CoRSeqV3-C: a novel HIV-1 subtype C specific V3 sequence based coreceptor usage prediction algorithm

• Published in: Retrovirology Vol. 10; no. 1; p. 24
• Main Authors: Cashin, Kieran, Gray, Lachlan R, Jakobsen, Martin R, Sterjovski, Jasminka, Churchill, Melissa J, Gorry, Paul R
• Format: Journal Article
• Language: English
• Published: London BioMed Central 27.02.2013; BioMed Central Ltd
• Subjects: Algorithms; Amino acids; Analysis; Antibodies; Antiviral agents; Biomedical and Life Sciences; Biomedicine; Cancer Research; Care and treatment; Computational Biology - methods; Departments; Development and progression; Entropy; Genotype; Health aspects; HIV (Viruses); HIV Envelope Protein gp120 - genetics; HIV infection; HIV-1 - genetics; HIV-1 - physiology; Humans; Infections; Infectious Diseases; Molecular Biology - methods; Protein Structure; Receptors, HIV - analysis; Vaccine; Viral Tropism; Virology; Virology - methods; Viruses; HIV-1; subtype C; gp120; CXCR4; Coreceptor; CCR5; V3; Prediction algorithm
• ISSN: 1742-4690; 1742-4690
• DOI: 10.1186/1742-4690-10-24

Background The majority of HIV-1 subjects worldwide are infected with HIV-1 subtype C (C-HIV). Although C-HIV predominates in developing regions of the world such as Southern Africa and Central Asia, C-HIV is also spreading rapidly in countries with more developed economies and health care systems, whose populations are more likely to have access to wider treatment options, including the CCR5 antagonist maraviroc (MVC). The ability to reliably determine C-HIV coreceptor usage is therefore becoming increasingly more important. In silico V3 sequence based coreceptor usage prediction algorithms are a relatively rapid and cost effective method for determining HIV-1 coreceptor specificity. In this study, we elucidated the V3 sequence determinants of C-HIV coreceptor usage, and used this knowledge to develop and validate a novel, user friendly, and highly sensitive C-HIV specific coreceptor usage prediction algorithm. Results We characterized every phenotypically-verified C-HIV gp120 V3 sequence available in the Los Alamos HIV Database. Sequence analyses revealed that compared to R5 C-HIV V3 sequences, CXCR4-using C-HIV V3 sequences have significantly greater amino acid variability, increased net charge, increased amino acid length, increased frequency of insertions and substitutions within the GPGQ crown motif, and reduced frequency of glycosylation sites. Based on these findings, we developed a novel C-HIV specific coreceptor usage prediction algorithm (CoRSeq V3-C ), which we show has superior sensitivity for determining CXCR4 usage by C-HIV strains compared to all other available algorithms and prediction rules, including Geno2pheno [coreceptor] and WebPSSM SINSI -C, which has been designed specifically for C-HIV. Conclusions CoRSeq V3-C is now openly available for public use at http://www.burnet.edu.au/coreceptor . Our results show that CoRSeq V3-C is the most sensitive V3 sequence based algorithm presently available for predicting CXCR4 usage of C-HIV strains, without compromising specificity. CoRSeq V3-C may be potentially useful for assisting clinicians to decide the best treatment options for patients with C-HIV infection, and will be helpful for basic studies of C-HIV pathogenesis.