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Volume 47 Number 5
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Volume 47 Number 4 Volume 47 Number 5

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Research articles

ScienceAsia 47 (2021): 567-577 |doi: 10.2306/scienceasia1513-1874.2021.073


Influence of DNA extraction methods and 16S rRNA targeted hypervariable regions on microbial diversity profiling of dental plaque and saliva


Sree Sankar Darveekaran Naira,b, Pengfei Zhua, Yogendra Bhaskara,b, Fei Tenga,c,*

 
ABSTRACT:     The application of high-throughput sequencing has revolutionized our ability to investigate the microbiota composition of complex oral ecosystems. One such approach is through 16S rRNA sequencing. Deciphering this diverse microbial community using such approach is more accurate than traditional culture-based methods. Numerous factors such as primer selection, DNA extraction methods, and sequencing platforms may compromise the results. Therefore, these factors need to be considered carefully for studies such as microbial diversity analysis and microbial abundance determination. Here, we evaluated the effect of two DNA extraction methods (soil and swab DNA extraction kits) and targeted 16S rRNA hypervariable regions (V1V3 and V3V4) on plaque and saliva sample types to investigate the diverse microbes in oral samples of five Chinese citizens. Both of the extraction methods were successful in determining the relative abundance of microbes; however, relative abundance percentage of the species reported by the soil extraction method with the hypervariable region V1V3 is higher in both sample types. The relative taxonomical abundance of microbes at OTU level of species represented by the V3V4 region is lower; nonetheless, the number of unshared species identified is higher using this region. Both of the hypervariable regions identified unshared species in plaque and saliva sample types. Thus, choice of DNA extraction methods and hypervariable regions greatly influence the representation of oral microbial diversity in plaque and saliva. This study provides a guide to future studies to portray and quantify the human oral microbiota.

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a Single-Cell Center, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong 266101 China
b University of Chinese Academy of Science, Beijing 100049 China
c Department of Stomatology, Qingdao Municipal Hospital, Qingdao, Shandong 266101 China

* Corresponding author, E-mail: tengfei@qibebt.ac.cn

Received 7 Jun 2020, Accepted 3 May 2021