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When Parasites Catch Viruses: Viral Symbiont of a Protozoan Parasite Increases Virulence to Human Ho

Discussion in 'Other Health News and Research' started by Overstressed, Nov 20, 2012.

  1. Overstressed

    Overstressed Senior Member

    When Parasites Catch Viruses: Viral Symbiont of a Protozoan Parasite Increases Virulence to Human Host

    ScienceDaily (Nov. 7, 2012) — When humans have parasites, the organisms live in our bodies, co-opt our resources and cause disease. However, it turns out that parasites themselves can have their own co-habitants.

    Researchers from Harvard Medical School, Brigham and Women's Hospital and SUNY Upstate Medical University have found that the pathogenicity of the sexually transmitted protozoan parasiteTrichomonas vaginalis -- the cause of trichomoniasis -- is fueled by a viral invader. Trichomoniasis infections are more common than all bacterial STDs combined. Annually, trichomoniasis affects nearly 250 million people, typically as vaginitis in women and urethritis in men.
    "Trichomoniasis is associated with devastating consequences for women due to inflammation and related risks of reproductive disease," said Raina Fichorova, leader of the research team as well as associate professor of obstetrics, gynecology and reproductive biology at Brigham and Women's Hospital. "Our future goal is to determine how the viral symbiont and its inflammatory 'halo' affect the risk of preterm delivery and low birth weight."
    "This is only one of two incidents that we know of for which the pathogenicity of a protozoan virus has been characterized," said Max Nibert, Harvard Medical School professor of microbiology and immunology and co-author of the paper. "When found together, the result is an increase in virulence of the protozoan parasite to the human host, leading to exacerbated disease."
    This study, which was initiated by a Harvard Catalyst Pilot grant, will be published online in Public Library of Science (PLOS) One.
    Rather than invading human cells, Trichomonas vaginalisattaches to their surface and feeds on them, sometimes remaining asymptomatic for a period of time. The virus, called Trichomonasvirus, infects the protozoan and increases its pathogenic power by fueling virus-specific inflammatory responses.
    Moreover, carrying the protozoan parasite predisposes women to acquire sexually transmitted viruses, particularly HIV and human papillomavirus, or HPV, both of which can lead to serious diseases such as AIDS and cervical cancer, respectively. Fichorova and Nibert have recently obtained funding from the Harvard University Center for AIDS Research to find out if the virus itself is directly responsible for increased HIV risk.
    According to Nibert, the virus-parasite symbiosis is the norm rather than the exception with this particular protozoan. Upwards of 80 percent of Trichomonas vaginalis isolates carry the virus. "Unlike flu viruses, for example, this virus can't spread by jumping out of the cell into another one," said Nibert, who has pioneered molecular biology work on double-stranded RNA viruses, a category that includes Trichomonasvirus. "It just spreads between cells when they divide or mate."
    According to the researchers, it is this double-stranded nature of the viral genome that contributes to increased virulence of the protozoan parasite. "The double-stranded RNA seems important to the signaling process," added Nibert.
    Currently, trichomoniasis is treated with the antibiotic metronidazole. But this treatment is only effective on the protozoan. "When the medication is used, the dying or stressed protozoa release unharmed virions, which then signal to the human cells," explained Fichorova. As a result, the symptoms are aggravated, and this in turn might increase the danger it poses to pregnant women and their children.
    "Ahead is more research to better understand the viral cycle and structural features that might be vulnerable to drugs, which will lead to opening new doors for better treatment of trichomoniasis and related diseases," said Fichorova. "Our complementary expertise, interdisciplinary team efforts and strong collaboration is the key to our future success."
    Nibert added that basic research on Trichomonas vaginalis is not nearly as supported as he thinks it should be. "It is unfortunate that a human pathogen of such worldwide significance has been neglected to such a degree," he said.

    Personal note(in bold): this mechanism might explain how I might got ill. I catched this disease sexually, and it might explain why it's transferred easily. Where the virus itself might be difficult transferred from person to person, it can through an easy-to-catch-transfer-vector. My close family contacts are getting ill too.

    Best wishes,
    merylg, roller and natasa778 like this.
  2. Waverunner

    Waverunner Senior Member

    I hate parasites. I hope that diagnostics and treatment catch up to this problem.
    merylg and Overstressed like this.
  3. roller

    roller wiggle jiggle

    imo its wrong to think that we must have personally caught the viruses , pathogens or whatever...
    when your mother gave birth in an hospital she may have well contracted something like that.
    and would pass it on by breastfeeding, possibly.

    the medical statements on how diseases are transmitted or what they cause in the body
    couldnt have been more unreliable to outright false, one must say.
    their parotting has been proven wrong too often.

    an 'STD' can be transmitted in many ways.

    this parasite/virus infects the soft tissues.
    then vaginal inflammation is a sure thing, but it obviously settles in other human tissue as well.

    im surprised, that this pathogen got so little attention.
  4. roller

    roller wiggle jiggle

    perhaps a lot of these 'new' uncontrollable infections started in hospitals.
    particularly when giving birth. this produces large contamination areas.
    the microbe theory was rejected for decades.
    Last edited: Feb 7, 2016
    merylg likes this.

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