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Rationally-defined microbial consortia suppress multidrug-resistant proinflammatory Enterobacteriaceae via ecological control.
Honda, Kenya; Furuichi, Munehiro; Kawaguchi, Takaaki; Pust, Marie-Madlen; Yasuma-Mitobe, Keiko; Plichta, Damian; Hasegawa, Naomi; Ohya, Takashi; Bhattarai, Shakti; Sasajima, Satoshi; Yoshimasa, Aoto; Tuganbaev, Timur; Yaginuma, Mizuki; Ueda, Masahiro; Okahashi, Nobuyuki; Amafuji, Kimiko; Kiridooshi, Yuuko; Sugita, Kayoko; Strazar, Martin; Skelly, Ashwin; Suda, Wataru; Hattori, Masahira; Nakamoto, Nobuhiro; Caballero, Silvia; Norman, Jason; Olle, Bernat; Tanoue, Takeshi; Arita, Makoto; Bucci, Vanni; Atarashi, Koji; Xavier, Ramnik.
Afiliación
  • Honda K; Keio University School of Medicine.
  • Furuichi M; Keio University School of Medicine.
  • Kawaguchi T; Keio University School of Medicine.
  • Pust MM; Broad Institute of MIT and Harvard.
  • Yasuma-Mitobe K; Keio University School of Medicine.
  • Plichta D; Broad Institute.
  • Hasegawa N; Keio University School of Medicine.
  • Ohya T; Keio University School of Medicine.
  • Bhattarai S; UMass Chan Medical School.
  • Sasajima S; Keio University School of Medicine.
  • Yoshimasa A; JSR-Keio University Medical and Chemical Innovation Center.
  • Tuganbaev T; Keio University School of Medicine.
  • Yaginuma M; Keio University School of Medicine.
  • Okahashi N; Osaka Universtiy.
  • Amafuji K; Keio University School of Medicine.
  • Kiridooshi Y; JSR Corp.
  • Sugita K; Keio University School of Medicine.
  • Strazar M; Broad Institute of MIT and Harvard.
  • Skelly A; Keio University School of Medicine.
  • Suda W; RIKEN Center for Integrative Medical Sciences.
  • Hattori M; RIKEN IMS.
  • Nakamoto N; Keio University School of Medicine.
  • Caballero S; Immunology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center.
  • Norman J; Vedanta Biosciences Inc.
  • Olle B; Vedanta Biosciences.
  • Tanoue T; Keio University School of Medicine.
  • Arita M; RIKEN Center for Integrative Medical Sciences.
  • Bucci V; UMass Chan Medical School.
  • Atarashi K; Keio University School of Medicine.
  • Xavier R; Massachusetts General Hospital.
Res Sq ; 2023 Oct 23.
Article en En | MEDLINE | ID: mdl-37961431
ABSTRACT
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 damage1,2. Gram-negative Enterobacteriaceae gut pathobionts are particularly recalcitrant to conventional antibiotic treatment3,4, though an emerging body of evidence suggests that manipulation of the commensal microbiota may be a practical alternative therapeutic strategy5-7. 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.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Res Sq Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Res Sq Año: 2023 Tipo del documento: Article