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Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana

To determine effects of cryptococcal meningitis (CM) on human immunodeficiency virus (HIV)-1C cerebrospinal fluid (CSF) viral escape, CSF/plasma viral discordance, and drug resistance mutation (DRM) discordance between CSF and plasma compartments, we compared CSF and plasma viral load (VL) and DRMs...

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Autores principales: Kelentse, Nametso, Moyo, Sikhulile, Mogwele, Mompati, Lechiile, Kwana, Moraka, Natasha O., Maruapula, Dorcas, Seatla, Kaelo K., Esele, Lerato, Molebatsi, Kesaobaka, Leeme, Tshepo B., Lawrence, David S., Musonda, Rosemary, Kasvosve, Ishmael, Harrison, Thomas S., Jarvis, Joseph N., Gaseitsiwe, Simani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544309/
https://www.ncbi.nlm.nih.gov/pubmed/33031315
http://dx.doi.org/10.1097/MD.0000000000022606
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author Kelentse, Nametso
Moyo, Sikhulile
Mogwele, Mompati
Lechiile, Kwana
Moraka, Natasha O.
Maruapula, Dorcas
Seatla, Kaelo K.
Esele, Lerato
Molebatsi, Kesaobaka
Leeme, Tshepo B.
Lawrence, David S.
Musonda, Rosemary
Kasvosve, Ishmael
Harrison, Thomas S.
Jarvis, Joseph N.
Gaseitsiwe, Simani
author_facet Kelentse, Nametso
Moyo, Sikhulile
Mogwele, Mompati
Lechiile, Kwana
Moraka, Natasha O.
Maruapula, Dorcas
Seatla, Kaelo K.
Esele, Lerato
Molebatsi, Kesaobaka
Leeme, Tshepo B.
Lawrence, David S.
Musonda, Rosemary
Kasvosve, Ishmael
Harrison, Thomas S.
Jarvis, Joseph N.
Gaseitsiwe, Simani
author_sort Kelentse, Nametso
collection PubMed
description To determine effects of cryptococcal meningitis (CM) on human immunodeficiency virus (HIV)-1C cerebrospinal fluid (CSF) viral escape, CSF/plasma viral discordance, and drug resistance mutation (DRM) discordance between CSF and plasma compartments, we compared CSF and plasma viral load (VL) and DRMs in individuals with HIV-associated CM in Botswana. This cross-sectional study utilized 45 paired CSF/plasma samples from participants in a CM treatment trial (2014–2016). HIV-1 VL was determined and HIV-1 protease and reverse transcriptase genotyping performed. DRMs were determined using the Stanford HIV database. CSF viral escape was defined as HIV-1 ribonucleic acid ≥0.5 log(10) higher in CSF than plasma and VL discordance as CSF VL > plasma VL. HIV-1 VL was successfully measured in 39/45 pairs, with insufficient sample volume in 6; 34/39 (87.2%) participants had detectable HIV-1 in plasma and CSF, median 5.1 (interquartile range: 4.7–5.7) and 4.6 (interquartile range:3.7–4.9) log(10) copies/mL, respectively (P≤.001). CSF viral escape was present in 1/34 (2.9%) and VL discordance in 6/34 (17.6%). Discordance was not associated with CD4 count, antiretroviral status, fungal burden, CSF lymphocyte percentage nor mental status. Twenty-six of 45 (57.8%) CSF/plasma pairs were successfully sequenced. HIV-1 DRM discordance was found in 3/26 (11.5%); 1 had I84IT and another had M46MI in CSF only. The third had K101E in plasma and V106 M in CSF. Our findings suggest that HIV-1 escape and DRM discordance may occur at lower rates in participants with advanced HIV-disease and CM compared to those with HIV associated neurocognitive impairment.
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spelling pubmed-75443092020-10-30 Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana Kelentse, Nametso Moyo, Sikhulile Mogwele, Mompati Lechiile, Kwana Moraka, Natasha O. Maruapula, Dorcas Seatla, Kaelo K. Esele, Lerato Molebatsi, Kesaobaka Leeme, Tshepo B. Lawrence, David S. Musonda, Rosemary Kasvosve, Ishmael Harrison, Thomas S. Jarvis, Joseph N. Gaseitsiwe, Simani Medicine (Baltimore) 4850 To determine effects of cryptococcal meningitis (CM) on human immunodeficiency virus (HIV)-1C cerebrospinal fluid (CSF) viral escape, CSF/plasma viral discordance, and drug resistance mutation (DRM) discordance between CSF and plasma compartments, we compared CSF and plasma viral load (VL) and DRMs in individuals with HIV-associated CM in Botswana. This cross-sectional study utilized 45 paired CSF/plasma samples from participants in a CM treatment trial (2014–2016). HIV-1 VL was determined and HIV-1 protease and reverse transcriptase genotyping performed. DRMs were determined using the Stanford HIV database. CSF viral escape was defined as HIV-1 ribonucleic acid ≥0.5 log(10) higher in CSF than plasma and VL discordance as CSF VL > plasma VL. HIV-1 VL was successfully measured in 39/45 pairs, with insufficient sample volume in 6; 34/39 (87.2%) participants had detectable HIV-1 in plasma and CSF, median 5.1 (interquartile range: 4.7–5.7) and 4.6 (interquartile range:3.7–4.9) log(10) copies/mL, respectively (P≤.001). CSF viral escape was present in 1/34 (2.9%) and VL discordance in 6/34 (17.6%). Discordance was not associated with CD4 count, antiretroviral status, fungal burden, CSF lymphocyte percentage nor mental status. Twenty-six of 45 (57.8%) CSF/plasma pairs were successfully sequenced. HIV-1 DRM discordance was found in 3/26 (11.5%); 1 had I84IT and another had M46MI in CSF only. The third had K101E in plasma and V106 M in CSF. Our findings suggest that HIV-1 escape and DRM discordance may occur at lower rates in participants with advanced HIV-disease and CM compared to those with HIV associated neurocognitive impairment. Lippincott Williams & Wilkins 2020-10-09 /pmc/articles/PMC7544309/ /pubmed/33031315 http://dx.doi.org/10.1097/MD.0000000000022606 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 4850
Kelentse, Nametso
Moyo, Sikhulile
Mogwele, Mompati
Lechiile, Kwana
Moraka, Natasha O.
Maruapula, Dorcas
Seatla, Kaelo K.
Esele, Lerato
Molebatsi, Kesaobaka
Leeme, Tshepo B.
Lawrence, David S.
Musonda, Rosemary
Kasvosve, Ishmael
Harrison, Thomas S.
Jarvis, Joseph N.
Gaseitsiwe, Simani
Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title_full Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title_fullStr Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title_full_unstemmed Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title_short Differences in human immunodeficiency virus-1C viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in Botswana
title_sort differences in human immunodeficiency virus-1c viral load and drug resistance mutation between plasma and cerebrospinal fluid in patients with human immunodeficiency virus-associated cryptococcal meningitis in botswana
topic 4850
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7544309/
https://www.ncbi.nlm.nih.gov/pubmed/33031315
http://dx.doi.org/10.1097/MD.0000000000022606
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