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    Home > Food News > Nutrition News > The first "living drug": "living drug" invented to treat drug-resistant infections

    The first "living drug": "living drug" invented to treat drug-resistant infections

    • Last Update: 2021-10-21
    • Source: Internet
    • Author: User
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    Image: Scanning electron microscope image of Mycoplasma pneumoniae cells, a small bacteria naturally adapted to human lungs



    Researchers from the Center for Genome Regulation (CRG) and Pulmobiotics SL created the first "living drug" to treat antibiotic-resistant bacteria that grow on the surface of medical implants


    The experimental treatment was tested on infection catheters in vitro, in vitro and in vivo, and successfully treated infections for all three test methods


    This discovery is an important first step in the development of new treatments for infections affecting medical implants such as catheters, pacemakers, and prosthetic joints


    The research was published today in the journal Molecular Systems Biology


    This new treatment specifically targets biofilms, which are groups of bacterial cells attached to the surface


    Staphylococcus aureus is one of the most common biofilm-related bacteria


    The authors of the study hypothesized that introducing organisms that directly produce enzymes near biofilms is a safer and cheaper way to treat infections


    The researchers chose to modify Mycoplasma pneumoniae, a common bacteria that lacks cell walls, to make it easier to release therapeutic molecules that fight infections, while helping it evade detection by the human immune system


    First, the Mycoplasma pneumoniae is modified so that it does not cause disease


    The researchers' primary goal is to use this modified bacteria to treat the biofilm around the breathing tube, because Mycoplasma pneumoniae naturally adapts to the lungs


    The modified bacteria may also be used in other diseases for a long time


    DOI

    10.


    Article title

    Engineering a genome-reduced bacterium to eliminate Staphylococcus aureus biofilms in vivo

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