Rationally-defined microbial consortia suppress multidrug-resistant proinflammatory Enterobacteriaceae via ecological control.
Kenya HondaMunehiro FuruichiTakaaki KawaguchiMarie-Madlen PustKeiko Yasuma-MitobeDamian Rafal PlichtaNaomi HasegawaTakashi OhyaShakti BhattaraiSatoshi SasajimaAoto YoshimasaTimur TuganbaevMizuki YaginumaMasahiro UedaNobuyuki OkahashiKimiko AmafujiYuuko KiridooshiKayoko SugitaMartin StražarAshwin N SkellyWataru SudaMasahira HattoriNobuhiro NakamotoSilvia CaballeroJason M NormanBernat OlleTakeshi TanoueMakoto AritaVanni BucciKoji AtarashiRamnik J XavierPublished in: Research square (2023)
Persistent colonization and outgrowth of pathogenic organisms in the intestine may occur due to long-term antibiotic usage or inflammatory conditions, which perpetuate dysregulated immunity and tissue damage 1,2 . Gram-negative Enterobacteriaceae gut pathobionts are particularly recalcitrant to conventional antibiotic treatment 3,4 , though an emerging body of evidence suggests that manipulation of the commensal microbiota may be a practical alternative therapeutic strategy 5-7 . In this study, we rationally isolated and down-selected commensal bacterial consortia from healthy human stool samples capable of strongly and specifically suppressing intestinal Enterobacteriaceae . One of the elaborated consortia, consisting of 18 commensal strains, effectively controlled ecological niches by regulating gluconate availability, thereby reestablishing colonization resistance and alleviating antibiotic-resistant Klebsiella -driven intestinal inflammation in mice . Harnessing these microbial activities in the form of live bacterial therapeutics may represent a promising solution to combat the growing threat of proinflammatory, antimicrobial-resistant bacterial infection.
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