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CCR5-∆32, CCR2-64I, SDF1-3'A, and IFNλ4 rs12979860 and rs8099917 gene polymorphisms in individuals with HIV-1, HIV/HTLV-1, and HIV/HTLV-2 in São Paulo, Brazil 巴西圣保罗地区HIV-1、HIV/HTLV-1和HIV/HTLV-2患者的CCR5-∆32、CCR2-64I、SDF1-3'A和ifn - λ4 rs12979860和rs8099917基因多态性
Pub Date : 2023-06-05 DOI: 10.54034/mic.e1855
Adele Caterino-de-Araujo, Karoline R. Campos, Emylenne C. Cabral-de-Oliveira, Ana Kelly S. Rodrigues, Rafael X. Silva, Bruna V. Azevedo, Rosa M. N. Marcusso
Background. Chemokine and chemokine-receptor polymorphisms have been associated with protection against HIV infection and delayed progression to AIDS, whereas polymorphisms in IFNλ4 (formerly IL28B) have been associated with human T-lymphotropic virus 1 (HTLV-1)-associated myelopathy (HAM) development. Evolutionary selection against ancestral genes differs among human populations, resulting in varying risks of acquiring and developing viral diseases. Methods. DNA samples from 434 patients infected with HIV-1 and/or co-infected with HTLV-1/-2, and samples from 74 HIV and HTLV non-infected individuals from São Paulo, Brazil, were divided into five groups: HIV-naïve, n=160; HIV-ART, n=180; HIV/HTLV-1, n=53; HIV/HTLV-2, n=41; and control, n=74. These samples were analyzed for CCR5-∆32 deletion, CCR2-64I, SDF1-3'A, and IFNλ4 rs12979860 and rs8099917 single nucleotide polymorphisms using PCR and PCR-RFLP techniques. These polymorphisms' genotype and allele frequencies were calculated and compared among groups using logistic regression analysis. Results. All polymorphism profiles described in the literature were detected in this study. The wild-type genotype predominated in all genes analyzed except for IFNλ4 rs12979860. Statistical differences in allele frequencies among groups were detected in the CCR5 and CCR2 genes, with a high frequency of ∆32 in HIV-naïve vs. HIV-ART (OR 2.45, P=0.037) and a minus mutant allele A (CCR2-64I) in HIV-naïve vs. HIV/HTLV-1 (OR 1.90, P=0.048), HIV-ART vs. HIV/HTLV-1 (OR 2.62, P=0.003), and HIV/ART vs. HIV/HTLV-2 (OR 2.42, P=0.016). Conclusions. The polymorphism profiles detected in the study groups corroborate the profiles described in racial admixed populations. High CCR2-64I mutant allele frequencies were detected in HIV/HTLV-1/-2 co-infected individuals, and CCR5-∆32 showed predictive value for ART initiation.
背景。趋化因子和趋化因子受体多态性与预防HIV感染和延迟发展为艾滋病有关,而ifn - λ4(以前称为IL28B)的多态性与人类t淋巴细胞嗜病毒1 (HTLV-1)相关脊髓病(HAM)的发展有关。针对祖先基因的进化选择因人群而异,导致获得和发展病毒性疾病的风险各不相同。方法。将来自巴西圣保罗的434例HIV-1和/或HTLV-1/ 2合并感染者和74例HIV和HTLV未感染者的DNA样本分为5组:HIV-naïve, n=160;HIV-ART n = 180;艾滋病毒/ htlv 1, n = 53个;艾滋病毒/ HTLV-2 n = 41;对照组n=74。采用PCR和PCR- rflp技术分析CCR5-∆32缺失、CCR2-64I、SDF1-3'A和ifn - λ4 rs12979860和rs8099917单核苷酸多态性。计算这些多态性的基因型和等位基因频率,并采用logistic回归分析进行组间比较。结果。本研究检测了文献中描述的所有多态性谱。除ifn - λ4 rs12979860外,其余基因均以野生型为主。CCR5和CCR2基因的等位基因频率在组间存在统计学差异,HIV-naïve与HIV-ART的等位基因频率为∆32 (OR 2.45, P=0.037), HIV-naïve与HIV/HTLV-1的等位基因频率为δ 32 (OR 1.90, P=0.048), HIV-ART与HIV/HTLV-1的等位基因频率为δ 2- 64i (OR 2.62, P=0.003), HIV/ART与HIV/HTLV-2的等位基因频率为δ 2.42, P=0.016)。结论。在研究组中检测到的多态性谱证实了在种族混合人群中描述的谱。在HIV/HTLV-1/ 2共感染个体中检测到高CCR2-64I突变等位基因频率,CCR5-∆32对ART启动具有预测价值。
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Microbes, infection and chemotherapy
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