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Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis

Trichomonas vaginalis is the parasitic protozoan residing in human urogenital tract causing trichomoniasis, which is the leading non-viral sexually transmitted disease. It has cosmopolitan distribution throughout the globe and affects both men and women. Lifecycle of the parasite has been traditiona...

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Autores principales: Beri, Divya, Yadav, Priya, Devi, H. R. Nandini, Narayana, Chinmaya, Gadara, Darshak, Tatu, Utpal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972724/
https://www.ncbi.nlm.nih.gov/pubmed/32010634
http://dx.doi.org/10.3389/fcimb.2019.00430
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author Beri, Divya
Yadav, Priya
Devi, H. R. Nandini
Narayana, Chinmaya
Gadara, Darshak
Tatu, Utpal
author_facet Beri, Divya
Yadav, Priya
Devi, H. R. Nandini
Narayana, Chinmaya
Gadara, Darshak
Tatu, Utpal
author_sort Beri, Divya
collection PubMed
description Trichomonas vaginalis is the parasitic protozoan residing in human urogenital tract causing trichomoniasis, which is the leading non-viral sexually transmitted disease. It has cosmopolitan distribution throughout the globe and affects both men and women. Lifecycle of the parasite has been traditionally described as consisting of motile and symptom-causing trophozoites. Chemical and temperature perturbations in trophozoites have been shown to aid conversion to pseudocysts, which is poorly investigated. In the current study, we show the formation of viable cyst-like structures (CLS) in stationary phase of T. vaginalis axenic culture. We used a fluorescent stain called calcofluor white, which specifically binds to chitin and cellulose-containing structures, to score for T. vaginalis CLS. Using flow cytometry, we demonstrated and quantitated the processes of encystation as well as excystation; thus, completing the parasite's lifecycle in vitro without any chemical/temperature alterations. Like cysts from other protozoan parasites such as Entamoeba histolytica and Giardia lamblia, T. vaginalis CLS appeared spherical, immotile, and resistant to osmotic lysis and detergent treatments. Ultrastructure of CLS demonstrated by Transmission Electron Microscopy showed a thick electron-dense deposition along its outer membrane. To probe the physiological role of CLS, we exposed parasites to vaginal pH and observed that trophozoites took this as a cue to convert to CLS. Further, upon co- culturing with cells of cervical origin, CLS rapidly excysted to form trophozoites which abrogated the cervical cell monolayer in a dose-dependent manner. To further corroborate the presence of two distinct forms in T. vaginalis, we performed two-dimensional gel electrophoresis and global, untargeted mass spectrometry to highlight differences in the proteome with trophozoites. Interestingly, CLS remained viable in chlorinated swimming pool water implicating the possibility of its role as environmentally resistant structures involved in non-sexual mode of parasite transmission. Finally, we showed that symptomatic human patient vaginal swabs had both T. vaginalis trophozoites and CLS; thus, highlighting its importance in clinical infections. Overall, our study highlights the plasticity of the pathogen and its rapid adaption when subjected to stressful environmental cues and suggests an important role of CLS in the parasite's life cycle, pathogenesis and transmission.
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spelling pubmed-69727242020-02-01 Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis Beri, Divya Yadav, Priya Devi, H. R. Nandini Narayana, Chinmaya Gadara, Darshak Tatu, Utpal Front Cell Infect Microbiol Cellular and Infection Microbiology Trichomonas vaginalis is the parasitic protozoan residing in human urogenital tract causing trichomoniasis, which is the leading non-viral sexually transmitted disease. It has cosmopolitan distribution throughout the globe and affects both men and women. Lifecycle of the parasite has been traditionally described as consisting of motile and symptom-causing trophozoites. Chemical and temperature perturbations in trophozoites have been shown to aid conversion to pseudocysts, which is poorly investigated. In the current study, we show the formation of viable cyst-like structures (CLS) in stationary phase of T. vaginalis axenic culture. We used a fluorescent stain called calcofluor white, which specifically binds to chitin and cellulose-containing structures, to score for T. vaginalis CLS. Using flow cytometry, we demonstrated and quantitated the processes of encystation as well as excystation; thus, completing the parasite's lifecycle in vitro without any chemical/temperature alterations. Like cysts from other protozoan parasites such as Entamoeba histolytica and Giardia lamblia, T. vaginalis CLS appeared spherical, immotile, and resistant to osmotic lysis and detergent treatments. Ultrastructure of CLS demonstrated by Transmission Electron Microscopy showed a thick electron-dense deposition along its outer membrane. To probe the physiological role of CLS, we exposed parasites to vaginal pH and observed that trophozoites took this as a cue to convert to CLS. Further, upon co- culturing with cells of cervical origin, CLS rapidly excysted to form trophozoites which abrogated the cervical cell monolayer in a dose-dependent manner. To further corroborate the presence of two distinct forms in T. vaginalis, we performed two-dimensional gel electrophoresis and global, untargeted mass spectrometry to highlight differences in the proteome with trophozoites. Interestingly, CLS remained viable in chlorinated swimming pool water implicating the possibility of its role as environmentally resistant structures involved in non-sexual mode of parasite transmission. Finally, we showed that symptomatic human patient vaginal swabs had both T. vaginalis trophozoites and CLS; thus, highlighting its importance in clinical infections. Overall, our study highlights the plasticity of the pathogen and its rapid adaption when subjected to stressful environmental cues and suggests an important role of CLS in the parasite's life cycle, pathogenesis and transmission. Frontiers Media S.A. 2020-01-14 /pmc/articles/PMC6972724/ /pubmed/32010634 http://dx.doi.org/10.3389/fcimb.2019.00430 Text en Copyright © 2020 Beri, Yadav, Devi, Narayana, Gadara and Tatu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Beri, Divya
Yadav, Priya
Devi, H. R. Nandini
Narayana, Chinmaya
Gadara, Darshak
Tatu, Utpal
Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title_full Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title_fullStr Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title_full_unstemmed Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title_short Demonstration and Characterization of Cyst-Like Structures in the Life Cycle of Trichomonas vaginalis
title_sort demonstration and characterization of cyst-like structures in the life cycle of trichomonas vaginalis
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972724/
https://www.ncbi.nlm.nih.gov/pubmed/32010634
http://dx.doi.org/10.3389/fcimb.2019.00430
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