<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mikasi SG</submitter><funding>Poliomyelitis Research Foundation</funding><funding>South African Research Chairs Initiative of the Department of Science and Innovation</funding><funding>Higher Education Department, next Generation of Programme</funding><funding>South African Research Chairs Initiative of the Department of Science and Innovation (DSI)</funding><funding>National Research Foundation</funding><funding>South African Medical Research Council</funding><funding>Department of Science and Technology, Republic of South Africa</funding><funding>Harry Crossley Foundation</funding><pagination>379</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8063366</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The Integrase (IN) strand transfer inhibitor (INSTI), Dolutegravir (DTG), has been given the green light to form part of first-line combination antiretroviral therapy (cART) by the World Health Organization (WHO). DTG containing regimens have shown a high genetic barrier against HIV-1 isolates carrying specific resistance mutations when compared with other class of regimens.&lt;h4>Methods&lt;/h4>We evaluated the HIV-1 CRF02_AG IN gene sequences from Cameroon for the presence of resistance-associated mutations (RAMs) against INSTIs and naturally occurring polymorphisms (NOPs), using study sequences (n = 20) and (n = 287) sequences data derived from HIV Los Alamos National Laboratory database. The possible impact of NOPs on protein structure caused by HIV-1 CRF02_AG variations w</pubmed_abstract><journal>BMC infectious diseases</journal><pubmed_title>Interaction analysis of statistically enriched mutations identified in Cameroon recombinant subtype CRF02_AG that can influence the development of Dolutegravir drug resistance mutations.</pubmed_title><pmcid>PMC8063366</pmcid><funding_grant_id>17/49</funding_grant_id><funding_grant_id>64751</funding_grant_id><funding_grant_id>UID: 113547</funding_grant_id><pubmed_authors>Isaacs D</pubmed_authors><pubmed_authors>Jacobs GB</pubmed_authors><pubmed_authors>Chitongo R</pubmed_authors><pubmed_authors>Mikasi SG</pubmed_authors><pubmed_authors>Cloete R</pubmed_authors><pubmed_authors>Ikomey GM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interaction analysis of statistically enriched mutations identified in Cameroon recombinant subtype CRF02_AG that can influence the development of Dolutegravir drug resistance mutations.</name><description>&lt;h4>Background&lt;/h4>The Integrase (IN) strand transfer inhibitor (INSTI), Dolutegravir (DTG), has been given the green light to form part of first-line combination antiretroviral therapy (cART) by the World Health Organization (WHO). DTG containing regimens have shown a high genetic barrier against HIV-1 isolates carrying specific resistance mutations when compared with other class of regimens.&lt;h4>Methods&lt;/h4>We evaluated the HIV-1 CRF02_AG IN gene sequences from Cameroon for the presence of resistance-associated mutations (RAMs) against INSTIs and naturally occurring polymorphisms (NOPs), using study sequences (n = 20) and (n = 287) sequences data derived from HIV Los Alamos National Laboratory database. The possible impact of NOPs on protein structure caused by HIV-1 CRF02_AG variations w</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-22T15:49:02.784Z</modification><creation>2022-02-09T16:06:33.606Z</creation></dates><accession>S-EPMC8063366</accession><cross_references><pubmed>33892628</pubmed><doi>10.1186/s12879-021-06059-x</doi></cross_references></HashMap>