SignificanceIn a polymicrobial battlefield where different species compete for nutrients and colonization niches, antimicrobial compounds are the sword and shield of commensal microbes in competition with invading pathogens and each other. The identification of an -produced genotoxin, colibactin, and its specific targeted killing of enteric pathogens and commensals, including and , sheds light on our understanding of intermicrobial interactions in the mammalian gut. Our findings elucidate the mechanisms through which genotoxins shape microbial communities and provide a platform for probing the larger role of enteric multibacterial interactions regarding infection and disease outcomes.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931321 | PMC |
http://dx.doi.org/10.1073/pnas.2121180119 | DOI Listing |
Proc Natl Acad Sci U S A
March 2022
Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104.
SignificanceIn a polymicrobial battlefield where different species compete for nutrients and colonization niches, antimicrobial compounds are the sword and shield of commensal microbes in competition with invading pathogens and each other. The identification of an -produced genotoxin, colibactin, and its specific targeted killing of enteric pathogens and commensals, including and , sheds light on our understanding of intermicrobial interactions in the mammalian gut. Our findings elucidate the mechanisms through which genotoxins shape microbial communities and provide a platform for probing the larger role of enteric multibacterial interactions regarding infection and disease outcomes.
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