the predominant cariogenic strains but was not identified in our initial screening. Five positive clones were retrieved. In conclusion, our improved functional metagenomics screening method helped in the identification of important acid resistance genes, thereby providing new insights into the mechanism underlying caries formation as well as in the prevention and treatment of early childhood caries (ECC).

摘要

耐酸性是有助于致龋菌在龋齿环境中存活的关键特性之一,但迄今为止仅鉴定出少数几个赋予耐酸性的基因。功能宏基因组学提供了一种系统方法,用于研究共生DNA以鉴定编码目标功能的基因。在此,宿主菌株大肠杆菌DH10B和构建的双向转录载体pSKII-lacZ有助于构建宏基因组文库,从8名儿童的龋损龈上菌斑中克隆了46.6 Mb的宏基因组DNA,并筛选了致死功能。筛选鉴定出2个阳性克隆,其表现出与阳性对照相似的耐酸表型。生物信息学分析表明,这两个基因编码一种ATP/GTP结合蛋白和一种苹果酸脱氢酶。此外,我们还对变形链球菌进行了功能筛选,因为它是主要的致龋菌株之一,但在我们的初始筛选中未被鉴定出来。获得了5个阳性克隆。总之,我们改进的功能宏基因组学筛选方法有助于鉴定重要的耐酸性基因,从而为龋齿形成的潜在机制以及幼儿龋齿(ECC)的预防和治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea81/5795652/847280c3f17b/ZJOM_A_1424455_F0001_C.jpg

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