| Literature DB >> 31378677 |
Won Jong Kim1, Dustin Higashi1, Maira Goytia2, Maria A Rendón1, Michelle Pilligua-Lucas3, Matthew Bronnimann1, Jeanine A McLean4, Joseph Duncan5, David Trees4, Ann E Jerse3, Magdalene So6.
Abstract
The mucosa is colonized with commensal Neisseria. Some of these niches are sites of infection for the STD pathogen Neisseria gonorrhoeae (Ngo). Given the antagonistic behavior of commensal bacteria toward their pathogenic relatives, we hypothesized that commensal Neisseria may negatively affect Ngo colonization. Here, we report that commensal species of Neisseria kill Ngo through a mechanism based on genetic competence and DNA methylation state. Specifically, commensal-triggered killing occurs when the pathogen takes up commensal DNA containing a methylation pattern that it does not recognize. Indeed, any DNA will kill Ngo if it can enter the cell, is differentially methylated, and has homology to the pathogen genome. Consistent with these findings, commensal Neisseria elongata accelerates Ngo clearance from the mouse in a DNA-uptake-dependent manner. Collectively, we propose that commensal Neisseria antagonizes Ngo infection through a DNA-mediated mechanism and that DNA is a potential microbicide against this highly drug-resistant pathogen.Entities:
Keywords: DNA killing of pathogens; DNA uptake; commensal Neisseria; pathogenic Neisseria
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Year: 2019 PMID: 31378677 PMCID: PMC6728082 DOI: 10.1016/j.chom.2019.07.003
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023