Higher viral load may explain the dominance of CRF02―AG in the molecular epidemiology of HIV in Ghana
Identifieur interne : 000040 ( PascalFrancis/Curation ); précédent : 000039; suivant : 000041Higher viral load may explain the dominance of CRF02―AG in the molecular epidemiology of HIV in Ghana
Auteurs : Lucia Fischetti [Royaume-Uni] ; Ohene Opare-Sem [Ghana] ; Daniel Candotti [Royaume-Uni] ; Helen Lee [Royaume-Uni] ; Jean-Pierre Allain [Royaume-Uni]Source :
- AIDS : (London) [ 0269-9370 ] ; 2004.
Descripteurs français
- Pascal (Inist)
- SIDA, Réaction chaîne polymérase, Charge virale, Epidémiologie moléculaire, Ghana, Virus immunodéficience humaine, Virus HIV1, Arbre phylogénétique, Plasma sanguin, Asymptomatique, Donneur sang, Homme, Prévalence, RNA-directed DNA polymerase, Forme moléculaire, Pouvoir infectant, Reverse transcriptase.
- Wicri :
English descriptors
- KwdEn :
Abstract
Phylogenetic analysis of Ghanaian plasma samples from 84 asymptomatic candidate blood donors and 150 AIDS patients revealed a 63% prevalence of HIV-1 CRF02―AG. HIV-1 viral load in both populations was quantified using real-time reverse transcriptase-polymerase chain reaction. In asymptomatic candidate blood donors infected with CRF02―AG, the viral load was significantly higher than in donors infected with other HIV-1 molecular forms. A higher viral load of CRF02―AG is compatible with higher infectivity and prevalence.
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<term>Molecular epidemiology</term>
<term>Molecular form</term>
<term>Phylogenetic tree</term>
<term>Polymerase chain reaction</term>
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<front><div type="abstract" xml:lang="en">Phylogenetic analysis of Ghanaian plasma samples from 84 asymptomatic candidate blood donors and 150 AIDS patients revealed a 63% prevalence of HIV-1 CRF02―AG. HIV-1 viral load in both populations was quantified using real-time reverse transcriptase-polymerase chain reaction. In asymptomatic candidate blood donors infected with CRF02―AG, the viral load was significantly higher than in donors infected with other HIV-1 molecular forms. A higher viral load of CRF02―AG is compatible with higher infectivity and prevalence.</div>
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<s2>FE</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="09" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="09" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="09" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="10" i2="X" l="FRE"><s0>Exploration microbiologique</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="ENG"><s0>Microbiological investigation</s0>
<s5>37</s5>
</fC07>
<fC07 i1="10" i2="X" l="SPA"><s0>Análisis microbiológico</s0>
<s5>37</s5>
</fC07>
<fC07 i1="11" i2="X" l="FRE"><s0>Immunopathologie</s0>
<s5>38</s5>
</fC07>
<fC07 i1="11" i2="X" l="ENG"><s0>Immunopathology</s0>
<s5>38</s5>
</fC07>
<fC07 i1="11" i2="X" l="SPA"><s0>Inmunopatología</s0>
<s5>38</s5>
</fC07>
<fC07 i1="12" i2="X" l="FRE"><s0>Immunodéficit</s0>
<s5>39</s5>
</fC07>
<fC07 i1="12" i2="X" l="ENG"><s0>Immune deficiency</s0>
<s5>39</s5>
</fC07>
<fC07 i1="12" i2="X" l="SPA"><s0>Inmunodeficiencia</s0>
<s5>39</s5>
</fC07>
<fC07 i1="13" i2="X" l="FRE"><s0>Biologie moléculaire</s0>
<s5>41</s5>
</fC07>
<fC07 i1="13" i2="X" l="ENG"><s0>Molecular biology</s0>
<s5>41</s5>
</fC07>
<fC07 i1="13" i2="X" l="SPA"><s0>Biología molecular</s0>
<s5>41</s5>
</fC07>
<fN21><s1>031</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>
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