PT  - JOURNAL ARTICLE
AU  - Anna Cuscó
AU  - Carlotta Catozzi
AU  - Joaquim Viñes
AU  - Armand Sánchez
AU  - Olga Francino
TI  - Microbiota profiling with long amplicons using Nanopore sequencing: full-length 16S rRNA gene and whole rrn operon
AID  - 10.1101/450734
DP  - 2018 Jan 01
TA  - bioRxiv
PG  - 450734
4099  - http://biorxiv.org/content/early/2018/10/24/450734.short
4100  - http://biorxiv.org/content/early/2018/10/24/450734.full
AB  - Background Profiling microbiome on low biomass samples is challenging for metagenomics since these samples are prone to present DNA from other sources, such as the host or the environment. The usual approach is sequencing specific hypervariable regions of the 16S rRNA gene, which fails to assign taxonomy to genus and species level. Here, we aim to assess long-amplicon PCR-based approaches for assigning taxonomy at the genus and species level. We use Nanopore sequencing with two different markers: full-length 16S rRNA (∼1,500 bp) and the whole rrn operon (16S rRNA gene – ITS – 23S rRNA gene; 4,500 bp).Methods We sequenced a clinical isolate of Staphylococcus pseudintermedius, two mock communities (HM-783D, Bei Resources; D6306, ZymoBIOMICS™) and two pools of lowbiomass samples (dog skin). Nanopore sequencing was performed on MinION™ (Oxford Nanopore Technologies) using 1D PCR barcoding kit. Sequences were pre-processed, and data were analyzed using WIMP workflow on EPI2ME (ONT) or Minimap2 software with rrn database.Results Full-length 16S rRNA and the rrn operon retrieved the microbiota composition from the bacterial isolate, the mock communities and the complex skin samples, even at the genus and species level. For Staphylococcus pseudintermedius isolate, when using EPI2ME, the amplicons were assigned to the correct bacterial species in ∼98% of the cases with rrn operon as the marker, and ∼68% of the cases with 16S rRNA gene respectively. In both skin microbiota samples, we detected many species with an environmental origin. In chin, we found different Pseudomonas species in high abundance, whereas in dorsal skin there were more taxa with lower abundances.Conclusions Both full-length 16S rRNA and the rrn operon retrieved the microbiota composition of simple and complex microbial communities, even from the low-biomass samples such as dog skin. For an increased resolution at the species level, rrn operon would be the best choice.