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Development of early life gut resistome and mobilome across gestational ages and microbiota-modifying treatments

Bargheet, A. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
Klingenberg, C. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
Esaiassen, E. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
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Hjerde, E. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
Cavanagh, J. P. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
Bengtsson-Palme, Johan, 1985 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för infektionssjukdomar,Institute of Biomedicine, Department of Infectious Medicine,University of Gothenburg,Chalmers tekniska högskola,Chalmers University of Technology
Pettersen, V. K. (författare)
Universitetet i Tromsø – Norges arktiske universitet,University of Tromsø – The Arctic University of Norway
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 (creator_code:org_t)
2023
2023
Engelska.
Ingår i: Ebiomedicine. - 2352-3964. ; 92
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Gestational age (GA) and associated level of gastrointestinal tract maturation are major factors driving the initial gut microbiota composition in preterm infants. Besides, compared to term infants, premature infants often receive antibiotics to treat infections and probiotics to restore optimal gut microbiota. How GA, antibiotics, and probiotics modulate the microbiota’s core characteristics, gut resistome and mobilome, remains nascent. Methods We analysed metagenomic data from a longitudinal observational study in six Norwegian neonatal intensive care units to describe the bacterial microbiota of infants of varying GA and receiving different treatments. The cohort consisted of probiotic-supplemented and antibiotic-exposed extremely preterm infants (n = 29), antibiotic-exposed very preterm (n = 25), antibiotic-unexposed very preterm (n = 8), and antibiotic-unexposed full-term (n = 10) infants. The stool samples were collected on days of life 7, 28, 120, and 365, and DNA extraction was followed by shotgun metagenome sequencing and bioinformatical analysis. Findings The top predictors of microbiota maturation were hospitalisation length and GA. Probiotic administration rendered the gut microbiota and resistome of extremely preterm infants more alike to term infants on day 7 and ameliorated GA-driven loss of microbiota interconnectivity and stability. GA, hospitalisation, and both microbiota-modifying treatments (antibiotics and probiotics) contributed to an elevated carriage of mobile genetic elements in preterm infants compared to term controls. Finally, Escherichia coli was associated with the highest number of antibiotic-resistance genes, followed by Klebsiella pneumoniae and Klebsiella aerogenes. Interpretation Prolonged hospitalisation, antibiotics, and probiotic intervention contribute to dynamic alterations in resistome and mobilome, gut microbiota characteristics relevant to infection risk.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Nyckelord

Extremely preterm infants
Probiotics
Gestational age
Gut microbiota
Resistome
Mobilome
resistance
supplementation
association
General & Internal Medicine
Research & Experimental Medicine
Extremely preterm infants

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