Entamoeba gingivalis Exerts Severe Pathogenic Effects on the Oral Mucosa.

Autor: Bao X; Charité-University Medicine Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Dental and Craniofacial Sciences, Department of Periodontology, Oral Medicine and Oral Surgery, Berlin, Germany., Weiner J 3rd; Core Unit Bioinformatics, Berlin Institute of Health, Berlin, Germany., Meckes O; Eye of Science, Nicole Ottawa & Oliver Meckes GbR, Reutlingen, Germany., Dommisch H; Charité-University Medicine Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Dental and Craniofacial Sciences, Department of Periodontology, Oral Medicine and Oral Surgery, Berlin, Germany., Schaefer AS; Charité-University Medicine Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute for Dental and Craniofacial Sciences, Department of Periodontology, Oral Medicine and Oral Surgery, Berlin, Germany.
Jazyk: angličtina
Zdroj: Journal of dental research [J Dent Res] 2021 Jul; Vol. 100 (7), pp. 771-776. Date of Electronic Publication: 2021 Apr 01.
DOI: 10.1177/00220345211004498
Abstrakt: The protozoan Entamoeba gingivalis colonizes the healthy oral mucosa with a prevalence of 15%. Colonization can be asymptomatic, and it is considered not pathogenic. However, it is able to invade lacerated oral mucosa, where it ingests fragments of live cells, suggesting pathogenous potential. Here, we characterized the transcriptomes of gingival cells after infection with E. gingivalis using RNA sequencing and observed pathogen interaction with the epithelial monolayer barrier by scanning electron microscopy. In epithelial and fibroblast cells, strongest differential expression showed gene set "chemokines and inflammatory molecules in myeloid cells" (area under the curve [AUC] = 0.9, effect size 5.15, adjusted P = 3.1 × 10 -19 ) and "cell cycle and growth arrest" (AUC = 0.91, effect size = 4.56, adjusted P = 4.8 × 10 -9 ), respectively. The most upregulated genes were TNF (fold change 430) and IL8 (fold change 359) in epithelial cells and ZN331 (fold change 18) in fibroblasts. We showed that E. gingivalis killed live epithelial cells by trogocytosis, demonstrating strong pathogenic potential.
Databáze: MEDLINE