B3704 - An exploration of the relationship of early-life microbiome patterns and susceptibility to future infections - 25/05/2021

B number: 
B3704
Principal applicant name: 
Claire Woodall | Bristol Medical School: Population Health Sciences (UK)
Co-applicants: 
Professor Alastair Hay
Title of project: 
An exploration of the relationship of early-life microbiome patterns and susceptibility to future infections
Proposal summary: 

Often termed the ‘lost organ’ the human gut contains trillions of microbes. A rich, diverse gut microbiota is considered to promote health, whereas a microbiota with reduced diversity is associated with gut inflammation and disease. Many factors affect gut microbes including host genetics, injury, diet, infection and antibiotics; the use of the latter being associated with the increased risk of obesity, cancer, asthma and diabetes in children.

The development of gut microbiota begins before the infant is born with maternal factors such as infection and birth-mode. Then at birth microbial gut colonization begins, continually developing for about 3 years, until the microbiota becomes more stable and adult-like. The gut microbiota in children under 3 years of age fluctuates and is more impressionable to environmental factors than the adult microbiota. During this time children experience significant developmental changes that influence their health status and gut microbiome. Children also suffer more infectious diseases and associated antibiotic usage, than adults. Studies indicate that most, but not all, bacterial species recover during the 6 months post-antibiotic treatment and that specific early-life exposures to antibiotics, caesarean section and formula feeding disrupts gut microbiome establishment.

It has been suggested there is an early-life ‘critical window’ of development during which the microbiota is disrupted beyond repair favouring susceptibility to future health issues. A major concern is permanent loss of beneficial bacteria after repeated early life infections and associated antibiotics, with cumulative effects increasing susceptibility to emerging health issues and infections.

Impact of research: 
The likely impact for this community-based prospective cohort study is the link between the identified microbiome patterns and subsequent infection susceptibility. There are published studies that describe the association between targeted factors and disruptions to the early-life gut microbiome. However, there are no published studies describing associated factors that influence the ‘critical window’ of early-life microbiome development which then increase future susceptibility to later-life infections and emerging health issues. The identification of specific early-life microbiome patterns with the permanent loss of beneficial bacteria that children take forward with them through-out life will have a huge effect on their life. This study will reveal ground-breaking developments to identify children most vulnerable to susceptibility to later-life infections. A combination of being able to perform both a cross-section and longitudinal microbiome study is very rare and will greatly enhance our understanding of topical trends in clinical microbiome. In particular, the prediction of clinical outcomes through microbial biomarkers represents an active and promising area of research.
Date proposal received: 
Thursday, 21 January, 2021
Date proposal approved: 
Monday, 25 January, 2021
Keywords: 
Microbiology - Bacteriology, Infection, Microbial Bioinformatics, Microbiome