Clade homogeneity and Pol gene polymorphisms in chronically HIV-1 infected antiretroviral treatment naive patients after the roll out of ART in Ethiopia
© Mulu et al.; licensee BioMed Central Ltd. 2014
Received: 28 February 2014
Accepted: 18 March 2014
Published: 22 March 2014
Despite the increasing use of antiretroviral treatment (ART) recent data on frequency and pattern of drug resistance mutations in Ethiopia is not available. Furthermore with increasing mobility of people HIV-1 subtypes other than the predominant subtype C may likely be introduced from the neighbouring countries. This study was aimed to determine the molecular characterization and pre-antiretroviral treatment resistance mutations among HIV-1 chronically infected ART naïve patients after the roll out of ART in Ethiopia.
Viral RNA was determined in 160 baseline plasma samples. The entire PR and the first 335 codons (76%) of the RT regions of the pol gene of the HIV-1 genome (N = 160) were amplified and sequenced using an in-house assay. Genotypic drug resistance was defined as the presence of one or more resistance-related mutations as specified by the consensus mutation of Stanford University HIVDB and the International Antiviral Society (IAS) mutation lists.
A predominance of HIV-1 subtype C (98.7%) was observed. The level of drug resistance is found to be 5.6% and 13.1% according to the Stanford University HIVDB drug resistance interpretation algorithms and the International Antiviral Society mutation lists, respectively. Mutations conferring simultaneous resistance to NRTIs and NNRTIs were not detected and no major PR mutation was found. However, a high rate of polymorphic changes both in PR and RT regions were observed. Moreover, twenty four (15%) monophyletic transmission clusters with bootstrap value of 99% were found.
Strong evidence for consistent HIV-1C clade homogeneity and low influx of other variant into the country was found. The level of drug resistance observed in chronically infected treatment naïve patients which exceeds the WHO estimates suggests the need for incorporation of HIV-1 drug resistance testing prior to ART initiation. The occurrence of monophyletic transmission clusters affecting (24/160) individuals indicates their potential risk related practice. Thus, an intensified public health intervention program and monitoring of HIV drug resistance testing appears indispensible.
KeywordsAntiretroviral drug resistance HIV subtype Protease Reveres transcriptase
In response to the global HIV-1 epidemic and to achieve universal access for the treatment of HIV-1 infected individuals in resource limited countries, antiretroviral treatment (ART) has been scaled up in the past decade . However, the emergence of drug resistant variants  and their transmission to newly infected individuals has been documented . Studies from industrialized countries have shown a decline or a stabilized incidence in transmitted drug resistance (TDRs) with time related to nonucleoside reverse-transcriptase inhibitors (NNRTIs) [4, 5]. On contrary, available data from African countries showed an increasing trend on the prevalence of TDR over time after the roll out of ART in the region [4–6].
In Ethiopia, TDR before the introduction of ART (2002) and one year after its introduction (2005) was reported well below 3% [7, 8]. Nevertheless, data on drug resistance mutation after the scale up of ART are not available. With the increasing availability of ART in Ethiopia in recent years, the prevalence of TDRs will presumably also increase. Previous studies have shown that, HIV-1C is predominantly circulating in 99% of the infected individuals in Ethiopia unlike other sub-Saharan-Eastern African countries [9, 10]. However, with increasing mobility and migration of people, HIV-1 variants may be introduced and intermixed from the neighbouring countries where subtypes A, D, G as well as recombinant forms in Kenya and subtype D in Sudan are co-circulating [9, 10].
HIV pol gene encodes the reverse-transcriptase (RT), protease (PR) and integrase enzymes that are the major targets of antiretroviral therapy . As drug-regimens used in Southern and Eastern African countries, where non-B subtypes are predominately circulating mostly consist of NNRTIs and NRTIs in the 1st with addition of protease inhibitors (PIs) in 2nd line, understanding of drug-resistance patterns in pol gene among non-B subtypes may help to optimize the selection of first-line regimens and limit the acquisition of cross-resistance. The objectives of the current study is to determine the HIV-1 genetic diversity and to identify the pattern of antiretroviral drug resistance mutations in pol gene of HIV-1 isolated from chronically infected treatment naïve Ethiopian patients.
HIV-1 chronically infected treatment naïve patients (N = 160) with advanced diseases (WHO clinical stages III and IV)  above 18 years of age and seeking care and treatment at Gondar University Hospital for the first time, Northwest Ethiopia in 2008/2009 were recruited consecutively. Patients were excluded for the following reasons: pregnant or had taken single dose nevirapine (NVP) for prevention of mother to child transmission (PMTCT) or patients with known chronic illness or any previous ART use.
Five ml venous blood was collected in vacutainer tubes containing ethylene diamine tetraacetic acid (EDTA). Baseline CD4+ T cell count was measured using the FACSCount flow cytometer (Becton Dickinson, San Jose, CA, USA) following the manufacturer’s protocol. Plasma was separated by centrifugation and stored at −40°C.
RNA extraction and plasma viral load determination
RNA extraction was done with the Abbott m2000sp automated sample preparation system using mSample preparation system RNA kit. Plasma viral load was determined with Abbott m2000rt Quantitative RealTime HIV-1 assay (Abbott Molecular, Des Plaines, IL, USA) with a lower detection limit of 40 copies/ml.
Reverse transcription and PCR amplification for polgene sequencing
List of in-house primers used for pol genome amplification and genotypic drug-resistance testing
Purified PCR products were subjected to direct sequencing of both sense and antisense strands using Big Dye Terminator Cycle Sequencing Ready Reaction kit (Applied Biosystems, Foster City, CA, USA). For each sample, six separate sequencing reactions were done using the two inner PCR primers (HIVpcrFor2 and HIVpcrRev2) and four additional internal primers: HIVseq1, HIVseq2, HIVseq3 and HIVseq4 (Table 1) which allowed a double coverage of the pol region. All primer positions are matched to HIV-1HXB2 (GenBank accession number K03455). Both forward and reverse overlapping sequences were manually edited with the Geneious software version 5.4 .
Pol gene sequences were aligned with reference subtypes (A-D, F-H, J, K, circulating recombinant forms (CRFs) and SIV) obtained from HIV Sequence Database at Los Alamos (http://www.hiv.lanl.gov) accessed on September 24, 2013. Phylogenetic inferences were performed by the neighbour-joining method with 1,000 bootstrap replicates under Kimura’s two-parameter correction using MEGA 5. The evolutionary distances were computed using the Maximum Composite Likelihood method and are in the units of the number of base substitutions per site .
Drug resistance analysis
The existing drug resistance interpretation algorithms use lists of amino acid mutations that are associated with drug resistance, derived largely from research of HIV-1B infected individuals [16–20]. With this limitation, in this study genotypic drug resistance was defined as the presence of one or more resistance-related mutations, as specified by the consensus mutation of Stanford University HIVDB (http://hivdb.stanford.edu) accessed on September 24, 2013 and the latest definition of the International Antiviral Society (IAS) mutation lists .
Age, sex, WHO clinical stage, CD4+ T cell count and HIV RNA level were included in the statistical analysis using SPSS statistical software (Version 17, USA). Student t test was used and a p-value of < 0.05 was considered statistically significant.
Ethical clearance and written informed consent from the University of Gondar Ethical Review Committee (RPO/55/291/00) and each study subjects was obtained, respectively.
Sociodemographic, immunological and virological profile of chronically HIV-1 infected patients from Northwest Ethiopia
Male no. (%)
Female no. (%)
Total no. (%)
WHO clinical status
CD4+ T cell count (cells/mm3)
HIV RNA level (copies/ml)
Genotypic drug resistance
Resistance conferring mutations in the RT gene among chronically infected patients from Northwest Ethiopia
ETR, DLV, EFV, NVP
AZT, D4T, ABC, DDI, TDF
ABC, ddI, FTC, 3TC, d4T, TDF
DLV, EFV, ETR, NVP
EFV, ETR, NVP, RPV
EFV, ETR, NVP, RPV
Polymorphisms at known drug resistance positions of HIV-1 subtype B among chronically infected patients from Northwest Ethiopia (N = 160)
Number of cases
Five patients had NNRTI resistance (K101E in one, Y188H in one, G190A in two and M230I in one patient) according to the Stanford University drug resistance database and IAS mutation lists (Table 3). In addition, according to IAS (Table 3) etravirine resistance associated mutations V90I and E138A/G were observed in 3 (1.9%) and 10 (6.5%) of the patients, respectively which increase the overall magnitude of NNRTI resistance to 10.6% (17/160). One patient had both K101E (in both IAS and/or Stanford algorithms) and E138A mutations (in IAS algorithm).
As indicated in Table 4, a polymorphic mutation K101R was observed in another patient. The polymorphic mutation K103R which occurs in 1-2% of untreated persons and reduces NVP, DLV and EFV susceptibility was also observed in one patient. In addition, highly unusual mutations at known subtype B drug resistance position conferring resistance to NNRTI were observed (Table 4). In 23.7% (38/160) of the patients a polymorphic change from A to S at codon 98 was observed, a substitution that was recently introduced into the ANRS algorithm as conferring resistance to nevirapine in subtype C only (http://www.hivfrenchresistance.org).
In both algorithms, four patients (2.6%) had NRTI resistance-associated mutations. K65R was observed in one patient. Mutations at position 210 from L to W and at 219 from K to E were observed in two and one patient, respectively. A revertant mutation T215A was also observed in 3 (1.9%) of the patients. Moreover atypical mutations at known subtype B drug resistance positions (Table 4) conferring resistance to NRTI were observed at positions M41 (2.3%), D67 (2.3%), Q151 (1.5%), M184 (3.1%) and T215 (2%).
Drug resistance versus immunological and virological data
Characteristics of patients with and without transmitted drug resistance
Patients with resistance mutations
Patients without resistance mutations
Age (mean ± SEM)
32.7 ± 1.7
32.9 ± 0.78
CD4+ T cellsa
141 ± 21.5
178 ± 9.3
Plasma viral loadb
4.98 ± 0.13
4.73 ± 0.06
This study provides the first description of HIV-1 drug resistance in chronically infected ART naive patients after the scale up of ART in Ethiopia and shows an increase in magnitude of TDR with expanded access of ART in the country and is in line with reports from eastern and southern African countries [4, 6]. The results also highlight the need to scale up PIs in the country. The two fold variation in the magnitude of drug resistance between IAS drug resistance mutations lists (13.1%) and HIVDB DR Interpretation algorithm (5.6%) indicates the difficulty of interpreting drug resistance mutation in subtype C isolates [16–20]. The level of drug resistance in the current study is significantly higher than the previous report from the same area (3.3%) sampled in 2002  but similar with findings from other eastern and southern Africa countries after the roll out of ART [4–6] which support the notion that scaling up of ART in Africa will drive the emergence of TDR. The findings also imply that many HIV infected individuals receiving ART are continuing to exercise risk related behaviour which is in line with behavioural study in Ethiopia  and an eventual increase of TDR cases is anticipated in the country. Thus, an intensified public health intervention program directed at such patients to prevent TDR viruses is warranted.
In contrast to a previous report among pregnant women from central Ethiopia  and other African countries in which TDR was interpreted based on the WHO HIV drug resistance threshold survey, the frequency of resistant associated mutation in the current study is higher than the WHO HIV drug resistance threshold survey report  which is similar with a recent study from Tanzania . Nevertheless, it is difficult to directly compare the data from these studies since there were differences in the inclusion criteria, the representativeness of the samples and the resistance algorithms used for interpretation. The current study was a hospital based study among chronically infected patients seeking treatment but the studies for WHO TDR surveillance were based on recently seroconverted individuals below 25 years of age with CD4+ T cell counts of >500 cells/ml and primigravida women.
Although the mutations associated with resistance to NNRTIs in subtype C isolates in this study were similar with previous studies from other African countries [4, 6] different patterns and frequencies of specific mutations were observed with 10.3% prevalence of drug resistance to this drug classes according to the IAS resistance mutation list. The detection of mutations conferring resistance to NVP (G190A and Y188H) in 4 patients is high compared with previous report from Ethiopia [7, 8] and other African countries [4, 6] before the scale up ART which may be associated with the prophylactic use of single dose NVP for the PMTCT in the country  and the low genetic threshold for resistance to NNRTI. It is also worse enough to detect etravirine associated mutations (V90I, K101E and E138A) in 8.4% of the patients in areas where etravirine is yet not available. This is much higher than the previous reports [7, 8] indicating the higher evolutionary rate of HIV-1C in Ethiopia and that HIV-1 variants containing these mutations are circulating in the absence of etravirine in the country. Thus, the introduction of etravirine in African countries where subtype C is predominantly circulating needs attention.
The 2.6% frequency of resistance mutation to NRTIs is low compared with studies from other African countries [4, 6]. Low rate of K65R mutation which causes intermediate resistance to most of the NRTIs and low level resistance to d4T [24, 25] was observed in one patient and could be due to the recent availability of tenofovir in Ethiopia. Although this mutation is relatively uncommon, there has been an increase in its prevalence in some countries as a result of the widespread clinical use of tenofovir [26–29]. Moreover, despite the wide use of thymidine analogs (zidovidine or stavudine) in Ethiopia, thymidine analog mutations were observed in low frequency unlike previous similar studies .
The absence of major drug resistance mutation in PR region is consistent with previous studies [4–7] and might be related to the late introduction and limited access of this drug class in the region. However, the rate of minor mutations (Table 4) is consistent with the previous studies among subtype C isolates [17, 30–32]. Although the clinical significance of these natural polymorphisms in non-B subtypes is controversial , it is suggested that they may influence the risk of treatment failure, as it does for clade B viruses  and may facilitate the selection of different pathways and/or a more rapid emergence of drug resistance and treatment failure [32, 35].
The present data clearly shows the predominance (98.7%) of HIV-1 subtype C in Ethiopia similar with previous reports [7–10] and provides a strong evidence for consistent HIV-1C clade homogeneity in the country for the past 4 decades. The reason for the predominance of subtype C in Ethiopia cannot be given with absolute certainty. However, it can be speculated that this subtype when introduced first into the country, has rapidly saturated the commercial sex workers network [9, 10, 35]. Although, the lack of other subtypes suggest a low influx of subtypes from neighbouring countries [9, 10] the rare findings of the inter-subtype recombinant CD and CK may have epidemiological contribution to HIV epidemic in Ethiopia. Moreover, the 15% monophyletic transmission clusters observed in current isolates imply that many HIV infected individuals are exercising risk related behaviour and highlights the importance of understanding transmission dynamics of HIV-1 subtype C in the population.
In conclusion, there is strong evidence for consistent HIV-1C clade homogeneity and low influx of other HIV-1 subtypes to Ethiopia for the past 4 decades. The observed level of drug resistance which exceeds the WHO’s estimates suggests the need for routine HIV-1 genotypic drug resistance testing for treatment naïve patients and supports the hypothesis that scaling-up of ART in resource limited settings drive the development of drug resistance. The absence of major drug resistance mutations in PR gene suggest for scaling-up of PIs in Ethiopia. The occurrence of monophyletic transmission clusters in 15% of individuals indicate their potential of risk related practice and thus, an intensified public health intervention program targeting such individuals is warranted.
Nucleotide sequences are deposited in National Centre for Biotechnology Information (NCBI), USA GenBank (Accession Number: KF026059-KF026220).
The authors would like to thank all study participants. Expert technical assistance by Sandra Bergs and Janka Rätzke is gratefully acknowledged. This work was partly supported by German Academic Exchange Service (DAAD), Association of Sponsors and Friends of Leipzig University, and HIV/AIDS Prevention and Control Office of Amhara Regional State, Ethiopia.
- Braitstein P, Brinkhof MW, Dabis F, Schechter M, Boulle A, Miotti P, Wood R, Laurent C, Sprinz E, Seyler C, Bangsberg DR, Balestre E, Sterne JA, May M, Egger M, ART-LINC Collaboration, ART-CC groups: Mortality of HIV-1-infected patients in the first year of antiretroviral therapy: comparison between low-income and high-income countries. Lancet. 2006, 367: 817-824.View ArticlePubMedGoogle Scholar
- Novak RM, Chen L, MacArthur RD, Baxter JD, Huppler Hullsiek K, Peng G, Xiang Y, Henely C, Schmetter B, Uy J, van den Berg-Wolf M, Kozal M, Terry Beirn Community Programs for Clinical Research on AIDS 058 Study Team: Prevalence of antiretroviral drug resistance mutations in chronically HIV-infected treatment naïve patients: implications for routine resistance screening before initiation of antiretroviral therapy. Clin Infect Dis. 2005, 40: 468-474. 10.1086/427212.View ArticlePubMedGoogle Scholar
- Pillay D, Bhaskaran K, Jurriaans S, Prins M, Masquelier B, Dabis F, Gifford R, Nielsen C, Pedersen C, Balotta C, Rezza G, Ortiz M, de Mendoza C, Kücherer C, Poggensee G, Gill J, Porter K, CASCADE Virology Collaboration: The impact of transmitted drug resistance on the natural history of HIV infection and response to first-line therapy. AIDS. 2006, 20: 21-28.View ArticlePubMedGoogle Scholar
- Frentz E, Boucher CAB, Vijver D: Temporal changes in the epidemiology of transmission of drug resistance HIV-1 across the world. AIDS Rev. 2012, 14: 17-27.PubMedGoogle Scholar
- Vercauteren J, Wensing AM, van de Vijver DA, Albert J, Balotta C, Hamouda O, Kücherer C, Struck D, Schmit JC, Asjö B, Bruckova M, Camacho RJ, Clotet B, Coughlan S, Grossman Z, Horban A, Korn K, Kostrikis L, Nielsen C, Paraskevis D, Poliak M, Puchhammer-Stöckl E, Riva C, Ruiz L, Salminen M, Schuurman R, Sonnerborg A, Stanekova D, Stanojevic M, Vandamme AM, et al: Transmission of drug-resistant HIV-1 is stabilizing in Europe. J Infect Dis. 2009, 200 (10): 1503-1508. 10.1086/644505. doi:10.1086/644505View ArticlePubMedGoogle Scholar
- Gupta RK, Jordan MR, Sultan BJ, Hill A, Davis DH, Gregson J, Sawyer AW, Hamers RL, Ndembi N, Pillay D, Bertagnolio S: Global trends in antiretroviral resistance in treatment-naïve individuals with HIV after rollout of antiretroviral treatment in resource-limited settings: a global collaborative study and meta-regression analysis. Lancet. 2012, 6736: 61038-61041.Google Scholar
- Kassu A, Fujino M, Matsuda M, Nishizawa M, Ota F, Sugiura W: Molecular epidemiology of HIV-1 in treatment naive patients in North Ethiopia. AIDS Res Hum Retroviruses. 2007, 23: 564-568. 10.1089/aid.2006.0270.View ArticlePubMedGoogle Scholar
- Abegaz WE, Grossman Z, Wolday D, Ram D, Kaplan J, Sibide K, Wuhib T, Ismael S, Nkengasong J, Mekonen T, Berhanu H, Messele T, Lulseged S, Maayan S, Mengistu Y: Threshold survey evaluating transmitted HIV drug resistance among public antenatal clinic clients in Addis Ababa, Ethiopia. Antivir Ther. 2008, 13 (Suppl 2): 89-94.PubMedGoogle Scholar
- Hemelaar J, Gouwsb E, Ghysb DP, WHO-UNAIDS Network for HIV isolation and characterization: Global trends in molecular epidemiology of HIV-1 during 2000–2007. AIDS. 2011, 25: 679-689. 10.1097/QAD.0b013e328342ff93.View ArticlePubMedPubMed CentralGoogle Scholar
- Lihana WR, Ssemwanga D, Abimiku A, Ndimbi A: Update on HIV-1 diversity in Africa: A decade in review. AIDS Rev. 2012, 14: 83-100.PubMedGoogle Scholar
- Wainberg MA, Zaharatos GA, Brenner BG: Mechanisms of disease development of antiretroviral drug resistance. N Engl J Med. 2011, 365: 37-46. 10.1056/NEJMicm1104783.View ArticleGoogle Scholar
- World Health Organization: Interim WHO clinical staging of HIV/AIDS & HIV/AIDS case definitions for surveillance: African region. 2005, Switzerland: World Health Organization, http://www.who.int/hiv/pub/guidelines/clinicalstaging.pdf,Google Scholar
- Mulu A, Liebert UG, Maier M: Virological efficacy and immunological recovery among Ethiopian HIV-1 infected adults and children. BMC Infect Dis. 2014, 14 (1): 28-10.1186/1471-2334-14-28. doi:10.1186/1471-2334-14-28View ArticlePubMedPubMed CentralGoogle Scholar
- Drummond AJ, Ashton B, Buxton S, Cheung M, Cooper A, Duran C, Field M, Heled J, Kearse M, Markowitz S, Moir R, Stones-Havas S, Sturrock S, Thierer T, Wilson A: Geneious v5.4. 2011, http://www.geneious.com,Google Scholar
- Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: Molecular evolutionary genetics analysis using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods. Mol Biol Evol. 2011, 28: 2731-2739. 10.1093/molbev/msr121.View ArticlePubMedPubMed CentralGoogle Scholar
- Johnson AV, Calvez V, Günthard HF, Paredes R, Pillay D, Shater R, Wensing AM, Richman DD: Update of the drug resistance mutations in HIV-1: International AIDS Society-USA. Top HIV Med. 2013, 21: 6-14.Google Scholar
- Kantor R, Katzenstein DA, Efron B, Carvalho AP, Wynhoven B, Cane P, Clarke J, Sirivichayakul S, Soares MA, Snoeck J, Pillay C, Rudich H, Rodrigues R, Holguin A, Ariyoshi K, Bouzas MB, Cahn P, Sugiura W, Soriano V, Brigido LF, Grossman Z, Morris L, Vandamme AM, Tanuri A, Phanuphak P, Weber JN, Pillay D, Harrigan PR, Camacho R, Schapiro JM, et al: Impact of HIV-1 subtype and antiretroviral therapy on protease and reverse transcriptase genotype: Results of a global collaboration. PLoS Med. 2005, 2: e112-10.1371/journal.pmed.0020112. doi:10.1371/journal.pmed.0020112View ArticlePubMedPubMed CentralGoogle Scholar
- Philip CA, Kantor R: Transmitted drug resistance in non-subtype B HIV-1 infection. HIV Ther. 2009, 3: 447-465. 10.2217/hiv.09.30.View ArticleGoogle Scholar
- Martinez-Cajas JL, Pai NP, Klein MB, Wainberg MA: Differences in resistance mutations among HIV-1 non-subtype B infections: a systematic review of evidence (1996–2008). J Int AIDS Coc. 2009, 12: 11-19. 10.1186/1758-2652-12-11.View ArticleGoogle Scholar
- Shafer RW, Rhee SY, Pillay D, Miller V, Sandstrom P, Schapiro JM, Kuritzkes DR, Bennett D: HIV-1 protease and reverse transcriptase mutations for drug resistance surveillance. AIDS. 2007, 21: 215-223. 10.1097/QAD.0b013e328011e691.View ArticlePubMedPubMed CentralGoogle Scholar
- Dessie Y, Gerbaba M, Bedru A, Davey G: Risky sexual practice and related factors among ART attendees in Addis Ababa public hospital Ethiopia: a cross-sectional study. BMC Public Health. 2011, 11: 422-10.1186/1471-2458-11-422. doi:10.1186/1471-2458-11-422View ArticlePubMedPubMed CentralGoogle Scholar
- World Health Organization HIVDR status report. http://www.who.int/hiv/topics/drugresistance/status/en/index.html,
- Kasang C, Kalluvya S, Majinge C, Stich A, Bodem J, Kongola G, Jacobs GB, Mlewa M, Mildner M, Hensel I, Horn A, Preiser W, van Zyl G, Klinker H, Koutsilieri E, Rethwilm A, Scheller C, Weissbrich B: HIV drug resistance (HIVDR) in antiretroviral therapy-naive patients in Tanzania not eligible for WHO Threshold HIVDR Survey is dramatically high. PLoS One. 2011, 6: e23091-10.1371/journal.pone.0023091. doi:10.1371/journal.pone.0023091View ArticlePubMedPubMed CentralGoogle Scholar
- Johnson JA, Li JF, Wei X, Lipscomb J, Irlbeck D, Craig C, Smith A, Bennett DE, Monsour M, Sandstrom P, Lanier ER, Heneine W: Minority HIV-1 drug resistance mutations are present in antiretroviral treatment-naïve populations and associate with reduced treatment efficacy. PLoS Med. 2008, 5: 158-165. 10.1371/journal.pmed.0050158. doi:10.1371/journal.pmed.0050158View ArticleGoogle Scholar
- Waters É, Nelson M, Mandalia S, Bowe M, Powles T, Gazzard B, Stebbing J: The risks and incidence of K65R and L74V mutations and subsequent virologic response. Clin Infect Dis. 2008, 46: 96-100. 10.1086/523001.View ArticlePubMedGoogle Scholar
- Gallant JE, Rodriguez AE, Weinberg WG, Young B, Berger DS, Lim ML, Liao Q, Ross L, Johnson J, Shaefer MS, ESS30009 Study: Early virologic non-response to tenofovir, abacavir and lamivudine in HIV-infected antiretroviral-naive subjects. J Infect Dis. 2005, 192: 1921-1930. 10.1086/498069.View ArticlePubMedGoogle Scholar
- Pillay V, Pillay C, Kantor R, Venter F, Levin L, Morris L: HIV type 1 subtypes C drug resistance among paediatric and adult South African patients failing antiretroviral therapy. AIDS Res Hum Retroviruses. 2008, 24: 1449-1454. 10.1089/aid.2008.0180.View ArticlePubMedGoogle Scholar
- Hawkins CA, Chaplin B, Idoko J, Ekong E, Adewole I, Gashau W, Murphy RL, Kanki P, APIN Plus/Harvard PEPFAR Team: 2009: Clinical and genotypic findings in HIV infected patients with the K65R mutation failing first-line antiretroviral therapy in Nigeria. J Acquir Immune Defic Syndr. 2009, 52: 228-234. 10.1097/QAI.0b013e3181b06125.View ArticlePubMedPubMed CentralGoogle Scholar
- Turner D, Shahar E, Katchman E, Kedem E, Matus N, Katzir M, Hassoun G, Pollack S, Kessner R, Wainberg MA, Avidor B: Prevalence of the K65R Resistance Reverse Transcriptase Mutation in Different HIV-1 Subtypes in Israel. J Med Virol. 2009, 81: 1509-1512. 10.1002/jmv.21567.View ArticlePubMedGoogle Scholar
- Baxter JD, Schapiro JM, Boucher CA, Kohlbrenner VM, Hall DB, Scherer JR, Mayers DL: Genotypic changes in human immunodeficiency virus type 1 protease associated with reduced susceptibility and virologic response to the protease inhibitor tipranavir. J Virol. 2006, 80: 10794-10801. 10.1128/JVI.00712-06.View ArticlePubMedPubMed CentralGoogle Scholar
- Holguin A, Paxinos E, Hertogs K, Womac C, Soriano V: Impact of frequent natural polymorphisms at the protease gene on the in vitro susceptibility to protease inhibitors in HIV-1 non-B subtypes. J Clin Virol. 2004, 31: 215-220. 10.1016/j.jcv.2004.03.015.View ArticlePubMedGoogle Scholar
- Wainberg MA, Brenner BG: The Impact of HIV Genetic polymorphisms and subtype differences on the occurrence of resistance to antiretroviral drugs. Mol Biol Int. 2012, 256982-doi:10.1155/2012/256982Google Scholar
- Taylor BS, Sobieszczyk ME, McCutchan FE, Hammer SM: The challenge of HIV-1 subtype diversity. N Engl J Med. 2008, 358: 1590-1602. 10.1056/NEJMra0706737. doi:10.1056/NEJMra0706737View ArticlePubMedPubMed CentralGoogle Scholar
- Holguin A, Sune C, Hamy F, Soriano V, Klimkait T: Natural polymorphisms in the protease gene modulate the replicative capacity of non-B HIV-1 variants in the absence of drug pressure. J Clin Virol. 2008, 36: 264-270.View ArticleGoogle Scholar
- Tsega E, Mengesha B, Nordenfêrt E, Hansson BG, Lindberg J: Serologically survey of human immunodeficiency virus infection in Ethiopia. Ethiop Med J. 1988, 26: 179-184.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2334/14/158/prepub
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