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
UT WoS
EID Scopus
Klíčová slova anglicky
Trichomonasvirus; TVV; exosome; extracellular vesicle; proteomics; tsRNA
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
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