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DeClercq, V.

Publications and source records attributed to DeClercq, V..

3 recordsLinked to original sources

Effect of bedrest on the human gut and oral microbiome: implications for frailty

The physiological effects of spaceflight resemble those of ageing and prolonged inactivity, and ground-based microgravity analogs have emerged as promising models for studying frailty. The human microbiome is increasingly recognised for its role in age-associated decline, although precise mechanisms remain unclear. Here, we evaluate the gut and oral microbiomes of twenty-two participants, aged 55-65, who were enrolled in a head-down tilt bedrest (HDBR) study, the first Canadian HDBR study conducted in an older cohort. Participants were randomly assigned to an inactivity or multi-modality exercise intervention group for fourteen days of HDBR, followed by seven days of rehabilitation and additional follow-up appointments. Gut (n=343) and oral (n=344) taxonomic profiles were generated using V4/V5 16S rRNA gene sequencing from fecal and salivary samples collected throughout the study. Gut functional profiles were generated using metagenomic (n=86) and metabolomic (n=83) data. Frailty was measured using a 36-item frailty index. Inactivity-associated changes to the gut microbiome during HDBR included decreasing -diversity, decreasing Akkermansia and Lactobacillus, and increasing Bacteroides. Exercise-associated changes included increasing gut Roseburia. Interestingly, oral microbiome {beta}-diversity was more strongly associated with frailty than the gut. We conclude that inactivity-associated changes to the human microbiome could contribute to the early stages of frailty development, and that exercise can serve as an effective countermeasure against these effects. These results may inform strategies to preserve the health of both older adults facing prolonged periods of inactivity, as well as astronauts during longer space exploration missions. IMPORTANCEHealthy ageing carries significant demographic, economic, and public health implications globally, and both physical activity and human-associated microorganisms play important roles in its trajectory. Using microgravity simulation in older adults as a human frailty model, we show that short periods of inactivity could have significant effects on these microbial communities, particularly in the gut, which could further contribute to multi-system physiological decline and frailty pathogenesis. Participants who completed a daily, multi-modality exercise intervention did not exhibit these changes, which may help protect both older adults facing periods of inactivity and astronauts in the advent of longer space exploration missions. Interestingly, our results suggested that oral bacteria may be a more sensitive indicator of individual frailty levels than gut bacteria. Future research should ensure that functional aspects of human-associated microbial communities are thoroughly investigated, as these may offer deeper insight into their contributions to age-related decline.

microbiology↗

Investigating the oral microbiome in retrospective and prospective cases of prostate, colon, and breast cancer.

The human microbiome has been proposed as a useful biomarker for several different human diseases including various cancers. To answer this question, we examined salivary samples from two Canadian population cohorts, the Atlantic Partnership for Tomorrows Health project (PATH) and Albertas Tomorrow Project (ATP). Sample selection was then divided into both a retrospective and prospective case control design examining individuals with prostate, breast, or colon cancer. In total 89 retrospective and 260 prospective cancer cases were matched to non-cancer controls and saliva samples were sequenced using 16S rRNA gene sequencing to compare bacterial diversity, and taxonomic composition. We found no significant differences in alpha or beta diversity across any of the three cancer types and two study designs. Although retrospective colon cancer samples did show evidence on visual clustering in weighted beta diversity metrics. Differential abundance analysis of individual taxon showed several taxa that were associated with previous cancer diagnosis in all three groupings within the retrospective study design. However, only one genus (Ruminococcaceae UCG-014) in breast cancer and one ASV (Fusobacterium periodonticum) in colon cancer was identified by more than one differential abundance (DA) tool. In prospective cases of disease three ASVs were associated with colon cancer, one ASV with breast cancer, and one ASV with prostate cancer. None overlapped between the two different study cohorts. Attempting to identify microbial signals using Random Forest classification showed relatively low levels of signal in both prospective and retrospective cases of breast and prostate cancer (AUC range: 0.394-0.665). Contrastingly, colon cancer did show signal in our retrospective analysis (AUC: 0.745) and in one of two prospective cohorts (AUC: 0.717). Overall, our results indicate that it is unlikely that reliable oral microbial biomarkers of disease exist in the context of both breast and prostate cancer. However, they do suggest that further research into the relationship between the oral microbiome and colon cancer could be fruitful. Particularly in the context of early disease progression and risk of cancer development.

microbiology↗

Assessing the variation within the oral microbiome of healthy adults

Over 1000 different species of microbes have been found to live within the human oral cavity where they play important roles in maintaining both oral and systemic health. Several studies have identified the core members of this microbial community, however, the factors that determine oral microbiome composition are not well understood. In this study we exam the salivary oral microbiome of 1049 Atlantic Canadians using 16S rRNA gene sequencing in order to determine which dietary, lifestyle, and anthropometric features play a role in shaping microbial community composition. Features that were identified as being significantly associated with overall composition were then additionally examined for genera and amplicon sequence variants that were associated with these features. Several associations were replicated in an additional secondary validation dataset. Overall, we found that several anthropometric measurements including waist hip ratio, height, and fat free mass, as well as age and sex, were associated with oral microbiome composition in both our exploratory and validation cohorts. We were unable to validate dietary impacts on the oral microbiome but did find evidence to suggest potential contributions from factors such as the number of vegetable and refined grain servings an individual consumes. Interestingly, each one of these factors on their own were associated with only minor shifts in the oral microbiome suggesting that future biomarker identification for several diseases associated with the oral microbiome may be undertaken without the worry of confounding factors obscuring biological signal. ImportanceThe human oral cavity is inhabited by a diverse community of microbes known as the human oral microbiome. These microbes play a role in maintaining both oral and systemic health and as such have been proposed to be useful biomarkers of disease. However, to identify these biomarkers, we first need to determine the composition and variation of the healthy oral microbiome. Within this report we investigate the oral microbiome of 1049 healthy individuals to determine which genera and amplicon sequence variants are commonly found between individual oral microbiomes. We then further investigate how lifestyle, anthropometric, and dietary choices impact overall microbiome composition. Interestingly, the results from this investigation showed that while many features were significantly associated with oral microbiome composition no single biological factor explained a variation larger than 2%. These results indicate that future work on biomarker detection may be encourage by the lack of strong confounding factors.

microbiology↗