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. Author manuscript; available in PMC: 2016 Feb 25.
Published in final edited form as: Nature. 2010 Apr 1;464(7289):673. doi: 10.1038/464673c

Public database for HIV drug resistance in southern Africa

Tulio de Oliveira 1, Robert W Shafer 2, Christopher Seebregts 3
PMCID: PMC4767176  NIHMSID: NIHMS759321  PMID: 20360715

The Opinion article by S. Karim and Q. Karim laments the lack of an effective conduit between South Africa’s AIDS research and its prevention and treatment policies and programmes (Nature 463, 733–734; 2010). We would like to draw attention to an HIV-1 drug-resistance database, a scientific resource for regional and global HIV research that will enhance surveillance programmes in southern Africa.

The database was established by investigators from the Southern African Treatment and Resistance Network (SATuRN), in collaboration with researchers from the United States and Europe. SATuRN will provide national departments of health with high-quality, up-to-date information to guide delivery of antiretroviral therapy, helping to ensure the long-term success of antiretroviral treatment programmes.

As part of this network, we have installed a South African mirror of the Stanford HIV Drug Resistance Database (HIVDB). This mirror (www.bioafrica.net/saturn) will be continuously updated and released to local investigators in a curated and readily analysable form, in the context of more than 120,000 sequences already in the Stanford HIVDB. Neighbouring countries that share subtype C as the predominant virus (the strain fuelling southern Africa’s AIDS epidemic) are also providing data.

The mirror will ensure that subtype-C sequences are analysed according to standard state-of-the-art technologies developed by Stanford HIVDB. It will help patient management, allowing quick identification of resistant strains and systematic tracking both of resistance patterns and of prevalence and distribution of resistance mutations within different population groups. It will inform decisions about new drugs, diagnostics and treatment strategies in southern Africa. Already, the data show that resistance in newly infected individuals is still very low (under 5%), as is the accumulation of thymidine-analogue mutations that can limit the effectiveness of second-line antiretroviral therapy.

Investigators, clinicians and laboratories wishing to take part in the collaboration should contact the authors.

Contributor Information

Tulio de Oliveira, Email: tdeoliveira@africacentre.ac.za, Africa Centre for Health and Population Studies, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.

Robert W. Shafer, Division of Infectious Diseases, Department of Medicine, Stanford University, USA

Christopher Seebregts, Biomedical Informatics Research, Medical Research Council, South Africa.

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