| Literature DB >> 33741997 |
Savannah Mwesigwa1, Lesedi Williams2, Gaone Retshabile2, Eric Katagirya1, Gerald Mboowa1, Busisiwe Mlotshwa2, Samuel Kyobe1, David P Kateete1, Eddie Mujjwiga Wampande1, Misaki Wayengera1, Sununguko Wata Mpoloka2, Angella N Mirembe3, Ishmael Kasvosve2, Koketso Morapedi2, Grace P Kisitu3, Adeodata R Kekitiinwa3, Gabriel Anabwani4, Moses L Joloba1, Enock Matovu5, Julius Mulindwa5, Harry Noyes6, Gerrit Botha7, Chester W Brown8, Graeme Mardon9, Mogomotsi Matshaba4,9, Neil A Hanchard10,11.
Abstract
Human immunodeficiency virus (HIV) infection remains a significant public health burden globally. The role of viral co-infection in the rate of progression of HIV infection has been suggested but not empirically tested, particularly among children. We extracted and classified 42 viral species from whole-exome sequencing (WES) data of 813 HIV-infected children in Botswana and Uganda categorised as either long-term non-progressors (LTNPs) or rapid progressors (RPs). The Ugandan participants had a higher viral community diversity index compared to Batswana (p = 4.6 × 10-13), and viral sequences were more frequently detected among LTNPs than RPs (24% vs 16%; p = 0.008; OR, 1.9; 95% CI, 1.6-2.3), with Anelloviridae showing strong association with LTNP status (p = 3 × 10-4; q = 0.004, OR, 3.99; 95% CI, 1.74-10.25). This trend was still evident when stratified by country, sex, and sequencing platform, and after a logistic regression analysis adjusting for age, sex, country, and the sequencing platform (p = 0.02; q = 0.03; OR, 7.3; 95% CI, 1.6-40.5). Torque teno virus (TTV), which made up 95% of the Anelloviridae reads, has been associated with reduced immune activation. We identify an association between viral co-infection and prolonged AIDs-free survival status that may have utility as a biomarker of LTNP and could provide mechanistic insights to HIV progression in children, demonstrating the added value of interrogating off-target WES reads in cohort studies.Entities:
Year: 2021 PMID: 33741997 PMCID: PMC7979878 DOI: 10.1038/s41525-021-00185-w
Source DB: PubMed Journal: NPJ Genom Med ISSN: 2056-7944 Impact factor: 8.617