Cargando…

Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs

Background: Preterm infants are born with an immature immune system, limited passive immunity, and are at risk of developing bacteremia and sepsis in the postnatal period. We hypothesized that enteral feeding, with or without added immunoglobulins, improves the clinical response to systemic infectio...

Descripción completa

Detalles Bibliográficos
Autores principales: Bæk, Ole, Brunse, Anders, Nguyen, Duc Ninh, Moodley, Arshnee, Thymann, Thomas, Sangild, Per Torp
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267211/
https://www.ncbi.nlm.nih.gov/pubmed/32536925
http://dx.doi.org/10.3389/fimmu.2020.01019
_version_ 1783541434680344576
author Bæk, Ole
Brunse, Anders
Nguyen, Duc Ninh
Moodley, Arshnee
Thymann, Thomas
Sangild, Per Torp
author_facet Bæk, Ole
Brunse, Anders
Nguyen, Duc Ninh
Moodley, Arshnee
Thymann, Thomas
Sangild, Per Torp
author_sort Bæk, Ole
collection PubMed
description Background: Preterm infants are born with an immature immune system, limited passive immunity, and are at risk of developing bacteremia and sepsis in the postnatal period. We hypothesized that enteral feeding, with or without added immunoglobulins, improves the clinical response to systemic infection by coagulase negative staphylococci. Methods: Using preterm cesarean delivered pigs as models for preterm infants, we infused live Staphylococcus epidermidis (SE, 5 × 10(9) colony forming units per kg) systemically 0–3 days after birth across five different experiments. SE infection responses were assessed following different gestational age at birth (preterm vs. term), enteral milk diets (bovine colostrum, infant formula with or without added porcine plasma) and with/without systemic immunoglobulins. Pigs infected with SE were assessed 12–48 h for clinical variables, blood bacteriology, chemistry, hematology, and gut dysfunction (intestinal permeability, necrotizing enterocolitis lesions). Results: Adverse clinical responses and increased mortality were observed in preterm vs. term pigs, when infected with SE just after birth. Feeding bovine colostrum just after birth improved blood SE clearance and clinical status (improved physical activity and intestinal structure, fewer bone marrow bacteria), relative to pigs fed infant formula. A few days later, clinical responses to SE bacteremia (hematology, neutrophil phagocytic capacity, T cell subsets) were less severe, and less affected by different milk diets, with or without added immunoglobulins. Conclusion: Prematurity increases the sensitivity of newborn pigs to SE bacteremia, potentially causing sepsis. Sensitivity to systemic SE infection decreases rapidly in the days after preterm birth. Both age and diet (parenteral nutrition, colostrum, milk, formula) may influence gut inflammation, bacterial translocation and systemic immune development in the days after birth in preterm newborns.
format Online
Article
Text
id pubmed-7267211
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-72672112020-06-12 Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs Bæk, Ole Brunse, Anders Nguyen, Duc Ninh Moodley, Arshnee Thymann, Thomas Sangild, Per Torp Front Immunol Immunology Background: Preterm infants are born with an immature immune system, limited passive immunity, and are at risk of developing bacteremia and sepsis in the postnatal period. We hypothesized that enteral feeding, with or without added immunoglobulins, improves the clinical response to systemic infection by coagulase negative staphylococci. Methods: Using preterm cesarean delivered pigs as models for preterm infants, we infused live Staphylococcus epidermidis (SE, 5 × 10(9) colony forming units per kg) systemically 0–3 days after birth across five different experiments. SE infection responses were assessed following different gestational age at birth (preterm vs. term), enteral milk diets (bovine colostrum, infant formula with or without added porcine plasma) and with/without systemic immunoglobulins. Pigs infected with SE were assessed 12–48 h for clinical variables, blood bacteriology, chemistry, hematology, and gut dysfunction (intestinal permeability, necrotizing enterocolitis lesions). Results: Adverse clinical responses and increased mortality were observed in preterm vs. term pigs, when infected with SE just after birth. Feeding bovine colostrum just after birth improved blood SE clearance and clinical status (improved physical activity and intestinal structure, fewer bone marrow bacteria), relative to pigs fed infant formula. A few days later, clinical responses to SE bacteremia (hematology, neutrophil phagocytic capacity, T cell subsets) were less severe, and less affected by different milk diets, with or without added immunoglobulins. Conclusion: Prematurity increases the sensitivity of newborn pigs to SE bacteremia, potentially causing sepsis. Sensitivity to systemic SE infection decreases rapidly in the days after preterm birth. Both age and diet (parenteral nutrition, colostrum, milk, formula) may influence gut inflammation, bacterial translocation and systemic immune development in the days after birth in preterm newborns. Frontiers Media S.A. 2020-05-27 /pmc/articles/PMC7267211/ /pubmed/32536925 http://dx.doi.org/10.3389/fimmu.2020.01019 Text en Copyright © 2020 Bæk, Brunse, Nguyen, Moodley, Thymann and Sangild. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bæk, Ole
Brunse, Anders
Nguyen, Duc Ninh
Moodley, Arshnee
Thymann, Thomas
Sangild, Per Torp
Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title_full Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title_fullStr Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title_full_unstemmed Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title_short Diet Modulates the High Sensitivity to Systemic Infection in Newborn Preterm Pigs
title_sort diet modulates the high sensitivity to systemic infection in newborn preterm pigs
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267211/
https://www.ncbi.nlm.nih.gov/pubmed/32536925
http://dx.doi.org/10.3389/fimmu.2020.01019
work_keys_str_mv AT bækole dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs
AT brunseanders dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs
AT nguyenducninh dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs
AT moodleyarshnee dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs
AT thymannthomas dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs
AT sangildpertorp dietmodulatesthehighsensitivitytosystemicinfectioninnewbornpretermpigs