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


Journal

Nature medicine
ISSN: 1546-170X
Titre abrégé: Nat Med
Pays: United States
ID NLM: 9502015

Informations de publication

Date de publication:
11 2019
Historique:
received: 05 10 2018
accepted: 03 10 2019
pubmed: 9 11 2019
medline: 21 1 2020
entrez: 9 11 2019
Statut: ppublish

Résumé

Late-onset sepsis (LOS) is thought to result from systemic spread of commensal microbes from the intestines of premature infants. Clinical use of probiotics for LOS prophylaxis has varied owing to limited efficacy, reflecting an incomplete understanding of relationships between development of the intestinal microbiome, neonatal dysbiosis and LOS. Using a model of LOS, we found that components of the developing microbiome were both necessary and sufficient to prevent LOS. Maternal antibiotic exposure that eradicated or enriched transmission of Lactobacillus murinus exacerbated and prevented disease, respectively. Prophylactic administration of some, but not all Lactobacillus spp. was protective, as was administration of Escherichia coli. Intestinal oxygen level was a major driver of colonization dynamics, albeit via mechanisms distinct from those in adults. These results establish a link between neonatal dysbiosis and LOS, and provide a basis for rational selection of probiotics that modulate primary succession of the microbiome to prevent disease.

Identifiants

pubmed: 31700190
doi: 10.1038/s41591-019-0640-y
pii: 10.1038/s41591-019-0640-y
pmc: PMC7250008
mid: NIHMS1563256
doi:

Substances chimiques

Protective Agents 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1772-1782

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR003096
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI007051
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA013148
Pays : United States
Organisme : NIDDK NIH HHS
ID : F30 DK105680
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR050948
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001417
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008361
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

Liu, L. et al. Global, regional, and national causes of child mortality in 2000–13, with projections to inform post-2015 priorities: an updated systematic analysis. Lancet 385, 430–440 (2015).
pubmed: 25280870
Stoll, B. J. et al. Trends in care practices, morbidity, and mortality of extremely preterm neonates, 1993–2012. JAMA 314, 1039–1051 (2015).
pubmed: 26348753 pmcid: 4787615
Dong, Y. & Speer, C. P. Late-onset neonatal sepsis: recent developments. Arch. Dis. Child. Fetal Neonatal Ed. 100, F257–F263 (2015).
pubmed: 25425653
Kuppala, V., Meinzen-Derr, J. & Morrow, A. Prolonged initial empirical antibiotic treatment is associated with adverse outcomes in premature infants. J. Pediatr. 159, 720–725 (2011).
pubmed: 21784435 pmcid: 3193552
Fajardo, C., Alshaikh, B. & Harabor, A. Prolonged use of antibiotics after birth is associated with increased morbidity in preterm infants with negative cultures. J. Matern. Fetal Neonatal Med. 64, 1–7 (2018).
Gibson, M. K. et al. Developmental dynamics of the preterm infant gut microbiota and antibiotic resistome. Nat. Microbiol. 1, 16024 (2016).
pubmed: 27572443 pmcid: 5031140
Yassour, M. et al. Natural history of the infant gut microbiome and impact of antibiotic treatment on bacterial strain diversity and stability. Sci. Transl. Med. 8, 343ra81 (2016).
pubmed: 27306663 pmcid: 5032909
Parm, Ü., Metsvaht, T., Ilmoja, M.-L. & Lutsar, I. Gut colonization by aerobic microorganisms is associated with route and type of nutrition in premature neonates. Nutr. Res. 35, 496–503 (2015).
pubmed: 25922115
Bokulich, N. A. et al. Antibiotics, birth mode, and diet shape microbiome maturation during early life. Sci. Transl. Med. 8, 343ra82 (2016).
pubmed: 27306664 pmcid: 5308924
Korpela, K. et al. Intestinal microbiota development and gestational age in preterm neonates. Sci. Rep. 8, 2453 (2018).
pubmed: 29410448 pmcid: 5802739
Tarr, P. I. & Warner, B. B. Gut bacteria and late-onset neonatal bloodstream infections in preterm infants. Semin. Fetal Neonatal Med. 21, 388–393 (2016).
pubmed: 27345372
Graham, P. L., Della-Latta, P., Wu, F., Zhou, J. & Saiman, L. The gastrointestinal tract serves as the reservoir for Gram-negative pathogens in very low birth weight infants. Pediatr. Infect. Dis. J. 26, 1153–1156 (2007).
pubmed: 18043457
Knoop, K. A. et al. Microbial antigen encounter during a preweaning interval is critical for tolerance to gut bacteria. Sci. Immunol. 2, eaao1314 (2017).
pubmed: 29246946 pmcid: 5759965
Kim, Y.-G. et al. Neonatal acquisition of Clostridia species protects against colonization by bacterial pathogens. Science 356, 315–319 (2017).
pubmed: 28428425 pmcid: 6082366
Tourneur, E. & Chassin, C. Neonatal immune adaptation of the gut and its role during infections. Clin. Dev. Immunol. 2013, 270301–270317 (2013).
pubmed: 23737810 pmcid: 3659470
Dermyshi, E. et al. The ‘golden age’ of probiotics: a systematic review and meta-analysis of randomized and observational studies in preterm infants. Neonatology 112, 9–23 (2017).
van den Akker, C. H. P. et al. Probiotics for preterm infants: a strain-specific systematic review and network meta-analysis. J. Pediatr. Gastroenterol. Nutr. 67, 103–122 (2018).
pubmed: 29384838
Deshmukh, H. S. et al. The microbiota regulates neutrophil homeostasis and host resistance to Escherichia coli K1 sepsis in neonatal mice. Nat. Med. 20, 524–530 (2014).
pubmed: 24747744 pmcid: 4016187
Ulas, T. et al. S100-alarmin-induced innate immune programming protects newborn infants from sepsis. Nat. Immunol. 18, 622–632 (2017).
pubmed: 28459433
Howe, K. et al. Development of stable reporter system cloning luxCDABE genes into chromosome of Salmonella enterica serotypes using Tn7 transposon. BMC Microbiol. 10, 197 (2010).
pubmed: 20653968 pmcid: 2918591
Langstraat, J., Bohse, M. & Clegg, S. Type 3 fimbrial shaft (MrkA) of Klebsiella pneumoniae, but not the fimbrial adhesin (MrkD), facilitates biofilm formation. Infect. Immun. 69, 5805–5812 (2001).
pubmed: 11500458 pmcid: 98698
Ko, K. S. The contribution of capsule polysaccharide genes to virulence of Klebsiella pneumoniae. Virulence 8, 485–486 (2017).
pubmed: 27715471
Pamer, E. G. Resurrecting the intestinal microbiota to combat antibiotic-resistant pathogens. Science 352, 535–538 (2016).
pubmed: 27126035 pmcid: 4984266
Patel, S. & Bernice, F. Vancomycin. in StatPearls https://www.ncbi.nlm.nih.gov/pubmed/29083794 (StatPearls Publishing, 2018).
Miranda, J. C. et al. Gentamicin absorption during prophylactic use for necrotizing enterocolitis. Dev. Pharmacol. Ther. 7, 303–306 (1984).
pubmed: 6478984
Milani, C. et al. Phylotype-level profiling of lactobacilli in highly complex environments by means of an internal transcribed spacer-based metagenomic approach. Appl. Environ. Microbiol. 84, e00706–e00718 (2018).
pubmed: 29728382 pmcid: 6029092
Eren, A. M. et al. Oligotyping: differentiating between closely related microbial taxa using 16S rRNA gene data. Methods Ecol. Evol. 4, 1111–1119 (2013).
pmcid: 3864673
Ammor, M. S., Belén Flórez, A. & Mayo, B. Antibiotic resistance in non-enterococcal lactic acid bacteria and bifidobacteria. Food Microbiol. 24, 559–570 (2007).
pubmed: 17418306
Elkins, C. A. & Mullis, L. B. Bile-mediated aminoglycoside sensitivity in Lactobacillus species likely results from increased membrane permeability attributable to cholic acid. Appl. Environ. Microbiol. 70, 7200–7209 (2004).
pubmed: 15574918 pmcid: 535180
Yassour, M. et al. Strain-level analysis of mother-to-child bacterial transmission during the first few months of life. Cell Host Microbe 24, 146–154 (2018).
pubmed: 30001517 pmcid: 6091882
Ferretti, P. et al. Mother-to-infant microbial transmission from different body sites shapes the developing infant gut microbiome. Cell Host Microbe 24, 133–145 (2018).
pubmed: 30001516 pmcid: 6716579
Taft, D. H. et al. Center variation in intestinal microbiota prior to late-onset sepsis in preterm infants. PloS One 10, e0130604 (2015).
pubmed: 26110908 pmcid: 4482142
Madan, J. C. et al. Gut microbial colonisation in premature neonates predicts neonatal sepsis. Arch. Dis. Child. Fetal Neonatal Ed. 97, F456–F462 (2012).
pubmed: 22562869 pmcid: 3724360
Mai, V. et al. Distortions in development of intestinal microbiota associated with late onset sepsis in preterm infants. PloS One 8, e52876 (2013).
pubmed: 23341915 pmcid: 3544792
Litvak, Y., Byndloss, M. X. & Baumler, A. J. Colonocyte metabolism shapes the gut microbiota. Science 362, eaat9076 (2018).
pubmed: 30498100 pmcid: 6296223
Rivera-Chávez, F. et al. Depletion of butyrate-producing Clostridia from the gut microbiota drives an aerobic luminal expansion of Salmonella. Cell Host Microbe 19, 443–454 (2016).
pubmed: 27078066 pmcid: 4832419
Cramton, S. E., Ulrich, M., Götz, F. & Döring, G. Anaerobic conditions induce expression of polysaccharide intercellular adhesin in Staphylococcus aureus and Staphylococcus epidermidis. Infect. Immun. 69, 4079–4085 (2001).
pubmed: 11349079 pmcid: 98472
Byndloss, M. X. & Baumler, A. J. The germ-organ theory of non-communicable diseases. Nat. Rev. Microbiol. 16, 103–110 (2018).
pubmed: 29307890
Lodinová-Zádniková, R. & Sonnenborn, U. Effect of preventive administration of a nonpathogenic Escherichia coli strain on the colonization of the intestine with microbial pathogens in newborn infants. Biol. Neonate 71, 224–232 (1997).
pubmed: 9129791
Birchenough, G. M. H. et al. Altered innate defenses in the neonatal gastrointestinal tract in response to colonization by neuropathogenic Escherichia coli. Infect. Immun. 81, 3264–3275 (2013).
pubmed: 23798529 pmcid: 3754193
Grozdanov, L. et al. Analysis of the genome structure of the nonpathogenic probiotic Escherichia coli strain Nissle 1917. J. Bacteriol. 186, 5432–5441 (2004).
pubmed: 15292145 pmcid: 490877
Reed, B. D., Schibler, K. R., Deshmukh, H., Ambalavanan, N. & Morrow, A. L. The impact of maternal antibiotics on neonatal disease. J. Pediatr. 197, 97–103 (2018).
pubmed: 29551319 pmcid: 6028045
Schulman, J. et al. Neonatal intensive care unit antibiotic use. Pediatrics 135, 826–833 (2015).
pubmed: 25896845
Rao, S. C., Athalye-Jape, G. K., Deshpande, G. C., Simmer, K. N. & Patole, S. K. Probiotic supplementation and late-onset sepsis in preterm infants: a meta-analysis. Pediatrics 137, e20153684 (2016).
pubmed: 26908700
Viswanathan, S., Lau, C., Akbari, H., Hoyen, C. & Walsh, M. C. Survey and evidence-based review of probiotics used in very low birth weight preterm infants within the United States. J. Perinatol. 36, 1106–1111 (2016).
pubmed: 27583387
Suez, J., Zmora, N., Segal, E. & Elinav, E. The pros, cons, and many unknowns of probiotics. Nat. Med. 25, 716–729 (2019).
Segers, M. E. & Lebeer, S. Towards a better understanding of Lactobacillus rhamnosus GG–host interactions. Microb. Cell Fact. 13, S7 (2014).
pubmed: 25186587 pmcid: 4155824
Panigrahi, P. et al. A randomized synbiotic trial to prevent sepsis among infants in rural India. Nature 548, 407–412 (2017).
Kelly, C. J. et al. Crosstalk between microbiota-derived short-chain fatty acids and intestinal epithelial HIF augments tissue barrier function. Cell Host Microbe 17, 662–671 (2015).
pubmed: 25865369 pmcid: 4433427
Byndloss, M. X. et al. Microbiota-activated PPAR-γ signaling inhibits dysbiotic Enterobacteriaceae expansion. Science 357, 570–575 (2017).
pubmed: 28798125 pmcid: 5642957
Lee, A. & Gemmell, E. Changes in the mouse intestinal microflora during weaning: role of volatile fatty acids. Infect. Immun. 5, 1–7 (1972).
pubmed: 4656353 pmcid: 422310
Hosny, M., Cassir, N. & La Scola, B. Updating on gut microbiota and its relationship with the occurrence of necrotizing enterocolitis. Hum. Microbiome J. 4, 14–19 (2017).
Corsini, I. et al. Peroxisome proliferator-activated receptor-γ agonist pioglitazone reduces the development of necrotizing enterocolitis in a neonatal preterm rat model. Pediatr. Res. 81, 364–368 (2017).
pubmed: 27973471
Friedman, E. S. et al. Microbes versus chemistry in the origin of the anaerobic gut lumen. Proc. Natl Acad. Sci. USA 115, 4170–4175 (2018).
de Goffau, M. C. et al. Human placenta has no microbiome but can contain potential pathogens. Nature 572, 329–334 (2019).
pubmed: 31367035
Pedersen, M. B., Gaudu, P., Lechardeur, D., Petit, M.-A. & Gruss, A. Aerobic respiration metabolism in lactic acid bacteria and uses in biotechnology. Annu. Rev. Food Sci. Technol. 3, 37–58 (2012).
pubmed: 22385163
Wilck, N. et al. Salt-responsive gut commensal modulates T
pubmed: 29143823 pmcid: 6070150
Singh, A. K., Hertzberger, R. Y. & Knaus, U. G. Hydrogen peroxide production by lactobacilli promotes epithelial restitution during colitis. Redox Biol. 16, 11–20 (2018).
pubmed: 29471162 pmcid: 5835490
Lee, Y.-S. et al. Microbiota-derived lactate accelerates intestinal stem-cell-mediated epithelial development. Cell Host Microbe 24, 833–846 (2018).
pubmed: 30543778
Litvak, Y. et al. Commensal Enterobacteriaceae protect against Salmonella colonization through oxygen competition. Cell Host Microbe 25, 128–139 (2019).
pubmed: 30629913
Hinsa, S. M., Espinosa-Urgel, M., Ramos, J. L. & O'Toole, G. A. Transition from reversible to irreversible attachment during biofilm formation by Pseudomonas fluorescens WCS365 requires an ABC transporter and a large secreted protein. Mol. Microbiol. 49, 905–918 (2003).
pubmed: 12890017
McKenzie, G. J. & Craig, N. L. Fast, easy and efficient: site-specific insertion of transgenes into enterobacterial chromosomes using Tn7 without need for selection of the insertion event. BMC Microbiol. 6, 39 (2006).
pubmed: 16646962 pmcid: 1475584
Kumar, R. et al. Getting started with microbiome analysis: sample acquisition to bioinformatics. Curr. Protoc. Hum. Genet. 82, 18.8.1–18.8.29 (2014).
Segata, N. et al. Metagenomic biomarker discovery and explanation. Genome Biol. 12, R60 (2011).
pubmed: 21702898 pmcid: 3218848
Meadow, J. q2oligo—convert QIIME files into oligotyping subsets. GitHub https://github.com/jfmeadow/q2oligo (2014).
Bergey, D. H. Bergey's Manual of Systematics of Archaea and Bacteria. Bergey's Manual Trust https://doi.org/10.1002/9781118960608 (2015).
Ormerod, K. L. et al. Genomic characterization of the uncultured Bacteroidales family S24-7 inhabiting the guts of homeothermic animals. Microbiome 4, 36 (2016).
pubmed: 27388460 pmcid: 4936053
Tegtmeier, D., Riese, C., Geissinger, O., Radek, R. & Brune, A. Breznakia blatticola gen. nov. sp. nov. and Breznakia pachnodae sp. nov., two fermenting bacteria isolated from insect guts, and emended description of the family Erysipelotrichaceae. Syst. Appl. Microbiol. 39, 319–329 (2016).
pubmed: 27270136
Weingarten, R. A. et al. Genomic analysis of hospital plumbing reveals diverse reservoir of bacterial plasmids conferring carbapenem resistance. mBio 9, e02011–e02017 (2018).
pubmed: 29437920 pmcid: 5801463
Nurk, S. et al. Assembling single-cell genomes and mini-metagenomes from chimeric MDA products. J. Comput. Biol. 20, 714–737 (2013).
pubmed: 24093227 pmcid: 3791033
Koren, S. et al. Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation. Genome Res. 27, 722–736 (2017).
pubmed: 28298431 pmcid: 5411767
Treangen, T. J., Ondov, B. D., Koren, S. & Phillippy, A. M. The harvest suite for rapid core-genome alignment and visualization of thousands of intraspecific microbial genomes. Genome Biol. 15, 524 (2014).
pubmed: 25410596 pmcid: 4262987
Wyres, K. L. et al. Identification of Klebsiella capsule synthesis loci from whole genome data. Microb. Genomics 2, 1–15 (2016).
Johnson, R. C. et al. Investigation of a cluster of Sphingomonas koreensis infections. N. Engl. J. Med. 379, 2529–2539 (2018).
pubmed: 30586509 pmcid: 6322212
Wood, D. E. & Salzberg, S. L. Kraken: ultrafast metagenomic sequence classification using exact alignments. Genome Biol. 15, R46 (2014).
pubmed: 24580807 pmcid: 4053813
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Meth. 9, 357–359 (2012).
Bates, D., Mächler, M., Bolker, B. & Walker, S. Fitting linear mixed-effects models using lme4. J. Stat. Software 1, 1–48 (2015).

Auteurs

Jeffrey R Singer (JR)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA. jrsinger@uab.edu.

Emily G Blosser (EG)

Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Obstetrics and Gynecology, Ochsner Health System, New Orleans, LA, USA.

Carlene L Zindl (CL)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.

Daniel J Silberger (DJ)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.

Sean Conlan (S)

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

Vincent A Laufer (VA)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.

Daniel DiToro (D)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA.

Clay Deming (C)

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

Ranjit Kumar (R)

Center for Clinical and Translational Science Informatics Institute, University of Alabama at Birmingham, Birmingham, AL, USA.

Casey D Morrow (CD)

Department of Cell Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.

Julia A Segre (JA)

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

Michael J Gray (MJ)

Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL, USA.

David A Randolph (DA)

Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.
Division of Neonatal-Perinatal Medicine, Rocky Mountain Hospital for Children, Denver, CO, USA.

Casey T Weaver (CT)

Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, USA. cweaver@uab.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH