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1.
Braz. j. med. biol. res ; 45(2): 104-112, Feb. 2012. ilus, tab
Article in English | LILACS | ID: lil-614579

ABSTRACT

Few studies have reported the molecular epidemiological characterization of HIV-1 in the Northern region of Brazil. The present study reports the molecular and epidemiological characterization of 31 HIV-1 isolates from blood donors from the State of Amazonas who donated blood between April 2006 and March 2007. Serum/plasma samples from all donors were screened for HIV antibodies by ELISA and the results confirmed by Western blot analysis. Genomic DNA was extracted from the buffy coat using the Super Quik-Gene-DNA Isolation kit. Nested PCR was performed on the env, gag, and pol regions of HIV-1 using the Gene Amp PCR System 9700. Sequencing reactions were performed using the inner PCR primers and the DYEnamic™ ET Dye Terminator Kit, and phylogenetic analysis was performed using the gag, pol, and env gene sequences. We collected samples from 31 blood donors who tested positive for HIV-1 in confirmatory experiments. The male:female ratio of blood donors was 3.4:1, and the mean age was 32.4 years (range: 19 to 61 years). Phylogenetic analysis showed that subtype B is the most prevalent among Northern Brazilian HIV-1-seropositive blood donors. One HIV-1 subtype C and one circulating recombinant form (CRF_BF) of HIV-1 were identified in the State of Amazonas. This is the first study showing the occurrence of a possible "homogenous" subtype C in this region of Brazil. This finding could contribute to a better characterization of the HIV-1 strains that circulate in the country.


Subject(s)
Adult , Female , Humans , Middle Aged , Young Adult , Blood Donors , HIV Infections/virology , HIV-1 , Base Sequence , Blotting, Western , Brazil/epidemiology , Enzyme-Linked Immunosorbent Assay , Genes, env/genetics , Genes, gag/genetics , Genes, pol/genetics , HIV Infections/epidemiology , HIV-1 , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction
2.
Indian J Pathol Microbiol ; 2005 Jul; 48(3): 337-40
Article in English | IMSEAR | ID: sea-74485

ABSTRACT

Screening of drug-resistant variants is very important for the effective clinical management of HIV-infected patients and development of new strategies. The present study was aimed to detect codon-184 mutations in the pol-gene of HIV leading to resistance to lamivudine (3-TC) by nested cum ARMS-PCR approach in 10 treated and 9 treatment naive patients. For correlation the whole blood CD4/CD8 cell counts and the soluble TNFRII levels in plasma were also determined. Of the 19 patients tested, mutant variants were observed in 2 patients (Met Val in one and Met Val & lle in second) both being treated with 3-TC. No mutations were detected in the treatment-naive patients. The results confirmed that, drug resistant variants of codon-184 emerge rapidly in patients receiving 3-TC containing regimens including our population, which is mainly infected with subtypeC of the virus that could be detected along with wild viral population using sensitive approaches such as ARMS-PCR.


Subject(s)
Anti-HIV Agents/pharmacology , Antiretroviral Therapy, Highly Active , CD4 Lymphocyte Count , Codon , Drug Resistance, Viral , Drug Therapy, Combination , Genes, pol/genetics , HIV Infections/drug therapy , HIV Reverse Transcriptase/drug effects , HIV-1/drug effects , Humans , Incidence , India/epidemiology , Lamivudine/pharmacology , Mutation , Reverse Transcriptase Inhibitors/pharmacology
3.
Southeast Asian J Trop Med Public Health ; 2002 Dec; 33(4): 818-21
Article in English | IMSEAR | ID: sea-33146

ABSTRACT

HIV-1 drug resistance may limit the use of antiretrovirals when attempting to reduce the vertical transmission rate. Establishing the prevalence of the HIV-1 mutations associated with antiretroviral resistance in pregnant women will enable clinicians to maximize the chances of preventing vertical transmission. In order to determine the prevalence of HIV-1 resistant strains among antiretroviral-naive pregnant Thai women, the nucleotide sequences of the HIV-1 polymerase (pol) gene were evaluated. The plasma samples were collected from the women during the 34th week of pregnancy: numerous secondary mutations could be found in the reverse transcriptase (RT) and protease gene, while no primary mutations in the pol gene were found. The result also showed that by detecting the delta32bp deletion within the CCR 5 locus, it was evident that none of HIV-1 infected individuals had homozygous or heterozygous delta32bp deletions of the CCR5 gene; moreover, no CCR5 gene mutations were found in any individual.


Subject(s)
Adolescent , Adult , Anti-HIV Agents/therapeutic use , Drug Resistance, Viral/genetics , Endopeptidases/genetics , Molecular Epidemiology , Female , Gene Deletion , Genes, pol/genetics , HIV Infections/drug therapy , HIV Reverse Transcriptase/genetics , HIV-1/genetics , Heterozygote , Homozygote , Humans , Infectious Disease Transmission, Vertical/prevention & control , Mutation/genetics , Phylogeny , Population Surveillance , Pregnancy , Pregnancy Complications, Infectious/drug therapy , Prevalence , RNA, Viral/genetics , Receptors, CCR5/genetics , Reverse Transcriptase Polymerase Chain Reaction , Thailand/epidemiology
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