2005
DOI: 10.1590/s0074-02762005000800008
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A genotyping study of human immunodeficiency virus type-1 drug resistance in a small Brazilian municipality

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Cited by 11 publications
(4 citation statements)
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“…This information fills a gap about the level F/28B -L10I, A71T L210W -AZT, d4T --FJ594182 MSM/2007 M/26/B -Q58E, I85V --TPV --FJ594183 MSM/2008 M/31/B M46I, L90M L33I --FPV, of primary resistance in this geographic region of the country and contrasts with mostly lower levels of resistance reported in other areas. 23,2,[24][25][26][27][28][29] Brazil is a continental country where recent reports from the northeast and southeast regions have shown very high levels of primary drug resistance. 30,31 These studies together with ours indicate Brazilian areas with higher prevalence rates of primary drug resistance.…”
Section: Discussionmentioning
confidence: 99%
“…This information fills a gap about the level F/28B -L10I, A71T L210W -AZT, d4T --FJ594182 MSM/2007 M/26/B -Q58E, I85V --TPV --FJ594183 MSM/2008 M/31/B M46I, L90M L33I --FPV, of primary resistance in this geographic region of the country and contrasts with mostly lower levels of resistance reported in other areas. 23,2,[24][25][26][27][28][29] Brazil is a continental country where recent reports from the northeast and southeast regions have shown very high levels of primary drug resistance. 30,31 These studies together with ours indicate Brazilian areas with higher prevalence rates of primary drug resistance.…”
Section: Discussionmentioning
confidence: 99%
“…The samples were amplified for the gp120 C2-V3 region using a nested PCR protocol with ED5/ED12 and ED31/ED33 oligonucleotide sets respectively as outer and inner primers [15], generating a fragment of approximately 564 bp. Similarly, for the pol gene we amplified a 1 Kb fragment covering the protease (PR) and part of the reverse transcriptase (RT) using the outer DP10/LR54 and inner DP16/LR49 primer sets as previously described [16,17]. The samples were amplified in the thermocycler GeneAmp ® PCR System 9700 (Perkin Elmer - Norwalk, USA) using the following conditions: 3 cycles at 97°C for 1 minute, 55°C for 1 min, 72°C for 2 minutes.…”
Section: Methodsmentioning
confidence: 99%
“…Nucleotide sequencing and phylogenetic reconstructions -After signed informed consent, blood samples were collected, DNA was extracted from peripheral blood mononuclear cells, and the sequence of a single fragment (around 1000 nucleotides) of HIV-1 polymerase gene encompassing the whole protease (PR) and reverse transcriptase (RT) amino acids 1-230 was generated using a previously described in-house protocol (Eyer-Silva & Morgado 2005). In spite of being a relatively conserved region of the HIV-1 genome, the polymerase gene has been shown to contain enough phylogenetic signal for subtyping analysis (Cornelissen et al 1997) and to allow studies of epidemiologic relationships between populations, groups and people (Hue et al 2004, Eyer-Silva & Morgado 2006.…”
Section: Patients Materials and Methodsmentioning
confidence: 99%