Literature DB >> 28428425

Neonatal acquisition of Clostridia species protects against colonization by bacterial pathogens.

Yun-Gi Kim1,2, Kei Sakamoto3,2, Sang-Uk Seo3,2, Joseph M Pickard3,2, Merritt G Gillilland4, Nicholas A Pudlo5, Matthew Hoostal4, Xue Li4, Thomas D Wang6, Taylor Feehley7, Andrew T Stefka7, Thomas M Schmidt4,5, Eric C Martens5, Shinji Fukuda8,9, Naohiro Inohara3, Cathryn R Nagler7, Gabriel Núñez1,2.   

Abstract

The high susceptibility of neonates to infections has been assumed to be due to immaturity of the immune system, but the mechanism remains unclear. By colonizing adult germ-free mice with the cecal contents of neonatal and adult mice, we show that the neonatal microbiota is unable to prevent colonization by two bacterial pathogens that cause mortality in neonates. The lack of colonization resistance occurred when Clostridiales were absent in the neonatal microbiota. Administration of Clostridiales, but not Bacteroidales, protected neonatal mice from pathogen infection and abrogated intestinal pathology upon pathogen challenge. Depletion of Clostridiales also abolished colonization resistance in adult mice. The neonatal bacteria enhanced the ability of protective Clostridiales to colonize the gut.
Copyright © 2017, American Association for the Advancement of Science.

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Year:  2017        PMID: 28428425      PMCID: PMC6082366          DOI: 10.1126/science.aag2029

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  16 in total

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2.  Challenges in infant immunity: implications for responses to infection and vaccines.

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Review 6.  Innate immune function by Toll-like receptors: distinct responses in newborns and the elderly.

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7.  Transitions in oral and intestinal microflora composition and innate immune receptor-dependent stimulation during mouse development.

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Journal:  PLoS Biol       Date:  2007-06-26       Impact factor: 8.029

Review 10.  Global causes of diarrheal disease mortality in children <5 years of age: a systematic review.

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Journal:  PLoS One       Date:  2013-09-04       Impact factor: 3.240

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  78 in total

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5.  Preventing dysbiosis of the neonatal mouse intestinal microbiome protects against late-onset sepsis.

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8.  MAIT cells are imprinted by the microbiota in early life and promote tissue repair.

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Review 10.  Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease.

Authors:  Joseph M Pickard; Melody Y Zeng; Roberta Caruso; Gabriel Núñez
Journal:  Immunol Rev       Date:  2017-09       Impact factor: 12.988

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