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Brazilian Journal of Infectious Diseases

Print version ISSN 1413-8670On-line version ISSN 1678-4391

Braz J Infect Dis vol.11 no.1 Salvador Feb. 2007

http://dx.doi.org/10.1590/S1413-86702007000100008 

ORIGINAL PAPERS

 

Identification and characterization of previously described epitopes in HIV-1 subtypes B, C, F and BF in Brazil

 

 

Artur Trancoso Lopo de QueirozI, II; Luciane Amorim SantosI, II; Domingos Ramon MoreauI; Tulio de OliveiraIII; David I. WatkinsIV; Bernardo Galvão-CastroI, II; Luiz Carlos Junior AlcantaraI, II

IAdvanced Public Health Laboratory, Gonçalo Moniz Research Center, Oswaldo Cruz Foundation, Salvador, BA, Brazil
IIBahia School of Medicine and Public Health/Foundation for Development of Science, Salvador, BA, Brazil
IIIDepartment of Zoology, University of Oxford, Oxford, United Kingdom
IVUniversity of Wisconsin Medical School, Department of Pathology, Madison, USA

Address for correspondence

 

 


ABSTRACT

Genetic analysis of HIV-1 is essential to improve treatment strategies and select epitopes for vaccine programs. The objective of this study was to determine whether known CD4+ and CD8+ epitopes were present in Brazilian HIV-1 strains. We used previously described CD8+ and CD4+ epitopes from the Los Alamos laboratory to search for these epitopes in the Brazilian sequences using the HIVbase program and we compared the frequency results with the analyses using physical-chemical profile tools from Network Protein Sequence Analysis (NPSA), and the SYFPEITHI program. Furthermore, this analysis was carried out with the Prosite tool using the GeneDoc program and ds/dn analyses using the Synonymous Nonsynonymous Analysis Program (SNAP). The HIVbase epitope mapping demonstrated that 30 CD8+ and 6 CD4+ epitopes were present in the Brazilian sequences at a high frequency. Only two of these epitopes were heavily glycosylated. Interestingly, ds/dn analyses showed evidence of purifying selective pressure. These types of analyses could be useful for the assessment of possible vaccine efficiency in populations.

Key-Words: HIV-1, env, vaccine, epitope.


 

 

HIV-1, identified as the etiological agent of AIDS [1], contributes to the development of immunodeficiency. Its biological complexity and high mutation rate have made the design of a vaccine to control the pandemic difficult. CD8+ T lymphocyte responses are largely responsible for controlling viral replication during both acute and chronic infection [2-4]. The antibody responses appears much later and select a mutant virus [5]. Mutations in CTL epitopes and sites recognized by antibodies and acquisition of glycosylation sites are escape mechanisms that allow the virus to replicate and infect more cells [5-7].

The mapping of epitopes in diverse virus proteins and the identification of possible modifications can provide useful information to aid vaccine development. For example, mutations in the TW10 and SL9 Gag epitopes result in a fitness cost to the virus [7], and this kind of information is very useful for the vaccine development process. The use of bioinformatics software can identify escaping epitopes. Bioinformatics programs have been developed for diverse areas including protein analysis, physical-chemical characteristics, MHC binding databases, and posttranslational modification. The use of these programs to study the molecular epidemiology and genetic variation of the HIV-1 epidemic in Brazil may provide important information about the epidemic in this country. This information could be important in the design of an effective vaccine as well as for antiretroviral treatment. The objective of this study was to characterize genetic variation in previously identified epitopes in the Brazilian HIV-1 env sequences.

 

Materials and Methods

Sequences of all of the Brazilian HIV-1 strains (3,813) were collected from GenBank and added to the HIVbase Database [8]. Epitope mapping analyses were performed as described in the HIV Immunology and HIV/SIV Los Alamos Vaccine Databases [9]. We selected and analyzed only the env region, consisting of 2,644 sequences from gp120: C1V1=51; C2=59; C3=200; V3loop=515; and gp41=50. The alignment of these sequences was carried out using the ClustalX [10] software. Genedoc [11] software was used to edit and translate the alignment, and the potential site analyses were performed using the Prosite [12] tool. For selective pressure analysis, we used the Synonymous Nonsynonymous Analysis Program (SNAP) [13] from Los Alamos. The proportion of synonymous substitutions per potential synonymous site and the proportion of nonsynonymous substitutions per potential nonsynonymous site were calculated using the Nei and Gojobori method [14]. Prediction of cellular epitopes was made with the SYFPEITHI online database [15]. Identification of Antibody epitopes and their physical-chemical characteristics were carried out using the Physico-chemical profiles program of the Network Protein Sequence Analysis (NPSA) [16-20].

 

Results

HIVbase epitope mapping showed that thirty CD8+ (Table 1) and six CD4+ (Table 2) epitopes had a high frequency and showed varying degrees of conservation in the Brazilian HIV sequence. However, the SYPETEITHI analysis was restricted to the following HLA alleles: HLA-A*03, -A*6801, -A*2402 and -A*0201. Two of the epitopes in this program had several N-glycosylation sites (CTRPNNNTRK at amino acid position 296 to 305, at a frequency of 96.2%, and NCGGEFFYCN at amino acid position 377 to 386 with a frequency of 84.5%). The ds/dn ratio was high in some of the CD8+ epitopes. This high ratio suggests that these particular epitopes may either not be under positive selection or are maintained under functional constraints.

The subtype B epitopes were the most conserved ones, especially in the C1 and C3 regions, followed by subtype F. In the V3loop region, subtype F was the most conserved one. However, none of the most frequent mutations were associated with the loss of N-glycosylation site at this position. The gp41 was the most conserved region among the subtypes and this can be explained by the absence of variable regions in this protein. Epitopes in this region showed high ds/dn ratios but these ratios were lower than the gp120 epitopes. This epitope conservation and the high ds/dn ratio suggest that these regions may be important for viral fitness. Mutations in this region might change the protein structure, reducing the infection capacity of the virus.

The epitope VPVWKEATTTL is associated with a rapid progression HLA allele, HLA-B35 [4] and exhibited low variation in non-C subtypes. Interestingly, this epitope was highly variable in B/F recombinants. This suggests that CTL may be exerting selective pressure on this subtype.

The regions involved in N-glycosylation were highly conserved. These sites are potentially important for the functioning of these proteins, and mutation in these regions might affect viral function.

 

Conclusion

An ideal vaccine would contain epitopes that would engender strong immune responses against the functionally important regions. Escape from these vaccine-induced immune responses would compromise viral fitness. Additionally, it will be important to continue analyzing epitope variability in other viral proteins in the HIV-1 strains circulating in Brazil as any eventual vaccine for use in Brazil will need to be relevant to the viruses in Brazil.

 

Acknowledgements

ATLQ and LAS contributed equally to this work. We are grateful to Elisabeth Deliege for her technical assistance.

 

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Address for correspondence:
Dr. Luiz Carlos J. Alcantara
Advanced Public Health Laboratory, Gonçalo Moniz Research Center, Oswaldo Cruz Foundation
Rua Waldemar Falcão 121, Candeal
Salvador, Bahia, Brazil. Zip code: 40296-610
Telephone # 55 71 3176 2246/3176 2213
Fax # 55 71 3176 2300
E-mail: lalcan@cpqgm.fiocruz.br

Received on 27 October 2006; revised 22 January 2007.
Financial Support: This project was partially supported by the Fundação de Amparo a Pesquisa do Estado da Bahia (FAPESB, grant number 303/03) and PN-DST/AIDS, Ministério da Saúde, Brasil (grant number 306 and 307/04).

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