A Surveillance on Protease Inhibitor Resistance-Associated Mutations Among Iranian HIV-1 Patients

被引:5
|
作者
Nasiri-Tajabadi, Zeynab [1 ]
Salim, Farah Bokharaei [2 ]
Najafzadeh, Mohammad-Javad [3 ,4 ]
Kalantari, Saeed [5 ]
Garshasbi, Saba [6 ]
Jamehdar, Saeid Amel [1 ,7 ]
Farsiani, Hadi [1 ,7 ]
Mazaheri, Zahra [1 ]
Sankian, Mojtaba [8 ]
Youssefi, Masoud [1 ,7 ]
机构
[1] Mashhad Univ Med Sci, Fac Med, Dept Microbiol & Virol, Mashhad, Iran
[2] Iran Univ Med Sci, Dept Virol, Tehran, Iran
[3] Mashhad Univ Med Sci, Fac Med, Dept Parasitol & Mycol, Mashhad, Iran
[4] Mashhad Univ Med Sci, Ghaem Hosp, Fac Med, Canc Mol Pathol Res Ctr, Mashhad, Iran
[5] Iran Univ Med Sci, Dept Infect Dis & Trop Med, Tehran, Iran
[6] Iran Univ Med Sci, HIV Lab, Deputy Hlth, Natl Ctr, Tehran, Iran
[7] Mashhad Univ Med Sci, Antimicrobial Resistance Res Ctr, Mashhad, Iran
[8] Mashhad Univ Med Sci, Immunol Res Ctr, Avicenna Res Inst, Mashhad, Iran
来源
ARCHIVES OF CLINICAL INFECTIOUS DISEASES | 2018年 / 13卷 / 06期
关键词
Mutation; Drug Resistance; HIV; Protease Inhibitor;
D O I
10.5812/archcid.69153
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: Drug resistance is emerging as one of the greatest challenges in the development of effective treatment for HIV infection. The importance of clinical studies in this field stems from the world wide growing of treatment drug-resistant mutations. Objectives: This study was performed to determine the HIV subtype and the resistance mutations to the protease inhibitors in both untreated HIV patients and patients under treatment with protease inhibitors (PIs) in Iran. Methods: The study was conducted on two groups of participants. The first group consisted of 25 HIV patients who did not receive any antiretroviral treatment. The second group included 25 HIV patients who have being treated with a combination of protease inhibitors. After genome extraction, a nested polymerase chain reaction was performed to amplify the protease gene. Upon confirmation using electrophoresis, the amplicons or PCR products were sequenced and analyzed to determine the drug resistance mutations as well as the viral subtypes. Results: Nomutations were found in the first group; however, 32% of the samples in the second group had PI related drug-resistance mutations. The major mutations were V82A and M46I, which were seen in 12% of the samples, while the minor mutation F53L was seen in 16% of the samples. The subtype analysis showed that 94% of the samples were subtype CRF35_AD, and 6% were of defined as subtype A. Conclusions: The present study reports updates on the mutations related to protease resistance in Iranian HIV patients receiving treatment. Our data, as well as existing reports, support the need for the optimization of treatment to prevent emergence of resistant viruses and a search for new antiretroviral drug candidates for HIV patients.
引用
收藏
页数:6
相关论文
共 50 条
  • [31] HIV-1 drug resistance-associated mutations among HIV-1 infected drug-naive antenatal clinic attendees in rural Kenya
    Kiptoo, Michael
    Brooks, James
    Lihana, Raphael W.
    Sandstrom, Paul
    Ng'ang'a, Zipporah
    Kinyua, Joyceline
    Lagat, Nancy
    Okoth, Fredrick
    Songok, Elijah M.
    BMC INFECTIOUS DISEASES, 2013, 13
  • [32] Molecular epidemiology and prevalence of drug resistance-associated mutations in newly diagnosed HIV-1 patients in Cameroon
    Nkengafac, A. D.
    Tina, S.
    Sua, F.
    Mason, T.
    Auyuketta, N.
    Oben, S.
    ANTIVIRAL THERAPY, 2007, 12 : S50 - S50
  • [33] Molecular epidemiology and prevalence of drug resistance-associated mutations in newly diagnosed HIV-1 patients in Cameroon
    Nkengafac, A. D.
    Tina, S.
    Sua, F.
    Mason, T.
    Auyuketta, N.
    Oben, S.
    ANTIVIRAL THERAPY, 2007, 12 (05) : S50 - S50
  • [34] Molecular epidemiology and prevalence of drug resistance-associated mutations in newly diagnosed HIV-1 patients in Portugal
    Palma, A. C.
    Araujo, F.
    Duque, V.
    Borges, F.
    Paixao, M. T.
    Camacho, R.
    INFECTION GENETICS AND EVOLUTION, 2007, 7 (03) : 391 - 398
  • [35] Zero prevalence of primary drug resistance-associated mutations to protease inhibitors in HIV-1 drug-naive patients in and around Aligarh, India
    Azam, Mohd
    Malik, Abida
    Rizvi, Meher
    Rai, Arvind
    JOURNAL OF INFECTION IN DEVELOPING COUNTRIES, 2014, 8 (01): : 79 - 85
  • [36] Collinearity of protease mutations in HIV-1 samples with high-level protease inhibitor class resistance
    Babrzadeh, Farbod
    Varghese, Vici
    Pacold, Mary
    Liu, Tommy F.
    Nyren, Pal
    Schiffer, Celia
    Fessel, W. Jeffrey
    Shafer, Robert W.
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2013, 68 (02) : 414 - 418
  • [37] The cumulative occurrence of resistance mutations in the HIV-1 protease gene is associated with failure of salvage therapy with ritonavir and saquinavir in protease inhibitor-experienced patients
    Karmochkine, M
    Mohamed, AS
    Piketty, C
    Ginsburg, C
    Raguin, G
    Schneider-Fauveau, V
    Gutmann, L
    Kazatchkine, MD
    Belec, L
    ANTIVIRAL RESEARCH, 2000, 47 (03) : 179 - 188
  • [38] Drug Resistance Mutations Alter Dynamics of Inhibitor-Bound HIV-1 Protease
    Cai, Yufeng
    Myint, Wazo
    Paulsen, Janet L.
    Schiffer, Celia A.
    Ishima, Rieko
    Yilmaz, Nese Kurt
    JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2014, 10 (08) : 3438 - 3448
  • [39] Replicative fitness in vivo of HIV-1 variants with multiple drug resistance-associated mutations
    Devereux, HL
    Emery, VC
    Johnson, MA
    Loveday, C
    JOURNAL OF MEDICAL VIROLOGY, 2001, 65 (02) : 218 - 224
  • [40] HIV-1 drug resistance-associated mutations among HIV-1 infected drug-naïve antenatal clinic attendees in rural Kenya
    Michael Kiptoo
    James Brooks
    Raphael W Lihana
    Paul Sandstrom
    Zipporah Ng’ang’a
    Joyceline Kinyua
    Nancy Lagat
    Fredrick Okoth
    Elijah M Songok
    BMC Infectious Diseases, 13