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Endobiont Viruses Sensed by the Human Host – Beyond Conventional Antiparasitic Therapy
Author(s) -
Rai. Fichorova,
Yu Jin Lee,
Hidemi S. Yamamoto,
Yuko Takagi,
Gary R. Hayes,
Russell P. Goodman,
Xenia Chepa-Lotrea,
Olivia R. Buck,
Ryan Murray,
Tomasz Kula,
David Beach,
Bibhuti N. Singh,
Max L. Nibert
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0048418
Subject(s) - trichomoniasis , trichomonas vaginalis , biology , proinflammatory cytokine , protozoan infection , trichomonas , metronidazole , immunology , interferon , virology , pathogen , human pathogen , protozoan parasite , coinfection , microbiology and biotechnology , virus , antibiotics , medicine , parasite hosting , inflammation , gene , genetics , pathology , world wide web , computer science
Wide-spread protozoan parasites carry endosymbiotic dsRNA viruses with uncharted implications to the human host. Among them, Trichomonas vaginalis , a parasite adapted to the human genitourinary tract, infects globally ∼250 million each year rendering them more susceptible to devastating pregnancy complications (especially preterm birth), HIV infection and HPV-related cancer. While first-line antibiotic treatment (metronidazole) commonly kills the protozoan pathogen, it fails to improve reproductive outcome. We show that endosymbiotic Trichomonasvirus , highly prevalent in T. vaginalis clinical isolates, is sensed by the human epithelial cells via Toll-like receptor 3, triggering Interferon Regulating Factor -3, interferon type I and proinflammatory cascades previously implicated in preterm birth and HIV-1 susceptibility. Metronidazole treatment amplified these proinflammatory responses. Thus, a new paradigm targeting the protozoan viruses along with the protozoan host may prevent trichomoniasis-attributable inflammatory sequelae.

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