Tracing the Impact of Public Health Interventions on HIV-1 Transmission in Portugal Using Molecular Epidemiology

Author:

Vasylyeva Tetyana I12,du Plessis Louis1,Pineda-Peña Andrea C345,Kühnert Denise6,Lemey Philippe7,Vandamme Anne-Mieke37,Gomes Perpétua89,Camacho Ricardo J7,Pybus Oliver G1,Abecasis Ana B3,Faria Nuno R1ORCID

Affiliation:

1. Department of Zoology, University of Oxford, United Kingdom

2. New College, University of Oxford, United Kingdom

3. Center for Global Health and Tropical Medicine, Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa

4. Molecular Biology and Immunology Department, Fundación Instituto de Inmunología de Colombia

5. Basic Sciences Department, Universidad del Rosario, Bogotá, Colombia

6. Max Planck Institute for the Science of Human History, Jena, Germany

7. Laboratory for Clinical and Epidemiological Virology, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Belgium

8. Laboratory of Molecular Biology, LMCBM, SPC, Hospital de Egas Moniz–Centro Hospitalar de Lisboa Ocidental, Lisbon

9. Center for Interdisciplinary Research Egas Moniz, CiiEM, Almada, Portugal

Abstract

Abstract Background Estimation of temporal changes in human immunodeficiency virus (HIV) transmission patterns can help to elucidate the impact of preventive strategies and public health policies. Methods Portuguese HIV-1 subtype B and G pol genetic sequences were appended to global reference data sets to identify country-specific transmission clades. Bayesian birth-death models were used to estimate subtype-specific effective reproductive numbers (Re). Discrete trait analysis (DTA) was used to quantify mixing among transmission groups. Results We identified 5 subtype B Portuguese clades (26–79 sequences) and a large monophyletic subtype G Portuguese clade (236 sequences). We estimated that major shifts in HIV-1 transmission occurred around 1999 (95% Bayesian credible interval [BCI], 1998–2000) and 2000 (95% BCI, 1998–2001) for subtypes B and G, respectively. For subtype B, Re dropped from 1.91 (95% BCI, 1.73–2.09) to 0.62 (95% BCI,.52–.72). For subtype G, Re decreased from 1.49 (95% BCI, 1.39–1.59) to 0.72 (95% BCI, .63–.8). The DTA suggests that people who inject drugs (PWID) and heterosexuals were the source of most (>80%) virus lineage transitions for subtypes G and B, respectively. Conclusions The estimated declines in Re coincide with the introduction of highly active antiretroviral therapy and the scale-up of harm reduction for PWID. Inferred transmission events across transmission groups emphasize the importance of prevention efforts for bridging populations.

Funder

Wellcome Trust

Seventh Framework Programme

European Research Council

Research Foundation Flanders

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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