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Oral Microbiome Homogeneity Across Diverse Human Groups from Southern Africa: First Results from Southwestern Angola and Zimbabwe

Overview
Journal BMC Microbiol
Publisher Biomed Central
Specialty Microbiology
Date 2023 Aug 18
PMID 37596536
Authors
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Abstract

Background: While the human oral microbiome is known to play an important role in systemic health, its average composition and diversity patterns are still poorly understood. To gain better insights into the general composition of the microbiome on a global scale, the characterization of microbiomes from a broad range of populations, including non-industrialized societies, is needed. Here, we used the portion of non-human reads obtained through an expanded exome capture sequencing approach to characterize the saliva microbiomes of 52 individuals from eight ethnolinguistically diverse southern African populations from Angola (Kuvale, Kwepe, Himba, Tjimba, Kwisi, Twa, !Xun) and Zimbabwe (Tshwa), including foragers, food-producers, and peripatetic groups (low-status communities who provide services to their dominant neighbors).

Results: Our results indicate that neither host genetics nor livelihood seem to influence the oral microbiome profile, with Neisseria, Streptococcus, Prevotella, Rothia, and Porphyromonas being the five most frequent genera in southern African groups, in line with what has been shown for other human populations. However, we found that some Tshwa and Twa individuals display an enrichment of pathogenic genera from the Enterobacteriaceae family (i.e. Enterobacter, Citrobacter, Salmonella) of the Proteobacteria phylum, probably reflecting deficient sanitation and poor health conditions associated with social marginalization.

Conclusions: Taken together, our results suggest that socio-economic status, rather than ethnolinguistic affiliation or subsistence mode, is a key factor in shaping the salivary microbial profiles of human populations in southern Africa.

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References
1.
Li S, Su B, He Q, Wu H, Zhang T . Alterations in the oral microbiome in HIV infection: causes, effects and potential interventions. Chin Med J (Engl). 2021; 134(23):2788-2798. PMC: 8667981. DOI: 10.1097/CM9.0000000000001825. View

2.
. Structure, function and diversity of the healthy human microbiome. Nature. 2012; 486(7402):207-14. PMC: 3564958. DOI: 10.1038/nature11234. View

3.
Rabe A, Salazar M, Michalik S, Fuchs S, Welk A, Kocher T . Metaproteomics analysis of microbial diversity of human saliva and tongue dorsum in young healthy individuals. J Oral Microbiol. 2019; 11(1):1654786. PMC: 6720020. DOI: 10.1080/20002297.2019.1654786. View

4.
De Filippis F, Vannini L, La Storia A, Laghi L, Piombino P, Stellato G . The same microbiota and a potentially discriminant metabolome in the saliva of omnivore, ovo-lacto-vegetarian and Vegan individuals. PLoS One. 2014; 9(11):e112373. PMC: 4221475. DOI: 10.1371/journal.pone.0112373. View

5.
Love M, Huber W, Anders S . Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014; 15(12):550. PMC: 4302049. DOI: 10.1186/s13059-014-0550-8. View