TY - JOUR
T1 - Antibiotics, pediatric dysbiosis, and disease
AU - Vangay, Pajau
AU - Ward, Tonya
AU - Gerber, Jeffrey S.
AU - Knights, Dan
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/5/13
Y1 - 2015/5/13
N2 - Antibiotics are by far the most common medications prescribed for children. Recent epidemiological data suggests an association between early antibiotic use and disease phenotypes in adulthood. Antibiotic use during infancy induces imbalances in gut microbiota, called dysbiosis. The gut microbiome's responses to antibiotics and its potential link to disease development are especially complex to study in the changing infant gut. Here, we synthesize current knowledge linking antibiotics, dysbiosis, and disease and propose a framework for studying antibiotic-related dysbiosis in children. We recommend future studies into the microbiome-mediated effects of antibiotics focused on four types of dysbiosis: loss of keystone taxa, loss of diversity, shifts in metabolic capacity, and blooms of pathogens. Establishment of a large and diverse baseline cohort to define healthy infant microbiome development is essential to advancing diagnosis, interpretation, and eventual treatment of pediatric dysbiosis. This approach will also help provide evidence-based recommendations for antibiotic usage in infancy.
AB - Antibiotics are by far the most common medications prescribed for children. Recent epidemiological data suggests an association between early antibiotic use and disease phenotypes in adulthood. Antibiotic use during infancy induces imbalances in gut microbiota, called dysbiosis. The gut microbiome's responses to antibiotics and its potential link to disease development are especially complex to study in the changing infant gut. Here, we synthesize current knowledge linking antibiotics, dysbiosis, and disease and propose a framework for studying antibiotic-related dysbiosis in children. We recommend future studies into the microbiome-mediated effects of antibiotics focused on four types of dysbiosis: loss of keystone taxa, loss of diversity, shifts in metabolic capacity, and blooms of pathogens. Establishment of a large and diverse baseline cohort to define healthy infant microbiome development is essential to advancing diagnosis, interpretation, and eventual treatment of pediatric dysbiosis. This approach will also help provide evidence-based recommendations for antibiotic usage in infancy.
UR - http://www.scopus.com/inward/record.url?scp=84929300450&partnerID=8YFLogxK
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U2 - 10.1016/j.chom.2015.04.006
DO - 10.1016/j.chom.2015.04.006
M3 - Review article
C2 - 25974298
AN - SCOPUS:84929300450
SN - 1931-3128
VL - 17
SP - 553
EP - 564
JO - Cell Host and Microbe
JF - Cell Host and Microbe
IS - 5
ER -