Literature DB >> 28334218

Reconciliation between operational taxonomic units and species boundaries.

Mohamed Mysara1,2,3,4, Peter Vandamme5, Ruben Props6, Frederiek-Maarten Kerckhof6, Natalie Leys1, Nico Boon6, Jeroen Raes3,4, Pieter Monsieurs1.   

Abstract

The development of high-throughput sequencing technologies has revolutionised the field of microbial ecology via 16S rRNA gene amplicon sequencing approaches. Clustering those amplicon sequencing reads into operational taxonomic units (OTUs) using a fixed cut-off is a commonly used approach to estimate microbial diversity. A 97% threshold was chosen with the intended purpose that resulting OTUs could be interpreted as a proxy for bacterial species. Our results show that the robustness of such a generalised cut-off is questionable when applied to short amplicons only covering one or two variable regions of the 16S rRNA gene. It will lead to biases in diversity metrics and makes it hard to compare results obtained with amplicons derived with different primer sets. The method introduced within this work takes into account the differential evolutional rates of taxonomic lineages in order to define a dynamic and taxonomic-dependent OTU clustering cut-off score. For a taxonomic family consisting of species showing high evolutionary conservation in the amplified variable regions, the cut-off will be more stringent than 97%. By taking into consideration the amplified variable regions and the taxonomic family when defining this cut-off, such a threshold will lead to more robust results and closer correspondence between OTUs and species. This approach has been implemented in a publicly available software package called DynamiC. © FEMS 2017. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  16S rRNA amplicon sequencing; 16S rRNA metagenomics; DynamiC; OTU clustering; microbial biodiversity; next generation sequencing; operational taxonomic units (OTUs)

Mesh:

Substances:

Year:  2017        PMID: 28334218      PMCID: PMC5812548          DOI: 10.1093/femsec/fix029

Source DB:  PubMed          Journal:  FEMS Microbiol Ecol        ISSN: 0168-6496            Impact factor:   4.194


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