<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">WJA</journal-id><journal-title-group><journal-title>World Journal of AIDS</journal-title></journal-title-group><issn pub-type="epub">2160-8814</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/wja.2016.64019</article-id><article-id pub-id-type="publisher-id">WJA-72476</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Qualitative Detection of Proviral-DNA of HIV-1 in Infants to Determine the Efficacy of Antiretroviral Therapy in the Prevention of Vertical Transmission of HIV-1 in The Gambia
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Lamin</surname><given-names>B. Cham</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pape</surname><given-names>Mbacké Sembene</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Pa</surname><given-names>Ousman Bah</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Musa</surname><given-names>Ceesay</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ebrima</surname><given-names>Joof</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abou</surname><given-names>Kebbeh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Massamba</surname><given-names>Gueye</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ebrima</surname><given-names>Njie</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Bakary</surname><given-names>Sanneh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>National Public Health Laboratories, Ministry of Health and Social Welfare, Kotu Layout, Kotu, The Gambia</addr-line></aff><aff id="aff2"><addr-line>Université Cheikh Anta Diop de Dakar, Dakar, Senegal</addr-line></aff><aff id="aff4"><addr-line>University of The Gambia, Sere Kunda, The Gambia</addr-line></aff><aff id="aff3"><addr-line>National AIDS Control Program, Ministry of Health and Social Welfare, Dar es Salaam, Tanzania</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>laminbcham@gmail.com(LBC)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>04</day><month>11</month><year>2016</year></pub-date><volume>06</volume><issue>04</issue><fpage>169</fpage><lpage>177</lpage><history><date date-type="received"><day>October</day>	<month>20,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>November</month>	<year>27,</year>	</date><date date-type="accepted"><day>December</day>	<month>1,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The priority of The Gambia government is to eliminate maternal to child transmission of HIV and in line with this priority, the country implemented an antiretroviral therapy (ART) program. With this, all HIV infected pregnant and breastfeeding mothers and infants have access to ARV drugs. This study aims to determine the prevalence of vertical transmission of HIV among women receiving the ARV drugs. Dried blood spot samples were collected from 109 HIV-exposed infants enrolled in 13 PMTCT sites across the country. A qualitative detection of proviral-DNA of HIV-1 was performed using the RealTime Abbott PCR assay. Data from 105 mothers were analyzed using SPSS version 16.0 and association of risk factors to PCR results were analyzed using (Crosstabs) Pearson Chi-Square. The p-value of significant was set at p &lt; 0.05. This study has found that the prevalence of vertical transmission of HIV is 0.0% (0/64) among women that received the ARV prophylaxis then started ART, 7.1% (2/28) among mothers that received HIV prophylaxis only, and 38.4% (5/13) among women who neither receive HIV-prophylaxis nor ART during pregnancy or breastfeeding. Other risk factors of vertical transmission such as late initiation of treatment, default during treatment and first born of twins were found to be significantly associated with vertical transmission p = 0.001, p = 0.022 and p = 0.000 respectively. This study has found that the early intervention of ART at the onset of pregnancy through breastfeeding can eliminates Maternal to Child transmission of HIV-1and a high risk of vertical transmission was found among women who neither receive prophylaxis nor ART. If the effectiveness of the antiretroviral therapy is maintain, The Gambia, in the near future will attain the WHO’s goal to eliminate maternal to child transmission of HIV.
 
</p></abstract><kwd-group><kwd>ARV Drugs</kwd><kwd> ART</kwd><kwd> Prophylaxis</kwd><kwd> Maternal to Child (Vertical) Transmission</kwd><kwd> PCR</kwd><kwd> HIV-Exposed Infants</kwd><kwd> The Gambia</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>The climatic and other environmental factors of the African continent encourage the adaptation and survival of most micro-organisms (pathogens inclusive). This has caused infectious diseases to be a major challenge in the socio-economic status of countries in the Sub-Saharan Africa. One of the leading pathogenic viruses that cause serious public health challenge is the Human Immunodeficiency Virus (HIV).</p><p>The Human Immunodeficiency Virus (HIV) is an etiological cause of Acquired Immunodeficiency Syndrome (AIDS) [<xref ref-type="bibr" rid="scirp.72476-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref4">4</xref>] which is a major worldwide threat particularly in Africa as it continues to claim millions of lives and still remind incurable. Globally, over 35.4 million people are living with the HIV and about 63% - 70% of the HIV infected individuals at the end of 2012 are living in Sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.72476-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref6">6</xref>] . The Sub-Saharan Africa represent 10% of the world’s population but unfortunately 67% of HIV infected adults and 90% of HIV infected children live in Sub-Saharan Africa and about three quarters of all AIDS deaths occurred in this region [<xref ref-type="bibr" rid="scirp.72476-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref8">8</xref>] . It is estimated that roughly there are 7000 new HIV infections every day and nearly 97% of these, come from developing countries and about 60% are from Sub-Saharan Africa [<xref ref-type="bibr" rid="scirp.72476-ref4">4</xref>] .</p><p>The Gambia has a population of 1.8 million with a growth rate of 3.3% and the current HIV prevalence is at 1.57% for HIV-1 and 0.26% for HIV-2. The Gambia like other West African countries has a low prevalence of HIV. It was first diagnosed in May 1986 and by 1999, there were 810 new cases detected [<xref ref-type="bibr" rid="scirp.72476-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref8">8</xref>] . The HIV-1 has a prevalence of 0.6% in 1993 to 2.1% in 2004, then later drop to 1.1% in 2005 and then shot to 2.8% in 2006. The prevalence was then stabilized between 2.8% to 1.57% from 2006 to 2013 due to the intervention of different HIV prevention and control programs [<xref ref-type="bibr" rid="scirp.72476-ref8">8</xref>] .</p><p>The priority of the government of The Gambia is to reduce the HIV prevalence to less than 1% and in line to this priority. The Gambia has developed different means of preventing of HIV infections. Among them, it is the Elimination of Mother to Child Transmission of HIV. With this program, the country has aimed at reducing transmission from mother to child to less than 4%.</p><p>The Prevention of mother To Child Transmission (PMTCT) program in The Gambia provides free and easy access to ARV drugs to all HIV infected pregnant and breastfeeding women and their children. The national coverage of the PMTCT program is very wide across the country. About 60% of these patients are enrolled in the public health facilities and 40% in private facilities. Forty four percent (44%) of the patients are enrolled in two urban sites showing the concentration of the services in major urban areas, yet a massive decentralization of PMTCT sites have been done in 2016 [<xref ref-type="bibr" rid="scirp.72476-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref8">8</xref>] . This treatment was initially monitored using a routine CD4 analysis and now all patients on ART are run for viral load.</p><p>The antiretroviral drugs used in The Gambia are combination of Nucleoside Reverse Transcriptase Inhibitors (NRTIs), Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) and Protease Inhibitors (PIs). The NRTIs used are Zidovudine (AZT), Abacavir (ABC), Emtricitabin and Tenofovir (TDF) and the NNRTIs used are Niverapine (NVP), Efavirenz (EFV) and the protease inhibitorsare Liponavir (LPV) or Ritonavir [<xref ref-type="bibr" rid="scirp.72476-ref7">7</xref>] . The dosages for pregnant and breast feeding mother and children infected with HIV-1 differ from those of HIV-2. This is because HIV-2 is naturally resistant to NNRTIs.</p><p>・ Adult with HIV-1: TDF + 3TC + EFV (alternative; AZT + 3TC + NVP/LPV).</p><p>・ Adults with HIV-2; AZT + 3TC + TDF (alternative; AZT + 3TC + ABC/LPV).</p><p>・ Children: AZT syrup twice daily or NVP dose daily.</p><p>In addition to the PMTCT, HIV patients receiving the ARV drugs are also given Clotrimazole as a prophylaxis for opportunistic infections. Despite this recent optimization of antiretroviral drugs, the country continues to register new HIV pediatric infections.</p><p>In August 2015, The Gambia established a new molecular biology laboratory (DNA &amp; RNA PCR) purposely for the early infant diagnostic (EID) for HIV and monitoring the adherence of patients receiving the antiretroviral drugs. With this, all children born and breastfeeding from HIV infected mothers are tested (using PCR) at birth or during breastfeeding. Though EID is very challenging because of the cost and complexity of collecting, transporting and testing of biological samples but it is crucial for the timely initiation of ARVs to reduce child mortality [<xref ref-type="bibr" rid="scirp.72476-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref10">10</xref>] .</p></sec><sec id="s2"><title>2. Methodology</title><sec id="s2_1"><title>2.1. Ethical Consideration</title><p>This study was reviewed and approved by The Gambia Scientific and Ethic Committee and the reference number of ethical clearance certificate is SCC1475v2. It was also approved and funded by the National AIDS Secretariat (NAS) and all data for the analysis were abstracted from their routine collected HIV information in The Gambia.</p></sec><sec id="s2_2"><title>2.2. Inclusion and Exclusion Criteria</title><p>Infants born and breastfeeding from HIV-1 infected mothers were included in this study. Since the RealTime Abbott PCR used in The Gambia can only detect the HIV-1 proviral DNA, thus infants born and breastfeeding from HIV-2 or HIV-1&amp;2 infected mothers were excluded from this study</p></sec><sec id="s2_3"><title>2.3. Study Subjects and Design</title><p>A total number of 109 samples were collected from infants born and breastfeeding from HIV infected mother receiving the combined ARVs drugs as lifelong therapy between May-August 2016. Few drops of infant’s blood sample (50 uL) were collected on a Whatman 903 card, air dry, stored at 10 C and transported to the National Public Health Laboratories (Reference Lab) in a form of Dried Blood Spot (DBS). These samples we collected from 6 hospitals and 7 health centers across the country. These includes Bansang Hospital, Bwiam Hospital, Jammeh Foundation Hospital, Edward Francis Small Teaching Hospital, Serekunda General Hospital and Farafenni Hospital, Hands on Care Health Center, Sibanor Health center, SOS Health center, Soma Health center, Kudang Health center, Kuntaur health center and Basse Health Center.</p></sec><sec id="s2_4"><title>2.4. Data Collection and Analysis</title><p>Each mother was given an identification number and data on HIV related issues were abstracted from HIV treatment sites. Information such as mother’s age, date of delivery, number of parity, number of infected child, duration of breastfeeding, treatment site, date of initiation of ARVs, duration on ARVs, CD4 cell count before delivery, last viral load etc. These categorical data were analyzed using SPSS version 16.0 software. Pearson Chi-square test by Crosstabs method was used to determine the association of risk factors. The statistical significant value was set at p &lt; 0.05.</p></sec><sec id="s2_5"><title>2.5. DNA Extraction and Detection of Proviral DNA</title><p>Two to three circles of about 50 uL were cut from the What man 903 card and transferred into a 50 mL falcon tube and 1.7 mL of mLysis<sub>DNA</sub> buffer was added to each sample. Reagent such as mLysisbuffer, mWash1 solution, mWash2 solution, Micro-par- ticles (Magnetic particles), and Elution buffer were used during DNA extraction. 70% ethanol was added to both the mLysis buffer and the mWash solutions, 35 mL of ethanol was added to a 70 mL of mlysis buffer, 23 mL ethanol was added to a 46 mL of mWash1 and 70 mL ethanol was added to a 46 mL of mWash2. 750 uL of the Internal Control (IC) was added to each bottle of the mLysis buffer ethanol solution. 13mL of mMicropaticles (Magnetic particles) and 11 mL of Elution buffer were also used.</p><p>The Amplification Master-mix consist of 271 uL of HIV-1 Activation reagent, 979 uL of HIV-1 Oligonucleotide and a Thermostable DNA polymerase enzyme reagents were used for HIV-1 proviral-DNA amplification. These reagents were thaw at 15*C and loaded into the m2000sp machine. An Abbott 96-wells Optical Reaction plate (PCR- plate) was place on the Epperdorf PCR cooler, a disposable deep-well plate and disposable tips were also loaded to the m2000sp machine.</p><p>After the extracted nucleic acid were transferred to the PCR Optical reaction plate, the PCR plate was sealed and transferred to the m2000 rt machine for the reverse transcription of HIV-1 RNA to cDNA and detection of any extracted HIV-1 proviral-DNA.</p></sec></sec><sec id="s3"><title>3. Results</title><p>Between May-July 2016, a total number of 109 HIV-exposed infants whose mothers are currently receiving the combined antiretroviral therapy were tested to evaluate the prevalence of vertical transmission of HIV-1 using the Reverse Transcriptase Polymerase Chain Reaction (rt-PCR) technique. Out of these 109 HIV-1 exposed infants, 7 (6.4%) were found positive.</p><sec id="s3_1"><title>3.1. Baseline Characteristic of Infants and Their Mothers</title><p>All the 109 HIV exposed infants were on exclusive breastfeeding. Among these, 47.7% (52/109) have exclusively breastfed for 02 months, 25.6% (29/109) for 02 to 04 months, and 25.7% (28/109) have exclusively breastfed for 06 months. Among these infants, 10 infants were born as twins. Among the 105 mothers, 60.9% (64/105) mothers received the HIV prophylaxis then started ART during pregnancy and breastfeeding, 26.6% (28/105) mothers received only prophylaxis during pregnancy and breastfeeding and 12.3% (13/105) mothers never receive prophylaxis or ART during pregnancy and breastfeeding. Among these, 15.2% (16/105) mothers had late to start prophylaxis or ART (after 03 months of breastfeeding) and 18.1% (19/105) mothers defaulted treatment at some time during pregnancy or breastfeeding.</p></sec><sec id="s3_2"><title>3.2. Prevalence of Mother to Child Transmission of HIV</title><p>This study has found the prevalence of vertical transmission of HIV-1 is 0.0% (0/64) among mothers that received prophylaxis then started ART during pregnancy and breastfeeding, 7.1% (2/28) among mother that received only prophylaxis during pregnancy and breastfeeding and 38.4% (5/13) among mothers that never receive prophylaxis or ARVs during pregnancy and first 03 months of breastfeeding as shown in <xref ref-type="table" rid="table1">Table 1</xref>.</p></sec><sec id="s3_3"><title>3.3. Risk Factors of Vertical Transmission of HIV-1 in The Gambia</title><p>It was also found out that 15.8% (3/19) were positive among women that defaulted treatment at some time during pregnancy or breastfeeding while 31.2% (5/16) were positive among women who late to start prophylaxis/ART (started after 03 months of breastfeeding). These were found to be significantly associated with vertical transmission with p = 0.022 and p = 0.001 respectively.</p><p>The study has also found that 40% (2/5) were positive among first born of twins with a p = 0.000 (very significant association). All HIV-exposed infants are put on ART from birth and during breastfeeding and no HIV-infant mortality was registered since the intervention of ARVs in both rural and urban settings. <xref ref-type="table" rid="table2">Table 2</xref> shows the risk factors associated with vertical transmission of HIV-1 in The Gambia.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Rate of vertical transmission of HIV-1</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Total</th><th align="center" valign="middle" >HIV+</th><th align="center" valign="middle" >HIV−</th><th align="center" valign="middle" >Rate %</th></tr></thead><tr><td align="center" valign="middle" >Mother received HIV-prophylaxis then started ART during pregnancy and breastfeeding</td><td align="center" valign="middle" >64</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >64</td><td align="center" valign="middle" >0.0%</td></tr><tr><td align="center" valign="middle" >Mother received only HIV-prophylaxis during pregnancy and breastfeeding</td><td align="center" valign="middle" >28</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >26</td><td align="center" valign="middle" >7.1%</td></tr><tr><td align="center" valign="middle" >Mother never receive HIV-prophylaxis or ART during pregnancy or first 3 months of breastfeeding</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >38.4%</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Risk factors associated with vertical transmission of HIV-1 in The Gambia</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Total</th><th align="center" valign="middle" >HIV+</th><th align="center" valign="middle" >HIV−</th><th align="center" valign="middle" >Rate %</th><th align="center" valign="middle" >p-value</th></tr></thead><tr><td align="center" valign="middle" >Mother late to start prophylaxis or ARV (after 3 months of breastfeeding)</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >11</td><td align="center" valign="middle" >31.2%</td><td align="center" valign="middle" >p = 0.001</td></tr><tr><td align="center" valign="middle" >Mother defaulted treatment at some time during pregnancy or breastfeeding</td><td align="center" valign="middle" >19</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >15.8%</td><td align="center" valign="middle" >p = 0.022</td></tr><tr><td align="center" valign="middle" >First born of a twins</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >40%</td><td align="center" valign="middle" >p = 0.000</td></tr><tr><td align="center" valign="middle" >Exclusive breastfeeding</td><td align="center" valign="middle" >109</td><td align="center" valign="middle" >7</td><td align="center" valign="middle" >102</td><td align="center" valign="middle" >_</td><td align="center" valign="middle" >Not Sig.</td></tr></tbody></table></table-wrap><p>All the 109 infants (100%) were on exclusive breastfeeding and no Mixed-feeding or Formula-feeding was found. No risk association was done since all the 109 infants were on exclusive breastfeeding.</p></sec><sec id="s3_4"><title>3.4. Vertical Transmission among Health Facilities in The Gambia</title><p><xref ref-type="fig" rid="fig1">Figure 1</xref> shows the rate of vertical transmission of HIV-1 is higher in Soma Health Center and Sibanor Health Center where each facility representing 28.6% of the total number of positive infants. Brikama Health Center (Hands on Care), Serrekunda General Hospital and Basse Major Health Center represent 14.3% each while no vertical transmission was registered from other health facilities.</p></sec></sec><sec id="s4"><title>4. Discussion</title><p>This study has found the prevalence of vertical transmission of HIV among women that received the HIV prophylaxis then start ART (as a lifelong therapy) during pregnancy and breastfeeding is at 0.0%, while 7.1%, among those that received HIV prophylaxis only, and unlike HIV infected women who never receive HIV-prophylaxis or ART during pregnancy or breastfeeding, the rate of vertical transmission is at 38.4% (as described in <xref ref-type="table" rid="table1">Table 1</xref>). A similar study done in Nigeria [<xref ref-type="bibr" rid="scirp.72476-ref1">1</xref>] and Burkina Faso [<xref ref-type="bibr" rid="scirp.72476-ref4">4</xref>] , both revealed a vertical transmission rate of 0.0% among women receiving ART while 4.8% and 1.75% among women who received only prophylaxis respectively. As shown in <xref ref-type="table" rid="table2">Table 2</xref>, risk factors of vertical transmission such as late initiation of treatment, default during treatment and first born of twin were found to be significantly associated with vertical transmission, p = 0.001, p = 0.022 and p = 0.000 respectively.</p><p>Late initiation of treatment and default during treatment are considered as the highest risk factors, 71% mothers of the infected infants started the therapy after three months of breastfeeding while 39% mothers of infected infants have defaulted treatment at certain point during treatment. This has also conceded with a similar observation made in Thailand, approximately 83% of HIV infected infants were born to mothers that lately initiate the ART and 59% among these women are living in rural setting. This was related to limited PMTCT/ART sites in the rural settings in Thailand [<xref ref-type="bibr" rid="scirp.72476-ref11">11</xref>] . Thus establishment of more PMTCT/ART sites and decentralization of these sites would reduce the default of treatment among these women.</p><p>This research has also revealed out a very significant association (p = 0.000) between first born of twins and vertical transmission of HIV-1 (<xref ref-type="table" rid="table2">Table 2</xref>). Approximately 29%</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Vertical transmission of HIV among health facilities</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-5200366x2.png"/></fig><p>(2/7) positive infants are first born twin, though only one of the mothers received HIV prophylaxis and the other never received prophylaxis or ARVs. According to [<xref ref-type="bibr" rid="scirp.72476-ref12">12</xref>] this could be associated with complications and higher risk of contracting maternal blood during delivery of the first born. The probability that breastfeeding is related to the increase in risk of transmission could not be establish, because all the 109 infants are/were on exclusive breastfeeding.</p><p>In addition, all the 105 mothers (100%) are given Cotrimazole (amoxicillin as alternative) as prophylaxis for opportunistic infections, this study has found out that defaulting during treatment is also related to the occurrence of opportunistic infection as 77.5% of patients that defaulted treatment at a point during treatment experience an opportunistic infections. Approximately 34% of mothers with positive infants were found to lost to follow up, with this regards, a proper uptake of HIV drugs should be ensure and a strengthening of follow-up of HIV pregnant women should be enhance.</p><p>Several similar studies done in Africa such as in Burkina Faso, Kenya, Nigeria, Tanzania and in Thailand, [<xref ref-type="bibr" rid="scirp.72476-ref4">4</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.72476-ref15">15</xref>] respectively, have all reported a low prevalence (less than 4%) of vertical transmission among women on ART and in addition, researches have revealed that the intervention of ARVs will not only reduce vertical transmission but it can reduce the risk of heterosexual transmission of HIV.</p></sec><sec id="s5"><title>5. Conclusion</title><p>This study has found that the early intervention of ART at the onset of pregnancy through breastfeeding can eliminate Maternal to Child transmission of HIV and a high risk of vertical transmission was found among women who neither receive prophylaxis nor ART. This provides evidence of the effectiveness of the ART program, however, if the effectiveness of the antiretroviral therapy is maintain, The Gambia, in the near future will attain the WHO’s goal to eliminate Maternal to Child transmission of HIV.</p></sec><sec id="s6"><title>6. Limitations of This Study</title><p>The RealTime Abbott PCR used in The Gambia can only detect proviral-DNA of HIV- 1 thus only HIV-1 patients were included in this study. Lack of enough information on mother’s CD4/CD8 cell count and viral load, however, the analysis would have been strengthened by including these variables.</p></sec><sec id="s7"><title>7. Recommendations</title><p>Though the intervention of ARVs drastically reduce vertical transmission of HIV, however, the HIV virus has a high resistance rate capacity and can develop resistance to most of these ARV drugs, which could limit future treatment. Thus, a constant monitoring and surveillance of HIV drug resistance is required.</p></sec><sec id="s8"><title>Acknowledgements</title><p>The author wishes to acknowledge Prof. Pape Mback&#233; SEMBENE and the study team at the National AIDS Control Program and National Public Health Laboratory for all the laboratory and field work. We wish to acknowledge the study participants for their willingness to participate.</p></sec><sec id="s9"><title>Funding</title><p>This study was funded and supported by the National AIDS Secretariat, National AIDS Control Program and the Ministry of Higher Education, Research, Science &amp; Technology (MoHERST) of The Gambia.</p></sec><sec id="s10"><title>Cite this paper</title><p>Cham, L.B., Sembene, P.M., Bah, P.O., et al. (2016) Qualitative Detection of Proviral-DNA of HIV-1 in Infants to Determine the Efficacy of Antiretroviral Therapy in the Prevention of Vertical Transmission of HIV-1 in The Gambia. World Journal of AIDS, 6, 169-177. http://dx.doi.org/10.4236/wja.2016.64019</p></sec></body><back><ref-list><title>References</title><ref id="scirp.72476-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Anoje, C., Aiyenigba, B., Suzuki, C., Badru, T., Akpoigbe, K., Odo, M. Chabikuli, O.N. (2012) Reducing Mother-to-Child Transmission of HIV: Findings from an Early Infant Diagnosis Program in South-South Region of Nigeria. BMC Public Health, 12, 184.  
https://doi.org/10.1186/1471-2458-12-184</mixed-citation></ref><ref id="scirp.72476-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Idele, P., Gillespie, A., Porth, T., Suzuki, C., Mahy, M., Kasedde, S. and Luo, C. (2014) Epidemiology of HIV and AIDS among Adolescents: Current Status, Inequities, and Data Gaps. Journal of Acquired Immune Deficiency Syndromes, 66, 144-153.  
https://doi.org/10.1097/QAI.0000000000000176</mixed-citation></ref><ref id="scirp.72476-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Mercier-delarue, S., Vray, M., Plantier, C., Maillard, T., Adjout, Z. and De Olivera, F. (2014) Higher Specificity of Nucleic Acid Sequence-Based Amplification Isothermal Technology than of Real-Time PCR for Quantification of HIV-1 RNA on Dried Blood Spots. Journal of Clinical Microbiology, 52, 52-56. https://doi.org/10.1128/JCM.01848-13</mixed-citation></ref><ref id="scirp.72476-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Sagna, T., Bisseye, C., Compaore, T.R., Therese, S., Djigma, F.W., Ouermi, D. and Simpore, J. (2015) Prevention of Mother-to-Child HIV-1 Transmission in Burkina Faso: Evaluation of Vertical Transmission by PCR, Molecular Characterization of Subtypes and Determination of Antiretroviral Drugs Resistance. Global Health Action, 8, Article ID: 26065.  
https://doi.org/10.3402/gha.v8.26065</mixed-citation></ref><ref id="scirp.72476-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Sarita, N., Wand, H., Abbai, N.S. and Ramjee, G. (2014) High Prevalence and Incidence of Sexually Transmitted Infections among Women Living in Kwazulu-Natal, South Africa. AIDS Research and Therapy, 11, 31. http://www.pubmedcentral.nih.gov 
https://doi.org/10.1186/1742-6405-11-31</mixed-citation></ref><ref id="scirp.72476-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Jamieson, D.J., Chasela, C.S., Hudgens, M.G., King, C.C., Athena, P., Kayira, D., et al. (2013) Maternal and Infant Antiretroviral Regimens to Prevent Postnatal HIV-1 Transmission: 48-Week Follow-Up of the BAN Randomised Controlled Trial. The Lancet, 379, 2449- 2458. https://doi.org/10.1016/S0140-6736(12)60321-3</mixed-citation></ref><ref id="scirp.72476-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Ministry of Health and Social Welfare &amp; World Health Organization (2015) Guidelines for Antiretroviral Therapy for the Prevention and Treatment of HIV in The Gambia. Banjul.</mixed-citation></ref><ref id="scirp.72476-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">National AIDS Secretariat (NAS), The Gambia Report on National Strategic Plan for HIV and AIDS 2014/2015 to 2019/2020. Draft Zero, 3 December 2013.</mixed-citation></ref><ref id="scirp.72476-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Kerr, R.J.S., Player, G., Fiscus, S.A., Nelson, J.A.E., Hill, C. and Carolina, N. (2009) Qualitative Human Immunodeficiency Virus RNA Analysis of Dried Blood Spots for Diagnosis of Infections in Infants. Journal of Clinical Microbiology, 47, 220-222.  
https://doi.org/10.1128/JCM.01521-08</mixed-citation></ref><ref id="scirp.72476-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Smit, P.W., Sollis, K.A., Fiscus, S., Ford, N., Vitoria, M., Essajee, S. and Peeling, R.W. (2014) Systematic Review of the Use of Dried Blood Spots for Monitoring HIV Viral Load and for Early Infant Diagnosis. PLoS ONE, 9, 1-8. https://doi.org/10.1371/journal.pone.0086461</mixed-citation></ref><ref id="scirp.72476-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Naiwatanakul, T., Voramongkol, N., Punsuwan, N., Lolekha, R., Gass, R., Thaisri, H. and Bhakeecheep, S. (2016) Uptake of Early Infant Diagnosis in Thailand’s National Program for Preventing Mother-to-Child HIV Transmission and Linkage to Care, 2008-2011. Journal of the International AIDS Society, 19, Article ID: 20511.  
https://doi.org/10.7448/ias.19.1.20511</mixed-citation></ref><ref id="scirp.72476-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Caplan, A., Prazuck, T., Chaillon, A., Niang, M., Barin, F., Rouzioux, C. and Hocqueloux, L. (2013) HIV-DNA in the Genital Tract of Women on Long-Term Effective Therapy Is Associated to Residual Viremia and Previous AIDS-Defining Illnesses. PLoS ONE, 8, e69686.  
https://doi.org/10.1371/journal.pone.0069686</mixed-citation></ref><ref id="scirp.72476-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Goggin, K., Wexler, C., Nazir, N., Staggs, V. S., Gautney, B., Okoth, V. and Ruff, A. (2016) Predictors of Infant Age at Enrollment in Early Infant Diagnosis Services in Kenya. AIDS and Behavior, 20, 2141-2150. https://doi.org/10.1007/s10461-016-1404-z</mixed-citation></ref><ref id="scirp.72476-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Negedu-momoh, O.R., Olonitola, O.S., Odama, L.E., Inabo, H.I., Mbah, H.A., Kasembeli, A.N. and Agwale, S.M. (2014) Antiretroviral-Drug Resistant Mutations and Genetic Diversity in HIV-1 Infected Individuals in Nigeria. World Journal of AIDS, 4, 187-197.  
https://doi.org/10.4236/wja.2014.42024</mixed-citation></ref><ref id="scirp.72476-ref15"><label>15</label><mixed-citation publication-type="other" xlink:type="simple">Nuwagaba-Biribonwoha, H., Werq-semo, B., Abdallah, A., Cunningham, A., Gamaliel, J. G., Mtunga, S. and Abrams, E.J. (2010) Introducing a Multi-Site Program for Early Diagnosis of HIV Infection among HIV-Exposed Infants in Tanzania. BMC Pediatrics, 10, 44.  
https://doi.org/10.1186/1471-2431-10-44</mixed-citation></ref></ref-list></back></article>