Metagenomic next-generation sequencing of samples from pediatric febrile illness in Tororo, Uganda.
Akshaya RameshSara NakielnyJennifer HsuMary KyohereOswald ByaruhangaCharles de BourcyRebecca EggerBoris DimitrovYun-Fang JuanJonathan SheuJames WangKatrina KalantarCharles LangelierTheodore RuelArthur MpimbazaMichael R WilsonPhilip J RosenthalJoseph L DerisiPublished in: PloS one (2019)
Febrile illness is a major burden in African children, and non-malarial causes of fever are uncertain. In this retrospective exploratory study, we used metagenomic next-generation sequencing (mNGS) to evaluate serum, nasopharyngeal, and stool specimens from 94 children (aged 2-54 months) with febrile illness admitted to Tororo District Hospital, Uganda. The most common microbes identified were Plasmodium falciparum (51.1% of samples) and parvovirus B19 (4.4%) from serum; human rhinoviruses A and C (40%), respiratory syncytial virus (10%), and human herpesvirus 5 (10%) from nasopharyngeal swabs; and rotavirus A (50% of those with diarrhea) from stool. We also report the near complete genome of a highly divergent orthobunyavirus, tentatively named Nyangole virus, identified from the serum of a child diagnosed with malaria and pneumonia, a Bwamba orthobunyavirus in the nasopharynx of a child with rash and sepsis, and the genomes of two novel human rhinovirus C species. In this retrospective exploratory study, mNGS identified multiple potential pathogens, including 3 new viral species, associated with fever in Ugandan children.
Keyphrases
- plasmodium falciparum
- endothelial cells
- young adults
- induced pluripotent stem cells
- respiratory syncytial virus
- mental health
- pluripotent stem cells
- acute kidney injury
- urinary tract infection
- intensive care unit
- cross sectional
- south africa
- emergency department
- risk assessment
- antibiotic resistance genes
- acute care
- cell free