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.

Základní údaje

Originální název

Double-Stranded RNA Viruses Are Released From Trichomonas vaginalis Inside Small Extracellular Vesicles and Modulate the Exosomal Cargo

Autoři

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 a Jan TACHEZY

Vydání

Frontiers in Microbiology, Switzerland, Frontiers Research Foundation, 2022, 1664-302X

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10606 Microbiology

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 5.200

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:90127/22:00140166

Organizační jednotka

CIISB II

EID Scopus

Klíčová slova anglicky

Trichomonasvirus; TVV; exosome; extracellular vesicle; proteomics; tsRNA

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 6. 5. 2025 08:41, Mgr. Eva Dubská

Anotace

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.

Návaznosti

90127, velká výzkumná infrastruktura
Název: CIISB II