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Seroprevalence of six different viruses among pregnant women and blood donors in rural and urban Burkina Faso: A comparative analysis

Identifieur interne : 000314 ( Istex/Corpus ); précédent : 000313; suivant : 000315

Seroprevalence of six different viruses among pregnant women and blood donors in rural and urban Burkina Faso: A comparative analysis

Auteurs : Ellen Collenberg ; Thierry Ouedraogo ; Jean Ganamé ; Helmut Fickenscher ; Gisela Kynast-Wolf ; Heiko Becher ; Bocar Kouyaté ; Hans-Georg Kr Usslich ; Lassana Sangaré ; Denis M. Tebit

Source :

RBID : ISTEX:1B2094DD645C5F08A46BFF5CD6C0E2B1DC4351D7

English descriptors

Abstract

A seroprevalence study was carried out of six different human pathogenic viruses, namely human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), human T‐cell leukemia virus (HTLV), human herpesvirus type 8 (HHV‐8), and dengue virus among pregnant women and blood donors from rural (Nouna) and urban (Ouagadougou) Burkina Faso, West Africa. A total of 683 samples from blood donors (n = 191) and pregnant women (n = 492) were collected from both sites and screened for the different virus infection markers resulting in the following prevalence values for Nouna or Ouagadougou, respectively: HIV 3.6/4.6, anti‐HBV core (anti‐HBc) 69.6/76.4, HBV surface antigen (HBsAg)14.3/17.3, HCV 2.2/1.5, HTLV 1.4/0.5, HHV‐8 11.5/13.5, dengue virus 26.3/36.5. Individuals aged ≥25 years were more likely to be infected with HIV than those below 24 years (P < 0.05). Infection with HIV increased the likelihood of co‐infection with other viruses, such as HHV‐8, HBV and HTLV. Co‐infection studies involving five viruses (HBV‐HBsAg, HHV‐8, HIV, HCV, and HTLV) showed that 4.8% (33/683) of the studied population were dually infected, with HBsAg+ HHV‐8 (13/33), HBsAg+HIV (8/33) and HIV+HHV‐8 (8/33) being the most common co‐infections. Of the population studied 0.6% (4/683) was triply infected, the most common infection being with HBV+HIV+HHV‐8 (3/4). There was no difference in the prevalence of HIV, anti‐HBc, HBsAg, HCV, HTLV, and HHV‐8 either among blood donors or pregnant women in urban or rural setting, while dengue virus prevalence was relatively lower in rural (26.3%) than in urban (36.5%) Burkina Faso. J. Med. Virol. 78:683–692, 2006. © 2006 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/jmv.20593

Links to Exploration step

ISTEX:1B2094DD645C5F08A46BFF5CD6C0E2B1DC4351D7

Le document en format XML

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<div type="abstract" xml:lang="en">A seroprevalence study was carried out of six different human pathogenic viruses, namely human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), human T‐cell leukemia virus (HTLV), human herpesvirus type 8 (HHV‐8), and dengue virus among pregnant women and blood donors from rural (Nouna) and urban (Ouagadougou) Burkina Faso, West Africa. A total of 683 samples from blood donors (n = 191) and pregnant women (n = 492) were collected from both sites and screened for the different virus infection markers resulting in the following prevalence values for Nouna or Ouagadougou, respectively: HIV 3.6/4.6, anti‐HBV core (anti‐HBc) 69.6/76.4, HBV surface antigen (HBsAg)14.3/17.3, HCV 2.2/1.5, HTLV 1.4/0.5, HHV‐8 11.5/13.5, dengue virus 26.3/36.5. Individuals aged ≥25 years were more likely to be infected with HIV than those below 24 years (P < 0.05). Infection with HIV increased the likelihood of co‐infection with other viruses, such as HHV‐8, HBV and HTLV. Co‐infection studies involving five viruses (HBV‐HBsAg, HHV‐8, HIV, HCV, and HTLV) showed that 4.8% (33/683) of the studied population were dually infected, with HBsAg+ HHV‐8 (13/33), HBsAg+HIV (8/33) and HIV+HHV‐8 (8/33) being the most common co‐infections. Of the population studied 0.6% (4/683) was triply infected, the most common infection being with HBV+HIV+HHV‐8 (3/4). There was no difference in the prevalence of HIV, anti‐HBc, HBsAg, HCV, HTLV, and HHV‐8 either among blood donors or pregnant women in urban or rural setting, while dengue virus prevalence was relatively lower in rural (26.3%) than in urban (36.5%) Burkina Faso. J. Med. Virol. 78:683–692, 2006. © 2006 Wiley‐Liss, Inc.</div>
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<affiliation>Current Address: Institut fuer Infektionsmedizin, Universitaetsklinikum Kiel, Brunswiker Str. 4, 24105 Kiel, Germany.</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Gisela</namePart>
<namePart type="family">Kynast‐Wolf</namePart>
<affiliation>Abteilung Tropenhygiene und Öffentliches Gesundheitswesen, Universitaetsklinikum Heidelberg, Heidelberg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Heiko</namePart>
<namePart type="family">Becher</namePart>
<affiliation>Abteilung Tropenhygiene und Öffentliches Gesundheitswesen, Universitaetsklinikum Heidelberg, Heidelberg, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Bocar</namePart>
<namePart type="family">Kouyaté</namePart>
<affiliation>Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Hans‐Georg</namePart>
<namePart type="family">Kräusslich</namePart>
<affiliation>Abteilung Virologie, Universitaetsklinikum Heidelberg, Heidelberg, Germany</affiliation>
<affiliation>Abteilung Virologie, Universitaetsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.===</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Lassana</namePart>
<namePart type="family">Sangaré</namePart>
<affiliation>Laboratoire Bacterio‐Virologie, Centre Hospitalier Universitaire Yalgado Ouedraogo, Ouagadougou, Burkina Faso</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Denis M.</namePart>
<namePart type="family">Tebit</namePart>
<affiliation>Abteilung Virologie, Universitaetsklinikum Heidelberg, Heidelberg, Germany</affiliation>
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<dateIssued encoding="w3cdtf">2006-05</dateIssued>
<dateValid encoding="w3cdtf">2006-01-09</dateValid>
<copyrightDate encoding="w3cdtf">2006</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract lang="en">A seroprevalence study was carried out of six different human pathogenic viruses, namely human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), human T‐cell leukemia virus (HTLV), human herpesvirus type 8 (HHV‐8), and dengue virus among pregnant women and blood donors from rural (Nouna) and urban (Ouagadougou) Burkina Faso, West Africa. A total of 683 samples from blood donors (n = 191) and pregnant women (n = 492) were collected from both sites and screened for the different virus infection markers resulting in the following prevalence values for Nouna or Ouagadougou, respectively: HIV 3.6/4.6, anti‐HBV core (anti‐HBc) 69.6/76.4, HBV surface antigen (HBsAg)14.3/17.3, HCV 2.2/1.5, HTLV 1.4/0.5, HHV‐8 11.5/13.5, dengue virus 26.3/36.5. Individuals aged ≥25 years were more likely to be infected with HIV than those below 24 years (P < 0.05). Infection with HIV increased the likelihood of co‐infection with other viruses, such as HHV‐8, HBV and HTLV. Co‐infection studies involving five viruses (HBV‐HBsAg, HHV‐8, HIV, HCV, and HTLV) showed that 4.8% (33/683) of the studied population were dually infected, with HBsAg+ HHV‐8 (13/33), HBsAg+HIV (8/33) and HIV+HHV‐8 (8/33) being the most common co‐infections. Of the population studied 0.6% (4/683) was triply infected, the most common infection being with HBV+HIV+HHV‐8 (3/4). There was no difference in the prevalence of HIV, anti‐HBc, HBsAg, HCV, HTLV, and HHV‐8 either among blood donors or pregnant women in urban or rural setting, while dengue virus prevalence was relatively lower in rural (26.3%) than in urban (36.5%) Burkina Faso. J. Med. Virol. 78:683–692, 2006. © 2006 Wiley‐Liss, Inc.</abstract>
<note type="funding">Deutsche Forschungsgemeinschaft (SFB 544, project A6)</note>
<subject lang="en">
<genre>keywords</genre>
<topic>HIV</topic>
<topic>HBV</topic>
<topic>HCV</topic>
<topic>HTLV</topic>
<topic>HHV‐8</topic>
<topic>dengue virus epidemiology</topic>
</subject>
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<titleInfo>
<title>Journal of Medical Virology</title>
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<titleInfo type="abbreviated">
<title>J. Med. Virol.</title>
</titleInfo>
<genre type="journal">journal</genre>
<subject>
<genre>article-category</genre>
<topic>Research Article</topic>
</subject>
<identifier type="ISSN">0146-6615</identifier>
<identifier type="eISSN">1096-9071</identifier>
<identifier type="DOI">10.1002/(ISSN)1096-9071</identifier>
<identifier type="PublisherID">JMV</identifier>
<part>
<date>2006</date>
<detail type="volume">
<caption>vol.</caption>
<number>78</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>5</number>
</detail>
<extent unit="pages">
<start>683</start>
<end>692</end>
<total>10</total>
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<identifier type="istex">1B2094DD645C5F08A46BFF5CD6C0E2B1DC4351D7</identifier>
<identifier type="DOI">10.1002/jmv.20593</identifier>
<identifier type="ArticleID">JMV20593</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2006 Wiley‐Liss, Inc.</accessCondition>
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<recordOrigin>Wiley Subscription Services, Inc., A Wiley Company</recordOrigin>
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