HIV Subtypes and Drug-resistance-associated Mutations in US Blood Donors, 2015–2020

Abstract Background Monitoring genotypes of HIV infections in blood donors may provide insights into infection trends in the general population. Methods HIV RNA was extracted from plasma samples of blood donors confirmed as HIV positive by blood screening nucleic acid and antibody tests. HIV genome...

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Veröffentlicht in:Open Forum Infectious Diseases 2024-07, Vol.11 (7), p.ofae343
Hauptverfasser: Custer, Brian, Altan, Eda, Montalvo, Leilani, Coyne, Alison, Grebe, Eduard, Deng, Xutao, Stone, Mars, Delwart, Eric, Bakkour, Sonia, Hailu, Benyam, Reik, Rita, Kessler, Debra, Stramer, Susan L, Busch, Michael P
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container_issue 7
container_start_page ofae343
container_title Open Forum Infectious Diseases
container_volume 11
creator Custer, Brian
Altan, Eda
Montalvo, Leilani
Coyne, Alison
Grebe, Eduard
Deng, Xutao
Stone, Mars
Delwart, Eric
Bakkour, Sonia
Hailu, Benyam
Reik, Rita
Kessler, Debra
Stramer, Susan L
Busch, Michael P
description Abstract Background Monitoring genotypes of HIV infections in blood donors may provide insights into infection trends in the general population. Methods HIV RNA was extracted from plasma samples of blood donors confirmed as HIV positive by blood screening nucleic acid and antibody tests. HIV genome target regions were amplified using nested real time-polymerase chain reaction followed by next-generation sequencing. Sequences were compared to those in the Los Alamos National Laboratory (LANL) database. Sequences were also assessed for drug resistance mutations (DRM) using the Stanford HIV DRM Database. Results From available HIV-positive donations collected between 1 September 2015 and 31 December 2020, 563 of 743 (75.8%) were successfully sequenced; 4 were subtype A, 543 subtype B, 5 subtype C, 1 subtype G, 5 circulating recombinant forms (CRF), and 2 were subtype B and D recombinants. Overall, no significant differences between blood donor and available LANL genotypes were found, and the genotypes of newly acquired versus prevalent HIV infections in donors were similar. The proportion of non-B subtypes and CRF remained a small fraction, with no other subtype or CRF representing more than 1% of the total. DRM were identified in 122 (21.6%) samples with protease inhibitor, nucleoside reverse transcriptase inhibitor and non-nucleoside reverse transcriptase inhibitor DRMs identified in 4.9%, 4.6% and 14.0% of samples, respectively. Conclusions HIV genetic diversity and DRM in blood donors appear representative of circulating HIV infections in the US general population and may provide more information on infection diversity than sequences reported to LANL, particularly for recently transmitted infections.
doi_str_mv 10.1093/ofid/ofae343
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Methods HIV RNA was extracted from plasma samples of blood donors confirmed as HIV positive by blood screening nucleic acid and antibody tests. HIV genome target regions were amplified using nested real time-polymerase chain reaction followed by next-generation sequencing. Sequences were compared to those in the Los Alamos National Laboratory (LANL) database. Sequences were also assessed for drug resistance mutations (DRM) using the Stanford HIV DRM Database. Results From available HIV-positive donations collected between 1 September 2015 and 31 December 2020, 563 of 743 (75.8%) were successfully sequenced; 4 were subtype A, 543 subtype B, 5 subtype C, 1 subtype G, 5 circulating recombinant forms (CRF), and 2 were subtype B and D recombinants. Overall, no significant differences between blood donor and available LANL genotypes were found, and the genotypes of newly acquired versus prevalent HIV infections in donors were similar. The proportion of non-B subtypes and CRF remained a small fraction, with no other subtype or CRF representing more than 1% of the total. DRM were identified in 122 (21.6%) samples with protease inhibitor, nucleoside reverse transcriptase inhibitor and non-nucleoside reverse transcriptase inhibitor DRMs identified in 4.9%, 4.6% and 14.0% of samples, respectively. Conclusions HIV genetic diversity and DRM in blood donors appear representative of circulating HIV infections in the US general population and may provide more information on infection diversity than sequences reported to LANL, particularly for recently transmitted infections.</description><identifier>ISSN: 2328-8957</identifier><identifier>EISSN: 2328-8957</identifier><identifier>DOI: 10.1093/ofid/ofae343</identifier><identifier>PMID: 38994445</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Analysis ; Antibodies ; Blood donors ; Digital rights (Intellectual property) ; Disease transmission ; DNA polymerases ; Drug resistance ; Drug therapy ; Efavirenz ; Epidemiology and Disease Surveillance ; Genomics ; Health aspects ; HIV (Viruses) ; HIV infection ; Infection ; Laboratories ; Phylogeny ; Protease inhibitors ; Proteases ; RNA ; Viral antibodies</subject><ispartof>Open Forum Infectious Diseases, 2024-07, Vol.11 (7), p.ofae343</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2024</rights><rights>The Author(s) 2024. 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Methods HIV RNA was extracted from plasma samples of blood donors confirmed as HIV positive by blood screening nucleic acid and antibody tests. HIV genome target regions were amplified using nested real time-polymerase chain reaction followed by next-generation sequencing. Sequences were compared to those in the Los Alamos National Laboratory (LANL) database. Sequences were also assessed for drug resistance mutations (DRM) using the Stanford HIV DRM Database. Results From available HIV-positive donations collected between 1 September 2015 and 31 December 2020, 563 of 743 (75.8%) were successfully sequenced; 4 were subtype A, 543 subtype B, 5 subtype C, 1 subtype G, 5 circulating recombinant forms (CRF), and 2 were subtype B and D recombinants. Overall, no significant differences between blood donor and available LANL genotypes were found, and the genotypes of newly acquired versus prevalent HIV infections in donors were similar. The proportion of non-B subtypes and CRF remained a small fraction, with no other subtype or CRF representing more than 1% of the total. DRM were identified in 122 (21.6%) samples with protease inhibitor, nucleoside reverse transcriptase inhibitor and non-nucleoside reverse transcriptase inhibitor DRMs identified in 4.9%, 4.6% and 14.0% of samples, respectively. 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Methods HIV RNA was extracted from plasma samples of blood donors confirmed as HIV positive by blood screening nucleic acid and antibody tests. HIV genome target regions were amplified using nested real time-polymerase chain reaction followed by next-generation sequencing. Sequences were compared to those in the Los Alamos National Laboratory (LANL) database. Sequences were also assessed for drug resistance mutations (DRM) using the Stanford HIV DRM Database. Results From available HIV-positive donations collected between 1 September 2015 and 31 December 2020, 563 of 743 (75.8%) were successfully sequenced; 4 were subtype A, 543 subtype B, 5 subtype C, 1 subtype G, 5 circulating recombinant forms (CRF), and 2 were subtype B and D recombinants. Overall, no significant differences between blood donor and available LANL genotypes were found, and the genotypes of newly acquired versus prevalent HIV infections in donors were similar. The proportion of non-B subtypes and CRF remained a small fraction, with no other subtype or CRF representing more than 1% of the total. DRM were identified in 122 (21.6%) samples with protease inhibitor, nucleoside reverse transcriptase inhibitor and non-nucleoside reverse transcriptase inhibitor DRMs identified in 4.9%, 4.6% and 14.0% of samples, respectively. Conclusions HIV genetic diversity and DRM in blood donors appear representative of circulating HIV infections in the US general population and may provide more information on infection diversity than sequences reported to LANL, particularly for recently transmitted infections.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>38994445</pmid><doi>10.1093/ofid/ofae343</doi><orcidid>https://orcid.org/0000-0001-6251-366X</orcidid><orcidid>https://orcid.org/0000-0001-7046-7245</orcidid><orcidid>https://orcid.org/0000-0001-5619-2767</orcidid><oa>free_for_read</oa></addata></record>
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subjects Analysis
Antibodies
Blood donors
Digital rights (Intellectual property)
Disease transmission
DNA polymerases
Drug resistance
Drug therapy
Efavirenz
Epidemiology and Disease Surveillance
Genomics
Health aspects
HIV (Viruses)
HIV infection
Infection
Laboratories
Phylogeny
Protease inhibitors
Proteases
RNA
Viral antibodies
title HIV Subtypes and Drug-resistance-associated Mutations in US Blood Donors, 2015–2020
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