Le SIDA au Ghana (serveur d'exploration)

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Infectious DNA clone of HIV type 1 A/G recombinant (CRF02―AG) replicable in peripheral blood mononuclear cells

Identifieur interne : 000134 ( PascalFrancis/Corpus ); précédent : 000133; suivant : 000135

Infectious DNA clone of HIV type 1 A/G recombinant (CRF02―AG) replicable in peripheral blood mononuclear cells

Auteurs : Mikako Takahoko ; Minoru Tobiume ; Koichi Ishikawa ; William Ampofo ; Naoki Yamamoto ; Michiyuki Matsuda ; Masashi Tatsumi

Source :

RBID : Pascal:02-0322075

Descripteurs français

English descriptors

Abstract

We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0889-2229
A02 01      @0 ARHRE7
A03   1    @0 AIDS res. hum. retroviruses
A05       @2 17
A06       @2 11
A08 01  1  ENG  @1 Infectious DNA clone of HIV type 1 A/G recombinant (CRF02―AG) replicable in peripheral blood mononuclear cells
A11 01  1    @1 TAKAHOKO (Mikako)
A11 02  1    @1 TOBIUME (Minoru)
A11 03  1    @1 ISHIKAWA (Koichi)
A11 04  1    @1 AMPOFO (William)
A11 05  1    @1 YAMAMOTO (Naoki)
A11 06  1    @1 MATSUDA (Michiyuki)
A11 07  1    @1 TATSUMI (Masashi)
A14 01      @1 Department of Pathology, Research Institute, International Medical Center of Japan @2 Tokyo 162-8644 @3 JPN @Z 1 aut. @Z 2 aut. @Z 6 aut.
A14 02      @1 Noguchi Memorial Institute for Medical Research, University of Ghana @2 Legon @3 GHA @Z 3 aut. @Z 4 aut.
A14 03      @1 Department of Microbiology, Tokyo Medical and Dental University @2 Tokyo 113-8519 @3 JPN @Z 5 aut.
A14 04      @1 Department of Veterinary Science, National Institute of Infectious Diseases @2 Tokyo 162-8640 @3 JPN @Z 7 aut.
A20       @1 1083-1087
A21       @1 2001
A23 01      @0 ENG
A43 01      @1 INIST @2 20934 @5 354000099074040120
A44       @0 0000 @1 © 2002 INIST-CNRS. All rights reserved.
A45       @0 12 ref.
A47 01  1    @0 02-0322075
A60       @1 P
A61       @0 A
A64 01  1    @0 AIDS research and human retroviruses
A66 01      @0 USA
C01 01    ENG  @0 We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.
C02 01  X    @0 002B06D01
C02 02  X    @0 002A05C04
C02 03  X    @0 002A05
C03 01  X  FRE  @0 Virus HIV1 @2 NW @5 01
C03 01  X  ENG  @0 HIV-1 virus @2 NW @5 01
C03 01  X  SPA  @0 HIV-1 virus @2 NW @5 01
C03 02  X  FRE  @0 Cellule sanguine @5 05
C03 02  X  ENG  @0 Blood cell @5 05
C03 02  X  SPA  @0 Célula sanguínea @5 05
C03 03  X  FRE  @0 Sang @5 06
C03 03  X  ENG  @0 Blood @5 06
C03 03  X  SPA  @0 Sangre @5 06
C03 04  X  FRE  @0 Isolat @5 07
C03 04  X  ENG  @0 Isolate @5 07
C03 04  X  SPA  @0 Aislado @5 07
C03 05  X  FRE  @0 Ghana @2 NG @5 08
C03 05  X  ENG  @0 Ghana @2 NG @5 08
C03 05  X  SPA  @0 Ghana @2 NG @5 08
C03 06  X  FRE  @0 Phylogenèse @5 09
C03 06  X  ENG  @0 Phylogeny @5 09
C03 06  X  SPA  @0 Filogénesis @5 09
C03 07  X  FRE  @0 Recombinaison @5 10
C03 07  X  ENG  @0 Recombination @5 10
C03 07  X  SPA  @0 Recombinación @5 10
C03 08  X  FRE  @0 Point cassure @5 11
C03 08  X  ENG  @0 Breakpoint @5 11
C03 08  X  SPA  @0 Punto ruptura @5 11
C03 09  X  FRE  @0 Transfection @5 12
C03 09  X  ENG  @0 Transfection @5 12
C03 09  X  SPA  @0 Transfección @5 12
C03 10  X  FRE  @0 Infection @5 14
C03 10  X  ENG  @0 Infection @5 14
C03 10  X  SPA  @0 Infección @5 14
C03 11  X  FRE  @0 Récepteur chimiokine CCR5 @5 67
C03 11  X  ENG  @0 CCR5 chemokine receptor @5 67
C03 11  X  SPA  @0 Receptor quimioquina CCR5 @5 67
C03 12  X  FRE  @0 Utilisation @5 68
C03 12  X  ENG  @0 Use @5 68
C03 12  X  SPA  @0 Utilización @5 68
C03 13  X  FRE  @0 Phytohémagglutinine @2 NK @2 FR @5 69
C03 13  X  ENG  @0 Phytohemagglutinin @2 NK @2 FR @5 69
C03 13  X  SPA  @0 Fitohemaglutinina @2 NK @2 FR @5 69
C03 14  X  FRE  @0 Réplication @5 70
C03 14  X  ENG  @0 Replication @5 70
C03 14  X  SPA  @0 Replicación @5 70
C07 01  X  FRE  @0 Virus immunodéficience humaine @2 NW
C07 01  X  ENG  @0 Human immunodeficiency virus @2 NW
C07 01  X  SPA  @0 Human immunodeficiency virus @2 NW
C07 02  X  FRE  @0 Lentivirus @2 NW
C07 02  X  ENG  @0 Lentivirus @2 NW
C07 02  X  SPA  @0 Lentivirus @2 NW
C07 03  X  FRE  @0 Retroviridae @2 NW
C07 03  X  ENG  @0 Retroviridae @2 NW
C07 03  X  SPA  @0 Retroviridae @2 NW
C07 04  X  FRE  @0 Virus @2 NW
C07 04  X  ENG  @0 Virus @2 NW
C07 04  X  SPA  @0 Virus @2 NW
C07 05  X  FRE  @0 Afrique @2 NG
C07 05  X  ENG  @0 Africa @2 NG
C07 05  X  SPA  @0 Africa @2 NG
N21       @1 182
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 02-0322075 INIST
ET : Infectious DNA clone of HIV type 1 A/G recombinant (CRF02―AG) replicable in peripheral blood mononuclear cells
AU : TAKAHOKO (Mikako); TOBIUME (Minoru); ISHIKAWA (Koichi); AMPOFO (William); YAMAMOTO (Naoki); MATSUDA (Michiyuki); TATSUMI (Masashi)
AF : Department of Pathology, Research Institute, International Medical Center of Japan/Tokyo 162-8644/Japon (1 aut., 2 aut., 6 aut.); Noguchi Memorial Institute for Medical Research, University of Ghana/Legon/Ghana (3 aut., 4 aut.); Department of Microbiology, Tokyo Medical and Dental University/Tokyo 113-8519/Japon (5 aut.); Department of Veterinary Science, National Institute of Infectious Diseases/Tokyo 162-8640/Japon (7 aut.)
DT : Publication en série; Niveau analytique
SO : AIDS research and human retroviruses; ISSN 0889-2229; Coden ARHRE7; Etats-Unis; Da. 2001; Vol. 17; No. 11; Pp. 1083-1087; Bibl. 12 ref.
LA : Anglais
EA : We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.
CC : 002B06D01; 002A05C04; 002A05
FD : Virus HIV1; Cellule sanguine; Sang; Isolat; Ghana; Phylogenèse; Recombinaison; Point cassure; Transfection; Infection; Récepteur chimiokine CCR5; Utilisation; Phytohémagglutinine; Réplication
FG : Virus immunodéficience humaine; Lentivirus; Retroviridae; Virus; Afrique
ED : HIV-1 virus; Blood cell; Blood; Isolate; Ghana; Phylogeny; Recombination; Breakpoint; Transfection; Infection; CCR5 chemokine receptor; Use; Phytohemagglutinin; Replication
EG : Human immunodeficiency virus; Lentivirus; Retroviridae; Virus; Africa
SD : HIV-1 virus; Célula sanguínea; Sangre; Aislado; Ghana; Filogénesis; Recombinación; Punto ruptura; Transfección; Infección; Receptor quimioquina CCR5; Utilización; Fitohemaglutinina; Replicación
LO : INIST-20934.354000099074040120
ID : 02-0322075

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Pascal:02-0322075

Le document en format XML

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<div type="abstract" xml:lang="en">We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.</div>
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</fA44>
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<s0>12 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>02-0322075</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>AIDS research and human retroviruses</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002B06D01</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002A05C04</s0>
</fC02>
<fC02 i1="03" i2="X">
<s0>002A05</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Virus HIV1</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>HIV-1 virus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>HIV-1 virus</s0>
<s2>NW</s2>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Cellule sanguine</s0>
<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Blood cell</s0>
<s5>05</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Célula sanguínea</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Sang</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Blood</s0>
<s5>06</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Sangre</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Isolat</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Isolate</s0>
<s5>07</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Aislado</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Ghana</s0>
<s2>NG</s2>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Ghana</s0>
<s2>NG</s2>
<s5>08</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Ghana</s0>
<s2>NG</s2>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Phylogenèse</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>Phylogeny</s0>
<s5>09</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Filogénesis</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Recombinaison</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Recombination</s0>
<s5>10</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Recombinación</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Point cassure</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Breakpoint</s0>
<s5>11</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Punto ruptura</s0>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Transfection</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Transfection</s0>
<s5>12</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Transfección</s0>
<s5>12</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Infection</s0>
<s5>14</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Infection</s0>
<s5>14</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Infección</s0>
<s5>14</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Récepteur chimiokine CCR5</s0>
<s5>67</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>CCR5 chemokine receptor</s0>
<s5>67</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Receptor quimioquina CCR5</s0>
<s5>67</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Utilisation</s0>
<s5>68</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Use</s0>
<s5>68</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Utilización</s0>
<s5>68</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Phytohémagglutinine</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>69</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Phytohemagglutinin</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>69</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Fitohemaglutinina</s0>
<s2>NK</s2>
<s2>FR</s2>
<s5>69</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Réplication</s0>
<s5>70</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Replication</s0>
<s5>70</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Replicación</s0>
<s5>70</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Virus immunodéficience humaine</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Human immunodeficiency virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Human immunodeficiency virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Afrique</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Africa</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Africa</s0>
<s2>NG</s2>
</fC07>
<fN21>
<s1>182</s1>
</fN21>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 02-0322075 INIST</NO>
<ET>Infectious DNA clone of HIV type 1 A/G recombinant (CRF02―AG) replicable in peripheral blood mononuclear cells</ET>
<AU>TAKAHOKO (Mikako); TOBIUME (Minoru); ISHIKAWA (Koichi); AMPOFO (William); YAMAMOTO (Naoki); MATSUDA (Michiyuki); TATSUMI (Masashi)</AU>
<AF>Department of Pathology, Research Institute, International Medical Center of Japan/Tokyo 162-8644/Japon (1 aut., 2 aut., 6 aut.); Noguchi Memorial Institute for Medical Research, University of Ghana/Legon/Ghana (3 aut., 4 aut.); Department of Microbiology, Tokyo Medical and Dental University/Tokyo 113-8519/Japon (5 aut.); Department of Veterinary Science, National Institute of Infectious Diseases/Tokyo 162-8640/Japon (7 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>AIDS research and human retroviruses; ISSN 0889-2229; Coden ARHRE7; Etats-Unis; Da. 2001; Vol. 17; No. 11; Pp. 1083-1087; Bibl. 12 ref.</SO>
<LA>Anglais</LA>
<EA>We constructed an infectious DNA clone of the HIV-1 A/G recombinant 97GH-AG2, which was isolated in Ghana in 1997 and was classified originally as subtype A. By phylogenetic and recombination breakpoint analyses, p97GH-AG2 was grouped in the circulating form of A/G recombinants (CRF02―AG) and was found to contain the least amount of subtype G-derived region among the known CRF02―AG HIV-1 DNAs. This result suggests that CRF02―AG may be a predominant form in Ghana. Virions produced by transfection of p97GH-AG2 into 293T cells grew in phytohemagglutinin-stimulated peripheral blood mononuclear cells (PBMCs). 97GH-AG2 also replicated efficiently in CCR5-expressing HeLa cells, MAGICS, but only weakly in the parent MAGI cells, indicating that 97GH-AG2 uses mostly CCR5 as a coreceptor. Isolation of the first HIV-1 (CRF02―AG) DNA clone that replicates in PBMCs will accelerate the molecular analysis of this subtype.</EA>
<CC>002B06D01; 002A05C04; 002A05</CC>
<FD>Virus HIV1; Cellule sanguine; Sang; Isolat; Ghana; Phylogenèse; Recombinaison; Point cassure; Transfection; Infection; Récepteur chimiokine CCR5; Utilisation; Phytohémagglutinine; Réplication</FD>
<FG>Virus immunodéficience humaine; Lentivirus; Retroviridae; Virus; Afrique</FG>
<ED>HIV-1 virus; Blood cell; Blood; Isolate; Ghana; Phylogeny; Recombination; Breakpoint; Transfection; Infection; CCR5 chemokine receptor; Use; Phytohemagglutinin; Replication</ED>
<EG>Human immunodeficiency virus; Lentivirus; Retroviridae; Virus; Africa</EG>
<SD>HIV-1 virus; Célula sanguínea; Sangre; Aislado; Ghana; Filogénesis; Recombinación; Punto ruptura; Transfección; Infección; Receptor quimioquina CCR5; Utilización; Fitohemaglutinina; Replicación</SD>
<LO>INIST-20934.354000099074040120</LO>
<ID>02-0322075</ID>
</server>
</inist>
</record>

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