Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia

Antiretroviral (ARV) therapy has dramatically reduced morbidity and mortality in human immunodeficiency virus 1 (HIV-1) infected children. However, development of ARV resistance in these children is a major public health problem due to lack of availability of and access to new drugs. This study was...

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Main Authors: Suharni Mohamad, Zakuan Zainy Deris, Nik Khairulddin Yusoff, Tg Ahmad Akram Tg Mohd Ariffin, Rafidah Hanim Shueb
Format: Article
Language:English
Published: Elsevier
Series:Brazilian Journal of Infectious Diseases
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702012000300012&lng=en&tlng=en
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spelling doaj-dcee745a8c3d443b99328f689ce45cb92020-11-25T03:51:11ZengElsevierBrazilian Journal of Infectious Diseases1678-439116328428810.1590/S1413-86702012000300012S1413-86702012000300012Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, MalaysiaSuharni Mohamad0Zakuan Zainy Deris1Nik Khairulddin Yusoff2Tg Ahmad Akram Tg Mohd Ariffin3Rafidah Hanim Shueb4Universiti Putra MalaysiaUniversiti Putra MalaysiaHospital Raja Perempuan Zainab IIUniversiti Putra MalaysiaUniversiti Putra MalaysiaAntiretroviral (ARV) therapy has dramatically reduced morbidity and mortality in human immunodeficiency virus 1 (HIV-1) infected children. However, development of ARV resistance in these children is a major public health problem due to lack of availability of and access to new drugs. This study was conducted in order to identify circulating HIV subtypes and recombinant forms and evaluate the drug resistance mutation patterns in 18 HIV-1 infected children failing ARV treatment in Kelantan, Malaysia. Genotyping for codon 1-99 of protease (PR) and 1-250 of reverse transcriptase (RT) were performed by polymerase chain reaction (PCR) amplification and DNA sequencing. Subsequently, these were phylogenetically analyzed to determine the subtypes. CRF33_01B (44.4%) was found to be the predominant HIV subtype, followed by B (27.8%), CRF15_01B (16.7%) and CRF01_AE (11.1%) subtypes. The most prevalent RT mutations were T215F/V/Y (66.7%), D67G/N (55.6%), K219Q/E/R (44.4%), M184V/I (38.9%), K70R/E (27.8%) and M41L (27.8%), associated with nucleoside reverse transcriptase inhibitors (NRTI) resistance; and K103N (55.6%), G190A (33.3%), and K101P/E/H (27.8%) associated with non-nucleoside reverse transcriptase inhibitors (NNRTI) resistance. The results showed a possible emergence of CRF33_01B as current predominant subtypes/circulating recombinant forms (CRFs), and a high frequency of primary mutations among HIV-1 infected children after failure of ARV therapy in Kelantan, Malaysia.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702012000300012&lng=en&tlng=enHIV-1 subtyperesistance mutationchildren
collection DOAJ
language English
format Article
sources DOAJ
author Suharni Mohamad
Zakuan Zainy Deris
Nik Khairulddin Yusoff
Tg Ahmad Akram Tg Mohd Ariffin
Rafidah Hanim Shueb
spellingShingle Suharni Mohamad
Zakuan Zainy Deris
Nik Khairulddin Yusoff
Tg Ahmad Akram Tg Mohd Ariffin
Rafidah Hanim Shueb
Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
Brazilian Journal of Infectious Diseases
HIV-1 subtype
resistance mutation
children
author_facet Suharni Mohamad
Zakuan Zainy Deris
Nik Khairulddin Yusoff
Tg Ahmad Akram Tg Mohd Ariffin
Rafidah Hanim Shueb
author_sort Suharni Mohamad
title Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
title_short Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
title_full Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
title_fullStr Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
title_full_unstemmed Assessing subtypes and drug resistance mutations among HIV-1 infected children who failed antiretroviral therapy in Kelantan, Malaysia
title_sort assessing subtypes and drug resistance mutations among hiv-1 infected children who failed antiretroviral therapy in kelantan, malaysia
publisher Elsevier
series Brazilian Journal of Infectious Diseases
issn 1678-4391
description Antiretroviral (ARV) therapy has dramatically reduced morbidity and mortality in human immunodeficiency virus 1 (HIV-1) infected children. However, development of ARV resistance in these children is a major public health problem due to lack of availability of and access to new drugs. This study was conducted in order to identify circulating HIV subtypes and recombinant forms and evaluate the drug resistance mutation patterns in 18 HIV-1 infected children failing ARV treatment in Kelantan, Malaysia. Genotyping for codon 1-99 of protease (PR) and 1-250 of reverse transcriptase (RT) were performed by polymerase chain reaction (PCR) amplification and DNA sequencing. Subsequently, these were phylogenetically analyzed to determine the subtypes. CRF33_01B (44.4%) was found to be the predominant HIV subtype, followed by B (27.8%), CRF15_01B (16.7%) and CRF01_AE (11.1%) subtypes. The most prevalent RT mutations were T215F/V/Y (66.7%), D67G/N (55.6%), K219Q/E/R (44.4%), M184V/I (38.9%), K70R/E (27.8%) and M41L (27.8%), associated with nucleoside reverse transcriptase inhibitors (NRTI) resistance; and K103N (55.6%), G190A (33.3%), and K101P/E/H (27.8%) associated with non-nucleoside reverse transcriptase inhibitors (NNRTI) resistance. The results showed a possible emergence of CRF33_01B as current predominant subtypes/circulating recombinant forms (CRFs), and a high frequency of primary mutations among HIV-1 infected children after failure of ARV therapy in Kelantan, Malaysia.
topic HIV-1 subtype
resistance mutation
children
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1413-86702012000300012&lng=en&tlng=en
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