Blood virosphere in febrile Tanzanian children.
Samuel CordeyFlorian LaubscherMary-Anne HartleyThomas JunierKristina KeitelMylène DocquierNicolas GuexChristian IseliGael VieillePhilippe Le MercierAnne GleizesJosephine SamakaTarsis MlaganileFrank KagoroJohn MasimbaZamzam SaidHosiana TembaGasser H ElbannaCaroline TapparelMarie-Celine ZanellaIoannis XenariosJacques FellayValérie D'AcremontLaurent KaiserPublished in: Emerging microbes & infections (2021)
Viral infections are the leading cause of childhood acute febrile illnesses motivating consultation in sub-Saharan Africa. The majority of causal viruses are never identified in low-resource clinical settings as such testing is either not part of routine screening or available diagnostic tools have limited ability to detect new/unexpected viral variants. An in-depth exploration of the blood virome is therefore necessary to clarify the potential viral origin of fever in children. Metagenomic next-generation sequencing is a powerful tool for such broad investigations, allowing the detection of RNA and DNA viral genomes. Here, we describe the blood virome of 816 febrile children (<5 years) presenting at outpatient departments in Dar es Salaam over one-year. We show that half of the patients (394/816) had at least one detected virus recognized as causes of human infection/disease (13.8% enteroviruses (enterovirus A, B, C, and rhinovirus A and C), 12% rotaviruses, 11% human herpesvirus type 6). Additionally, we report the detection of a large number of viruses (related to arthropod, vertebrate or mammalian viral species) not yet known to cause human infection/disease, highlighting those who should be on the radar, deserve specific attention in the febrile paediatric population and, more broadly, for surveillance of emerging pathogens.Trial registration: ClinicalTrials.gov identifier: NCT02225769.
Keyphrases
- sars cov
- endothelial cells
- young adults
- induced pluripotent stem cells
- urinary tract infection
- emergency department
- pluripotent stem cells
- chemotherapy induced
- ejection fraction
- prognostic factors
- clinical trial
- intensive care unit
- end stage renal disease
- copy number
- liver failure
- chronic kidney disease
- nucleic acid
- public health
- optical coherence tomography
- single molecule
- clinical practice
- climate change
- real time pcr
- multidrug resistant
- microbial community
- human health
- cell free