2018
DOI: 10.1016/j.ibiod.2017.02.015
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Comparison of methods for identification of microbial communities in book collections: Culture-dependent (sequencing and MALDI-TOF MS) and culture-independent (Illumina MiSeq)

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Cited by 60 publications
(45 citation statements)
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“…A total of 13 DNA samples (6 from the mummy's surface, 3 from the internal organs, 1 from the skin crystal and 1 each from the chapel air, the sarcophagus air and the sarcophagus glass) were analysed by Illumina sequencing using the procedure given in Kraková et al (2018). The approach includes PCR amplification of the bacterial 16S rRNA gene V1-V4 region using primers 27f (5 0 -AGA GTT TGA TCC TGG CTC AG-3 0 ) and 685r (5 0 -TCT ACG CAT TTC ACC GCT AC-3 0 ) and amplification of the fungal 28S rRNA large-subunit D1/D2 region using the NL1/NL4 primer set (NL1: 5 0 -GCA TAT CAA TAA GCG GAG GAA AAG-3 0 ; NL4: 5 0 -GGT CCG TGT TTC AAG ACG G-3 0 ).…”
Section: Illumina Platform High-throughput Sequencingmentioning
confidence: 99%
“…A total of 13 DNA samples (6 from the mummy's surface, 3 from the internal organs, 1 from the skin crystal and 1 each from the chapel air, the sarcophagus air and the sarcophagus glass) were analysed by Illumina sequencing using the procedure given in Kraková et al (2018). The approach includes PCR amplification of the bacterial 16S rRNA gene V1-V4 region using primers 27f (5 0 -AGA GTT TGA TCC TGG CTC AG-3 0 ) and 685r (5 0 -TCT ACG CAT TTC ACC GCT AC-3 0 ) and amplification of the fungal 28S rRNA large-subunit D1/D2 region using the NL1/NL4 primer set (NL1: 5 0 -GCA TAT CAA TAA GCG GAG GAA AAG-3 0 ; NL4: 5 0 -GGT CCG TGT TTC AAG ACG G-3 0 ).…”
Section: Illumina Platform High-throughput Sequencingmentioning
confidence: 99%
“…The PCR product of the most common primer pair ITS1-ITS2 used for fungal identification (Iwen et al, 2002;Kõljalg et al, 2013) is too short and also too variable for truly universal primer design (von der Schulenburg et al, 2001). The low-throughput Sanger sequencing of the hypervariable D1-D2 region of 28S rRNA (Khot et al, 2009) or high-throughput Illumina sequencing of the transposon fragmented 28S rRNA (Kraková et al, 2018) still lacks the ability of precise fungal discrimination. The amplification and sequence of a large part of the ribosomal cluster in one fragment would be ideal.…”
Section: Microbial Communities' Analysismentioning
confidence: 99%
“…The bacteria of the group Propionibacterium/Cutibacterium are very frequently isolated from human skin, therefore is very likely that they have a human origin. Other bacteria of cutaneous origin, belonging to the genera Corynebacterium and Staphylococcus (Ramsey et al, 2016), present on the seal surface were also detected from several archive documents in the past (Puškárová et al, 2016;Kraková et al, 2018). Among these bacteria of presumed human origin Staphylococcus aureus previously showed the Pb resistance and sensitivity (Levinson et al, 1996) and evidenced the sorption of lead in the extracellular polymeric substance (Bhaskar and Bhosle, 2006).…”
Section: Microbial Communities' Analysismentioning
confidence: 99%
“…Moreover, a contemporaneous collection of animal skins bound together provides a 4 remarkable biological resource, which may inform upon the husbandry of the animals and in turn shed 5 light on the assembly of the codex. The utility of parchment documents as a store of biological 6 information is confirmed by a number of molecular studies, which have successfully retrieved DNA 7 sequences from parchments and produced comparisons with modern reference populations of cattle, 8 sheep and goat [1][2][3][4]. These analyses have utilised isolated parchment fragments, which are then digested 9…”
Section: Introductionmentioning
confidence: 99%
“…11 12 In the light of the vast potential afforded by ancient manuscripts several authors are experimenting with 13 non-destructive sampling of documents. Whilst most of these methods involve some form of 14 spectroscopic analysis, novel approaches which release molecules from the surface, such as the use of 15 synthetic gel films [5,6] have been reported, and this work can be seen as part of a wider push to develop 16 sampling methods for material culture [7][8][9][10][11]. These studies also form part of an increasingly 17 sophisticated analysis of the conservation status of objects, which includes analyses of the microflora 18 within buildings and upon objects.…”
Section: Introductionmentioning
confidence: 99%