| BMC Infectious Diseases | |
| High prevalence of CXCR4 usage among treatment-naive CRF01_AE and CRF51_01B-infected HIV-1 subjects in Singapore | |
| Research Article | |
| Li Lin1  Mei Ting Tan2  Wei Xin Khong2  Arlene Chua2  Kah Ying Ng2  Joe Yap Kwan2  Yee Sin Leo2  Palvinder Kaur2  Oon Tek Ng2  Kuan Kiat Chew2  Thomas C Quinn3  Oliver Laeyendecker3  | |
| [1] Department of Infectious Disease, Jurong General Hospital, 159964, Singapore, Singapore;Institute of Infectious Disease and Epidemiology, Communicable Disease Centre, Tan Tock Seng Hospital, 308433, Singapore, Singapore;Johns Hopkins School of Medicine, Baltimore, MD, USA;Laboratory of Immunoregulation, Division of Intramural Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, Baltimore, MD, USA; | |
| 关键词: CXCR4 usage; HIV-1; treatment-naïve; | |
| DOI : 10.1186/1471-2334-13-90 | |
| received in 2012-10-31, accepted in 2013-02-08, 发布年份 2013 | |
| 来源: Springer | |
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【 摘 要 】
BackgroundRecent studies suggest HIV-1 inter-subtype differences in co-receptor usage. We examined the correlation between HIV-1 subtype and co-receptor usage among treatment-naïve HIV-1 subjects in Singapore. Additionally, we investigated whether the subtype co-receptor association was influenced by stage of infection.MethodsV3 sequences of HIV-1 envelope protein gp120 were obtained from 110 HIV treatment-naïve patients and genotypic co-receptor tropism determination was performed using Geno2pheno. Two false-positive rate (FPR) cut-offs, 10% and 5.75% were selected for tropism testing.ResultsSubtype assignment of viral strains from 110 HIV-infected individuals based on partial sequencing of HIV-1 pol, gp120 and gp41 were as follows: 27 subtype B, 64 CRF01_AE, 10 CRF51_01B, and 9 other subtypes. At FPR=10%, 10 (100%) CRF51_01B-infected subjects and 26 (40.6%) CRF01_AE-infected subjects had CXCR4-using virus, compared to 7 (25.9%) subtype B subjects and 1 (11.1%) CRF33_01B-infected subject (P < 0.001). At FPR=5.75%, 10 (100%) CRF51_01B-infected subjects and 20 (31.3%) CRF01_AE-infected subjects had CXCR4-using virus, compared to 4 (14.8%) subtype B and 1 (11.1%) CRF33_01B-infected subjects (P < 0.001). Among those with evidence of seroconversion within 2 years prior to study enrolment, 100% of CRF51_01B-infected subjects had CXCR4-using virus, independent of Geno2pheno FPR.ConclusionCRF51_01B and CRF01_AE-infected individuals have higher prevalence of CXCR4-usage compared to subtype B infected individuals. Further studies examining these differences could help optimise the use of CCR5-antagonist in populations with these subtypes, and increase our understanding of HIV-1 biology.
【 授权许可】
CC BY
© Ng et al.; licensee BioMed Central Ltd. 2013
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202311109654993ZK.pdf | 181KB |
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