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Correction to: A comprehensive fungi-specific 18S rRNA gene sequence primer toolkit suited for diverse research issues and sequencing platforms
BMC Microbiology volume 19, Article number: 249 (2019)
- The original article was published in BMC Microbiology 2018 18:190
Correction to: BMC Microbiol
Following publication of the original article , we have been notified that three of the primer names identified as most promising candidates for fungal community surveys were incorrectly renamed following the primer nomenclature system proposed by Gargas & DePriest . Their positioning on the reference sequence had to be shifted 1bp towards the 3’-end (see Table 1 for the correct naming). The same error occurred in some primer names listed in the additional files (see attached Supplementary information).
As consequence, the number of identical nucleotides shared by the most promising primers and the newly designed blocking oligo sequences changed (see Table 2).
In this correction, the revised supplementary materials are included.
Banos, et al. A comprehensive fungi-specific 18S rRNA gene sequence primer toolkit suited for diverse research issues and sequencing platforms. BMC Microbiol. 2018;18:190. https://doi.org/10.1186/s12866-018-1331-4.
Gargas A, DePriest PT. A nomenclature for fungal PCR primers with examples from intron-containing SSU rDNA. Mycologia. 1996;88(5):745–8. https://doi.org/10.2307/3760969.
Additional file 3. List of the seven most promising primer pairs for biodiversity assessments identified by in silico PCR. Primer pairs are suitable for different sequencing methods dependent on the expected amplicon size. Sequence coverage rate of diverse fungal and non-fungal eukaryotic groups as revealed by in silico PCR.
Additional file 4. Annealing temperatures empirically evaluated for the most promising primer pairs. Two fungal strains, one of the Basidiomycota and one of the Ascomycota, served as template DNA. Intensity of the color indicates the strength of the amplification product detected by ethidium bromide staining. Red, template DNA from Taphrina deformans; Green, template DNA from Agaricus bisporus; *, optimal annealing temperature.
Additional file 11. Taxonomic composition of three environmental samples. Barchart indicates relative sequence abundance of the different fungal classes/subgroups amplified by the primer pair nu-SSU-1334-5′/nu-SSU-1648-3′ (FF390/FR-1). Others: Blastocladiomyetes, Glomeromycetes, Monoblepharidomycetes, Pucciniomycotina_Incertae sedis.
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Banos, S., Lentendu, G., Kopf, A. et al. Correction to: A comprehensive fungi-specific 18S rRNA gene sequence primer toolkit suited for diverse research issues and sequencing platforms. BMC Microbiol 19, 249 (2019). https://doi.org/10.1186/s12866-019-1628-y