AI Article Synopsis

  • The study highlights the issue of drug resistance mutations (DRM) to antiretroviral treatment (ART) in Brazil, where HIV prevalence is high and has seen an increase in the K65R mutation, particularly after switching from zidovudine to tenofovir in treatment regimens.
  • Researchers found a significant rise in the K65R mutation from 2.23% to 12.11%, correlating with higher viral loads in patients harboring this mutation.
  • There is a notable association between the K65R mutation and HIV-1 subtype C, indicating the need for careful monitoring of tenofovir-based treatment in populations with this subtype and specific HLA profiles.

Article Abstract

The success of antiretroviral treatment (ART) is threatened by the emergence of drug resistance mutations (DRM). Since Brazil presents the largest number of people living with HIV (PLWH) in South America we aimed at understanding the dynamics of DRM in this country. We analyzed a total of 20,226 HIV-1 sequences collected from PLWH undergoing ART between 2008-2017. Results show a mild decline of DRM over the years but an increase of the K65R reverse transcriptase mutation from 2.23% to 12.11%. This increase gradually occurred following alterations in the ART regimens replacing zidovudine (AZT) with tenofovir (TDF). PLWH harboring the K65R had significantly higher viral loads than those without this mutation ( < 0.001). Among the two most prevalent HIV-1 subtypes (B and C) there was a significant ( < 0.001) association of K65R with subtype C (11.26%) when compared with subtype B (9.27%). Nonetheless, evidence for K65R transmission in Brazil was found both for C and B subtypes. Additionally, artificial neural network-based immunoinformatic predictions suggest that K65R could enhance viral recognition by HLA-B27 that has relatively low prevalence in the Brazilian population. Overall, the results suggest that tenofovir-based regimens need to be carefully monitored particularly in settings with subtype C and specific HLA profiles.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157590PMC
http://dx.doi.org/10.3390/ijms22105304DOI Listing

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