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HIV-1 Drug-Resistance Surveillance among Treatment-Experienced and -Naïve Patients after the Implementation of Antiretroviral Therapy in Ghana

Identifieur interne : 000303 ( Pmc/Checkpoint ); précédent : 000302; suivant : 000304

HIV-1 Drug-Resistance Surveillance among Treatment-Experienced and -Naïve Patients after the Implementation of Antiretroviral Therapy in Ghana

Auteurs : Nicholas I. Nii-Trebi [Ghana] ; Shiro Ibe [Japon] ; Jacob S. Barnor [Ghana] ; Koichi Ishikawa [Japon] ; James A. M. Brandful [Ghana] ; Sampson B. Ofori [Ghana] ; Shoji Yamaoka [Japon] ; William K. Ampofo [Ghana] ; Wataru Sugiura [Japon]

Source :

RBID : PMC:3747072

Abstract

Background

Limited HIV-1 drug-resistance surveillance has been carried out in Ghana since the implementation of antiretroviral therapy (ART). This study sought to provide data on the profile of HIV-1 drug resistance in ART-experienced and newly diagnosed individuals in Ghana.

Methods

Samples were collected from 101 HIV-1-infected patients (32 ART-experienced cases with virological failure and 69 newly diagnosed ART-naïve cases, including 11 children), in Koforidua, Eastern region of Ghana, from February 2009 to January 2010. The pol gene sequences were analyzed by in-house HIV-1 drug-resistance testing.

Results

The most prevalent HIV-1 subtype was CRF02_AG (66.3%, 67/101) followed by unique recombinant forms (25.7%, 26/101). Among 31 ART-experienced adults, 22 (71.0%) possessed at least one drug-resistance mutation, and 14 (45.2%) had two-class-resistance to nucleoside and non-nucleoside reverse-transcriptase inhibitors used in their first ART regimen. Importantly, the number of accumulated mutations clearly correlated with the duration of ART. The most prevalent mutation was lamivudine-resistance M184V (n = 12, 38.7%) followed by efavirenz/nevirapine-resistance K103N (n = 9, 29.0%), and zidovudine/stavudine-resistance T215Y/F (n = 6, 19.4%). Within the viral protease, the major nelfinavir-resistance mutation L90M was found in one case. No transmitted HIV-1 drug-resistance mutation was found in 59 ART-naïve adults, but K103N and G190S mutations were observed in one ART-naïve child.

Conclusions

Despite expanding accessibility to ART in Eastern Ghana, the prevalence of transmitted HIV-1 drug resistance presently appears to be low. As ART provision with limited options is scaled up nationwide in Ghana, careful monitoring of transmitted HIV-1 drug resistance is necessary.


Url:
DOI: 10.1371/journal.pone.0071972
PubMed: 23977189
PubMed Central: 3747072


Affiliations:


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PMC:3747072

Le document en format XML

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<title>Background</title>
<p>Limited HIV-1 drug-resistance surveillance has been carried out in Ghana since the implementation of antiretroviral therapy (ART). This study sought to provide data on the profile of HIV-1 drug resistance in ART-experienced and newly diagnosed individuals in Ghana.</p>
</sec>
<sec>
<title>Methods</title>
<p>Samples were collected from 101 HIV-1-infected patients (32 ART-experienced cases with virological failure and 69 newly diagnosed ART-naïve cases, including 11 children), in Koforidua, Eastern region of Ghana, from February 2009 to January 2010. The
<italic>pol</italic>
gene sequences were analyzed by in-house HIV-1 drug-resistance testing.</p>
</sec>
<sec>
<title>Results</title>
<p>The most prevalent HIV-1 subtype was CRF02_AG (66.3%, 67/101) followed by unique recombinant forms (25.7%, 26/101). Among 31 ART-experienced adults, 22 (71.0%) possessed at least one drug-resistance mutation, and 14 (45.2%) had two-class-resistance to nucleoside and non-nucleoside reverse-transcriptase inhibitors used in their first ART regimen. Importantly, the number of accumulated mutations clearly correlated with the duration of ART. The most prevalent mutation was lamivudine-resistance M184V (
<italic>n</italic>
 = 12, 38.7%) followed by efavirenz/nevirapine-resistance K103N (
<italic>n</italic>
 = 9, 29.0%), and zidovudine/stavudine-resistance T215Y/F (
<italic>n</italic>
 = 6, 19.4%). Within the viral protease, the major nelfinavir-resistance mutation L90M was found in one case. No transmitted HIV-1 drug-resistance mutation was found in 59 ART-naïve adults, but K103N and G190S mutations were observed in one ART-naïve child.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Despite expanding accessibility to ART in Eastern Ghana, the prevalence of transmitted HIV-1 drug resistance presently appears to be low. As ART provision with limited options is scaled up nationwide in Ghana, careful monitoring of transmitted HIV-1 drug resistance is necessary.</p>
</sec>
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<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">PLoS One</journal-id>
<journal-id journal-id-type="iso-abbrev">PLoS ONE</journal-id>
<journal-id journal-id-type="publisher-id">plos</journal-id>
<journal-id journal-id-type="pmc">plosone</journal-id>
<journal-title-group>
<journal-title>PLoS ONE</journal-title>
</journal-title-group>
<issn pub-type="epub">1932-6203</issn>
<publisher>
<publisher-name>Public Library of Science</publisher-name>
<publisher-loc>San Francisco, USA</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">23977189</article-id>
<article-id pub-id-type="pmc">3747072</article-id>
<article-id pub-id-type="publisher-id">PONE-D-13-14356</article-id>
<article-id pub-id-type="doi">10.1371/journal.pone.0071972</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Research Article</subject>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Biology</subject>
<subj-group>
<subject>Microbiology</subject>
<subj-group>
<subject>Virology</subject>
<subj-group>
<subject>Viral Transmission and Infection</subject>
<subj-group>
<subject>Viral Load</subject>
</subj-group>
</subj-group>
</subj-group>
</subj-group>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Mathematics</subject>
<subj-group>
<subject>Statistics</subject>
<subj-group>
<subject>Biostatistics</subject>
</subj-group>
</subj-group>
</subj-group>
<subj-group subj-group-type="Discipline-v2">
<subject>Medicine</subject>
<subj-group>
<subject>Epidemiology</subject>
<subj-group>
<subject>Molecular Epidemiology</subject>
</subj-group>
</subj-group>
<subj-group>
<subject>Infectious Diseases</subject>
<subj-group>
<subject>Viral Diseases</subject>
<subj-group>
<subject>HIV</subject>
<subj-group>
<subject>HIV diagnosis and management</subject>
<subject>HIV epidemiology</subject>
<subject>Retrovirology and HIV immunopathogenesis</subject>
</subj-group>
</subj-group>
</subj-group>
</subj-group>
<subj-group>
<subject>Public Health</subject>
<subj-group>
<subject>Health Screening</subject>
</subj-group>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>HIV-1 Drug-Resistance Surveillance among Treatment-Experienced and -Naïve Patients after the Implementation of Antiretroviral Therapy in Ghana</article-title>
<alt-title alt-title-type="running-head">HIV-1 Drug-Resistance Surveillance in Ghana</alt-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Nii-Trebi</surname>
<given-names>Nicholas I.</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Ibe</surname>
<given-names>Shiro</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author" equal-contrib="yes">
<name>
<surname>Barnor</surname>
<given-names>Jacob S.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ishikawa</surname>
<given-names>Koichi</given-names>
</name>
<xref ref-type="aff" rid="aff4">
<sup>4</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Brandful</surname>
<given-names>James A. M.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ofori</surname>
<given-names>Sampson B.</given-names>
</name>
<xref ref-type="aff" rid="aff5">
<sup>5</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Yamaoka</surname>
<given-names>Shoji</given-names>
</name>
<xref ref-type="aff" rid="aff6">
<sup>6</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ampofo</surname>
<given-names>William K.</given-names>
</name>
<xref ref-type="aff" rid="aff3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sugiura</surname>
<given-names>Wataru</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="aff" rid="aff7">
<sup>7</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
</contrib-group>
<aff id="aff1">
<label>1</label>
<addr-line>Department of Medical Laboratory Sciences, School of Allied Health Sciences, University of Ghana, Accra, Ghana</addr-line>
</aff>
<aff id="aff2">
<label>2</label>
<addr-line>Department of Infection and Immunology, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan</addr-line>
</aff>
<aff id="aff3">
<label>3</label>
<addr-line>Department of Virology, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana</addr-line>
</aff>
<aff id="aff4">
<label>4</label>
<addr-line>AIDS Research Center, National Institute of Infectious Diseases, Tokyo, Japan</addr-line>
</aff>
<aff id="aff5">
<label>5</label>
<addr-line>Department of Medicine, Koforidua Regional Hospital, Koforidua, Ghana</addr-line>
</aff>
<aff id="aff6">
<label>6</label>
<addr-line>Department of Molecular Virology, Graduate School of Medicine, Tokyo Medical and Dental University, Tokyo, Japan</addr-line>
</aff>
<aff id="aff7">
<label>7</label>
<addr-line>Department of AIDS Research, Nagoya University Graduate School of Medicine, Nagoya, Japan</addr-line>
</aff>
<contrib-group>
<contrib contrib-type="editor">
<name>
<surname>Barbour</surname>
<given-names>Jason D.</given-names>
</name>
<role>Editor</role>
<xref ref-type="aff" rid="edit1"></xref>
</contrib>
</contrib-group>
<aff id="edit1">
<addr-line>University of Hawaii Manoa, United States of America</addr-line>
</aff>
<author-notes>
<corresp id="cor1">* E-mail:
<email>wsugiura@nnh.hosp.go.jp</email>
</corresp>
<fn fn-type="conflict">
<p>
<bold>Competing Interests: </bold>
The authors have declared that no competing interests exist.</p>
</fn>
<fn fn-type="con">
<p>Conceived and designed the experiments: NIN SI JSB KI JAMB SBO SY WKA WS. Performed the experiments: NIN SI JSB KI JAMB. Wrote the paper: NIN SI WS. Organized the study team: KI SY WKA WS. Enrolled patients into the study: SBO. Prepared a clinical database: NIN JSB KI SBO. Revised the manuscript critically JSB KI JAMB SBO SY WKA.</p>
</fn>
</author-notes>
<pub-date pub-type="collection">
<year>2013</year>
</pub-date>
<pub-date pub-type="epub">
<day>19</day>
<month>8</month>
<year>2013</year>
</pub-date>
<volume>8</volume>
<issue>8</issue>
<elocation-id>e71972</elocation-id>
<history>
<date date-type="received">
<day>7</day>
<month>4</month>
<year>2013</year>
</date>
<date date-type="accepted">
<day>7</day>
<month>7</month>
<year>2013</year>
</date>
</history>
<permissions>
<copyright-year>2013</copyright-year>
<copyright-holder>Nii-Trebi et al</copyright-holder>
<license>
<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
</license>
</permissions>
<abstract>
<sec>
<title>Background</title>
<p>Limited HIV-1 drug-resistance surveillance has been carried out in Ghana since the implementation of antiretroviral therapy (ART). This study sought to provide data on the profile of HIV-1 drug resistance in ART-experienced and newly diagnosed individuals in Ghana.</p>
</sec>
<sec>
<title>Methods</title>
<p>Samples were collected from 101 HIV-1-infected patients (32 ART-experienced cases with virological failure and 69 newly diagnosed ART-naïve cases, including 11 children), in Koforidua, Eastern region of Ghana, from February 2009 to January 2010. The
<italic>pol</italic>
gene sequences were analyzed by in-house HIV-1 drug-resistance testing.</p>
</sec>
<sec>
<title>Results</title>
<p>The most prevalent HIV-1 subtype was CRF02_AG (66.3%, 67/101) followed by unique recombinant forms (25.7%, 26/101). Among 31 ART-experienced adults, 22 (71.0%) possessed at least one drug-resistance mutation, and 14 (45.2%) had two-class-resistance to nucleoside and non-nucleoside reverse-transcriptase inhibitors used in their first ART regimen. Importantly, the number of accumulated mutations clearly correlated with the duration of ART. The most prevalent mutation was lamivudine-resistance M184V (
<italic>n</italic>
 = 12, 38.7%) followed by efavirenz/nevirapine-resistance K103N (
<italic>n</italic>
 = 9, 29.0%), and zidovudine/stavudine-resistance T215Y/F (
<italic>n</italic>
 = 6, 19.4%). Within the viral protease, the major nelfinavir-resistance mutation L90M was found in one case. No transmitted HIV-1 drug-resistance mutation was found in 59 ART-naïve adults, but K103N and G190S mutations were observed in one ART-naïve child.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Despite expanding accessibility to ART in Eastern Ghana, the prevalence of transmitted HIV-1 drug resistance presently appears to be low. As ART provision with limited options is scaled up nationwide in Ghana, careful monitoring of transmitted HIV-1 drug resistance is necessary.</p>
</sec>
</abstract>
<funding-group>
<funding-statement>This study was supported by a grant of the Japan Initiative for Global Research Network on Infectious Diseases from the Ministry of Education, Culture, Sports, Science and Technology of Japan to the University of Ghana; the Tokyo Medical and Dental University; a Grant-in-Aid for AIDS Research from the Ministry of Health, Labour and Welfare of Japan (H22-AIDS-004); and a grant from the HIV Research Trust, United Kingdom. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.</funding-statement>
</funding-group>
<counts>
<page-count count="8"></page-count>
</counts>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Ghana</li>
<li>Japon</li>
</country>
<region>
<li>Région de Kantō</li>
<li>Région du Grand Accra</li>
</region>
<settlement>
<li>Accra</li>
<li>Tokyo</li>
</settlement>
<orgName>
<li>Université du Ghana</li>
</orgName>
</list>
<tree>
<country name="Ghana">
<region name="Région du Grand Accra">
<name sortKey="Nii Trebi, Nicholas I" sort="Nii Trebi, Nicholas I" uniqKey="Nii Trebi N" first="Nicholas I." last="Nii-Trebi">Nicholas I. Nii-Trebi</name>
</region>
<name sortKey="Ampofo, William K" sort="Ampofo, William K" uniqKey="Ampofo W" first="William K." last="Ampofo">William K. Ampofo</name>
<name sortKey="Barnor, Jacob S" sort="Barnor, Jacob S" uniqKey="Barnor J" first="Jacob S." last="Barnor">Jacob S. Barnor</name>
<name sortKey="Brandful, James A M" sort="Brandful, James A M" uniqKey="Brandful J" first="James A. M." last="Brandful">James A. M. Brandful</name>
<name sortKey="Ofori, Sampson B" sort="Ofori, Sampson B" uniqKey="Ofori S" first="Sampson B." last="Ofori">Sampson B. Ofori</name>
</country>
<country name="Japon">
<noRegion>
<name sortKey="Ibe, Shiro" sort="Ibe, Shiro" uniqKey="Ibe S" first="Shiro" last="Ibe">Shiro Ibe</name>
</noRegion>
<name sortKey="Ishikawa, Koichi" sort="Ishikawa, Koichi" uniqKey="Ishikawa K" first="Koichi" last="Ishikawa">Koichi Ishikawa</name>
<name sortKey="Sugiura, Wataru" sort="Sugiura, Wataru" uniqKey="Sugiura W" first="Wataru" last="Sugiura">Wataru Sugiura</name>
<name sortKey="Sugiura, Wataru" sort="Sugiura, Wataru" uniqKey="Sugiura W" first="Wataru" last="Sugiura">Wataru Sugiura</name>
<name sortKey="Yamaoka, Shoji" sort="Yamaoka, Shoji" uniqKey="Yamaoka S" first="Shoji" last="Yamaoka">Shoji Yamaoka</name>
</country>
</tree>
</affiliations>
</record>

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