Shuhart Margaret C, Sullivan Daniel G, Bekele Kirubeal, Harrington Robert D, Kitahata Mari M, Mathisen Terri L, Thomassen Lisa V, Emerson Scott S, Gretch David R
Department of Medicine, University of Washington, Seattle, USA.
J Infect Dis. 2006 May 1;193(9):1211-8. doi: 10.1086/502974. Epub 2006 Mar 28.
Hepatitis C virus (HCV) quasispecies variability has been associated with liver disease progression. The effects of human immunodeficiency virus (HIV) coinfection and highly active antiretroviral therapy (HAART) on HCV quasispecies variability have not been firmly established.
We determined HCV quasispecies complexity and diversity in 69 subjects, 28 of whom were HIV infected, using clonal frequency analysis via heteroduplex mobility analysis of the second envelope gene hypervariable region. Nucleotide sequencing was performed for a small subset of subjects.
HIV-positive, HAART-naive subjects had significantly lower HCV quasispecies complexity and diversity than did both HIV-negative and HIV-positive HAART-treated subjects. In multivariate analysis, HIV infection predicted decreased complexity (P < .0001) and diversity (P = .001) of HCV quasispecies, whereas HAART predicted increased complexity (P = .013) and diversity (P = .026). For 4 of 6 patients, sequence analysis yielded data supporting the model that positive host pressure drives HCV quasispecies heterogeneity, although data favoring the hypothesis of selective outgrowth of the most fit variants were also observed.
HIV coinfection is associated with decreased HCV quasispecies variability, which appears to be reversed by effective HAART. Although HIV- and HAART-related effects on host immune pressure are likely to play a role in the observed differences in HCV genetic heterogeneity, other mechanisms may be operative.
丙型肝炎病毒(HCV)准种变异性与肝脏疾病进展相关。人类免疫缺陷病毒(HIV)合并感染及高效抗逆转录病毒治疗(HAART)对HCV准种变异性的影响尚未完全明确。
我们通过对69名受试者的第二个包膜基因高变区进行异源双链迁移率分析的克隆频率分析,测定了HCV准种的复杂性和多样性,其中28名受试者感染了HIV。对一小部分受试者进行了核苷酸测序。
未接受HAART治疗的HIV阳性受试者的HCV准种复杂性和多样性显著低于HIV阴性和接受HAART治疗的HIV阳性受试者。在多变量分析中,HIV感染预示着HCV准种复杂性(P <.0001)和多样性(P =.001)降低,而HAART预示着复杂性(P =.013)和多样性(P =.026)增加。对于6名患者中的4名,序列分析得出的数据支持宿主正向压力驱动HCV准种异质性的模型,尽管也观察到支持最适合变体选择性生长假说的数据。
HIV合并感染与HCV准种变异性降低相关,而有效的HAART似乎可以逆转这种情况。尽管HIV和HAART对宿主免疫压力的相关影响可能在观察到的HCV基因异质性差异中起作用,但其他机制可能也在起作用。