Nutrient Deficiency Promotes the Entry of Helicobacter pylori Cells into Candida Yeast Cells.
Kimberly Sánchez-AlonzoFabiola Silva-MieresLuciano Arellano-ArriagadaCristian Parra-SepúlvedaHumberto BernasconiCarlos T SmithVictor L CamposApolinaria García-CancinoPublished in: Biology (2021)
Helicobacter pylori, a Gram-negative bacterium, has as a natural niche the human gastric epithelium. This pathogen has been reported to enter into Candida yeast cells; however, factors triggering this endosymbiotic relationship remain unknown. The aim of this work was to evaluate in vitro if variations in nutrient concentration in the cultured medium trigger the internalization of H. pylori within Candida cells. We used H. pylori-Candida co-cultures in Brucella broth supplemented with 1%, 5% or 20% fetal bovine serum or in saline solution. Intra-yeast bacteria-like bodies (BLBs) were observed using optical microscopy, while intra-yeast BLBs were identified as H. pylori using FISH and PCR techniques. Intra-yeast H. pylori (BLBs) viability was confirmed using the LIVE/DEAD BacLight Bacterial Viability kit. Intra-yeast H. pylori was present in all combinations of bacteria-yeast strains co-cultured. However, the percentages of yeast cells harboring bacteria (Y-BLBs) varied according to nutrient concentrations and also were strain-dependent. In conclusion, reduced nutrients stresses H. pylori, promoting its entry into Candida cells. The starvation of both H. pylori and Candida strains reduced the percentages of Y-BLBs, suggesting that starving yeast cells may be less capable of harboring stressed H. pylori cells. Moreover, the endosymbiotic relationship between H. pylori and Candida is dependent on the strains co-cultured.
Keyphrases
- induced apoptosis
- helicobacter pylori
- cell cycle arrest
- candida albicans
- endothelial cells
- escherichia coli
- endoplasmic reticulum stress
- cell death
- signaling pathway
- high resolution
- gram negative
- mass spectrometry
- cystic fibrosis
- risk assessment
- cell proliferation
- staphylococcus aureus
- cell wall
- heavy metals
- optical coherence tomography
- replacement therapy