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

被引:0
|
作者
Custer, Brian [1 ,2 ]
Altan, Eda [1 ]
Montalvo, Leilani [1 ]
Coyne, Alison [1 ]
Grebe, Eduard [1 ]
Deng, Xutao [1 ,2 ]
Stone, Mars [1 ,2 ]
Delwart, Eric [1 ,2 ]
Bakkour, Sonia [3 ]
Hailu, Benyam [4 ]
Reik, Rita [5 ]
Kessler, Debra [6 ]
Stramer, Susan L. [7 ]
Busch, Michael P. [1 ,2 ]
机构
[1] Vitalant Res Inst, 360 Spear St,Suite 200, San Francisco, CA 94105 USA
[2] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA USA
[3] Grifols Diagnost Solut, Global Med Affairs Donor Screening, Emeryville, CA USA
[4] NHLBI, NIH, Div Blood Dis & Resources, Rockville, MD USA
[5] OneBlood, Sci Med Tech & Res, St Petersburg, FL USA
[6] New York Blood Ctr, Med Programs & Serv, New York, NY USA
[7] Infect Dis Consultant, North Potomac, MD USA
来源
OPEN FORUM INFECTIOUS DISEASES | 2024年 / 11卷 / 07期
基金
美国国家卫生研究院;
关键词
blood donors; blood screening; genetic sequence analysis; HIV; phylogenetics; HEPATITIS-C; INFECTIONS; TRANSMISSION; INSIGHTS; VIRUS;
D O I
10.1093/ofid/ofae343
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
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