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Identification of system-level features in HIV migration within a host.

Authors :
Goyal, Ravi
Goyal, Ravi
De Gruttola, Victor
Gianella, Sara
Caballero, Gemma
Porrachia, Magali
Ignacio, Caroline
Woodworth, Brendon
Smith, David
Chaillon, Antoine
Goyal, Ravi
Goyal, Ravi
De Gruttola, Victor
Gianella, Sara
Caballero, Gemma
Porrachia, Magali
Ignacio, Caroline
Woodworth, Brendon
Smith, David
Chaillon, Antoine
Source :
PLoS One; vol 18, iss 9
Publication Year :
2023

Abstract

OBJECTIVE: Identify system-level features in HIV migration within a host across body tissues. Evaluate heterogeneity in the presence and magnitude of these features across hosts. METHOD: Using HIV DNA deep sequencing data generated across multiple tissues from 8 people with HIV, we represent the complex dependencies of HIV migration among tissues as a network and model these networks using the family of exponential random graph models (ERGMs). ERGMs allow for the statistical assessment of whether network features occur more (or less) frequently in viral migration than might be expected by chance. The analysis investigates five potential features of the viral migration network: (1) bi-directional flow between tissues; (2) preferential migration among tissues in the same biological system; (3) heterogeneity in the level of viral migration related to HIV reservoir size; (4) hierarchical structure of migration; and (5) cyclical migration among several tissues. We calculate the Cohrans Q statistic to assess heterogeneity in the magnitude of the presence of these features across hosts. The analysis adjusts for missing data on body tissues. RESULTS: We observe strong evidence for bi-directional flow between tissues; migration among tissues in the same biological system; and hierarchical structure of the viral migration network. This analysis shows no evidence for differential level of viral migration with respect to the HIV reservoir size of a tissue. There is evidence that cyclical migration among three tissues occurs less frequent than expected given the amount of viral migration. The analysis also provides evidence for heterogeneity in the magnitude that these features are present across hosts. Adjusting for missing tissue data identifies system-level features within a host as well as heterogeneity in the presence of these features across hosts that are not detected when the analysis only considers the observed data. DISCUSSION: Identification of common features in vira

Details

Database :
OAIster
Journal :
PLoS One; vol 18, iss 9
Notes :
application/pdf, PLoS One vol 18, iss 9
Publication Type :
Electronic Resource
Accession number :
edsoai.on1410328771
Document Type :
Electronic Resource