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Smutna, T.

Publications and source records attributed to Smutna, T..

2 recordsLinked to original sources

The mannose 6-phosphate receptor system is ancient, widespread in eukaryotes, and functionally diversified in the human parasite Trichomonas vaginalis

In mammals, the mannose 6-phosphate (M6P) pathway tags newly synthesized hydrolases for delivery to the lysosomes. The pathway underlies healthy lysosomal function, but whether an equivalent system operates outside animals remains largely unexplored. Surveying 53 representative species, across eukaryotic supergroups we show that the M6P receptor (MPR), the phosphorylating enzyme GNPT, and the uncovering enzyme (UCE) form a statistically robust, co-occurring module across extant eukaryotic supergroups. In the human parasite Trichomonas vaginalis, this module has diversified into an expanded MPR family of seven paralogs, the largest reported within these 53 species, alongside a structurally minimal single GNPT gene, despite the complete absence of UCE. Using co-immunoprecipitation (co-IP), mass spectrometry and confocal microscopy, we demonstrate that MPRs and GNPT localise to the Golgi apparatus, and their interactomes show paralog-specific enrichment of distinct hydrolase cargo, adaptor complexes and the retromer complex proteins for retrieval of MPRs, presenting a full receptor-recycling cycle. Critically, mass spectrometry based glycomics directly detects mature M6P-modified N-glycans in T. vaginalis built on unique Man5GlcNAc2 structure with no trace of GlcNAc-capped intermediate, seen in mammalian cells. Together, these results provide evidence that M6P pathway is an ancient and widespread eukaryotic system, with its functionally diversified variant operating in T. vaginalis for lysosomal biogenesis.

molecular biology↗

Trichomonas vaginalis targets Lactobacillus jensenii via pseudopodia-independent phagocytosis and secreted lysozyme TvGH25

A low abundance or absence of protective lactobacilli during acute trichomoniasis is a well-known phenomenon that is associated with T. vaginalis (TV) infection. However, a crucial question that remains unanswered is whether alterations in the lactobacilli population precede TV infection or whether the parasite plays an active role in lactobacilli disappearance. Our findings showed that TV efficiently phagocytosed one of the dominant Lactobacillus species L. jensenii (LJ). Phagocytosis proceeds via a pseudopodia-independent mechanism reminiscent of sinking with a preference for viable cells. The presence of viable LJ leads to an increase in secretion of 27 TV proteins, including TvGH25 lysozyme. This enzyme cleaves peptidoglycan, a major component of the bacterial cell wall. TV overexpressing TvGH25 effectively lowers the bacterial cell count, evidencing the enzymes antimicrobial potential. These data support the notion that TV cells can suppress the Lactobacillus population through a combination of targeted secretory response and phagocytic activity, revealing novel potential targets for developing alternative therapeutic strategies against trichomoniasis. Significance StatementTrichomonas vaginalis (TV) is a sexually transmitted parasite that causes trichomoniasis and is connected to the disruption of the healthy vaginal microbiome, dominated by Lactobacillus species. However, the nature of the interactions between TV and Lactobacillus is poorly understood. In this study, we show that TV uses an unusual form of pseudopodia-independent phagocytosis to engulf L. jensenii alongside a targeted secretory response to the bacterial encounter, involving TvGH25 lysozyme. We found that TV acquired this enzyme by lateral gene transfer from bacteria and repurposed it against bacteria to degrade the major bacterial cell wall component peptidoglycan. TvGH25 thus represents an effective component of TVs antibacterial arsenal. Our findings provide new insights into the mechanistic disruption of the protective Lactobacillus microbiota.

microbiology↗