Jose-Abrego Alexis, Roman Sonia, Rebello Pinho João Renato, de Castro Vanessa Fusco Duarte, Panduro Arturo
Department of Molecular Biology in Medicine, Civil Hospital of Guadalajara, "Fray Antonio Alcalde," Guadalajara, Mexico.
Health Sciences Center, University of Guadalajara, Guadalajara, Mexico.
Front Microbiol. 2021 Mar 3;12:640889. doi: 10.3389/fmicb.2021.640889. eCollection 2021.
Hepatitis B virus (HBV) co-infection is possible in patients who are positive for human immunodeficiency virus (HIV) since both share similar transmission routes. Furthermore, through the continuous risk of exposure, they potentially can be infected by mixtures of distinct HBV genotypes which can result in the presence of two or more genotypes in a single patient. This study aimed to specify the frequency of mixtures of HBV genotypes and their potential clinic importance in HIV-infected Mexican patients. HBV infection was assessed by serological testing and molecular diagnostics. HBV mixtures were detected by multiplex PCR and DNA sequencing. Liver fibrosis was evaluated using transitional elastography, the Aspartate aminotransferase to Platelets Ratio Index score, and Fibrosis-4 score. Among 228 HIV-infected patients, 67 were positive for HBsAg. In 25 HBV/HIV co-infected patients, 44 HBV genotypes were found: H (50.0%, 22/44), G (22.7%, 10/44), D (15.9%, 6/44), A (9.1%, 4/44), and F (2.3%, 1/44). Among these, 44.0% (11/25) were single genotype, 36.0% (9/25) were dual and 20.0% (5/25) were triple genotype. The most frequent dual combination was G/H (44.4%, 4/9), while triple-mixtures were H/G/D (60.0%, 3/5). The increase in the number of genotypes correlated positively with age (Spearman's Rho = 0.53, = 0.0069) and negatively with platelet levels (Spearman's Rho = - 0.416, = 0.039). HBV viral load was higher in triply-infected than dually infected (31623.0 IU/mL vs. 1479.0 IU/mL, = 0.029) patients. Triple-mixed infection was associated with significant liver fibrosis (OR = 15.0 95%CI = 1.29 - 174.38, = 0.027). In conclusion, infection with mixtures of HBV genotypes is frequent in HIV patients causing significant hepatic fibrosis related to high viral load, especially in triple genotype mixtures.
由于人类免疫缺陷病毒(HIV)感染者和乙型肝炎病毒(HBV)感染者具有相似的传播途径,因此HIV阳性患者有可能同时感染HBV。此外,由于持续存在暴露风险,他们有可能感染不同HBV基因型的混合体,这可能导致单个患者体内存在两种或更多种基因型。本研究旨在明确HIV感染的墨西哥患者中HBV基因型混合体的频率及其潜在的临床重要性。通过血清学检测和分子诊断评估HBV感染情况。通过多重PCR和DNA测序检测HBV混合体。使用瞬时弹性成像、天冬氨酸氨基转移酶与血小板比值指数评分和纤维化-4评分评估肝纤维化情况。在228例HIV感染患者中,67例HBsAg呈阳性。在25例HBV/HIV合并感染患者中,共发现44种HBV基因型:H型(50.0%,22/44)、G型(22.7%,10/44)、D型(15.9%,6/44)、A型(9.1%,4/44)和F型(2.3%,1/44)。其中,44.0%(11/25)为单一基因型,36.0%(9/25)为双重基因型,20.0%(5/25)为三重基因型。最常见的双重组合是G/H型(44.4%,4/9),而三重混合体是H/G/D型(60.0%,3/5)。基因型数量的增加与年龄呈正相关(Spearman秩相关系数=0.53,P=0.0069),与血小板水平呈负相关(Spearman秩相关系数=-0.416,P=0.039)。三重感染患者的HBV病毒载量高于双重感染患者(31623.0 IU/mL对1479.0 IU/mL,P=0.029)。三重混合感染与显著肝纤维化相关(比值比=15.0,95%置信区间=1.29-174.38,P=0.027)。总之,HIV患者中HBV基因型混合体感染很常见,可导致与高病毒载量相关的显著肝纤维化,尤其是在三重基因型混合体中。