Background: To establish an infection in the vagina, Trichomonas vaginalis must adapt to various environmental cues for survival and further replication. Nutrient competition by lactobacilli, the major normal vaginal flora, is one of the mechanisms to limit the growth of other microorganisms. Additionally, lactobacilli produce H2O2 that can reduce the genital infections caused by other pathogens. Thus, the ability to overcome the metabolic stresses, such as glucose restriction (GR), as well as the oxidative stresses, is critical for T. vaginalis to establish an infection.
Methods: To gain insights into the molecular mechanisms of adaptation to GR, we utilized next-generation RNA sequencing (RNA-seq) to quantify the gene expression changes upon GR. Autophagy, a cytoprotective response to starvation, was monitored by using autophagy-specific staining, autophagy inhibition assay, and co-localization of autophagosomes with lysosomes.
Results: We demonstrated that GR promotes the survival of T. vaginalis. Besides, GR-cultivated cells exhibit higher H2O2 resistance. Our RNA-seq data revealed that genes involved in general energy metabolism were downregulated, whereas genes encoding glutamate metabolism-related aminotransferases were strikingly upregulated under GR. Furthermore, autophagy was first identified and characterized in T. vaginalis under GR.
Conclusions: These data suggest that GR induces a metabolic reprogramming, enhancing antioxidant ability and autophagy for cellular homeostasis to maintain survival.
General significance: Our work not only led to significant advances in understanding the transcriptional changes in response to GR but also provided possible strategies elicited by GR for T. vaginalis to adapt to the vaginal microenvironment.
Keywords: ADH; ALDO; ALT; Alanine aminotransferase; Alcohol dehydrogenase; Autophagy; CR; ENO; Enolase; Fructose-1,6-bisP aldolase; GAPDH; GDH; GK; GPI; GR; Glucokinase; Glucose phosphate isomerase; Glucose restriction; Glutamate dehydrogenase; Glyceraldehyde 3-P dehydrogenase; LDH; Lactate dehydrogenase; MDH; ME; Malate dehydrogenase; Malic enzyme; NGS; PEPCK; PFK; PGAM; PGK; PK; Phosphoenolpyruvate carboxykinase; Phosphofructokinase; Phosphoglycerate kinase; Pyruvate kinase; RNA sequencing; RNA-seq; ROS; Rbr; SOD; Superoxide dismutase; T. vaginalis; TPI; Thioredoxin peroxidase; Triose-phosphate isomerase; TrxP; caloric restriction; glucose restriction; next generation sequencing; phosphoglycerate mutase; reactive oxygen species; rubrerythrin.
© 2013.