dc.contributor.author | Akshaya Ramesh | |
dc.contributor.author | Sara Nakielny | |
dc.contributor.author | Jennifer Hsu | |
dc.contributor.author | Mary Kyohere | |
dc.contributor.author | Oswald Byaruhanga | |
dc.contributor.author | Charles F. A. de Bourcy | |
dc.contributor.author | Rebecca Egger | |
dc.contributor.author | Boris Dimitrov | |
dc.contributor.author | Yun-Fang Juan | |
dc.contributor.author | Jonathan Sheu | |
dc.contributor.author | James H.-C. Wang | |
dc.contributor.author | Katrina Kalantar | |
dc.contributor.author | Charles Langelier | |
dc.contributor.author | Theodore Ruel | |
dc.contributor.author | Arthur Mpimbaza | |
dc.contributor.author | Michael R. Wilson | |
dc.contributor.author | Philip J. Rosenthal | |
dc.contributor.author | Joeseph L DeRisi | |
dc.date.accessioned | 2021-01-11T13:51:44Z | |
dc.date.available | 2021-01-11T13:51:44Z | |
dc.date.issued | 2018 | |
dc.identifier.uri | https://combine.alvar.ug/handle/1/49512 | |
dc.description.abstract | Background: Febrile illness is a major burden in African children, and non-malarial causes of fever are uncertain. We built and employed IDseq, a cloud-based, open access, bioinformatics platform and service to identify microbes from metagenomic next-generation sequencing of tissue samples. In this pilot study, we evaluated blood, nasopharyngeal, and stool specimens from 94 children (aged 2-54 months) with febrile illness admitted to Tororo District Hospital, Uganda. Results: The most common pathogens identified were Plasmodium falciparum (51.1% of samples) and parvovirus B19 (4.4%) from blood; 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. Among other potential pathogens, we identified one novel orthobunyavirus, tentatively named Nyangole virus, from the blood of a child diagnosed with malaria and pneumonia, and Bwamba orthobunyavirus in the nasopharynx of a child with rash and sepsis. We also identified two novel human rhinovirus C species. Conclusions: This exploratory pilot study demonstrates the utility of mNGS and the IDseq platform for defining the molecular landscape of febrile infectious diseases in resource limited areas. These methods, supported by a robust data analysis and sharing platform, offer a new tool for the surveillance, diagnosis, and ultimately treatment and prevention of infectious diseases. | |
dc.publisher | Cold Spring Harbor Laboratory | |
dc.title | Etiology of fever in Ugandan children: identification of microbial pathogens using metagenomic next-generation sequencing and IDseq, a platform for unbiased metagenomic analysis | |
dc.type | Preprint | |
dc.identifier.doi | 10.1101/385005 | |
dc.identifier.mag | 2886470144 | |
dc.identifier.lens | 039-349-121-209-175 | |
dc.identifier.spage | 385005 | |
dc.subject.lens-fields | Etiology | |
dc.subject.lens-fields | Virology | |
dc.subject.lens-fields | Virus | |
dc.subject.lens-fields | Malaria | |
dc.subject.lens-fields | Sepsis | |
dc.subject.lens-fields | Orthobunyavirus | |
dc.subject.lens-fields | Parvovirus | |
dc.subject.lens-fields | Diarrhea | |
dc.subject.lens-fields | Rotavirus | |
dc.subject.lens-fields | Medicine |
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