期刊文献+
共找到4,798篇文章
< 1 2 240 >
每页显示 20 50 100
SARS coronavirus entry into host cells through a novel clathrin- and caveolae-independent endocytic pathway 被引量:51
1
作者 Wang,H Yang,P +4 位作者 Liu,K Guo,F Zhang,Y Zhang,G Jiang,C 《Cell Research》 SCIE CAS CSCD 2008年第2期290-301,共12页
While severe acute respiratory syndrome coronavirus (SARS-CoV)~as initially thought to enter cells through direct fusion with the plasma membrane, more recent evidence suggests that yirus entry may also involve endo... While severe acute respiratory syndrome coronavirus (SARS-CoV)~as initially thought to enter cells through direct fusion with the plasma membrane, more recent evidence suggests that yirus entry may also involve endocytosis. We have found that SARS-CoV enters cells viapH- and receptor-dependent endocytosis. Treatment of cells with either SARS-COV spike protein or spike-bearing pseudoviruses resulted in the translocation of angiotensin-converting enzyme 2 (ACE2), the functional receptor of SARS-CoV, from the cell surface to endosomes. In addition, the spike-bearing pseudoviruses and early endosome antigen 1 were found to colocalize in endosomes. Further analyses using specific endocytic path- way inhibitors and dominant-negative Epsl5 as well as caveolin-1 colocalization study suggested that virus entry was mediated by a clathrin- and caveolae-independent mechanism. Moreover, cholesterol- and sphingolipid-rich lipid raft microdomains in the plasma membrane, which have been shown to act as platforms for many physiological signaling pathways, were shown to be involved in virus entry. Endocytic entry of SARS-CoV may expand the cellular range of SARS-CoV infection, and our findings here contribute to the understanding of SARS-CoV pathogenesis, providing new information for anti-viral drug research. 展开更多
关键词 Severe Acute Respiratory Syndrome Coronavirus sars-CoV) ENDOCYTOSIS angiotensin-converting enzyme 2 (ACE2 lipid rafts
下载PDF
Chinese Medicine in Fighting against Covid-19: Role and Inspiration 被引量:9
2
作者 LI Jin-gen XU Hao 《Chinese Journal of Integrative Medicine》 SCIE CAS CSCD 2021年第1期3-6,共4页
Covid-19 pandemic has caused hundreds of thousands deaths and millions of infections and continued spreading violently.Although researchers are racing to find or develop effective drugs or vaccines,no drugs from moder... Covid-19 pandemic has caused hundreds of thousands deaths and millions of infections and continued spreading violently.Although researchers are racing to find or develop effective drugs or vaccines,no drugs from modern medical system have been proven effective and the high mutant rates of the virus may lead it resistant to whatever drugs or vaccines developed following modern drug development procedure.Current evidence has demonstrated impressive healing effects of several Chinese medicines(CMs)for Covid-19,which urges us to reflect on the role of CM in the era of modern medicine.Undoubtedly,CM could be promising resources for developing drug candidates for the treatment of Covid-19 in a way similar to the development of artemisinin.But the theory that builds CM,like the emphasis of driving away exogenous pathogen(virus,etc.)by restoring self-healing capacity rather than killing the pathogen directly from the inside and the'black-box'mode of diagnosing and treating patients,is as important,yet often ignored,an treasure as CM herbs and should be incorporated into modern medicine for future advancement and innovation of medical science. 展开更多
关键词 Chinese medicine Covid-19 sars-Co V-2 CORONAVIRUS herbal medicine
原文传递
几种SARS的中医治法对小鼠免疫系统功能影响的比较研究 被引量:8
3
作者 李灿东 王瑞国 +2 位作者 杜建 高碧珍 纪立金 《福建中医药》 2005年第3期1-2,共2页
为了探讨不同SARS的中医治法对环磷酰胺造成小鼠免疫系统功能抑制的影响。利用环磷酰胺造成小鼠免疫系统功能抑制的模型,用ELISA法检测其血清IgG和IgM、IFNγ和IL2,观察自拟固表解毒合剂和其它治法对其体液免疫和细胞免疫功能的影响。结... 为了探讨不同SARS的中医治法对环磷酰胺造成小鼠免疫系统功能抑制的影响。利用环磷酰胺造成小鼠免疫系统功能抑制的模型,用ELISA法检测其血清IgG和IgM、IFNγ和IL2,观察自拟固表解毒合剂和其它治法对其体液免疫和细胞免疫功能的影响。结果:固表解毒合剂可显著升高环磷酰胺造成免疫系统功能抑制的小鼠血清IgM、IFNγ和IL-2,且强于其它处方。结论:固表解毒法对环磷酰胺造成小鼠免疫系统功能抑制有明显增强作用,优于其它治法。 展开更多
关键词 中医治法 sars 小鼠 功能影响 免疫系统功能 ELISA法检测 IFN-γ 环磷酰胺 细胞免疫功能 IL-2 解毒合剂 血清IGG 血清IGM 体液免疫 增强作用 抑制 固表 解毒法
下载PDF
人ACE2转基因小鼠对SARS-CoV的易感性 被引量:6
4
作者 杨秀红 邓巍 +11 位作者 童攒 刘燕霞 张连峰 朱华 高虹 黄澜 刘亚莉 马春梅 徐艳峰 丁明孝 邓宏魁 秦川 《中国实验动物学报》 CAS CSCD 2007年第6期453-457,I0006,I0007,共7页
目的建立敏感的SARS小动物模型。方法通过显微注射技术,将编码SARS-CoV细胞受体的人血管紧张素转换酶(hACE2)基因导入小鼠的基因组中制备了hACE2转基因小鼠,在小鼠ACE2(mACE2)启动子的调控下,hACE2蛋白在转基因小鼠的肺脏、心脏、肾脏... 目的建立敏感的SARS小动物模型。方法通过显微注射技术,将编码SARS-CoV细胞受体的人血管紧张素转换酶(hACE2)基因导入小鼠的基因组中制备了hACE2转基因小鼠,在小鼠ACE2(mACE2)启动子的调控下,hACE2蛋白在转基因小鼠的肺脏、心脏、肾脏和小肠表达。我们观察了野生型和转基因小鼠在SARS冠状病毒接种后病原学和病理学方面的反应。结果在接种后第3天和第7天,病毒能够更有效地在转基因小鼠的肺脏复制,而且转基因小鼠出现更严重的肺损伤。肺组织的损伤包括肺间质充血、出血,单核细胞、淋巴细胞浸润及血浆蛋白的渗出,肺泡上皮细胞增生、脱落,此外,在转基因小鼠的某些器官还发现了血管炎、变性和坏死等病理变化。在转基因小鼠的肺上皮细胞、血管内皮细胞和脑神经细胞检测到病毒抗原。结论转基因小鼠比野生型小鼠对SARS病毒更易感,而且表现出更接近SARS患者的病理变化。 展开更多
关键词 sars病毒 ACE2 转基因小鼠 动物模型
下载PDF
SARS-CoV-2 induced intestinal responses with a biomimetic human gut-on-chip 被引量:6
5
作者 Yaqiong Guo Ronghua Luo +11 位作者 Yaqing Wang Pengwei Deng Tianzhang Song Min Zhang Peng Wang Xu Zhang Kangli Cui Tingting Tao Zhongyu Li Wenwen Chen Yongtang Zheng Jianhua Qin 《Science Bulletin》 SCIE EI CSCD 2021年第8期783-793,M0003,M0004,共13页
Coronavirus disease 2019(COVID-19), caused by severe acute respiratory syndrome coronavirus 2(SARSCo V-2), has become a global pandemic. Clinical evidence suggests that the intestine is another high-risk organ for SAR... Coronavirus disease 2019(COVID-19), caused by severe acute respiratory syndrome coronavirus 2(SARSCo V-2), has become a global pandemic. Clinical evidence suggests that the intestine is another high-risk organ for SARS-Co V-2 infection besides the lungs. However, a model that can accurately reflect the response of the human intestine to the virus is still lacking. Here, we created an intestinal infection model on a chip that allows the recapitulation of human relevant intestinal pathophysiology induced by SARSCo V-2 at organ level. This microengineered gut-on-chip reconstitutes the key features of the intestinal epithelium-vascular endothelium barrier through the three-dimensional(3 D) co-culture of human intestinal epithelial, mucin-secreting, and vascular endothelial cells under physiological fluid flow. The intestinal epithelium showed permissiveness for viral infection and obvious morphological changes with injury of intestinal villi, dispersed distribution of mucus-secreting cells, and reduced expression of tight junction(E-cadherin), indicating the destruction of the intestinal barrier integrity caused by virus.Moreover, the vascular endothelium exhibited abnormal cell morphology, with disrupted adherent junctions. Transcriptional analysis revealed abnormal RNA and protein metabolism, as well as activated immune responses in both epithelial and endothelial cells after viral infection(e.g., upregulated cytokine genes), which may contribute to the injury of the intestinal barrier associated with gastrointestinal symptoms. This human organ system can partially mirror intestinal barrier injury and the human response to viral infection, which is not possible in existing in vitro culture models. It provides a unique and rapid platform to accelerate COVID-19 research and develop novel therapies. 展开更多
关键词 Organ-on-a-chip COVID-19 sars-Co V-2 Microphysiological system Gastrointestinal infection
原文传递
SARS冠状病毒S2基因原核表达及免疫学特性 被引量:3
6
作者 周浩 龙北国 +4 位作者 张文炳 江丽芳 陈丽丹 贡树基 赵卫 《中国公共卫生》 CAS CSCD 北大核心 2007年第8期962-964,共3页
目的研究严重急性呼吸道综合征(SARS)冠状病毒S2蛋白表达并对其免疫学特性。方法克隆SARS冠状病毒S2基因,并在大肠埃希菌中表达谷胱甘肽硫转移酶(GST-S2)融合蛋白。通过免疫印迹(Westernblot)和酶联免疫吸附试验(ELISA)方法鉴定表达GST... 目的研究严重急性呼吸道综合征(SARS)冠状病毒S2蛋白表达并对其免疫学特性。方法克隆SARS冠状病毒S2基因,并在大肠埃希菌中表达谷胱甘肽硫转移酶(GST-S2)融合蛋白。通过免疫印迹(Westernblot)和酶联免疫吸附试验(ELISA)方法鉴定表达GST-S2融合蛋白的活性。结果通过原核系统表达的GST-S2融合蛋白可与谷胱甘肽硫转移酶(GST)多克隆抗体结合,并在85千道尔顿(KD)处出现特异性结合条带。GST-S2蛋白能与SARS患者恢复期血清反应,而不与正常人血清反应。结论本项研究获得了SARS冠状病毒GST-S2融合蛋白,它可与GST多克隆抗体特异性结合,并与SARS患者恢复期血清发生特异性反应。 展开更多
关键词 sars冠状病毒 S2基因 克隆
下载PDF
Pattern of Potential Laboratory Markers for COVID-19 in Eastern Sudan
7
作者 Nazik Sir El Khatim Bakhit Suliman Mohammed Omer Abaker Gibreel Mervat Sir El Khatim Bakhit Suliman 《Open Journal of Epidemiology》 2024年第3期508-516,共9页
Background: Coronavirus disease 2019 (COVID-19) is a recent global health crisis. One of the major issues of COVID-19 is its unpredictable manifestations and serious outcomes. Many hematological parameters are thought... Background: Coronavirus disease 2019 (COVID-19) is a recent global health crisis. One of the major issues of COVID-19 is its unpredictable manifestations and serious outcomes. Many hematological parameters are thought to change dramatically during the course of the disease. These include white blood cells, red blood cells, and platelets. This study aimed at evaluating certain laboratory results;peripheral blood lymphopenia, relative neutrophilia, high neutrophil-lymphocyte ratio, and elevated C-reactive protein as potential laboratory markers of COVID-19 in Eastern Sudanese patients. Methods: We, retrospectively, aimed at the evaluation of peripheral blood leucocytes count, neutrophil-lymphocyte ratio NLR and C-reactive protein (CRP) levels in confirmed COVID-19 eastern Sudanese patients during the course of the disease. Results: The mean total leucocytes count, % neutrophils count, absolute neutrophils count and C-reactive protein (CRP) were significantly higher (P. value = 0.000) in COVID-19 patients than in the control group while the mean % lymphocytes count and % mixed cells count were found to be significantly lower in COVID-19 patients than in the control group (P. value 0.000). Conclusion: Peripheral blood leucocyte alterations (simultaneous presence of lymphopenia, relative neutrophilia and high neutrophil lymphocyte ratio (NLR) along with elevated CRP levels may be valuable biomarkers associated with COVID-19 in Port Sudan city, Red Sea state, Sudan. These markers might be important in prediction, inspection of disease progression and prognosis. 展开更多
关键词 COVID-19 sars 2 WBCs CRP NLR Port Sudan
下载PDF
SARS冠状病毒S蛋白部分序列2的克隆与表达 被引量:4
8
作者 秦莉 吴少庭 +7 位作者 王西明 袁仕善 雷明军 潘辉榕 黄达娜 高世同 张仁利 屈伸 《中国人兽共患病杂志》 CAS CSCD 北大核心 2003年第5期17-19,136,共4页
目的 构建SARS冠状病毒棘突蛋白部分序列 2 (S2 )的原核表达质粒 ,分析其在大肠杆菌中的表达状况。方法 采用逆转录聚合酶链式反应技术从SARS冠状病毒基因组中扩增出编码S蛋白的第 2 170到 2 814位碱基的基因片段 ,克隆至 pMD18-T载体... 目的 构建SARS冠状病毒棘突蛋白部分序列 2 (S2 )的原核表达质粒 ,分析其在大肠杆菌中的表达状况。方法 采用逆转录聚合酶链式反应技术从SARS冠状病毒基因组中扩增出编码S蛋白的第 2 170到 2 814位碱基的基因片段 ,克隆至 pMD18-T载体 ,PCR筛选阳性克隆并测序。用限制性内切酶消化后 ,目的片段亚克隆至表达载体pGEX - 4T - 2 ,转化大肠杆菌JM10 9,PCR和双酶切鉴定转化菌落。将阳性菌落经IPTG诱导 ,SDS -PAGE和免疫印迹分析靶蛋白的表达。结果 RT -PCR扩增出S2特异片段 ,经测序与GenBank比对存在 1处碱基突变。S2基因片段亚克隆至表达载体 pGEX - 4T - 2构建成重组表达质粒 ,并在JM 10 9中表达了S2融合蛋白。结论 成功构建了SARS冠状病毒S2的重组表达质粒 ,并在大肠杆菌中表达了S2融合蛋白。 展开更多
关键词 sars 严重急性呼吸综合征 冠状病毒 S2蛋白 基因克隆 基因表达
下载PDF
SARS-CoV细胞受体的研究进展 被引量:4
9
作者 韩剑峰 秦鄂德 《军事医学科学院院刊》 CSCD 北大核心 2007年第1期74-77,共4页
严重急性呼吸综合征(severe acute respiratory syndrom e,SARS)是由SARS冠状病毒(SARS coronavirus,SARS-CoV)感染引起的一种新发严重急性呼吸系统传染病。SARS-CoV受体的阐明对于了解病毒的宿主与组织嗜性具有重要意义,同时也有助于... 严重急性呼吸综合征(severe acute respiratory syndrom e,SARS)是由SARS冠状病毒(SARS coronavirus,SARS-CoV)感染引起的一种新发严重急性呼吸系统传染病。SARS-CoV受体的阐明对于了解病毒的宿主与组织嗜性具有重要意义,同时也有助于了解病毒的致病机制以及研发阻止病毒结合受体的抗病毒药物。目前的研究发现SARS-CoV的受体包括血管紧张素转换酶2(ACE2)和CD209L,二者在SARS-CoV的感染致病过程中均发挥重要作用。本文综述了在SARS-CoV细胞受体结构与功能方面的研究进展。 展开更多
关键词 sars-COV 病毒受体 ACE2 CD209L
原文传递
SARS患者血清IL-2、IL-10和IL-12的检测 被引量:4
10
作者 郝娃 李卓 +2 位作者 郭新会 张可 郭雁宾 《现代免疫学》 CAS CSCD 北大核心 2004年第3期252-252,248,共2页
为了探讨细胞因子与SARS患者感染的关系 ,用ELISA的方法对急性期、恢复期SARS患者、慢性乙肝患者和正常人血清进行了IL 2、IL 10和IL 12水平检测 ,并对 14例急性期和恢复期SARS患者的白介素水平变化进行了配对分析。结果显示 :急性期SAR... 为了探讨细胞因子与SARS患者感染的关系 ,用ELISA的方法对急性期、恢复期SARS患者、慢性乙肝患者和正常人血清进行了IL 2、IL 10和IL 12水平检测 ,并对 14例急性期和恢复期SARS患者的白介素水平变化进行了配对分析。结果显示 :急性期SARS患者的IL 2、IL 10、IL 12水平显著高于恢复期患者及慢性乙肝患者和健康人的水平 (P <0 0 5 )。提示 :细胞因子在SARS感染中可能起重要作用。 展开更多
关键词 sars 细胞因子 IL-2 IL-10 IL-12
下载PDF
Molecular Phenomic Approaches to Deconvolving the Systemic Effects of SARS-CoV-2 Infection and Post-acute COVID-19 Syndrome 被引量:4
11
作者 Jeremy K.Nicholson 《Phenomics》 2021年第4期143-150,共8页
SARS COV-2 infection causes acute and frequently severe respiratory disease with associated multi-organ damage and systemic disturbances in many biochemical pathways.Metabolic phenotyping provides deep insights into t... SARS COV-2 infection causes acute and frequently severe respiratory disease with associated multi-organ damage and systemic disturbances in many biochemical pathways.Metabolic phenotyping provides deep insights into the complex immunopathological problems that drive the resulting COVID-19 disease and is also a source of novel metrics for assess-ing patient recovery.A multiplatform metabolic phenotyping approach to studying the pathology and systemic metabolic sequelae of COVID-19 is considered here,together with a framework for assessing post-acute COVID-19 Syndrome(PACS)that is a major long-term health consequence for many patients.The sudden emergence of the disease presents a biological discovery challenge as we try to understand the pathological mechanisms of the disease and develop effective mitigation strategies.This requires technologies to measure objectively the extent and sub-phenotypes of the disease at the molecular level.Spectroscopic methods can reveal metabolic sub-phenotypes and new biomarkers that can be monitored during the acute disease phase and beyond.This approach is scalable and translatable to other pathologies and provides as an exem-plar strategy for the investigation of other emergent zoonotic diseases with complex immunological drivers,multi-system involvements and diverse persistent symptoms. 展开更多
关键词 sars COV-2 COVID-19 Post-acute COVID-19 Syndrome(PACS)lSpectroscopy Metabolic Phenoconversion Phenoreversion
原文传递
SARS相关冠状病毒S2基因的克隆及其DNA疫苗的免疫效果 被引量:1
12
作者 郭瀛军 黄力 +5 位作者 王开宇 张术 陈祖欢 朱维佳 陈则 孙树汉 《第二军医大学学报》 CAS CSCD 北大核心 2003年第7期707-709,共3页
目的 :构建抗原基因为 SARS相关冠状病毒 (severe acute respiratory syndrome coronavirus,SARS- Co V) S2基因的DNA疫苗 ,将其接种小鼠后观察病毒特异性抗体产生情况。方法 :将合成的 S2基因片段克隆至真核表达载体 ,随之将质粒进行... 目的 :构建抗原基因为 SARS相关冠状病毒 (severe acute respiratory syndrome coronavirus,SARS- Co V) S2基因的DNA疫苗 ,将其接种小鼠后观察病毒特异性抗体产生情况。方法 :将合成的 S2基因片段克隆至真核表达载体 ,随之将质粒进行小鼠肌内接种免疫 ,定期检测血清中抗 SARS- Co V的病毒特异性抗体水平。结果 :疫苗接种后第 2周就能检测出病毒特异性抗体 ,随着时间的延续 ,抗体水平逐步升高 ,而空质粒对照组未检测出明显的特异性抗体。 结论 :以 S2为抗原基因的 DNA疫苗能诱导 展开更多
关键词 sars 冠状病毒 S2基因 基因克隆 DNA疫苗 免疫效果 严重急性呼吸综合征
下载PDF
Why lockdown?Why national unity?Why global solidarity?Simplified arithmetic tools for decision-makers,health professionals,journalists and the general public to explore containment options for the 2019 novel coronavirus 被引量:2
13
作者 Gerry F.Killeen Samson S.Kiware 《Infectious Disease Modelling》 2020年第1期442-458,共17页
As every country in the world struggles with the ongoing COVID-19 pandemic,it is essential that as many people as possible understand the epidemic containment,elimination and exclusion strategies required to tackle it... As every country in the world struggles with the ongoing COVID-19 pandemic,it is essential that as many people as possible understand the epidemic containment,elimination and exclusion strategies required to tackle it.Simplified arithmetic models of COVID-19 transmission,control and elimination are presented in user-friendly Shiny and Excel formats that allow non-specialists to explore,query,critique and understand the containment decisions facing their country and the world at large.Although the predictive model is broadly applicable,the simulations presented are based on parameter values representative of the United Republic of Tanzania,which is still early enough in its epidemic cycle and response to avert a national catastrophe.The predictions of these models illustrate(1)why ambitious lock-down interventions to crush the curve represent the only realistic way for individual countries to contain their national-level epidemics before they turn into outright catastrophes,(2)why these need to be implemented so early,so stringently and for such extended periods,(3)why high prevalence of other pathogens causing similar symptoms to mild COVID-19 precludes the use of contact tracing as a substitute for lock down interventions to contain and eliminate epidemics,(4)why partial containment strategies intended to merely flatten the curve,by maintaining epidemics at manageably low levels,are grossly unrealistic,and(5)why local elimination may only be sustained after lock down ends if imported cases are comprehensively excluded,so international co-operation to conditionally re-open trade and travel between countries certified as free of COVID-19 represents the best strategy for motivating progress towards pandemic eradication at global level.The three sequential goals that every country needs to emphatically embrace are contain,eliminate and exclude.As recently emphasized by the World Health Organization,success will require widespread genuine national unity and unprecedented global solidarity. 展开更多
关键词 CORONAVIRUS COVID-19 sars2 Severe acute respiratory syndrome coronavirus 2 sars-CoV-2 Model Epidemiology OUTBREAK ZOONOSIS Emerging infection
原文传递
High-throughput screening of SARS-CoV-2 main and papain-like protease inhibitors 被引量:2
14
作者 Yi Zang Mingbo Su +30 位作者 Qingxing Wang Xi Cheng Wenru Zhang Yao Zhao Tong Chen Yingyan Jiang Qiang Shen Juan Du Qiuxiang Tan Peipei Wang Lixin Gao Zhenming Jin Mengmeng Zhang Cong Li Ya Zhu Bo Feng Bixi Tang Han Xie Ming-Wei Wang Mingyue Zheng Xiaoyan Pan Haitao Yang Yechun Xu Beili Wu Leike Zhang Zihe Rao Xiuna Yang Hualiang Jiang Gengfu Xiao Qiang Zhao Jia Li 《Protein & Cell》 SCIE CSCD 2023年第1期17-27,共11页
The global COVID-19 coronavirus pandemic has infected over 109 million people,leading to over 2 million deaths up to date and still lacking of effective drugs for patient treatment.Here,we screened about 1.8 million s... The global COVID-19 coronavirus pandemic has infected over 109 million people,leading to over 2 million deaths up to date and still lacking of effective drugs for patient treatment.Here,we screened about 1.8 million small molecules against the main protease(M^(pro))and papain like protease(PL^(pro)),two major proteases in severe acute respiratory syndrome-coronavirus 2 genome,and identified 1851M^(pro)inhibitors and 205 PL^(pro)inhibitors with low nmol/l activity of the best hits.Among these inhibitors,eight small molecules showed dual inhibition effects on both M^(pro)and PL^(pro),exhibiting potential as better candidates for COVID-19 treatment.The best inhibitors of each protease were tested in antiviral assay,with over 40%of M^(pro)inhibitors and over 20%of PL^(pro)inhibitors showing high potency in viral inhibition with low cytotoxicity.The X-ray crystal structure of SARS-CoV-2 M^(pro)in complex with its potent inhibitor 4a was determined at 1.8Åresolution.Together with docking assays,our results provide a comprehensive resource for future research on anti-SARS-CoV-2 drug development. 展开更多
关键词 high-throughput screening sars CoV-2 MAIN papain-like proteases
原文传递
人血管紧张素转换酶2基因的克隆及其真核表达载体的构建 被引量:2
15
作者 肖洪广 高俊 +3 位作者 刘利东 林勇平 黄泽红 李宁 《热带医学杂志》 CAS 2006年第7期776-778,共3页
目的克隆人血管紧张素转换酶2基因(ACE2),并构建其真核表达载体。方法用Trizol试剂从人肺组织提取总RNA,然后经逆转录得到人ACE2的cDNA。半巢式PCR方法扩增人ACE2基因后,先进行T-A连接,转化感受态大肠杆菌DH5α,接种含IPTG和x-Gal平板... 目的克隆人血管紧张素转换酶2基因(ACE2),并构建其真核表达载体。方法用Trizol试剂从人肺组织提取总RNA,然后经逆转录得到人ACE2的cDNA。半巢式PCR方法扩增人ACE2基因后,先进行T-A连接,转化感受态大肠杆菌DH5α,接种含IPTG和x-Gal平板筛选重组子,并进一步亚克隆至真核表达质粒载体pcDNA3.1(+)。经PCR扩增、酶切和序列测定方法鉴定重组质粒。结果获得了人ACE2的编码基因,并成功构建了其真核表达载体。结论人血管紧张素转换酶2是SARS冠状病毒的功能受体,与SARS冠状病毒Spike蛋白上的受体结合域相结合,在SARS冠状病毒感染和传播中起重要作用,本工作为研究SARS冠状病毒感染及跨种属传播机制奠定了基础。 展开更多
关键词 sars冠状病毒 血管紧张素转换酶2 真核表达
下载PDF
Real-Time Analysis of COVID-19 Pandemic on Most Populated Countries Worldwide 被引量:2
16
作者 Meenu Gupta Rachna Jain +1 位作者 Akash Gupta Kunal Jain 《Computer Modeling in Engineering & Sciences》 SCIE EI 2020年第12期943-965,共23页
The spread of the Severe Acute Respiratory Syndrome Coronavirus 2(SARS-CoV-2)has already taken on pandemic extents,influencing even more than 200 nations in a couple of months.Although,regulation measures in China hav... The spread of the Severe Acute Respiratory Syndrome Coronavirus 2(SARS-CoV-2)has already taken on pandemic extents,influencing even more than 200 nations in a couple of months.Although,regulation measures in China have decreased new cases by over 98%,this decrease is not the situation everywhere,and most of the countries still have been affected by it.The objective of this research work is to make a comparative analysis of the top 5 most populated countries namely United States,India,China,Pakistan and Indonesia,from 1st January 2020 to 31st July 2020.This research work also targets to predict an increase in the number of deaths and total infected cases in these five countries.In our research,the performance of the proposed framework is determined by using three Machine Learning(ML)regression algorithms namely Linear Regression(LR),Support Vector Regression(SVR),andRandom Forest(RF)Regression.The proposed model is also validated upon the infected and death cases of further dates.The performance of these three algorithms is compared using the RootMean Square Error(RMSE)metrics.Random Forest algorithm shows best performance as compared to other proposed algorithms,with the lowest RMSE value in the prediction of total infected and total deaths cases for all the top five most populated countries. 展开更多
关键词 COVID-19 sars COV-2 country-wise analysis most populated countries PANDEMIC mortality rate
下载PDF
Exosomes: Emerging implementation of nanotechnology for detecting and managing novel corona virus-SARS-CoV-2 被引量:2
17
作者 Akhilesh Dubey Cynthia Lizzie Lobo +3 位作者 Ravi GS Amitha Shetty Srinivas Hebbar Sally AEl-Zahaby 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2022年第1期20-34,共15页
The spread of SARS-CoV-2 as an emerging novel coronavirus disease (COVID-19) had progressed as a worldwide pandemic since the end of 2019. COVID-19 affects firstly lungs tissues which are known for their very slow reg... The spread of SARS-CoV-2 as an emerging novel coronavirus disease (COVID-19) had progressed as a worldwide pandemic since the end of 2019. COVID-19 affects firstly lungs tissues which are known for their very slow regeneration. Afterwards, enormous cytokine stimulation occurs in the infected cells immediately after a lung infection which necessitates good management to save patients. Exosomes are extracellular vesicles of nanometric size released by reticulocytes on maturation and are known to mediate intercellular communications. The exosomal cargo serves as biomarkers in diagnosing various diseases;moreover, exosomes could be employed as nanocarriers in drug delivery systems. Exosomes look promising to combat the current pandemic since they contribute to the immune response against several viral pathogens. Many studies have proved the potential of using exosomes either as viral elements or host systems that acquire immune-stimulatory effects and could be used as a vaccine or drug delivery tool. It is essential to stop viral replication, prevent and reverse the massive storm of cytokine that worsens the infected patients’ situations for the management of COVID-19. The main benefits of exosomes could be;no cells will be introduced, no chance of mutation, lack of immunogenicity and the damaged genetic material that could negatively affect the recipient is avoided. Additionally, it was found that exosomes are static with no ability for in vivo reproduction. The current review article discusses the possibilities of using exosomes for detecting novel coronavirus and summarizes state of the art concerning the clinical trials initiated for examining the use of COVID-19 specific T cells derived exosomes and mesenchymal stem cells derived exosomes in managing COVID-19. 展开更多
关键词 EXOSOMES COVID-19 Specific T cell-derived exosomes Mesenchymal stem cells-derived EXOSOMES NANOTECHNOLOGY sars-Co V-2
下载PDF
SARS冠状病毒基础研究进展 被引量:2
18
作者 李怡棠 程桂芳 《生理科学进展》 CAS CSCD 北大核心 2005年第1期35-37,共3页
SARS(severeacuterespiratorysyndrome ,严重急性呼吸综合症 )是严重危害人类健康的传染病 ,现已发现其病原体为正链RNA冠状病毒 (coronavirus ,CoV) ,SARSCoV为一类新型的冠状病毒 ,至今没有有效对抗其感染的药物。本文从SARSCoV的功... SARS(severeacuterespiratorysyndrome ,严重急性呼吸综合症 )是严重危害人类健康的传染病 ,现已发现其病原体为正链RNA冠状病毒 (coronavirus ,CoV) ,SARSCoV为一类新型的冠状病毒 ,至今没有有效对抗其感染的药物。本文从SARSCoV的功能受体、蛋白酶、疫苗和RNA干扰技术在SARSCoV研究中的应用等方面综述了其基础研究进展 。 展开更多
关键词 sars CoV ACE2 3-C样蛋白 S蛋白 N蛋白
下载PDF
SARS病毒S蛋白S1和S2片段的合成及在大肠杆菌中的表达 被引量:1
19
作者 郑尚永 潘卫庆 《安徽农业科学》 CAS 北大核心 2011年第20期12208-12211,共4页
[目的]通过拼接完成对SARS S蛋白的上下游序列S1和S2的合成,并在大肠杆菌中表达,获得具活性的S1和S2蛋白。[方法]利用不对称PCR方法以及采用设计酶切位点将2个片段连接的方法合成SARS香港株S蛋白上下游2个片段S1和S2;构建S1和S2这2个基... [目的]通过拼接完成对SARS S蛋白的上下游序列S1和S2的合成,并在大肠杆菌中表达,获得具活性的S1和S2蛋白。[方法]利用不对称PCR方法以及采用设计酶切位点将2个片段连接的方法合成SARS香港株S蛋白上下游2个片段S1和S2;构建S1和S2这2个基因片段的原核表达载体,pET28a-S1和pET28a-S2,并转化BL21表达菌株,然后用IPTG诱导目的基因的表达并提取纯化目的蛋白。[结果]连接得到S1和S2这2个基因片段,并成功地在大肠杆菌中得到表达。[结论]该研究为后续SARS疫苗研究提供检测抗原奠定了基础。 展开更多
关键词 sars S蛋白 S1蛋白 S2蛋白 原核表达 纯化
下载PDF
严重急性呼吸综合征冠状病毒核衣壳蛋白对环氧合酶-2表达的影响 被引量:1
20
作者 祝成亮 李艳 +4 位作者 闫晓红 童永清 汪明 夏尊恩 刘芳 《中华传染病杂志》 CAS CSCD 北大核心 2010年第8期461-464,共4页
目的 探讨严重急性呼吸综合征冠状病毒(SARS-CoV)核衣壳蛋白对环氧合酶-2(COX-2)表达的影响.方法 将带有COX-2基因启动子的报告质粒分别与表达SARS-CoV基因组的单个基因的质粒共转染293T细胞,并测定荧光素酶的活性,采用RT-PCR和West... 目的 探讨严重急性呼吸综合征冠状病毒(SARS-CoV)核衣壳蛋白对环氧合酶-2(COX-2)表达的影响.方法 将带有COX-2基因启动子的报告质粒分别与表达SARS-CoV基因组的单个基因的质粒共转染293T细胞,并测定荧光素酶的活性,采用RT-PCR和Western印迹法检测COX-2 mRNA和蛋白表达的变化.结果 SARS-CoV核衣壳蛋白能显著激活COX-2基因启动子的活性,并在mRNA和蛋白水平上调COX-2的表达,且这种激活作用随着核衣壳蛋白浓度的增加而增强.结论 SARS-CoV核衣壳蛋白能特异性地激活COX-2的表达. 展开更多
关键词 sars病毒 核壳蛋白质类 环氧化酶2 基因表达
原文传递
上一页 1 2 240 下一页 到第
使用帮助 返回顶部