TY - JOUR
T1 - Prolonged hospitalization signature and early antibiotic effects on the nasopharyngeal resistome in preterm infants
AU - Dhariwal, Achal
AU - Rajar, Polona
AU - Salvadori, Gabriela
AU - Åmdal, Heidi Aarø
AU - Berild, Dag
AU - Saugstad, Ola Didrik
AU - Fugelseth, Drude
AU - Greisen, Gorm
AU - Dahle, Ulf
AU - Haaland, Kirsti
AU - Petersen, Fernanda Cristina
N1 - © 2024. The Author(s).
PY - 2024/7/17
Y1 - 2024/7/17
N2 - Respiratory pathogens, commonly colonizing nasopharynx, are among the leading causes of death due to antimicrobial resistance. Yet, antibiotic resistance determinants within nasopharyngeal microbial communities remain poorly understood. In this prospective cohort study, we investigate the nasopharynx resistome development in preterm infants, assess early antibiotic impact on its trajectory, and explore its association with clinical covariates using shotgun metagenomics. Our findings reveal widespread nasopharyngeal carriage of antibiotic resistance genes (ARGs) with resistomes undergoing transient changes, including increased ARG diversity, abundance, and composition alterations due to early antibiotic exposure. ARGs associated with the critical nosocomial pathogen Serratia marcescens persist up to 8-10 months of age, representing a long-lasting hospitalization signature. The nasopharyngeal resistome strongly correlates with microbiome composition, with inter-individual differences and postnatal age explaining most of the variation. Our report on the collateral effects of antibiotics and prolonged hospitalization underscores the urgency of further studies focused on this relatively unexplored reservoir of pathogens and ARGs.
AB - Respiratory pathogens, commonly colonizing nasopharynx, are among the leading causes of death due to antimicrobial resistance. Yet, antibiotic resistance determinants within nasopharyngeal microbial communities remain poorly understood. In this prospective cohort study, we investigate the nasopharynx resistome development in preterm infants, assess early antibiotic impact on its trajectory, and explore its association with clinical covariates using shotgun metagenomics. Our findings reveal widespread nasopharyngeal carriage of antibiotic resistance genes (ARGs) with resistomes undergoing transient changes, including increased ARG diversity, abundance, and composition alterations due to early antibiotic exposure. ARGs associated with the critical nosocomial pathogen Serratia marcescens persist up to 8-10 months of age, representing a long-lasting hospitalization signature. The nasopharyngeal resistome strongly correlates with microbiome composition, with inter-individual differences and postnatal age explaining most of the variation. Our report on the collateral effects of antibiotics and prolonged hospitalization underscores the urgency of further studies focused on this relatively unexplored reservoir of pathogens and ARGs.
KW - Humans
KW - Nasopharynx/microbiology
KW - Infant, Premature
KW - Anti-Bacterial Agents/pharmacology
KW - Infant, Newborn
KW - Prospective Studies
KW - Hospitalization
KW - Female
KW - Male
KW - Metagenomics/methods
KW - Infant
KW - Serratia marcescens/drug effects
KW - Microbiota/drug effects
KW - Drug Resistance, Bacterial/genetics
KW - Drug Resistance, Microbial/genetics
UR - http://www.scopus.com/inward/record.url?scp=85198969428&partnerID=8YFLogxK
U2 - 10.1038/s41467-024-50433-7
DO - 10.1038/s41467-024-50433-7
M3 - Journal article
C2 - 39019886
SN - 2041-1722
VL - 15
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6024
ER -