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Pathogenic Bacteroides fragilis strains can emerge from gut-resident commensals.
Oles, Renee E; Terrazas, Marvic Carrillo; Loomis, Luke R; Neal, Maxwell J; Paulchakrabarti, Mousumi; Zuffa, Simone; Hsu, Chia-Yun; Vasquez Ayala, Adriana; Lee, Michael H; Tribelhorn, Caitlin; Belda-Ferre, Pedro; Bryant, MacKenzie; Zemlin, Jasmine; Young, Jocelyn; Dulai, Parambir; Sandborn, William J; Sivagnanam, Mamata; Raffatellu, Manuela; Pride, David; Dorrestein, Pieter C; Zengler, Karsten; Choudhury, Biswa; Knight, Rob; Chu, Hiutung.
Afiliación
  • Oles RE; Department of Pathology, University of California, San Diego, La Jolla, CA.
  • Terrazas MC; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Loomis LR; Department of Pathology, University of California, San Diego, La Jolla, CA.
  • Neal MJ; Department of Pathology, University of California, San Diego, La Jolla, CA.
  • Paulchakrabarti M; Department of Bioengineering, University of California, San Diego, La Jolla, CA.
  • Zuffa S; GlycoAnalytics Core, University of California San Diego, San Diego, CA.
  • Hsu CY; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla.
  • Vasquez Ayala A; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA.
  • Lee MH; Department of Pathology, University of California, San Diego, La Jolla, CA.
  • Tribelhorn C; Department of Pathology, University of California, San Diego, La Jolla, CA.
  • Belda-Ferre P; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Bryant M; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Zemlin J; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Young J; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Dulai P; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla.
  • Sandborn WJ; Collaborative Mass Spectrometry Innovation Center, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, CA.
  • Sivagnanam M; Division of Gastroenterology, Hepatology and Nutrition, University of California, San Diego and Rady Children's Hospital, San Diego, CA.
  • Raffatellu M; Division of Gastroenterology, University of California, San Diego, La Jolla, CA.
  • Pride D; Division of Gastroenterology, Northwestern University, Chicago, Illinois.
  • Dorrestein PC; Division of Gastroenterology, University of California, San Diego, La Jolla, CA.
  • Zengler K; Center for Microbiome Innovation, University of California, San Diego, La Jolla, CA.
  • Choudhury B; Division of Gastroenterology, Hepatology and Nutrition, University of California, San Diego and Rady Children's Hospital, San Diego, CA.
  • Knight R; Division of Host-Microbe Systems and Therapeutics, Department of Pediatrics, University of California, San Diego, La Jolla, CA.
  • Chu H; Center for Microbiome Innovation, University of California, San Diego, La Jolla, CA.
bioRxiv ; 2024 Jun 19.
Article en En | MEDLINE | ID: mdl-38948766
ABSTRACT
Bacteroides fragilis is a prominent member of the human gut microbiota, playing crucial roles in maintaining gut homeostasis and host health. Although it primarily functions as a beneficial commensal, B. fragilis can become pathogenic. To determine the genetic basis of its duality, we conducted a comparative genomic analysis of 813 B. fragilis strains, representing both commensal and pathogenic origins. Our findings reveal that pathogenic strains emerge across diverse phylogenetic lineages, due in part to rapid gene exchange and the adaptability of the accessory genome. We identified 16 phylogenetic groups, differentiated by genes associated with capsule composition, interspecies competition, and host interactions. A microbial genome-wide association study identified 44 genes linked to extra-intestinal survival and pathogenicity. These findings reveal how genomic diversity within commensal species can lead to the emergence of pathogenic traits, broadening our understanding of microbial evolution in the gut.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Canadá
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