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Published on: March 8, 2012
[APOBEC3 hypermutations in HIV-1 infected cases in Turkey]
Murat Sayan1, Funda Simşek, Nurgül Ceran
1Kocaeli University Medical Faculty Hospital, Central Laboratory, PCR Unit, Kocaeli, Turkey. sayanmurat@hotmail.com.
Mikrobiyoloji Bulteni
|August 27, 2013
Summary
APOBEC3G/F hypermutations were found in 2.5% of Turkish HIV-1 strains, primarily in the reverse transcriptase gene. These findings offer insights into HIV-1 genetic diversity and host-pathogen interactions.
Area of Science:
- Virology
- Genetics
- Immunology
Background:
- Host genetic factors influence human immunodeficiency virus (HIV) pathogenesis.
- APOBEC3 (apolipoprotein B mRNA editing enzyme catalytic polypeptide like-3) proteins are endogenous antiviral factors that restrict HIV replication.
- APOBEC3G and APOBEC3F are key members of this family, known to induce hypermutation in viral genomes.
Purpose of the Study:
- To investigate the prevalence and characteristics of APOBEC3G/F-induced hypermutations in HIV-1 strains from Turkey.
- To analyze the specific locations and patterns of these hypermutations within the HIV-1 pol gene.
Main Methods:
- Analysis of HIV-1 pol gene sequences (reverse transcriptase and protease) from 515 HIV-1 infected patients in Turkey (2009-2012).
- Nested RT-PCR and direct sequencing were employed for genetic analysis.
- The HIVdb-Stanford algorithm was used to identify APOBEC3G/F hypermutations.
Main Results:
- Overall APOBEC3G/F hypermutations were detected in 2.5% (13/515) of HIV-1 pol gene sequences.
- Prevalence was 2% in antiretroviral-naive patients and 4.1% in patients on HAART.
- Hypermutations were predominantly located in the reverse transcriptase (RT) gene and associated with APOBEC3G.
Conclusions:
- APOBEC3G/F-mediated hypermutation occurs in HIV-1 strains within the Turkish population.
- The findings highlight the role of APOBEC3G in viral evolution and provide a baseline for future studies on HIV-1 genetic diversity in Turkey.
- Further research into hypermutation motifs and their relationship with HIV-1 subtypes is warranted.
