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Helminth parasites have been shown to have systemic effects in the host. Using shotgun metagenomic sequencing, we characterise the gut microbiome and resistome of 113 Zimbabwean preschool-aged children (1–5 years). We test the hypothesis that infection with the human helminth parasite,
Schistosoma haematobium
, is associated with changes in gut microbial and antimicrobial resistance gene abundance/diversity. Here, we show that bacteria phyla
Bacteroidetes
,
Firmicutes, Proteobacteria
, and fungi phyla
Ascomycota, Microsporidia, Zoopagomycota
dominate the microbiome. The abundance of
Proteobacteria
,
Ascomycota
, and
Basidiomycota
differ between schistosome-infected versus uninfected children. Specifically, infection is associated with increases in
Pseudomonas, Stenotrophomonas, Derxia, Thalassospira
,
Aspergillus, Tricholoma
, and
Periglandula
, with a decrease in
Azospirillum
. We find 262 AMR genes, from 12 functional drug classes, but no association with individual-specific data. To our knowledge, we describe a novel metagenomic dataset of Zimbabwean preschool-aged children, indicating an association between urogenital schistosome infection and changes in the gut microbiome.
Osakunor et al. show that infection of Zimbabwean preschool-aged children with
Schistosoma haematobium
correlates with abundance changes in
Pseudomonas, Stenotrophomonas, Derxia, Thalassospira, Aspergillus, Tricholoma, Periglandula
, and
Azospirillum
. This study provides a microbiome and resistome dataset of African preschool-aged children.