Ultrasmall episymbiotic Saccharibacteria suppresses gingival inflammation and bone loss through host bacterial modulation

Published: 18 September 2024| Version 1 | DOI: 10.17632/vp68zv9wj9.1
Contributors:
Otto Chipashvili, Daniel R. Utter,
, Yansong Ma,
,
, Yasmin Alayyoubi,
,
,
,
,
,
,

Description

Raw data accompanying the manuscript published in the linked Cell Host & Microbe URL published on DDMMYYYY. This dataset contains raw data from two related 16S rRNA amplicon sequencing projects, the first from whole human plaque samples ("Perio_3") and the second from ligatures soaked with PBS or experimental bacteria ("Ligature_microbiome"). Perio_3 also includes analyzed data ("Perio_3_analyzed") with the ASV representative sequences and counts by sample. Please see the STAR methods of the paper linked above for full experimental methods, the methods are described in brief here. Perio_3: Three periodontal patient plaque samples were resuspended by vortexing. 0.5 mL of the sample was pelleted and resuspended in 150 uL of phosphate buffer saline (PBS). Genomic DNA (gDNA) was isolated by MasterPure gram-positive DNA purification kit (Epicenter) according to the manufactory’s protocol with a slight modification of bead beating step. Briefly, 150 uL of PBS bacteria was mixed with 150 uL of Tris-EDTA (TE) buffer and transferred to a stock tube containing glass beads (Sigma G8772). The final concentration of lysozyme was added to the final concentration of 2 mg/mL, and incubated for 1 hour at 37C. Subsequently, the cells were disrupted by bead beater for 3 x 30 s each at 6 m/s speed with 1 minute short pauses at 4C. g DNA was isolated using the manufacturer’s protocol here on. Isolated gDNA was sent to Zymo sequencing core for sequencing of the V1-V3 region of the 16S rRNA gene using 250bp pair-end sequencing chemistry. Ligature_microbiome: Ligature from the mouse 2nd molar was removed and placed in 150 µL of sterile PBS buffer. Cells from the ligature was resuspended by vortexing the sample. 140 µL cells were mixed with 150 µL of TE buffer and the gDNA was isolated using MasterPure DNA isolation kit supplemented with bead beating. Isolated DNA was sent for 16S rRNA sequencing to Forsyth Institute or Zymo sequencing core. A static version of the code used for the microbiome analyses is included here as 'narrative_methods.html'

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Microbiome, Mouse Model, rRNA Analysis, Periodontal Disease

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