@article{fa4213c574dd413b8fd50eb2b3e45083,
title = "Age and environmental exposures influence the fecal bacteriome of young children with cystic fibrosis",
abstract = "Background: Mechanisms that facilitate early infection and inflammation in cystic fibrosis (CF) are unclear. We previously showed that young CF children with secondhand smoke exposure (SHSe) have increased susceptibility to respiratory infections. We aimed to define the impact of SHSe and other external factors upon the fecal bacteriome in early CF. Methods: Twenty CF infants and children were enrolled, clinical data recorded, and hair nicotine measured as an objective surrogate of SHSe. Fecal samples were collected at clinic visits and bacteriome 16S rRNA gene sequencing performed. Results: SHSe was associated with increased alpha diversity and increased relative abundance of Acinetobacter and Akkermansia, along with decreased Bifidobacterium and Lactobacillus. Recent antibiotic exposure predicted bacterial population structure in children less than 2 years of age and was associated with decreased Bacteroides relative abundance. Age was the strongest predictor of overall fecal bacterial composition and positively associated with Blautia and Parabacteroides. Weight for length was negatively associated with Staphylococcus relative abundance. Conclusions: SHSe and other external factors such as antibiotics appear to alter fecal bacterial composition in young CF children, but the strongest predictor of overall composition was age. These findings have implications for understanding the intestinal microbiome in young CF children.",
keywords = "cystic fibrosis (CF)",
author = "Loman, {Brett R.} and Shrestha, {Chandra L.} and Rohan Thompson and Groner, {Judith A.} and Asuncion Mejias and Ruoff, {Kathryn L.} and O'Toole, {George A.} and Bailey, {Michael T.} and Kopp, {Benjamin T.}",
note = "Funding Information: Thank you to Melinda Smith for assistance in sample procurement. Grant support provided by Nationwide Children's Hospital Intramural Grant (BTK, RT, and AM), American Academy of Pediatrics Julius B. Richmond Center New Investigator Grant (BTK), The Ohio State University Center for Clinical and Translational Science (National Center for Advancing Translational Sciences, Grant UL1TR002733), and by the Cystic Fibrosis Foundation (Cure CF Columbus Research Development Program, Grant MCCOY19RO). Support for KLR and GAO provided by NIDDK/P30‐DK117469 (DartCF; Dartmouth Cystic Fibrosis Research Center). We thank MBL for the fee‐for‐service sequencing, and Dr. Hilary Morrison for providing details of the methods. Funding Information: Thank you to Melinda Smith for assistance in sample procurement. Grant support provided by Nationwide Children's Hospital Intramural Grant (BTK, RT, and AM), American Academy of Pediatrics Julius B. Richmond Center New Investigator Grant (BTK), The Ohio State University Center for Clinical and Translational Science (National Center for Advancing Translational Sciences, Grant UL1TR002733), and by the Cystic Fibrosis Foundation (Cure CF Columbus Research Development Program, Grant MCCOY19RO). Support for KLR and GAO provided by NIDDK/P30-DK117469 (DartCF; Dartmouth Cystic Fibrosis Research Center). We thank MBL for the fee-for-service sequencing, and Dr. Hilary Morrison for providing details of the methods. Publisher Copyright: {\textcopyright} 2020 Wiley Periodicals, Inc.",
year = "2020",
month = jul,
day = "1",
doi = "10.1002/ppul.24766",
language = "English (US)",
volume = "55",
pages = "1661--1670",
journal = "Pediatric Pulmonology",
issn = "8755-6863",
publisher = "John Wiley & Sons, Ltd.",
number = "7",
}