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1.
对362名无症状高滴度HBsAg携带者用RIA法检测HBeAg、Anti-HBe、Anti-HCV、Anti-HDV。结果表明,HBeAg阳性率随HBsAg滴度的增高而增加,且有显著性差异(P<0.05)。重叠感染以HBV+HCV最高,占27.6%;其次是HBV+HDV,占9.1%;HBV+HCV+HDV最少,占6.4%。但是,以上重叠感染率均与HBsAg滴度及/或HBeAg阳性率高低无关(P>0.05)。调查显示,无症状HBsAg携带者中HBV+HCV,或HBV+HDV,或HBV+HCV+HDV的重叠感染均可发生。  相似文献   

2.
应用ELISA和PCR法检测502例乙肝病人血清,401例HBsAg阳性血清中,有114例(28.4%)抗-HCV和HCVRNA双项阳性,25例(6.2%)HCVRNA单项阳性;21例(5.2%)抗-HCV单项阳性。将HBsAg乙肝病人分成HBVDNA,HBeAg阳性组和HBVDNA,HBeAg阴性组。前者抗-HCV阳性率为11.6%~20.5%,HCVRNA阳性率为16.2%~20.5%。后者抗-HCV阳性率为20.2%~55.6%,HCVRNA阳性率为23%~60.3%。结果说明长期携带HBV者和慢性乙肝病人均可重叠HCV感染。HBVDNA阳性组抗-HCV和HCVRNA阳性率明显高于HBVDNA阳性组  相似文献   

3.
谭文杰  夏宁邵 《病毒学报》1998,14(2):114-120
通过逆转录-聚合酶链反应从我国河南省2例重叠感染HCV或HBV/HDV的献血啼中,分离到HBVNS5区的部分cDNA,对其进行序列分析比较,结果表明,河南株HGVNS5工核苷酸与两中国HGV主同源性高于国外代表株(88.5-90.6%),但由核苷酸推导的氨基酸的同源性都无明显的地区性区别。HGVNS5区氨基酸序列较保守,缺乏明显高变区,中国4株HGV在7384位发生了由C→T的变异,从而导致一个人  相似文献   

4.
中国河南株丁型肝炎病毒全基因组的cDNA克隆和序列分析   总被引:3,自引:0,他引:3  
从我国河南-抗丁型肝炎病毒抗原(anti-HDAg)及丁型肝炎病毒(HDv)RNA双阳性的HBsAg携带者血清中提取RNA,采用人工合成的引物进行逆转录和聚合酶链反应(PCR),获得了贯穿HDV全基因组的6个相互重叠的cDNA片段。经双脱氧末端终止法进行核苷酸序列分析,得到了长度为1674bp的我国人河南株HDVcDNA全序列。计算机分析表明,该株与我国台湾株(HDVIA型)、美国-1株(HDVIB型)、日本-1株(HDVⅡ型)和秘鲁-1株(HDVⅢ型)的核苷酸同源性分别为的94.3%、86.8%、75.4%和66.3%,氨基酸序列的同源性分别为89.7%、85.1%、71.9%和64.6%,并在核苷酸和推导的HDAg氨基酸序列中分别发现了5个和2个集中保守的区域。这些区域均与HDV的某些重要功能密切相关。  相似文献   

5.
作者应用抗HCVNS3区C33c抗原2B6株单克隆抗体和抗HBxAg多克隆抗体,采用ABC法对102例人原发性肝细胞肝癌(PHC)组织进行了HCV及HBV抗原定位研究。HCVC3。抗原及HBxAg在PHC中的阳性检出率分别是81.4%及74.5%,C33c抗原或HBxAg阳性占所检病例94.1%,相同病例二者同时阳性为61.8%。102例PHC中50例有癌旁肝组织,其C33c抗原和HBxAg的阳性检出率分别是62%和92%。HCVC33c抗原定位于肝癌细胞的胞浆内,胞核未见阳性信号。C33c抗原阳性细胞在PHC中呈散在、局灶分布为主,在癌旁肝组织呈弥漫分布为主。本文结果提示HCV感染在PHC的发生中可能起重要作用。  相似文献   

6.
肝硬变中丙型肝炎病毒C33c抗原及HBxAg的分布及意义   总被引:2,自引:0,他引:2  
应用抗HCVC33c抗原2B6株单克隆抗体和抗HBxAg多克隆抗体。以ABC法对86例肝硬变组织进行HCV及HBV相关抗原定位研究,HCVC33c抗原及HBxAg在肝硬变中的阳性率分别为76.7%及62.8%,C33c抗原和HBxAg阳性占所检病例88.4%,二者同时阳性为51.2%,HCVC33c抗原位于肝硬变组织的肝细胞胞桨内,充满整个胞桨,细胞核及胸膜未见阳性;阳性细胞呈弥温、局灶及散在分布  相似文献   

7.
新型HCV EIA诊断试剂盒的研制   总被引:3,自引:0,他引:3  
杨永平  曹经缓 《病毒学报》1994,10(2):118-127
丙型肝炎病毒(HCV)基因组结构区核壳蛋白(C)区抗原、膜蛋白E1和E2区抗原,以及非结构区NS3-NS5区抗原的区段,已经在原核细胞中获得有效的表达。同时,相应区段中的优势抗原表位肽也经化学合成法大规模地制备。HCV基因组上各区段抗原性的分析发现,由C区和NS3区分别编码的C抗原和C33c抗原是HCV基因组上两个优势抗原区段。其相应的抗体出现早(感染后6周可检出抗C33c抗体),阳转率高(约99%阳性检出率),特异性和重复性均优于其它区段抗原。以中国人HCV的C33c重组蛋白和分支状合成肽MAP-C-19为复合抗原,研制了适合我国抗HCV抗体检测的新型丙型肝炎病毒酶免疫测定(HCVELA)诊断试剂盒。它同当代美国Abbott/UBIHCVELA诊断试剂的符合率约98%,同加拿大YES公司HCVEIA诊断试剂的符合率约97.8%,阳性检出率提高了约2%,3次重复性达100%,表明其特异性、敏感性和重复性均达到了当代第二代JCVELA诊断试剂的水平。我国人群中抗HCV抗体的分布情况为:正常人群的检出率1%-2%;外科类住院病人检出率约28.8%;肝炎患者抗HCV阳性率为34.4%,慢活肝、肝硬化和重症肝炎患者  相似文献   

8.
本研究用PAP法、胸腺细胞增殖法、脾细胞增殖法,分别检测16例体外HBV感染和骨髓单个核细胞与16例慢性乙型肝炎患者体内感染的骨髓单个核细胞中的HBcAg和白细胞介素-1、白细胞介素-2的诱生活性。结果显示,体外HBV感染组成体内HBV感染组骨髓MNCs中HBcAg检出率分别为50%和43.7%。本实验结果表明,HBV在体外感染骨髓MNCs,且与体内自然感染相符,但光镜下未观察到致细胞病变效应。体  相似文献   

9.
本文通过逆转录(RT)-聚合酶链式反应(PCR),从两份分别来自湖南省娄底地区丙型肝炎病人和河北省秦皇岛市职业献血员丙型肝炎病毒(HCV)RNA打点杂交阳性的血清中,扩增并克隆到1段563bp的HCV基因组C区抗原基因C269/831,并通过PCR得到了3个表达片段C831、C801和C587。测定C269/831基因的全序列后发现,中国人HCV湖南分离株与HCV-Ⅰ型株HCV-US和Ⅱ型株HCV-BK在该基因区段的核苷酸/氨基酸序列的同源性,分别为90.3%/94.6%和95.2%/94.6%。利用原核高效表达载体pBV220在大肠杆菌中有效地表达了非融合的C区抗原基因重组蛋白CL、CM和CS。通过免疫筛选法及Westem印迹法对约占菌体可溶性蛋白11%的表达产物进行了鉴定。采用TritonX-100和盐析处理表达产物,再进行离子交换层析纯化,得到可用于检测HCV血清抗体的核壳蛋白(C)抗原。通过不同分子量抗原的表达,发现由C区N端89个氨基酸组成的多肽CS其抗原性与由158或168个氨基酸组成的多肽CM或CL相同,但抗原的稳定性和表达量显著优于后两种抗原。本研究为研制HCV抗体诊断试剂盒奠定了重要基础。  相似文献   

10.
对379例良、恶性肝组织进行的免疫组织化学研究显示,33%的慢性迁延性肝炎(6/18)、76%的慢性活动性肝炎(26/34)、92%的肝硬变(57/62)和97%的肝细胞性肝癌(HCC)(58/60)中有HBxAg表达,阳性率高于HBsAg或HBcAg。癌周肝中的HBxAg阳性率显著高于非癌周肝。与其它2种HBV抗原不同,HBxAg表达在细胞类型上有较明显的选择性,在肝小多角细胞(SPLC)、小细胞性不典型增生(SCD)及HCC中较强。与IGFⅡ、c-erbB-2、c-myc和EGF-R表达进行的对照研究表明HBxAg与IGFⅡ和c-erbB-2这2种HCC发生相关基因的表达关系密切。PCNA染色结果显示HBxAg阳性组织的细胞增殖活性显著高于HBxAg阴性组织。我们的结果还表明HBxAg表达与肝细胞不典型增生的发生和进展有关、提出HBVX基因可能通过其表达产物(HBxAg)首先激活IGFⅡ、c-erbB-2基因,继而引起显著的SPLC增生和SCD而参与HCC发生的.  相似文献   

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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases  相似文献   

14.
Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.  相似文献   

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Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.  相似文献   

18.
Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.  相似文献   

19.
The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.  相似文献   

20.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细  相似文献   

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