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国家自然科学基金(31072125)

作品数:5 被引量:6H指数:2
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抗微小隐孢子虫Apple结构域单克隆抗体的制备
2013年
采用PCR技术从已构建的微小隐孢子虫cDNA文库中扩增含Apple结构域基因,构建pGEX-4T-1-Apple重组质粒,并进行原核表达及纯化,得到分子质量大小约为34kDa的GST—Apple重组蛋白,以其为免疫原,免疫Balb/c小鼠,利用杂交瘤技术制备单克隆抗体,测定其免疫球蛋白亚类及效价,并用蛋白质印迹法(Western—blot)鉴定其特异性。结果共筛选出能稳定分泌抗重组Apple单克隆抗体的2株杂交瘤细胞株,抗体亚类均为IgGl,Western—blot分析显示2株单抗均能与重组蛋白GST—Apple发生特异性结合。为研究Apple结构域在隐孢子虫侵入过程中的功能提供有效工具。
张颖孔令聪张静赵权尹继刚
关键词:隐孢子虫单克隆抗体
ERG11 mutations associated with azole resistance in Candida albicans isolates from vulvovaginal candidosis patients
2015年
Objective: To investigate the azole susceptibility of Candida albicans(C.albicans)from vulvovaginal candidosis patients and to analyze the relationship between ERG11 gene mutations in these isolates and azole resistance.Methods: Three hundred and two clinical isolates of Candida species were collected.Azole susceptibility was tested in vitro in microdilution studies. The ERG11 genes of 17 isolates of C. albicans(2 susceptibles, 5 dose-dependent resistants and 10 resistants) were amplified and sequenced.Results: Of the 302 isolates collected, 70.2% were C. albicans, of which 8.5%, 3.8% and4.2% were resistant to fluconazole, itraconazole and voriconazole, respectively. In total,27 missense mutations were detected in ERG11 genes from resistant/susceptible dosedependent isolates. Among them, Y132 H, A114 S, and Y257 H substitutions were most prevalent and were known to cause fluconazole resistance. G464 S and F72 S also have been proved to cause fluconazole resistance. Two novel substitutions(T285A, S457P) in hotspot regions were identified.Conclusions: Twenty seven mutations in the ERG11 gene were identified in azoleresistant C. albicans isolates, which indicated a possible relation with the increase in resistance to azole drugs and the recurrence of vulvovaginal candidosis. The relationship of two novel substitutions(T285A, S457P) with fluconazole resistance needs to be further verified by site-directed mutagenesis.
Bin WangLi-Hua HuangJi-Xue ZhaoMan WeiHua FangDan-Yang WangHong-Fa WangJi-Gang YinMei Xiang
关键词:CANDIDAALBICANSAZOLESERG11
Detection of antibody responses in mice infected with Cryptosporidium parvum using four kinds of antigens
<正>Background:Cryptosporidium parvum is a protozoan parasite that causes diarrheal illness in a wide range of ...
Jing LiuTianyu ZhangKejie WangQingyan ShaoHuijun luNing JiangQijun ChenJigang Yin
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microRNA profiling in the parasite Neospora caninum using a high-throughput approach
Background:Neospora caninum is an important veterinary pathogen that causes spontaneous abortion in livestock....
Gang Liulijun JiaShoufa ZhangKejie WangQingyan ShaoTianyu ZhangHuijun luNing JiangQijun ChenJigang Yin
抗微小隐孢子虫TSP6蛋白单克隆抗体的制备与鉴定被引量:1
2013年
目的在大肠埃希菌中可溶性表达微小隐孢子虫TSP6抗原分子,并以其纯化产物为抗原,利用杂交瘤技术生产抗TSP6单克隆抗体(McAb)。方法将pGEX-4T-1-TSP6重组质粒转化大肠埃希菌BL21(DE3),经0.1mmol/LIPTG诱导表达后超声破菌,获得可溶性表达产物,通过Gluthathione-Sepharose 4B磁珠纯化蛋白质,以纯化的重组TSP6为抗原免疫BALB/c小鼠,采用杂交瘤技术进行细胞融合,用ELISA和有限稀释法筛选分泌高滴度McAb的杂交瘤细胞株,测定其免疫球蛋白亚类及效价,Western blot分析其特异性。结果筛选出2株杂交瘤细胞能稳定分泌抗TSP6单克隆抗体,经鉴定均为IgG1。Western blot分析显示,制备的单抗均能与相应的重组蛋白特异性结合。结论制备的抗TSP6杂交瘤细胞株能分泌高特异性的McAb。
张静赵继学韩福松高依然陆慧君姜宁尹继刚
关键词:微小隐孢子虫可溶性表达单克隆抗体
微小隐孢子虫TSP3蛋白质的表达与功能被引量:3
2015年
通过对微小隐孢子虫TSP3基因克隆构建原核表达载体,纯化TSP3 His-tag重组蛋白质免疫新西兰家兔,间接ELISA方法检测特异性血清效价并纯化多克隆抗体。纯化TSP3 GST-tag重组蛋白质并与HCT-8细胞进行共孵育,通过Western blot与间接ELISA检测细胞黏附特性。结果表明:成功构建了微小隐孢子虫p ET-TSP3和p GEX-TSP3重组表达质粒,并用亲和层析法成功纯化出较高质量的重组蛋白质。Cp TSP3重组蛋白质具有良好免疫原性,并能与HCT-8细胞黏附。
孙婷张星星余胜超刘刚尹继刚
关键词:微小隐孢子虫原核表达多克隆抗体细胞黏附
Detection of antibody responses in mice infected with Cryptosporidium parvum using four kinds of antigens
Background:Cryptosporidium parvum is a protozoan parasite that causes diarrheal illness in a wide range of mam...
Jing LiuTianyu ZhangKejie WangQingyan ShaoHuijun luNing JiangQijun ChenJigang Yin
骨髓间充质干细胞移植对小鼠急性肝功能衰竭的治疗作用被引量:2
2013年
目的:观察骨髓间充质干细胞(MSCs)移植对小鼠急性肝功能衰竭(ALF)的治疗作用,为MSCs的临床应用提供理论依据。方法:分离、纯化、扩增、鉴定小鼠MSCs,用CCl4灌胃制备稳定的小鼠ALF模型,将小鼠随机分为实验组和对照组,MSCs经尾静脉移植入实验组小鼠体内,对照组小鼠注入等量生理盐水,观察2组小鼠的活动、对外界反应及存活情况,检测2组小鼠血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)及总胆红素(TBIL),并进行病理学检测,免疫组织化学染色法检测肝脏白蛋白(ALB)表达。结果:流式细胞术检测,分离培养的MSCs 75.27%处于G0-G1期,而且MSCs强表达CD44,表达率为88.71%,基本不表达造血细胞表面标志物CD34。将MSCs移植入ALF小鼠体内后,实验组小鼠术后7d生存率为65%,明显高于对照组(25%)(P<0.01)。实验组与对照组小鼠血清ALT、AST及TBIL水平均明显升高,但实验组明显低于对照组,各时间点2组间比较差异有统计学意义(P<0.01)。实验组小鼠肝细胞坏死程度及炎细胞浸润等明显轻于对照组;7d后实验组小鼠病理组织学改善情况较对照组明显。免疫组织化学检测,7d后实验组小鼠肝组织中ALB表达明显高于对照组。结论:骨髓MSCs移植能明显改善ALF小鼠的肝功能,提高其生存率,提示骨髓MSCs移植对小鼠ALF具有明显的治疗作用。
赵继学王广义张海玉伏鑫
关键词:骨髓间充质干细胞急性肝衰竭
microRNA profiling in the parasite Neospora caninum using a high-throughput approach
<正>Background:Neospora caninum is an important veterinary pathogen that causes spontaneous abortion in livesto...
Gang Liulijun JiaShoufa ZhangKejie WangQingyan ShaoTianyu ZhangHuijun luNing JiangQijun ChenJigang Yin
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