Le SIDA au Ghana (serveur d'exploration)

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Vertical transmission of HIV in ghanaian women diagnosed in cord blood and post-natal samples

Identifieur interne : 000049 ( PascalFrancis/Curation ); précédent : 000048; suivant : 000050

Vertical transmission of HIV in ghanaian women diagnosed in cord blood and post-natal samples

Auteurs : Lucia Fischetti [Royaume-Uni] ; Kwabena Danso [Ghana] ; Albert Dompreh [Ghana] ; Victor Addo [Ghana] ; Lars Haaheim [Norvège] ; Jean-Pierre Allain [Royaume-Uni]

Source :

RBID : Pascal:06-0256799

Descripteurs français

English descriptors

Abstract

HIV RNA detection in the newborn is the main diagnostic tool for vertical transmission. Most infections are thought to occur peri- or post-natally, hence preventive antiviral therapy administered days before and during delivery. This study used cord blood for molecular diagnosis, examined viral load and HIV-1 subtypes as determinants of transmission, and compared molecular variability of maternal, cord blood, and post-natal quasispecies. Ninety-seven seropositive mother-cord blood paired plasmas from Ghana were tested for HIV RNA. Viral load was quantified and a subgroup of 45 random women samples was typed and subtyped. HIV-1 from infected pairs was cloned, sequenced, and analyzed phylogenetically. The prevalence of HIV infection in pregnant women was 3.3%. 13/97 cord blood samples (13.5%) contained HIV RNA. No correlation between either viral load at labor (range 103-107) or HIV-1 subtype and in utero transmission wasfound. In both transmitting and non-transmitting mothers, 56% of HIV-1 strains were CRF02_AG. In three pairs, maternal and cord blood quasispecies were closely related, suggesting late pregnancy or perinatal transmission, while in four pairs, genetic distances suggested transmission earlier during gestation. Maternal viral load and genotype did not correlate with HIV-1 pre-natal transmission. HIV infection during gestation appears relatively frequent.
pA  
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A03   1    @0 J. med. virol.
A05       @2 77
A06       @2 3
A08 01  1  ENG  @1 Vertical transmission of HIV in ghanaian women diagnosed in cord blood and post-natal samples
A11 01  1    @1 FISCHETTI (Lucia)
A11 02  1    @1 DANSO (Kwabena)
A11 03  1    @1 DOMPREH (Albert)
A11 04  1    @1 ADDO (Victor)
A11 05  1    @1 HAAHEIM (Lars)
A11 06  1    @1 ALLAIN (Jean-Pierre)
A14 01      @1 Department of Haematology, Division of Transfusion Medicine, University of Cambridge @2 Cambridge @3 GBR @Z 1 aut. @Z 6 aut.
A14 02      @1 Department of Obstetrics and Gynaecology, Komfo Anokye Teaching Hospital @2 Kumasi @3 GHA @Z 2 aut. @Z 4 aut.
A14 03      @1 Department of Microbiology, Komfo Anokye Teaching Hospital @2 Kumasi @3 GHA @Z 3 aut.
A14 04      @1 Department of Microbiology and Immunology, University of Bergen @2 Bergen @3 NOR @Z 5 aut.
A20       @1 351-359
A21       @1 2005
A23 01      @0 ENG
A43 01      @1 INIST @2 17422 @5 354000132096490040
A44       @0 0000 @1 © 2006 INIST-CNRS. All rights reserved.
A45       @0 1 p.1/4
A47 01  1    @0 06-0256799
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of medical virology
A66 01      @0 USA
C01 01    ENG  @0 HIV RNA detection in the newborn is the main diagnostic tool for vertical transmission. Most infections are thought to occur peri- or post-natally, hence preventive antiviral therapy administered days before and during delivery. This study used cord blood for molecular diagnosis, examined viral load and HIV-1 subtypes as determinants of transmission, and compared molecular variability of maternal, cord blood, and post-natal quasispecies. Ninety-seven seropositive mother-cord blood paired plasmas from Ghana were tested for HIV RNA. Viral load was quantified and a subgroup of 45 random women samples was typed and subtyped. HIV-1 from infected pairs was cloned, sequenced, and analyzed phylogenetically. The prevalence of HIV infection in pregnant women was 3.3%. 13/97 cord blood samples (13.5%) contained HIV RNA. No correlation between either viral load at labor (range 103-107) or HIV-1 subtype and in utero transmission wasfound. In both transmitting and non-transmitting mothers, 56% of HIV-1 strains were CRF02_AG. In three pairs, maternal and cord blood quasispecies were closely related, suggesting late pregnancy or perinatal transmission, while in four pairs, genetic distances suggested transmission earlier during gestation. Maternal viral load and genotype did not correlate with HIV-1 pre-natal transmission. HIV infection during gestation appears relatively frequent.
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C03 01  X  FRE  @0 Virus immunodéficience humaine @2 NW @5 01
C03 01  X  ENG  @0 Human immunodeficiency virus @2 NW @5 01
C03 01  X  SPA  @0 Human immunodeficiency virus @2 NW @5 01
C03 02  X  FRE  @0 Homme @5 02
C03 02  X  ENG  @0 Human @5 02
C03 02  X  SPA  @0 Hombre @5 02
C03 03  X  FRE  @0 Transmission verticale @5 05
C03 03  X  ENG  @0 Vertical transmission @5 05
C03 03  X  SPA  @0 Transmisión vertical @5 05
C03 04  X  FRE  @0 Femelle @5 06
C03 04  X  ENG  @0 Female @5 06
C03 04  X  SPA  @0 Hembra @5 06
C03 05  X  FRE  @0 Sang @5 07
C03 05  X  ENG  @0 Blood @5 07
C03 05  X  SPA  @0 Sangre @5 07
C03 06  X  FRE  @0 Ghana @2 NG @5 08
C03 06  X  ENG  @0 Ghana @2 NG @5 08
C03 06  X  SPA  @0 Ghana @2 NG @5 08
C03 07  X  FRE  @0 Charge virale @5 09
C03 07  X  ENG  @0 Viral load @5 09
C03 07  X  SPA  @0 Carga vírica @5 09
C03 08  X  FRE  @0 Soustype @5 10
C03 08  X  ENG  @0 Subtype @5 10
C03 08  X  SPA  @0 Subtipo @5 10
C07 01  X  FRE  @0 Lentivirus @2 NW
C07 01  X  ENG  @0 Lentivirus @2 NW
C07 01  X  SPA  @0 Lentivirus @2 NW
C07 02  X  FRE  @0 Retroviridae @2 NW
C07 02  X  ENG  @0 Retroviridae @2 NW
C07 02  X  SPA  @0 Retroviridae @2 NW
C07 03  X  FRE  @0 Virus @2 NW
C07 03  X  ENG  @0 Virus @2 NW
C07 03  X  SPA  @0 Virus @2 NW
C07 04  X  FRE  @0 Afrique @2 NG
C07 04  X  ENG  @0 Africa @2 NG
C07 04  X  SPA  @0 Africa @2 NG
N21       @1 163
N44 01      @1 OTO
N82       @1 OTO

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Pascal:06-0256799

Le document en format XML

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<div type="abstract" xml:lang="en">HIV RNA detection in the newborn is the main diagnostic tool for vertical transmission. Most infections are thought to occur peri- or post-natally, hence preventive antiviral therapy administered days before and during delivery. This study used cord blood for molecular diagnosis, examined viral load and HIV-1 subtypes as determinants of transmission, and compared molecular variability of maternal, cord blood, and post-natal quasispecies. Ninety-seven seropositive mother-cord blood paired plasmas from Ghana were tested for HIV RNA. Viral load was quantified and a subgroup of 45 random women samples was typed and subtyped. HIV-1 from infected pairs was cloned, sequenced, and analyzed phylogenetically. The prevalence of HIV infection in pregnant women was 3.3%. 13/97 cord blood samples (13.5%) contained HIV RNA. No correlation between either viral load at labor (range 10
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<sup>7</sup>
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<sup>3</sup>
-10
<sup>7</sup>
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</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Charge virale</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Viral load</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Carga vírica</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Soustype</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Subtype</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Subtipo</s0>
<s5>10</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Lentivirus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Retroviridae</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Virus</s0>
<s2>NW</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Afrique</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Africa</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Africa</s0>
<s2>NG</s2>
</fC07>
<fN21>
<s1>163</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
</record>

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