2022
DOI: 10.1186/s12866-022-02441-0
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Sediment-associated microbial community profiling: sample pre-processing through sequential membrane filtration for 16S rRNA amplicon sequencing

Abstract: Background Sequential membrane filtration as a pre-processing step for capturing sediment-associated microorganisms could provide good quality and integrity DNA that can be preserved and kept at ambient temperatures before community profiling through culture-independent molecular techniques. However, the effects of sample pre-processing via filtration on DNA-based profiling of sediment-associated microbial community diversity and composition are poorly understood. Specifically, the influences o… Show more

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Cited by 4 publications
(3 citation statements)
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“…Proteobacteria are reported in both HMs contaminated and uncontaminated regions (Ma et al, 2015;Yan et al, 2016). Previous studies documented the response of Proteobacteria to HMs contamination in polluted habitats (Hu et al, 2021;Liu et al, 2021b;Serrana and Watanabe, 2022). Bacteroidota (class Bacteroidia) and Cyanobacteria (class Cyanobacteria) were more abundant phyla in surface sediments of MA1.F with relative abundances of 23.91% and 26.40%, respectively.…”
Section: B a Figure 10mentioning
confidence: 87%
“…Proteobacteria are reported in both HMs contaminated and uncontaminated regions (Ma et al, 2015;Yan et al, 2016). Previous studies documented the response of Proteobacteria to HMs contamination in polluted habitats (Hu et al, 2021;Liu et al, 2021b;Serrana and Watanabe, 2022). Bacteroidota (class Bacteroidia) and Cyanobacteria (class Cyanobacteria) were more abundant phyla in surface sediments of MA1.F with relative abundances of 23.91% and 26.40%, respectively.…”
Section: B a Figure 10mentioning
confidence: 87%
“…The mixtures were incubated at 37 °C for 35 min, followed by heating at 100 °C for 15 min, and then centrifuged at 12,000 rpm for 10 min. The supernatant containing soluble DNA was used for amplifying the 16S rRNA gene using universal primers 16 s-F (AGAGTTTGATCCTGGCTCAG) and 16 s-R (GGTTACCTTGTTACGACTT) [ 42 ]. All PCR products were sent to Shanghai Maple Sequencing Co. for bi-directional sequencing, and the results were compared to the BLAST/NCBI website ( https://blast.ncbi.nlm.nih.gov/Blast.cgi ) to confirm their specificity to S. aureus .…”
Section: Methodsmentioning
confidence: 99%
“…The colony diversity of the mold culture samples was analyzed at FeiFan Standard Technical Service (Suzhou) Co., Ltd. Bacterial diversity was measured via the 16S rDNA method. [ 16 ] Fungal diversity was examined via the ITS method. [ 17 ] These procedures were performed as follows: (1) bacterial DNA and fungal RNA were extracted from the mold culture samples; (2) the universal primers of the bacterial DNA and the fungal RNA were added and PCR amplified; and (3) base sequences were tested, and bacterial genus was identified through evolutionary tree analysis.…”
Section: Methodsmentioning
confidence: 99%