ArticlePloS one2025
Replacing critical point drying with hexamethyldisilazane drying enhances the ultrastructural preservation of cell surface projections in the parasite Trichomonas vaginalis for scanning electron microscopy.
Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The cell surface of Trichomonas vaginalis, causative agent of human trichomoniasis, plays a pivotal role in parasite adhesion, motility, and intercellular communication. Scanning electron microscopy (SEM) is widely used to explore the surface projections involved in these processes; however, standard sample preparation via critical point drying (CPD) often damages delicate membrane projections. Here, we optimized a hexamethyldisilazane (HMDS) drying protocol as a reliable alternative to CPD for ultrastructural analysis of T. vaginalis using SEM. Both drying methods were compared in terms of image quality and artifact formation. HMDS drying significantly improved the preservation of fragile projections, such as filopodia-, cytoneme-, and lamellipodia-like structures, compared to CPD. Our results show that susceptibility to CPD-induced artifacts may vary among highly adherent T. vaginalis strains, highlighting the need for caution in SEM interpretation. In a strain previously CPD-characterized by exhibiting a low number of cytonemes, quantitative analyses revealed a marked increase in the number of parasites with filopodia and cytonemes upon HMDS, accompanied by a reduction in drying-associated artifacts. In contrast, other strains exhibited similar quantitative results for both methods, though HMDS demonstrated a slight qualitative enhancement. HMDS drying also enabled the identification of novel ultrastructural features of T. vaginalis, including (a) long (>20 µm) cytonemes forming network-like connections between parasites and host cells, and (b) thin posterior and axostylar cytoneme-like structures that seems involved in host cell adhesion. Moreover, HMDS provided better morphological preservation of amoeboid forms and enhanced visualization of parasite-host interactions, revealing membranous networks not previously observed with CPD. Altogether, this study demonstrates the importance of the drying methods for sample preparation and expands the approaches for parasite imaging, revealing HMDS as a valuable option that could provide new ultrastructural insights into the surface morphology and intercellular communication mechanisms of T. vaginalis.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.