RT Journal Article SR Electronic T1 Using MinION™ to characterize dog skin microbiota through full-length 16S rRNA gene sequencing approach JF bioRxiv FD Cold Spring Harbor Laboratory SP 167015 DO 10.1101/167015 A1 Anna Cuscó A1 Joaquim Viñes A1 Sara D’Andreano A1 Francesca Riva A1 Joaquim Casellas A1 Armand Sánchez A1 Olga Francino YR 2017 UL http://biorxiv.org/content/early/2017/07/21/167015.abstract AB The most common strategy to assess microbiota is sequencing specific hypervariable regions of 16S rRNA gene using 2nd generation platforms (such as MiSeq or Ion Torrent PGM). Despite obtaining high-quality reads, many sequences fail to be classified at the genus or species levels due to their short length. This pitfall can be overcome sequencing the full-length 16S rRNA gene (1,500bp) by 3rd generation sequencers.We aimed to assess the performance of nanopore sequencing using MinION™ on characterizing microbiota complex samples. First set-up step was performed using a staggered mock community (HM-783D). Then, we sequenced a pool of several dog skin microbiota samples previously sequenced by Ion Torrent PGM. Sequences obtained for full-length 16S rRNA with degenerated primers retrieved increased richness estimates at high taxonomic level (Bacteria and Archaea) that were missed with short-reads. Besides, we were able to obtain taxonomic assignments down to species level, although it was not always feasible due to: i) incomplete database; ii) primer set chosen; iii) low taxonomic resolution of 16S rRNA gene within some genera; and/or iv) sequencing errors. Nanopore sequencing of the full-length 16S rRNA gene using MinION™ with 1D sequencing kit allowed us inferring microbiota composition of a complex microbial community to lower taxonomic levels than short-reads from 2nd generation sequencers.