Purifying selection decreases the potential for Bangui orthobunyavirus outbreaks in humans.

Bangui virus bunyavirus febrile illness the Democratic Republic of the Congo virus discovery

Journal

Virus evolution
ISSN: 2057-1577
Titre abrégé: Virus Evol
Pays: England
ID NLM: 101664675

Informations de publication

Date de publication:
2023
Historique:
received: 25 10 2022
revised: 28 02 2023
accepted: 07 03 2023
medline: 8 4 2023
entrez: 7 4 2023
pubmed: 8 4 2023
Statut: epublish

Résumé

Pathogens carried by insects, such as bunyaviruses, are frequently transmitted into human populations and cause diseases. Knowing which spillover events represent a public health threat remains a challenge. Metagenomic next-generation sequencing (mNGS) can support infectious disease diagnostics by enabling the detection of any pathogen from clinical specimens. mNGS was performed on blood samples to identify potential viral coinfections in human immunodeficiency virus (HIV)-positive individuals from Kinshasa, the Democratic Republic of the Congo (DRC), participating in an HIV diversity cohort study. Time-resolved phylogenetics and molecular assay development assisted in viral characterization. The nearly complete genome of a novel orthobunyavirus related to Nyangole virus, a virus previously identified in neighboring Uganda, was assembled from a hepatitis B virus-positive patient. A quantitative polymerase chain reaction assay was designed and used to screen >2,500 plasma samples from Cameroon, the DRC, and Uganda, failing to identify any additional cases. The recent sequencing of a US Center for Disease Control Arbovirus Reference Collection revealed that this same virus, now named Bangui virus, was first isolated in 1970 from an individual in the Central African Republic. Time-scaled phylogenetic analyses of Bangui with the related Anopheles and Tanga serogroup complexes indicate that this virus emerged nearly 10,000 years ago. Pervasive and episodic models further suggest that this virus is under purifying selection and that only distant common ancestors were subject to positive selection events. This study represents only the second identification of a Bangui virus infection in over 50 years. The presumed rarity of Bangui virus infections in humans can be explained by its constraint to an avian host and insect vector, precluding efficient transmission into the human population. Our results demonstrate that molecular phylogenetic analyses can provide insights into the threat posed by novel or re-emergent viruses identified by mNGS.

Identifiants

pubmed: 37025159
doi: 10.1093/ve/vead018
pii: vead018
pmc: PMC10072187
doi:

Types de publication

Journal Article

Langues

eng

Pagination

vead018

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press.

Déclaration de conflit d'intérêts

G.S.O., L.J.P., T.V.M., K.-C.L., K.F., M.A.R., G.A.C., and M.G.B. are all employees and shareholders of Abbott Laboratories. C.Y.C. is the Director of the University of California San Francisco (UCSF)-Abbott Viral Diagnostics and Discovery Center and received research support from Abbott Laboratories for pathogen discovery. The remaining authors do not have conflicts of interest to disclose. No patents have been applied for, and no products are in development related to this research.

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Auteurs

Gregory S Orf (GS)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Lester J Perez (LJ)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Todd V Meyer (TV)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Ka-Cheung Luk (KC)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Kenn Forberg (K)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Mary A Rodgers (MA)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Abbas Hadji (A)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Linda James (L)

Université Protestante au Congo, Kinshasa, Democratic Republic of the Congo.

Samuel Mampunza (S)

Université Protestante au Congo, Kinshasa, Democratic Republic of the Congo.

Asmeeta Achari (A)

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.

Guixia Yu (G)

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.

Scot Federman (S)

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.

Charles Y Chiu (CY)

Department of Laboratory Medicine, University of California San Francisco, San Francisco, CA 94143, USA.
Department of Medicine, Division of Infectious Diseases, University of California San Francisco, San Francisco, CA 94143, USA.

Carole A McArthur (CA)

University of Missouri-Kansas City, Kansas City, MO 64110, USA.

Gavin A Cloherty (GA)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Michael G Berg (MG)

Abbott Laboratories and Abbott Pandemic Defense Coalition, Abbott Park, IL 60064, USA.

Classifications MeSH