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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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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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.</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. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</rights><rights>COPYRIGHT 2024 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c371t-dfa6a969b201ceaf3fd9359968addda56e02629322598bfb717fc2f7fd80c6303</cites><orcidid>0000-0001-6251-366X ; 0000-0001-7046-7245 ; 0000-0001-5619-2767</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11237352/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11237352/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1598,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38994445$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Custer, Brian</creatorcontrib><creatorcontrib>Altan, Eda</creatorcontrib><creatorcontrib>Montalvo, Leilani</creatorcontrib><creatorcontrib>Coyne, Alison</creatorcontrib><creatorcontrib>Grebe, Eduard</creatorcontrib><creatorcontrib>Deng, Xutao</creatorcontrib><creatorcontrib>Stone, Mars</creatorcontrib><creatorcontrib>Delwart, Eric</creatorcontrib><creatorcontrib>Bakkour, Sonia</creatorcontrib><creatorcontrib>Hailu, Benyam</creatorcontrib><creatorcontrib>Reik, Rita</creatorcontrib><creatorcontrib>Kessler, Debra</creatorcontrib><creatorcontrib>Stramer, Susan L</creatorcontrib><creatorcontrib>Busch, Michael P</creatorcontrib><creatorcontrib>Transfusion Transmissible Infections Monitoring System (TTIMS) Program</creatorcontrib><creatorcontrib>for the Transfusion Transmissible Infections Monitoring System (TTIMS) Program</creatorcontrib><title>HIV Subtypes and Drug-resistance-associated Mutations in US Blood Donors, 2015–2020</title><title>Open Forum Infectious Diseases</title><addtitle>Open Forum Infect Dis</addtitle><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.</description><subject>Analysis</subject><subject>Antibodies</subject><subject>Blood donors</subject><subject>Digital rights (Intellectual property)</subject><subject>Disease transmission</subject><subject>DNA polymerases</subject><subject>Drug resistance</subject><subject>Drug therapy</subject><subject>Efavirenz</subject><subject>Epidemiology and Disease Surveillance</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>HIV (Viruses)</subject><subject>HIV infection</subject><subject>Infection</subject><subject>Laboratories</subject><subject>Phylogeny</subject><subject>Protease inhibitors</subject><subject>Proteases</subject><subject>RNA</subject><subject>Viral antibodies</subject><issn>2328-8957</issn><issn>2328-8957</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kc1u1DAUhS0EolXpjjXKDhZN8U8cxyvUlp9WKmJRhq11Y18PRhl7sBOk7ngH3pAnwdUMVdkgS9fW9XeOrn0Iec7oKaNavE4-uFoARScekUMu-NAOWqrHD84H5LiUb5RSxqikSj8lB2LQuus6eUhWl1dfmptlnG-3WBqIrnmbl3WbsYQyQ7TYQinJBpjRNR-XGeaQYmlCbFY3zfmUUhWkmHI5aThl8vfPX5xy-ow88TAVPN7vR2T1_t3ni8v2-tOHq4uz69YKxebWeehB93qsUovghXdaSK37AZxzIHukvOdacC71MPpRMeUt98q7gdpeUHFE3ux8t8u4QWcxzhkms81hA_nWJAjm35sYvpp1-mEY40IJyavDq71DTt8XLLPZhGJxmiBiWooR9cOYknWCip7u0DVMaEL0qVrauhxugk0Rfaj9s4GqruNCqio42QlsTqVk9PeDMWru4jN38Zl9fBV_8fAx9_DfsCrwcgekZft_qz_9VqSc</recordid><startdate>202407</startdate><enddate>202407</enddate><creator>Custer, Brian</creator><creator>Altan, Eda</creator><creator>Montalvo, Leilani</creator><creator>Coyne, Alison</creator><creator>Grebe, Eduard</creator><creator>Deng, Xutao</creator><creator>Stone, Mars</creator><creator>Delwart, Eric</creator><creator>Bakkour, Sonia</creator><creator>Hailu, Benyam</creator><creator>Reik, Rita</creator><creator>Kessler, Debra</creator><creator>Stramer, Susan L</creator><creator>Busch, Michael P</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>7X8</scope><scope>5PM</scope><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></search><sort><creationdate>202407</creationdate><title>HIV Subtypes and Drug-resistance-associated Mutations in US Blood Donors, 2015–2020</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-dfa6a969b201ceaf3fd9359968addda56e02629322598bfb717fc2f7fd80c6303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Analysis</topic><topic>Antibodies</topic><topic>Blood donors</topic><topic>Digital rights (Intellectual property)</topic><topic>Disease transmission</topic><topic>DNA polymerases</topic><topic>Drug resistance</topic><topic>Drug therapy</topic><topic>Efavirenz</topic><topic>Epidemiology and Disease Surveillance</topic><topic>Genomics</topic><topic>Health aspects</topic><topic>HIV (Viruses)</topic><topic>HIV infection</topic><topic>Infection</topic><topic>Laboratories</topic><topic>Phylogeny</topic><topic>Protease inhibitors</topic><topic>Proteases</topic><topic>RNA</topic><topic>Viral antibodies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Custer, Brian</creatorcontrib><creatorcontrib>Altan, Eda</creatorcontrib><creatorcontrib>Montalvo, Leilani</creatorcontrib><creatorcontrib>Coyne, Alison</creatorcontrib><creatorcontrib>Grebe, Eduard</creatorcontrib><creatorcontrib>Deng, Xutao</creatorcontrib><creatorcontrib>Stone, Mars</creatorcontrib><creatorcontrib>Delwart, Eric</creatorcontrib><creatorcontrib>Bakkour, Sonia</creatorcontrib><creatorcontrib>Hailu, Benyam</creatorcontrib><creatorcontrib>Reik, Rita</creatorcontrib><creatorcontrib>Kessler, Debra</creatorcontrib><creatorcontrib>Stramer, Susan L</creatorcontrib><creatorcontrib>Busch, Michael P</creatorcontrib><creatorcontrib>Transfusion Transmissible Infections Monitoring System (TTIMS) Program</creatorcontrib><creatorcontrib>for the Transfusion Transmissible Infections Monitoring System (TTIMS) Program</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Open Forum Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Custer, Brian</au><au>Altan, Eda</au><au>Montalvo, Leilani</au><au>Coyne, Alison</au><au>Grebe, Eduard</au><au>Deng, Xutao</au><au>Stone, Mars</au><au>Delwart, Eric</au><au>Bakkour, Sonia</au><au>Hailu, Benyam</au><au>Reik, Rita</au><au>Kessler, Debra</au><au>Stramer, Susan L</au><au>Busch, Michael P</au><aucorp>Transfusion Transmissible Infections Monitoring System (TTIMS) Program</aucorp><aucorp>for the Transfusion Transmissible Infections Monitoring System (TTIMS) Program</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HIV Subtypes and Drug-resistance-associated Mutations in US Blood Donors, 2015–2020</atitle><jtitle>Open Forum Infectious Diseases</jtitle><addtitle>Open Forum Infect Dis</addtitle><date>2024-07</date><risdate>2024</risdate><volume>11</volume><issue>7</issue><spage>ofae343</spage><pages>ofae343-</pages><issn>2328-8957</issn><eissn>2328-8957</eissn><abstract>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.</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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