Longitudinal study of HIV protease mutations in oral tissues of selected patients

Twenty-nine HIV-1 infected patients from New Orleans were enrolled as a cohort for this study over a four and one half year period. HIV-1 protease gene (pro) sequences were amplified using DNA isolated from oral tissues (gingival cuff, buccal mucosa, tongue, palate) as well as saliva and peripheral...

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Main Authors: Peter J. Hickman, Janet E. Leigh, Paul L. Fidel. Jr, Ronald B. Luftig
Format: Article
Language:English
Published: Universidade Estadual de Campinas 2015-11-01
Series:Brazilian Journal of Oral Sciences
Subjects:
Online Access:https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641777
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spelling doaj-394eb4abf8604dd58e667a301a44a24b2021-07-15T14:01:27ZengUniversidade Estadual de CampinasBrazilian Journal of Oral Sciences1677-32252015-11-0131110.20396/bjos.v3i11.8641777Longitudinal study of HIV protease mutations in oral tissues of selected patientsPeter J. Hickman0Janet E. Leigh1Paul L. Fidel. Jr2Ronald B. Luftig3Louisiana State University Health Sciences CenterLouisiana State University Health Sciences CenterLouisiana State University Health Sciences CenterLouisiana State University Health Sciences CenterTwenty-nine HIV-1 infected patients from New Orleans were enrolled as a cohort for this study over a four and one half year period. HIV-1 protease gene (pro) sequences were amplified using DNA isolated from oral tissues (gingival cuff, buccal mucosa, tongue, palate) as well as saliva and peripheral blood mononuclear cells (PBMC). PCR products were directly sequenced using a combination of manual and automated methods, and nucleotide sequences were translated using the universal genetic code. Protein sequences obtained from independent amplifications of a particular patient at a given time were consolidated into a single consensus sequence and compared to HIV-1LAI to determine amino acid replacements. The major findings were: 1) each patient had a signature sequence that probably represented the predominant HIV–1 quasispecies; 2) over periods of 19 to 1673 days mutation patterns remained relatively stable within a given patient; and 3) although nearly 40% of the initial nonsynonymous replacements in the protease signature sequences were mutations known to impart resistance to protease inhibitors (PI), over time patients did not accumulate additional PIR mutationshttps://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641777HIV-1. Protease gene. Mutations
collection DOAJ
language English
format Article
sources DOAJ
author Peter J. Hickman
Janet E. Leigh
Paul L. Fidel. Jr
Ronald B. Luftig
spellingShingle Peter J. Hickman
Janet E. Leigh
Paul L. Fidel. Jr
Ronald B. Luftig
Longitudinal study of HIV protease mutations in oral tissues of selected patients
Brazilian Journal of Oral Sciences
HIV-1. Protease gene. Mutations
author_facet Peter J. Hickman
Janet E. Leigh
Paul L. Fidel. Jr
Ronald B. Luftig
author_sort Peter J. Hickman
title Longitudinal study of HIV protease mutations in oral tissues of selected patients
title_short Longitudinal study of HIV protease mutations in oral tissues of selected patients
title_full Longitudinal study of HIV protease mutations in oral tissues of selected patients
title_fullStr Longitudinal study of HIV protease mutations in oral tissues of selected patients
title_full_unstemmed Longitudinal study of HIV protease mutations in oral tissues of selected patients
title_sort longitudinal study of hiv protease mutations in oral tissues of selected patients
publisher Universidade Estadual de Campinas
series Brazilian Journal of Oral Sciences
issn 1677-3225
publishDate 2015-11-01
description Twenty-nine HIV-1 infected patients from New Orleans were enrolled as a cohort for this study over a four and one half year period. HIV-1 protease gene (pro) sequences were amplified using DNA isolated from oral tissues (gingival cuff, buccal mucosa, tongue, palate) as well as saliva and peripheral blood mononuclear cells (PBMC). PCR products were directly sequenced using a combination of manual and automated methods, and nucleotide sequences were translated using the universal genetic code. Protein sequences obtained from independent amplifications of a particular patient at a given time were consolidated into a single consensus sequence and compared to HIV-1LAI to determine amino acid replacements. The major findings were: 1) each patient had a signature sequence that probably represented the predominant HIV–1 quasispecies; 2) over periods of 19 to 1673 days mutation patterns remained relatively stable within a given patient; and 3) although nearly 40% of the initial nonsynonymous replacements in the protease signature sequences were mutations known to impart resistance to protease inhibitors (PI), over time patients did not accumulate additional PIR mutations
topic HIV-1. Protease gene. Mutations
url https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641777
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