# Diversity and composition of gut protist in young rural Zimbabwean children

**Authors:** Lorraine Tsitsi Pfavayi, Elopy Nimele Sibanda, Stephen Baker, Mark Woolhouse, Takafira Mduluza, Francisca Mutapi

PMC · DOI: 10.3389/frmbi.2024.1399160 · 2024-05-22

## TL;DR

This study explores gut protist diversity in young Zimbabwean children, finding that schistosome infection is linked to changes in protist composition.

## Contribution

The study provides new insights into gut protist diversity in rural Zimbabwean children and links schistosome infection to specific protist taxa.

## Key findings

- Blastocystis was the most abundant protist genus in the gut of preschool-aged children.
- Schistosoma hematobium infection was significantly associated with increased abundance of specific protist taxa.
- Pathogenic protists like E. histolytica and Cryptosporidium were present but at low prevalence.

## Abstract

The human gut microbiome harbours diverse species of archaea, bacteria, fungi, protists and viruses. To date, most gut microbiome studies have focused on bacteria, neglecting other microbial communities. Consequently, less is known about the diversity and abundance of the latter. Here, we aimed to characterise the diversity and composition of protists in the gut of preschool-aged children (PSAC) in rural Zimbabwe relative to host age, sex, and schistosome infection status.

The gut protist of 113 PSAC (1–5 years) was examined via shotgun metagenomic sequencing and analysed for diversity. Variation in protist abundance with host and environmental factors was analysed by permutational multivariate analysis of variance (PERMANOVA). To investigate how the composition of specific taxa varies across age, sex, nutritional measures and Schistosoma hematobium infection status, analysis of the composition of microbiomes (ANCOM) was used.

Eighty protist genera were identified, and the most abundant genera detected was Blastocystis. The prevalence of pathogenic protists was comparatively low, with 12.4% and 3.4% of the participants’ gut colonised by E. histolytica and Cryptosporidium, respectively. Of all the independent variables only S. haematobium infection showed significant relationship with the structure of the gut protist, being associated with increases in Peronospora, Pseudoperonospora, Plasmopara and Blastocystis (FDR= 0.009).

This study provides data on the prevalence and diversity of the gut protists in young Zimbabwean children with an emphasis on the host factors; age, sex and schistosome infection status. Our results showed no association between the host factors investigated, including anthropometric measures adjusted for age and the intestinal protist composition and structure, but S. haematobium infection status was associated with composition of specific taxa. There is a need for more studies determining how pathogenic protist interact with non-pathogenic protist in people exhibiting clinical symptoms to inform therapy and nutraceuticals.

## Linked entities

- **Species:** Blastocystis (taxon 12967), Peronospora (taxon 70742), Pseudoperonospora (taxon 143452), Plasmopara (taxon 4780)

## Full-text entities

- **Genes:** ST2 (suppression of tumorigenicity 2) [NCBI Gene 6761], ST3 (suppression of tumorigenicity 3) [NCBI Gene 6762] {aka CCTS, TSHL}
- **Diseases:** diarrhoeal disease (MESH:D004194), G. duodenalis (MESH:D005873), soil-transmitted helminths (MESH:D005242), amoebic colitis (MESH:D004404), S. haematobium infection (MESH:D012553), malnourished (MESH:D044342), death (MESH:D003643), PSAC (MESH:D015362), Crohn's disease (MESH:D003424), intestinal malabsorption (MESH:D008286), IBD (MESH:D015212), Schistosoma hematobium infection (MESH:D012555), Amoebiasis (MESH:D000562), flatulence (MESH:D005414), nausea (MESH:D009325), associated infections (MESH:D007239), Blastocystis (MESH:D016776), parasitic infections (MESH:D010272), vomiting (MESH:D014839), schistosome (MESH:D020818), inflammation (MESH:D007249), amoebic liver abscess (MESH:D008101), retardation of growth (MESH:D006130), infectious diseases (MESH:D003141), abdominal cramping (MESH:D003085), diarrhoea (MESH:D003967), fever (MESH:D005334), T1D (MESH:D003922), fatigue (MESH:D005221), Schistosomiasis (MESH:D012552), dysentery (MESH:D004403), anorexia (MESH:D000855)
- **Species:** gut metagenome (species) [taxon 749906], Plasmopara (genus) [taxon 4780], Entamoeba (genus) [taxon 5758], Schistosoma haematobium (species) [taxon 6185], Fenestella gardiennetii (species) [taxon 2499855], Blastocystis (genus) [taxon 12967], Schistosoma mansoni (species) [taxon 6183], Entamoeba histolytica (species) [taxon 5759], Entamoeba dispar (species) [taxon 46681], Giardia duodenalis (species) [taxon 5741], Peronospora (genus) [taxon 70742], Homo sapiens (human, species) [taxon 9606], Acanthamoeba (genus) [taxon 5754], Cryptosporidium (genus) [taxon 5806]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13019894/full.md

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Source: https://tomesphere.com/paper/PMC13019894