Matera Giovanni, Lamberti Angelo, Quirino Angela, Focà Domenico, Giancotti Aida, Barreca Giorgio S, Guadagnino Vincenzo, Liberto Maria Carla
Department of Medical Sciences, Institute of Microbiology, University of Catanzaro, Italy.
Diagn Microbiol Infect Dis. 2002 Mar;42(3):169-73. doi: 10.1016/s0732-8893(01)00350-9.
The aim of this study was to assess changes in the prevalence of hepatitis C virus (HCV) genotypes, focusing on genotype 4, by surveying population of chronic hepatitis C patients within an area of Southern Italy. HCV-RNA was detected in serum using two commercial hepatitis C RNA PCR assays (Amplicor Roche Diagnostic System, and AmpliSensor HCV, Nuclear Laser Medicine). PCR products were analyzed for genotyping using a reverse hybridization of the amplified product by a line probe assay (INNO LIPA, Innogenetics). In our Institution we have previously observed, in a period of 18 months (January 1997-May 1998) an initial increase of the genotype 4 which appeared in 3.3% of HCV patients versus a percentage of 1.3%, during 1996. Later data obtained from 702 HCV-RNA positive patients, collected from June 1998 until December 1999 indicated a 3.7% of genotype 4. This percentage increased until to 4.7% in the most recent period studied (January 2000-February 2001). Drug addiction, blood transfusion and sporadically acquired infections represented the most frequent risk factors. In the Calabria region, genotype 1b, the most prevalent isolate (53.3%) and genotype 2a/2c (26.2%) were associated with older age, confirming our previous study. Genotype 4 was the fifth most prevalent genotype observed, just after 3a and 1a subtypes. Spread of genotype 4 in Calabria region is mostly associated to older age when compared to genotype 3a and 1a, but is statistically associated with a younger group of patients when compared with genotype 1b. In conclusion we demonstrated a fourfold increased prevalence of HCV genotype 4 during the last 5 years.
本研究的目的是通过对意大利南部某地区慢性丙型肝炎患者群体进行调查,评估丙型肝炎病毒(HCV)基因型的流行变化情况,重点关注4型基因型。使用两种商用丙型肝炎RNA PCR检测方法(罗氏诊断系统的Amplicor和核激光医学的AmpliSensor HCV)在血清中检测HCV-RNA。通过线性探针分析(INNO LIPA,Innogenetics)对扩增产物进行反向杂交,以分析PCR产物的基因分型。在我们机构,此前在18个月期间(1997年1月至1998年5月)观察到4型基因型最初出现增长,1996年时4型基因型在HCV患者中的占比为3.3%,而1996年为1.3%。后来从1998年6月至1999年12月收集的702例HCV-RNA阳性患者的数据显示,4型基因型占3.7%。在最近研究期间(2000年1月至2001年2月),这一比例增至4.7%。药物成瘾、输血和偶发性感染是最常见的危险因素。在卡拉布里亚地区,最常见的分离株1b型基因型(53.3%)和2a/2c型基因型(26.2%)与年龄较大有关,这证实了我们之前的研究。4型基因型是观察到的第五大常见基因型,仅次于3a和1a亚型。与3a和1a基因型相比,4型基因型在卡拉布里亚地区的传播大多与年龄较大有关,但与1b型基因型相比,在统计学上与较年轻的患者群体有关。总之,我们证明在过去5年中HCV 4型基因型的流行率增加了四倍。