Ontology highlight
ABSTRACT: Objective
Targeted sequencing of 16S rDNA amplicons is routinely used for microbial community profiling but this method suffers several limitations such as bias affinity of universal primers and short read size. Gene capture by hybridization represents a promising alternative. Here we used a metagenomic extract from the pea aphid Acyrthosiphon pisum to compare the performances of two widely used PCR primer pairs with DNA capture, based on solution hybrid selection.Results
All methods produced an exhaustive description of the 8 bacterial taxa known to be present in this sample. In addition, the methods yielded similar quantitative results, with the number of reads strongly correlating with quantitative PCR controls. Both methods can thus be considered as qualitatively and quantitatively robust on such a sample with low microbial complexity.
SUBMITTER: Cariou M
PROVIDER: S-EPMC6042230 | biostudies-literature | 2018 Jul
REPOSITORIES: biostudies-literature
Cariou Marie M Ribière Céline C Morlière Stéphanie S Gauthier Jean-Pierre JP Simon Jean-Christophe JC Peyret Pierre P Charlat Sylvain S
BMC research notes 20180711 1
<h4>Objective</h4>Targeted sequencing of 16S rDNA amplicons is routinely used for microbial community profiling but this method suffers several limitations such as bias affinity of universal primers and short read size. Gene capture by hybridization represents a promising alternative. Here we used a metagenomic extract from the pea aphid Acyrthosiphon pisum to compare the performances of two widely used PCR primer pairs with DNA capture, based on solution hybrid selection.<h4>Results</h4>All met ...[more]