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81.
Tobiasch E Kehm R Bahr U Tidona CA Jakob NJ Handermann M Darai G Giese M 《Virus genes》2001,22(2):187-199
Equine arteritis virus (EAV) is a member of the Arteriviridae family, that includes lactate dehydrogenase-elevating virus (LDV), porcine reproductive and respiratory syndrome virus (PRRSV), and simian haemorrhagic fever virus (SHFV). Equine arteritis is a contagious disease of horses and is spread via respiratory or reproductive tract. The objective of the present study is to evaluate the possibility for developing a model system for prevention horses against an EAV infection by DNA vaccination. A cDNA bank from the RNA of EAV was established. This gene library contains the translation unit of the EAV open reading frames (ORF) 1 to 7. The identity of the cDNA was confirmed by nucleotide sequence analysis. Using this defined EAV cDNA gene library the cDNA sequence of the viral ORFs were molecularly cloned into the corresponding sites of well characterized and powerful expression vectors (pCR3.1, pDisplay, and/or pcDNA3.1/HisC).The capability of these recombinant plasmids expressing the gene products of the individual viral ORFs 3 to 5, and 7 in induction of an immune response in mouse system was investigated. The Balb/c mice (ten mice per assay) were inoculated with the DNA of the constructed expression vectors harboring and expressing the EAV cDNA of the viral ORFs. The Balb/c mice were injected with about 100 g DNA diluted in 100 l PBS. The DNA was injected subcutaneously and into the tibialis cranialis muscle (Musculus gastrocnemius). The mice were boosted 3 to 5 times with the same quantities of DNA and under the same conditions at about two week intervals. Control mice received the same amount of parental expression vectors via an identical route and frequency.The pre- and post-vaccinated sera of the individual animals were screened by neutralization tests (NT). Neutralizing antibodies against EAV were detected when the animals were inoculated with the DNA of the expression vectors harboring cDNA of the EAV ORFs 5 and 7. Highest NT-titers were observed when the animals were administered with the cDNA of ORF 5 and/or with the cDNA of the neutralization determinants of EAV that is located on the N-terminal ectodomain of the gene product of ORF 5 between the amino acid positions 1–121. These results obtained from these studies justified proofing the capability of the EAV cDNA sequences of the viral genes including ORFs 5 and 7 in the autologous animal system horse. 相似文献
82.
83.
Shichi D Kikkawa EF Ota M Katsuyama Y Kimura A Matsumori A Kulski JK Naruse TK Inoko H 《Tissue antigens》2005,66(3):200-208
Cardiomyopathy is a heart muscle disease with impaired stretch response that can result in severe heart failure and sudden death. A small proportion of hepatitis C virus (HCV)-infected patients may be predisposed to develop dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM). The molecular mechanisms involved in the predisposition remain unknown due in part to the lack of information on their genetic background. Because the human leukocyte antigen (HLA) region has a pivotal role in controlling the susceptibility to HCV-induced liver disease, we hypothesized that particular HLA alleles and/or non-HLA gene alleles within the human major histocompatibility complex (MHC) genomic region might control the predisposition to HCV-associated DCM (HCV-DCM) and/or HCV-associated HCM (HCV-HCM). Here, we present mapping results of the MHC-related susceptibility gene locus for HCV-associated cardiomyopathy by analyzing microsatellite and single nucleotide polymorphism markers. To delineate the susceptibility locus, we genotyped 44 polymorphic markers scattered across the entire MHC region in a total of 59 patients (21 HCV-DCM and 38 HCV-HCM) and 120 controls. We mapped HCV-DCM susceptibility to a non-HLA gene locus spanning from NFKBIL1 to MICA gene loci within the MHC class III-class I boundary region. Our results showed that HCV-DCM was more strongly associated with alleles of the non-HLA genes rather than the HLA genes themselves. In addition, no significant association was found between the MHC markers and HCV-HCM. This marked difference in the MHC-related disease susceptibility for HCV- associated cardiomyopathy strongly suggests that the development of HCV- DCM and HCV-HCM is under the control of different pathogenic mechanisms. 相似文献
84.
85.
Puri Beena Nelson William Porter Kevin R. Henchal Erik A. Hayes Curtis G. 《Virus genes》1998,17(1):85-88
We have determined the complete nucleotide sequence and the deduced amino acid polypeptide sequence of the genome of a dengue-1
(DEN-1) virus strain isolated from a patient on Nauru in the Western Pacific in 1974 (West Pac 74). The complete genome is
10,735 nucleotides in length and contains a single long open reading frame of 10,176 nucleotides encoding a polyprotein of
3392 amino acids. When compared to DEN-1 Singapore S275/90, the nucleotide and amino acid sequence homology are 94% and 97.8%,
respectively.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
86.
87.
Sugauchi F Orito E Kato H Suzuki S Kawakita S Sakamoto Y Fukushima K Akiba T Yoshihara N Ueda R Mizokami M 《Journal of medical virology》2003,69(1):33-40
Hepatitis B virus (HBV) genotypes have distinct geographical distribution. HBV sequences among hepatitis B carriers in Malawi have not been evaluated thus far. HBsAg serotype and genotype of HBV was determined in 20 serum samples from Malawian chronic HBV carriers, and two complete genomes and 13 entire pre-S2/S genes were sequenced directly. Genotype A HBV isolates were found in all of the samples, and serotype with adw2 and ayw2 were detected in three and 17 samples, respectively. In phylogenetic analyses, two complete genomes were classified into a subgroup A' that was described previously in South African isolates of the virus, and were separated from HBV isolates in Western countries with nucleotide differences ranging from 4.1-6.2%. The separation of subgroup A' was also evident in the tree topology of the entire pre-S1/S2, X and precore/core region, but not evident in the small-S region. The nucleotide divergences in subgroup A' were higher than those among genotype A without subgroup A' in the complete genomes as well as each of four open reading frames. All of the 13 pre-S2/S sequences were classified into the subgroup A', and clustered with known HBV isolates with ayw2 in carriers from South Africa and Zimbabwe. Three amino acids in the pre-S2/S gene were characteristic of subgroup A' with ayw2. In conclusion, unique HBV isolates of subgroup A' with ayw2 are prevalent in Malawi, and subgroup A' with a relatively higher nucleotide diversity may be a HBV isolate characteristic of the indigenous population of some African countries. 相似文献
88.
Micropuncture studies on the filtration rate of single superficial and juxtamedullary glomeruli in the rat kidney 总被引:28,自引:0,他引:28
Summary Single nephron filtration rates of superficial and juxtamedullary nephrons were determined in high and low sodium rats. Single nephron GFR was calculated from TF/P inulin and tubular flow rate in superficial nephrons and single juxtamedullary GFR from corresponding data in long loops of Henle. In low sodium rats superficial nephron GFR was 23.5±6.4 (SD)×10–6 ml/min×g KW, juxtamedullary nephron GFR was 58.2±13.6 and total kidney GFR (C
In) was 0.94±0.16 ml/min×g KW. Using these single nephron values, total kidney GFR and a total number of 30,000 glomeruli per kidney, the number of superficial and juxtamedullary glomeruli was calculated to be 23,267 and 6,733, respectively. During high sodium diet superficial nephron GFR increased to 38.1±11.3 and single juxtamedullary GFR decreased to 16.5±6.6, total kidney GFR increasing to 1.01±0.24. Calculation again revealed the same distribution of the two nephron types. End-proximal TF/P inulin in superficial nephrons was 2.36±0.36 in low sodium and 2.31±0.28 in high sodium rats. Loops of Henle TF/P inulin and intratubular flow rate were inversely related: the highest TF/P inulin values and lowest intratubular flow rates were found in the descending limb. These data quantify the distribution of superficial and juxtamedullary nephrons on a functional basis and suggest a mechanism by which the kidney adjusts sodium excretion by altering the contribution of each nephron type to total kidney GFR.Supported by the Deutsche Forschungsgemeinschaft and the U.S. Department of the Army, through its European Research Office. 相似文献
89.
A. S. Zagami G. A. Lambert 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1990,81(3):552-566
Summary Extracellular recordings were made in the thalamus of cats anaesthetized with chloralose and urethane following electrical,
mechanical and chemical stimulation of the superior sagittal sinus or middle meningeal artery. Facial receptive fields were
looked for using electrical and mechanical stimuli. The locations of fifty-six cells were verified histologically. Twenty
six cells were located in the ventroposteromedial nucleus (VPM) and six in its ventral periphery (VPMvp). All units in VPM
had facial receptive fields, usually involving the first trigeminal division. Cells with nociceptive receptive fields or responding
to the craniovascular application of bradykinin were often found in the periphery or “shell” region of VPM. Other craniovascular
nociceptive cells were found in VPMvp, in the posterior group and in the intralaminar complex. This study shows that craniovascular
afferents in the cat project to several thalamic nuclei and implicate VPM especially in craniovascular nociception. 相似文献
90.
目的:采用影像遗传学研究方法探索精神分裂症的影像遗传学特征。方法:在传统稀疏回归模型的基础上,改进
了其在不同范数条件下进行变量选择的能力,形成一种基于稀疏表示变量选择算法,并将该算法应用于208 个受试者的
41 236个功能磁共振成像数据和722 177个单核苷酸多态性数据的综合分析。通过对两类数据施加不同的权重因子,并
使用不同的Lp (p=0、0.5、1)范数分别对模型进行求解,筛选出两类数据在不同条件下的显著特征。结果:基因DAOA和
HTR2A在3种范数下均被筛选出。此外,在影像学数据方面,发现中央前回、枕上回、顶下缘角回、角回、内侧和旁扣带脑
回、后扣带回脑区与精神分裂症相关,此发现与先前精神分裂症的临床医学研究结果一致。结论:基于稀疏表示变量选择
方法应用于影像遗传学数据分析是一个有效可行的途径,为今后精神分裂症的影像遗传学研究提供了一种新的研究
思路。 相似文献