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细胞病变效应

细胞病变效应的相关文献在1993年到2020年内共计69篇,主要集中在基础医学、畜牧、动物医学、狩猎、蚕、蜂、中国医学 等领域,其中期刊论文67篇、会议论文2篇、专利文献139814篇;相关期刊57种,包括微生物学杂志、中国生物学文摘、中国病毒学等; 相关会议2种,包括第四次全国药用植物化学学术会议、中国微生物学会医学微生物的感染与免疫学术会议等;细胞病变效应的相关文献由273位作者贡献,包括叶亮英、崔保安、徐端红等。

细胞病变效应—发文量

期刊论文>

论文:67 占比:0.05%

会议论文>

论文:2 占比:0.00%

专利文献>

论文:139814 占比:99.95%

总计:139883篇

细胞病变效应—发文趋势图

细胞病变效应

-研究学者

  • 叶亮英
  • 崔保安
  • 徐端红
  • 李继安
  • 王学兵
  • 郑意
  • 顾小海
  • 顾绍庆
  • 任常宝
  • 冯旰珠
  • 期刊论文
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    • 摘要: 2020年4月19日,中国工程院院士李兰娟团队在MedRxiv上发布了未经同行审议的新论文。论文指出,新冠病毒已经出现了能够切实影响致病性的突变,药物和疫苗研发工作有必要把这些突变纳入考虑。论文重点结论:新冠病毒株的变异和多样性或被大大低估。不同变异毒株在细胞病变效应和病毒载量方面差异可达270倍。
    • 付辉; 安丽娜; 彭碧波
    • 摘要: 目的 比较4种不同的方法 对手足口病(hand-foot and mouth disease, HFMD)病原体肠病毒71型(enterovirus type71, EV71)感染的检测效果.方法 非洲绿猴肾细胞(Vero)培养至对数生长期后,加入EV71病毒株感染.分别采用细胞病变效应法(cytopathic effect,CPE)、实时荧光定量聚合酶链式反应(real time polymerase chain reaction, Real-Time PCR). Western blot和免疫荧光法检测病毒感染情况,并对4种检测结果 进行比较.结果 4种方法 均可检测到EV71的感染,其中CPE最经济实惠,但是检测周期长,需要至少96 h,并且对病毒活力要求高;Western blot和免疫荧光检测相近,72 h即可完成实验,但灵敏度低,对病毒量有一定要求;Real-Time PCR检测既快速灵敏性又高,48 h即可完成实验.结论不同的方法 各有其优缺点,需要根据不同的需要进行选择,达到快速准确诊断病原体的目的.%Objective To compare the effects of four different methods in the detection of pathogen enterovirus type 71(EV71 )of hand-foot and mouth disease (HFMD), and to provide reference for clinical detection. Methods African green monkey cells (Vero) were cultured until the logarithmic growth phase before they were infected with the EV71 strain. The cytopathic effect(CPE) method, real-time polymerase chain reaction (Real-Time PCR), Western blot and immunofluorescence were used respectively to detect the infection of EV71. The results of the four tests were compared. Results All the four methods were able to detect the infection of EV71. Among them, CPE was the most economical method, but its detection cycle was so long as to take at least 96 hours, and it required good vitality of the virus. The effect of detection of Western blot and immunofluorescence was similar, and the experiment could be completed in 72 hours, but their sensitivity was low and a relatively large amount of virus was required. Real-Time PCR detection was both quick and highly sensitive, and the experiment could be completed in 48 hours. Conclusions Each method has its own advantages and disadvantages. A method should be chosen according to different needs so as to make quick and accurate diagnosis of pathogens.
    • 郝嘉男1; 秦成峰12
    • 摘要: 细胞融合病毒最早由Stollar和Thomas和在埃及伊蚊细胞系(源自Peleg的蚊子胚胎)当中发现^[1]。他们将埃及伊蚊细胞的培养液低速离心,然后在上清液加入未稀释的白纹伊蚊单层细胞液。在室温孵育60分钟后,去除残留白纹伊蚊细胞液,培养液继续在28°C环境下用MM培养基培养。当细胞融合已经变得充分(约72小时后),低速离心培养液,获得的上清液即为细胞融合病毒的病毒液。通过梯度沉降速率实验对比Sindbis病毒^[2]发现,细胞融合病毒类似B类披膜病毒。经过脱氧胆酸盐和乙醚处理的细胞融合病毒在感染白纹伊蚊细胞后的细胞病变效应消失,提示细胞融合病毒具有包膜必需的脂类物质。在细胞融合病毒感染白纹伊蚊细胞后60小时,可以观察到明显的细胞病变效应(cytopathic effect,CPE),到76小时后90%以上的细胞出现CPE。通过观察细胞融合病毒的生长曲线,发现其在12小时之内有一段潜伏期类似B类披膜病毒,而通过电镜观察到病毒颗粒大小约为50nm,与B类披膜病毒类似^[3]。
    • 熊晓顺; 刘彩霞; 胡音音; 李向阳
    • 摘要: 目的 研究轮状病毒非结构蛋白4的86~175位氨基酸肽段(amino acid residues 86 to 175 of nonstructural protein 4,NSP486-175)对大鼠神经元细胞内钙离子的干扰及损伤作用.方法 利用前期制备好的活性NSP486-175蛋白处理原代培养的大鼠神经元细胞,观察蛋白质处理后细胞的形态变化,检测细胞培养液中乳酸脱氢酶(LDH)活性;Fluo-3 AM标记细胞内游离的钙离子,蛋白质处理细胞后,用激光共聚焦显微镜检测神经元细胞内钙离子浓度变化.结果 正常生长的神经元细胞胞体丰满,呈不规则形或梭形,细胞突起数量较多并且较长,纯化的NSP486-175蛋白刺激后的大鼠神经元细胞出现明显的细胞病变效应,细胞密度稀疏,细胞胞体皱缩,细胞突起数量减少;蛋白质处理组细胞培养液中的LDH活性均增大;外源性添加NSP486-175能引起神经元细胞内荧光强度和分布改变.结论NSP486-175 对大鼠神经元细胞具有损伤作用,这可能与它导致细胞内钙库释放引起的钙离子浓度升高有关,为轮状病毒肠道外播散感染和致病提供了一定的理论依据.%Objective To investigate the cytopathic effect of amino acid residues 86 to 175 of rotavirus nonstructural protein 4 (NSP486-175) on rat neurons and to analyze the underlying mechanism.MethodsPrimary cultured rat neurons were treated with NSP486-175 and the morphological changes induced in rat neurons were observed.Lactate dehydrogenase (LDH) activity in the culture supernatant of NSP486-175 treated-neurons was measured.Laser scanning confocal microscope was used to detect the concentration of intracellular Ca2+ labeled with Fluo-3 AM.Results Exogenous addition of NSP486-175 induced obvious cytopathic effect on rat neurons.The LDH activity in the culture supernatant of treated-neurons was stronger than that of the control group.The intensity and the distribution of fluorescence in neurons were altered after stimulation with NSP486-175.Conclusion NSP486-175 can induce the damage of rat neurons, which may be related to its role in increasing the concentration of intracellular Ca2+.This study may provide certain theoretical basis for understanding extra-intestinal spread and pathogenesis of rotavirus infection.
    • 宋风霞; 赵林清; 朱汝南; 邓洁; 宋秦伟; 王芳; 孙宇; 钱渊
    • 摘要: 目的研究CA16和EV71在4种细胞系中细胞病变作用的差异.方法随机选择滴度相似的EV71轻症、EV71重症和CA16轻症毒株各1株,分别感染RD、Vero、U251和SY5Y细胞,比较3株病毒在细胞病变的形态及程度、感染后的细胞存活率、病毒在细胞中的复制水平和病毒所致凋亡蛋白相关mRNA的表达水平等方面的差别.结果3株病毒的感染在同一细胞系中表现相似.镜下从形态学上无法对三株病毒加以区别;感染后病毒载量均表现为从高到低依次为Vero、RD、SY5Y细胞到U251细胞的顺序;病毒感染后细胞存活率的顺序与细胞内复制水平与相反,两者之间存在类似负相关的趋势.3株病毒的感染在3种细胞系中均有凋亡蛋白caspase-8、9和3相关mRNA的表达,提示可能3种细胞系中凋亡启动的途径相同.结论细胞水平的感染,提示这两种病毒感染所致临床表现的差异性并非单独由病毒所决定.%Objective To investigate the differences ofenterovirus 71 (EV71) and coxsackievirus A16 (CA16) infections in different cell lines.Methods Three virus strains with similar titers were used.Vero,RD,U251 and SY5Y cells were infected with these three selected virus strains,respectively.The pathogenicities of EV71 and CA 16 strains in the four types of cells were compared according to characterizes of infected cells in aspects of cell viability,cytopathic effect (CPE),virus loading and mRNA expression ofapoptins.Results Pathogenicities of the three strains within same cell line were similar.The three virus strains cannot be distinguished by their CPEs under microscopy.All of viral loads induced by the three viral infections in Vero cell were the highest one in the four cell lines,followed by RD,SY5Y and U251 cell.The cell viability rates had a trend of negative relationship with virus load,therefore,the order of cell viabilities after viral infections was in contrast to the viral loads.Infections by all of the three virus strains had caused mRNA expression of caspase-8,9 and 3 in the three host cells.The apoptotic pathways in three host cells caused by the three strains had no difference.Conclusions Comparison of infections induced by EV71 and CA16 in vitro suggested that the differences in clinical outcomes of the two viral infections are not determined solely by the virus.
    • 汪志; 孙彦阔; 陈耀; 冯松林; 冀池海; 刘乙兴; 李琪; 王少君; 张桂红
    • 摘要: 为了探索葛根连芩提取液体外抗猪繁殖与呼吸综合征病毒(PRRSV)的作用,在Marc-145细胞上进行相关抗病毒试验.在药物对Marc-145细胞的安全浓度范围内,通过细胞病变效应(CPE)来评价药物对PRRSV体外的抑制作用和阻断作用.结果显示,葛根连芩提取液对PRRSV有明显的体外阻断作用,而对PRRSV没有体外抑制作用.
    • 张耘实; 祁贤; 卢协勤; 刘星; 冯旰珠
    • 摘要: 为探讨栀子苷对甲型H1N1病毒的抑制效应,进行了相关体内外实验研究。体外实验中采用MTT法判定栀子苷对MDCK细胞的毒性作用。以帕拉米韦为阳性对照药,根据MTT比色值,观察栀子苷对甲型H1N1流感病毒感染的MDCK细胞的细胞病变效应(cytopathic effects,CPE),计算不同给药方式(预防给药、直接灭活及治疗给药)及不同药物剂量干预下,栀子苷对甲型H1N1流感病毒的抑制效率;体内实验以甲型H1N1流感病毒感染ICR小鼠,建立甲型H1N1流感病毒小鼠肺炎模型,比较栀子苷不同剂量干预下,小鼠肺指数、肺组织病理学检查及小鼠存活率。实验结果显示,栀子苷的细胞毒性小,其TD_(50)大于1 040μmol/L;栀子苷在预防、直接灭活及治疗给药方式下,对甲型H1N1流感病毒感染的MDCK细胞抗病毒EC_(50)分别为91.90、96.25和87.68μmol/L,对CPE有明显抑制作用;栀子苷可显著降低甲型H1N1流感病毒感染小鼠的肺指数、减轻肺组织炎症损伤、降低小鼠死亡率、延长生存时间。实验结果表明,栀子苷在体外能有效抑制甲型H1N1流感病毒对MDCK细胞的CPE,在体内能有效保护甲型H1N1流感病毒对小鼠肺部的攻击作用,可能为流感病毒的防治提供一个新的选择。
    • 赵秋敏; 郭晓芳; 左曙青; 周红宁; 张久松
    • 摘要: The aim of this study was to identify viral isolates obtained from mosquitoes in Yunnan Province of China.The newly obtained isolates were identified by RT-PCR using alphavirus universal primers.Four of five isolates were from Culex tritaeniorhynchus and the rest was from Anopheles sinensis.They induced obvious cytopathic effect on C6/36, Vero and BHK-21 cell lines, respectively.Nucleotide sequence analyses showed that five isolates had high homology with Getah virus (GETV) YN0540, HB0234, M1 strains of China, and South Korea, LEIV 17741 MPR strains, and Sagiyama virus, with 96.4%-99.2% identities.The nucleotide sequence identifies among the five new isolates were 98.4%-100%.Phylogenetic analysis showed that the new isolates were clustered with the GETVs.These results confirmed that the new isolates belonged to GETV.%本研究对前期从云南蚊虫获得的病毒分离物作进一步鉴定,以明确其分类地位。采用甲病毒通用引物进行RT-PCR检测,在5株病毒分离物扩增出目的基因片段。新分离株4株来自三带喙库蚊,1株来自中华按蚊。它们可使白蚊伊蚊细胞(C6/36)、猴肾细胞(Vero)及金黄地鼠肾细胞(BHK-21)发生规律性细胞病变。核苷酸序列分析显示5株病毒与盖塔病毒( Getah virus, GETV)同源性最高,与GETV中国云南YN0540株、河北株 HB0234、海南株 M1及南韩株、 LEIV MPR 株、鹭山病毒的同源性为96.4%~99.2%,5株病毒之间的同源性为98.4%~100%。系统进化分析结果显示,新分离株与上述GETV处于同一进化分支。以上结果证实5株病毒分离物为盖塔病毒。
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