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dc.contributor.authorPalanisamy, Navaneethan
dc.contributor.authorOsman, Nathan
dc.contributor.authorOhnona, Frédéric
dc.contributor.authorXu, Hong-Tao
dc.contributor.authorBrenner, Bluma
dc.contributor.authorMesplède, Thibault
dc.contributor.authorWainberg, Mark A
dc.date.accessioned2025-06-16T13:29:54Z
dc.date.available2025-06-16T13:29:54Z
dc.date.issued2017-01-07
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/629471/Does%20antiretroviral%20treatment%20change%20HIV-1%20codon%20usage%20patterns%20in%20its%20genes%20a%20preliminary%20bioinformatics%20study.pdf?sequence=2
dc.identifier.citationPalanisamy, N., Osman, N., Ohnona, F., Xu, H. T., Brenner, B., Mesplède, T., & Wainberg, M. A. (2017). Does antiretroviral treatment change HIV-1 codon usage patterns in its genes: a preliminary bioinformatics study. AIDS Research and Therapy, 14, 1-10. https://doi.org/10.1186/s12981-016-0130-yen_US
dc.identifier.issn1742-6405en_US
dc.identifier.doi10.1186/s12981-016-0130-yen_US
dc.identifier.urihttp://hdl.handle.net/10034/629471
dc.description.abstractBackground: Codon usage bias has been described for various organisms and is thought to contribute to the regulation of numerous biological processes including viral infections. HIV-1 codon usage has been previously shown to be different from that of other viruses and man. It is evident that the antiretroviral drugs used to restrict HIV-1 replication also select for resistance variants. We wanted to test whether codon frequencies in HIV-1 sequences from treatment-experienced patients differ from those of treatment-naive individuals due to drug pressure affecting codon usage bias. Results: We developed a JavaScript to determine the codon frequencies of aligned nucleotide sequences. Irrespective of subtypes, using HIV-1 pol sequences from 532 treatment-naive and 52 treatment-experienced individuals, we found that pol sequences from treatment-experienced patients had significantly increased AGA (arginine; p = 0.0002***) and GGU (glycine; p = 0.0001***), and decreased AGG (arginine; p = 0.0001***) codon frequencies. The same pattern was not observed when subtypes B and C sequences were analyzed separately. Additionally, irrespective of subtypes, using HIV-1 gag sequences from 524 treatment-naive and 54 treatment-experienced individuals, gag sequences from treatment-experienced patients had significantly increased CUA (leucine; p < 0.0001***), CAG (glutamine; p = 0.0006***), AUC (isoleucine; p < 0.0001***) and UCU (serine; p = 0.0005***), and decreased AUA (isoleucine; p = 0.0003***) and CAA (glutamine; p = 0.0006***) codon frequencies. Conclusion: Using pol and gag genes derived from the same HIV-1 genome, we show that antiretroviral therapy changed certain HIV-1 codon frequencies in a subtype specific way.en_US
dc.description.sponsorshipCanadian Institutes for Health Research (CIHR)en_US
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherSpringer Natureen_US
dc.relation.urlhttps://aidsrestherapy.biomedcentral.com/articles/10.1186/s12981-016-0130-yen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectHIV-1en_US
dc.subjectCodon usage frequencyen_US
dc.subjectBioinformaticsen_US
dc.subjectAntiretroviral therapyen_US
dc.subjectResistanceen_US
dc.subject.meshAnti-HIV Agents
dc.subject.meshBase Sequence
dc.subject.meshCodon
dc.subject.meshComputational Biology
dc.subject.meshDrug Resistance, Viral
dc.subject.meshGenes, pol
dc.subject.meshGenome, Viral
dc.subject.meshHIV Infections
dc.subject.meshHIV Integrase
dc.subject.meshHIV Protease
dc.subject.meshHIV-1
dc.subject.meshHumans
dc.subject.meshPhylogeny
dc.subject.meshSequence Analysis
dc.subject.meshVirus Replication
dc.subject.meshgag Gene Products, Human Immunodeficiency Virus
dc.subject.meshpol Gene Products, Human Immunodeficiency Virus
dc.subject.meshAnti-HIV Agents
dc.subject.meshBase Sequence
dc.subject.meshCodon
dc.subject.meshComputational Biology
dc.subject.meshDrug Resistance, Viral
dc.subject.meshGenes, pol
dc.subject.meshGenome, Viral
dc.subject.meshHIV Infections
dc.subject.meshHIV Integrase
dc.subject.meshHIV Protease
dc.subject.meshHIV-1
dc.subject.meshHumans
dc.subject.meshPhylogeny
dc.subject.meshSequence Analysis
dc.subject.meshVirus Replication
dc.subject.meshgag Gene Products, Human Immunodeficiency Virus
dc.subject.meshpol Gene Products, Human Immunodeficiency Virus
dc.subject.meshHumans
dc.subject.meshHIV-1
dc.subject.meshHIV Infections
dc.subject.meshHIV Protease
dc.subject.meshHIV Integrase
dc.subject.meshCodon
dc.subject.meshAnti-HIV Agents
dc.subject.meshSequence Analysis
dc.subject.meshComputational Biology
dc.subject.meshPhylogeny
dc.subject.meshDrug Resistance, Viral
dc.subject.meshVirus Replication
dc.subject.meshBase Sequence
dc.subject.meshGenes, pol
dc.subject.meshGenome, Viral
dc.subject.meshgag Gene Products, Human Immunodeficiency Virus
dc.subject.meshpol Gene Products, Human Immunodeficiency Virus
dc.titleDoes antiretroviral treatment change HIV-1 codon usage patterns in its genes: a preliminary bioinformatics studyen_US
dc.typeArticleen_US
dc.contributor.departmentUniversity of Heidelberg; McGill University AIDS Centreen_US
dc.identifier.journalAIDS Research and Therapyen_US
dc.date.updated2025-06-13T16:47:41Z
dc.identifier.volume14
dc.date.accepted2016-12-07
rioxxterms.identifier.projectN/Aen_US
rioxxterms.versionVoRen_US
rioxxterms.licenseref.startdate2017-01-07
rioxxterms.typeJournal Article/Review
dc.source.issue1
dc.source.beginpage2
dc.date.deposited2025-06-13en_US


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