Amino- and Carboxyl-Terminal CCR5 Mutations in Brazilian HIV-1-Infected Women and Homology Model of p.L55Q CCR5 Mutant

Genetic factors from an HIV-1 host can affect the rate of progression to AIDS and HIV infection. To investigate the frequency of mutations in the CCR5 gene, HIV-1 samples from infected women and uninfected individuals were selected for sequencing of the CCR5 gene regions encoding the N- and C-termin...

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Veröffentlicht in:AIDS research and human retroviruses 2015-07, Vol.31 (7), p.685-691
Hauptverfasser: Costa, Giselle Calasans de Souza, Nunes, Marcio Roberto T, Jesus, Jaqueline Goes, Novaes, Thiago, Cardoso, Jedson Ferreira, Sousa Júnior, Edivaldo Costa, Santos, Edson de Souza, Galvão-Castro, Bernardo, Zanette, Dalila Luciola, Gonçalves, Marilda de Souza, Alcantara, Luiz Carlos Junior
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Sprache:eng
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Zusammenfassung:Genetic factors from an HIV-1 host can affect the rate of progression to AIDS and HIV infection. To investigate the frequency of mutations in the CCR5 gene, HIV-1 samples from infected women and uninfected individuals were selected for sequencing of the CCR5 gene regions encoding the N- and C-terminal protein domains. Physicochemical CCR5 modeling and potential protein domain analysis were performed in order to evaluate the impact of the mutations found in the properties and structure of CCR5. The p.L55Q mutation in the N-terminal protein domain was observed only in uninfected individuals, with an allelic frequency of 1.8%. Physicochemical analysis revealed that the p.L55Q mutation magnified the flexibility and accessibility profiles and the modeling of CCR5 structures showed resulting in a small deviation to the right, as well as a hydrophobic to hydrophilic property alteration. The p.L55Q mutation also resulted in a slight modification of the electrostatic load of this region. Additionally, three novel silent mutations were found at the C-terminal coding region among HIV-1-infected women. The results suggest that the p.L55Q mutation might alter CCR5 conformation. Further studies should be conducted to verify the role of this mutation in HIV-1 susceptibility.
ISSN:0889-2229
1931-8405
DOI:10.1089/aid.2014.0140