Alvarado-Esquivel Cosme, Sablon Erwin, Conde-González Carlos-Jesús, Juárez-Figueroa Luis, Ruiz-Maya Lilia, Aguilar-Benavides Sergio
Faculty of Medicine, Universidad Juárez del Estado de Durango, Durango, Dgo, Mexico.
World J Gastroenterol. 2006 Oct 28;12(40):6540-5. doi: 10.3748/wjg.v12.i40.6540.
To determine the genotypes in Mexican hepatitis B virus (HBV) isolates and characterize their precore and core promoter mutations.
Forty-nine HBV isolates of Mexico obtained from sera of 15 hepatitis patients, 6 hemodialysis patients, 20 men seeking HIV testing, and 8 AIDS patients were analyzed. HBV isolates were amplified by PCR, and genotyped by line probe assay (INNO-LiPA HBV Genotyping; INNOGENETICS N V, Ghent, Belgium). HBV genotype confirmation was performed by DNA sequencing part of the sAg region. Precore and core promoter mutation characterization was performed by line probe assay (INNO-LiPA HBV PreCore; INNOGENETICS N V, Ghent, Belgium).
Overall, HBV genotype H was found in 37 (75.5%) out of the 49 isolates studied. HBV genotypes G, A, and D were found in 5 (10.2%), 4 (8.2%), and 3 (6.1%) isolates, respectively. HBV genotype H was predominant in isolates from hemodialysis patients (100%), hepatitis patients (80%), and men seeking HIV testing (75%), and accounted for half of infections in AIDS patients (50%). Six (12.2%) out of the 49 HBV isolates showed both wild type and mutant populations at precore codon 28. These mixed wild type and precore mutant populations were observed in one HBV genotype A isolate and in all HBV genotype G isolates. A dual variant core promoter mutation was observed in 1 (2%) of the isolates, which was genotype H.
HBV genotype H is highly predominant in HBV isolates of Mexico followed by genotypes G, A and D. A low frequency of precore and core promoter mutations is observed in HBV Mexican isolates.
确定墨西哥乙型肝炎病毒(HBV)分离株的基因型,并对其前核心区和核心启动子突变进行特征分析。
对从15例肝炎患者、6例血液透析患者、20例寻求HIV检测的男性以及8例艾滋病患者的血清中获得的49株墨西哥HBV分离株进行分析。通过PCR扩增HBV分离株,并采用线性探针分析(INNO-LiPA HBV基因分型;INNOGENETICS NV,比利时根特)进行基因分型。通过对sAg区域的部分DNA测序进行HBV基因型确认。采用线性探针分析(INNO-LiPA HBV前核心区;INNOGENETICS NV,比利时根特)对前核心区和核心启动子突变进行特征分析。
总体而言,在所研究的49株分离株中,37株(75.5%)为HBV基因型H。分别在5株(10.2%)、4株(8.2%)和3株(6.1%)分离株中发现了HBV基因型G、A和D。HBV基因型H在血液透析患者(100%)、肝炎患者(80%)和寻求HIV检测的男性(75%)的分离株中占主导地位,在艾滋病患者的感染中占一半(50%)。49株HBV分离株中有6株(12.2%)在前核心密码子28处同时显示野生型和突变型群体。这些野生型和前核心区突变型混合群体在1株HBV基因型A分离株和所有HBV基因型G分离株中均有观察到。在1株(2%)分离株中观察到双重变异核心启动子突变,该分离株为基因型H。
HBV基因型H在墨西哥HBV分离株中高度占主导地位,其次是基因型G、A和D。在墨西哥HBV分离株中观察到前核心区和核心启动子突变的频率较低。