J 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

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

90127, large research infrastructures
Name: CIISB II