Metagenomic Characterisation of the Gut Microbiome and Effect of Complementary Feeding on Bifidobacterium spp. in Australian Infants

Author:

Parkin Kimberley12ORCID,Palmer Debra J.12ORCID,Verhasselt Valerie13ORCID,Amenyogbe Nelly1,Cooper Matthew N.1,Christophersen Claus T.45ORCID,Prescott Susan L.246789ORCID,Silva Desiree24589ORCID,Martino David110ORCID

Affiliation:

1. Telethon Kids Institute, University of Western Australia, Nedlands, Perth, WA 6009, Australia

2. Medical School, University of Western Australia, Nedlands, Perth, WA 6009, Australia

3. Larsson-Rosenquist Foundation Centre for Immunology and Breastfeeding, Medical School, University of Western Australia, Nedlands, Perth, WA 6009, Australia

4. School of Molecular Life Sciences, Curtin University, Bentley, Perth, WA 6102, Australia

5. School of Medical and Health Sciences, Edith Cowen University, Joondalup, Perth, WA 6027, Australia

6. Joondalup Health Campus, Joondalup, Perth, WA 6027, Australia

7. Nova Institute for Health, Baltimore, MD 21231, USA

8. Department of Family and Community Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA

9. The ORIGINS Project, Telethon Kids Institute, Nedlands, Perth, WA 6009, Australia

10. School of Molecular Science, University of Western Australia, Nedlands, Perth, WA 6009, Australia

Abstract

Complementary feeding induces dramatic ecological shifts in the infant gut microbiota toward more diverse compositions and functional metabolic capacities, with potential implications for immune and metabolic health. The aim of this study was to examine whether the age at which solid foods are introduced differentially affects the microbiota in predominantly breastfed infants compared with predominantly formula-fed infants. We performed whole-genome shotgun metagenomic sequencing of infant stool samples from a cohort of six-month-old Australian infants enrolled in a nested study within the ORIGINS Project longitudinal birth cohort. Infants born preterm or those who had been administered antibiotics since birth were excluded. The taxonomic composition was highly variable among individuals at this age. Predominantly formula-fed infants exhibited a higher microbiome diversity than predominantly breastfed infants. Among the predominantly breastfed infants, the introduction of solid foods prior to five months of age was associated with higher alpha diversity than solid food introduction after six months of age, primarily due to the loss of Bifidobacterium infantis. In contrast, the age at which solid food was introduced was not associated with the overall change in diversity among predominantly formula-fed infants but was associated with compositional changes in Escherichia abundance. Examining the functional capacity of the microbiota in relation to these changes, we found that the introduction of solid foods after six months of age was associated with elevated one-carbon compound metabolic pathways in both breastfed and formula-fed infants, although the specific metabolic sub-pathways differed, likely reflecting different taxonomic compositions. Our findings suggest that the age of commencement of solid foods influences the gut microbiota composition differently in predominantly breastfed infants than in predominantly formula-fed infants.

Funder

Telethon Kids Institute Blue Sky Award

Family Larsson-Rosenquist Foundation

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3