Detailed Information on Publication Record
2022
Double-Stranded RNA Viruses Are Released From Trichomonas vaginalis Inside Small Extracellular Vesicles and Modulate the Exosomal Cargo
RADA, Petr, Ivan HRDY, Alois ZDRHA, Ravi Kumar NARAYANASAMY, Tamara SMUTNA et. al.Basic information
Original name
Double-Stranded RNA Viruses Are Released From Trichomonas vaginalis Inside Small Extracellular Vesicles and Modulate the Exosomal Cargo
Authors
RADA, Petr, Ivan HRDY, Alois ZDRHA, Ravi Kumar NARAYANASAMY, Tamara SMUTNA, Jana HORACKOVA, Karel HARANT, Vladimir BENES, Seow-Chin ONG, Chih-Yu TSAI, Hong-Wei LUO, Cheng-Hsun CHIU, Petrus TANG and Jan TACHEZY
Edition
Frontiers in Microbiology, Switzerland, Frontiers Research Foundation, 2022, 1664-302X
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10606 Microbiology
Country of publisher
Switzerland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 5.200
RIV identification code
RIV/00216224:14740/22:00128779
Organization unit
Central European Institute of Technology
UT WoS
000797822000001
Keywords in English
Trichomonasvirus; TVV; exosome; extracellular vesicle; proteomics; tsRNA
Tags
International impact, Reviewed
Změněno: 28/2/2023 19:25, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Trichomonas vaginalis is a parasitic protist that infects the human urogenital tract. During the infection, trichomonads adhere to the host mucosa, acquire nutrients from the vaginal/prostate environment, and release small extracellular vesicles (sEVs) that contribute to the trichomonad adherence and modulate the host-parasite communication. Approximately 40-70% of T. vaginalis strains harbor a double-stranded RNA virus called Trichomonasvirus (TVV). Naked TVV particles have the potential to stimulate a proinflammatory response in human cells, however, the mode of TVV release from trichomonads to the environment is not clear. In this report, we showed for the first time that TVV particles are released from T. vaginalis cells within sEVs. The sEVs loaded with TVV stimulated a higher proinflammatory response of human HaCaT cells in comparison to sEVs from TVV negative parasites. Moreover, a comparison of T. vaginalis isogenic TVV plus and TVV minus clones revealed a significant impact of TVV infection on the sEV proteome and RNA cargo. Small EVs from TVV positive trichomonads contained 12 enriched and 8 unique proteins including membrane-associated BspA adhesine, and about a 2.5-fold increase in the content of small regulatory tsRNA. As T. vaginalis isolates are frequently infected with TVV, the release of TVV via sEVs to the environment represents an important factor with the potential to enhance inflammation-related pathogenesis during trichomoniasis.
Links
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