成年牙周炎病人龈下菌斑优势菌群的探讨

本文用2种非选择性培养基和12种选择性培养基对17名北京市成年牙周炎病人和9名健康对照者龈下及龈沟菌斑菌群进行了培养、分离和鉴定。结果,牙周炎患者龈下菌斑的菌群主要由专性厌氧的革兰氏阴性杆菌组成(60.8％),优势菌为牙龈拟杆菌等;而对照组的菌群主要由兼性厌氧的革兰氏阳性球菌组成(69.2％),优势菌为链球菌属等。这种菌群构成,两组样本存在显著性差异,对于我们认识牙周炎的病原及有关微生态学问题可能有重要意义。     

依赖于DNA的RNA聚合酶与体外转录的研究 Ⅰ.酵母变异株20B-12 RNA聚合酶A和C的纯化及鉴定

从酵母变异株20B-12经过超声波处理、硫酸铵沉淀、DEAE纤维素和磷酸纤维素层析等步骤,纯化依赖于DNA的RNA聚合酶A和C,得到聚丙烯酰胺凝胶电泳均一的条带。其中不含DNase、RNase 和蛋白酶活力,无内源DNA。测定了 RNA 聚合酶A和C对α-鹅膏荤碱的敏感性。酶A在α-鹅膏荤碱为400μg/ml时,活性受到抑制,而酶C在该浓度时,几乎不受抑制。(NH_4)_2SO_4对酶A的最适浓度为20mM,对酶C有二个最适浓度,分别为40mM和240mM。无二价金属离子Mn~(2+)或Mg~(2+),酶A和C几乎无活力。两种酶最适Mn~(2+)浓度均为2.5mM,Mg~(2+)浓度均为5mM。两种酶以热变性小牛胸腺DNA为模板,测活性均较天然小牛胸腺DNA为模板时高。     

健康家兔肝脏内李司忒菌的分离鉴定

我们在健康家兔中发现有些动物的肝脏有灶性坏死,疑为李司忒菌感染所致,从而进行了细菌分离。结果培养出2株革兰氏阳性杆菌,经鉴定结果为单核细胞增多性李司忒菌1/2血清型。     

禽流感H5N1亚型病毒感染恒河猴模型的建立及禽流感发病机制初探

[目的]建立禽流感H5N1病毒感染恒河猴的动物模型,探讨禽流感在哺乳类动物的发病机制。[方法]通过“环甲膜穿刺术”经气管注射鸡胚培养的禽流感H5N1病毒(AF148678;ACGoose/Guangdong/11961H5N1)感染恒河猴,观察恒河猴染毒后出现的临床体征,用显微计数法检测外周血白细胞的动态变化,用ELISA检测禽流感病毒特异性抗体变化规律,用流式细胞仪检测外周血T淋巴细胞及其亚群的动态变化。在染毒后第1天、第3天、第10天和第14天分别剖杀染毒组恒河猴1只,HE染色观察主要组织器官的病理变化,用病毒分离、免疫组化和RT-PCR三种方法分析禽流感病毒侵袭机体的特点。[结果]临床症状和体征:急性起病,表现为发热,呼吸困难,精神状态下降,活动度明显减少,食欲下降,咳嗽,紫绀等,肺部听诊双肺可闻及干、湿音。1、病理特点:以肺部损伤为主,伴多器官病变。肺部的病变主要表现为弥漫性肺泡损伤,先后经历渗出期、增生期和纤维化期;在肝脏、肾脏和中枢神经系统中也观察到变性、坏死等病理变化。2、病毒侵袭机体的特点:病毒只在呼吸系统中复制,不在呼吸道以外的组织器官中复制;肺内支气管上皮细胞、肺泡上皮细胞和肺巨噬细胞是禽流感病毒侵犯的主要细胞类型。3、外周血象特点:外周血白细胞总数、淋巴细胞数出现短暂的下降,中性粒细胞数先升后降,但均于感染第7天后逐渐恢复到正常水平。4、抗体变化特点:感染后第7~11天,抗体水平持续快速升高;感染第11天后,抗体水平呈逐渐缓慢升高趋势(观察到染毒后50天为止)。5、细胞免疫特点:细胞免疫功能受损,表现为CD3+T淋巴细、CD3+CD4+T淋巴细胞和CD3+CD8+T淋巴细胞均出现短暂的下降,但这种细胞免疫功能受损是可逆的,到感染第7天后逐渐恢复回升至正常。[结论]1、恒河猴感染后的临床特点、病理变化、外周血象、免疫反应等均与人禽流感严重病例相类似,表明该模型是成功的,可为禽流感病毒在人体内致病机理的研究以及抗禽流感病毒的药物和疫苗评价提供最近似于人类的动物模型。2、综合本研究的实验结果,我们认为,H5N1禽流感毒主要攻击的对象为呼吸系统,不在呼吸道以外的组织器官中复制。禽流感病毒感染引起的急性弥漫性肺损伤是发病的中心环节,其发病可能经过病毒侵入、复制阶段,免疫损伤阶段和多器官功能损伤阶段。     

中国独活属花粉形态及分类学和进化意义

中国独活属约26种3变种。本文通过光学显微镜和扫描电镜观察,较系统地分析了21种2变种的花粉。研究结果表明:该属花粉基本为矩形类型,少数种具赤道收缩型。综合中国独活属形态解剖方面的相关特征,将中国独活属分为两大类群,并讨论了独活属的系统位置及其演化趋势。     

西双版纳竹类植物分布及其特点

本文应用民族植物学的方法和原理,调查和研究了分布于西双版纳的竹类植物。 竹类植物广泛分布于云南和东南亚地区。由于版纳优越的自然条件、独特的民族文化习俗和宗教信仰等方面的原因,生活在版纳的傣族和其他少数民族均有栽培、认识、利用竹类植物的传统习惯及较高的知识经验,使得版纳不仅具有大面积的天然竹林,而且具有许多人工竹林。 本文参阅了众多的竹类研究成果,整理了大量的野外调查、采集资料,充分肯定了前人对版纳竹类研究的价值,论述了分布于版纳的竹属,并应用植物区系的方法分析和探讨了版纳竹属的分布类型以及版纳与相关地区的竹类亲缘关系,认为:版纳竹类与东南亚关系最为密切,其次为滇西、滇东南,与滇中、华东有一定的联系,而与华南有着显著的差异。     

Cloning,Characterization and Primary Function Study of a Novel Gene,Cymg1,Related to Family 2 Cystatins

Cystatins are cysteine proteinase inhibitors,We found two expression sequence tags (ESTs),CA463109 and AV042522,from a mouse testis library using Digital differential display (DDD).By electricalhybridization,a novel gene,Cymgl(GenBank accession No.AY600990),which has a full length of 0.78 kb,and contains four exons and three introns,was cloned from a mouse testis eDNA library.The gene is locatedin the 2G3 area of chromosome 2.The full eDNA encompasses the entire open reading frame,encoding 141amino acid residues.The protein has a cysteine protease inhibitor domain that is related to the family 2cystatins but lacks critical consensus sites important for cysteine protease inhibition.These characteristicsare seen in the CRES subfamily,which are related to the family 2 cystatins and are expressed specifically inthe male reproductive tract.CYMG1 has a 44%(48/108)identity with mouse CRES and 30%(42/140)identity with mouse cystatin C.Northern blot analysis showed that the Cymgl is specifically expressed inadult mouse testes.Cell location studies showed that the GFP-tagged CYMG 1 protein was localized in thecytoplasm of HeLa cells,lmmunohistochemistry revealed that the CYMG1 protein was expressed in mousetestes spermatogonium,spermatocytes,round spermatids,elongating spermatids and spermatozoa.RT-PCRresults also showed that Cymgl was expressed in mouse testes and spermatogonium.The Cymgl expressionlevel varied in different developmental stages:it was low 1 week postpartum,steadily increased 2 to 5 weekspostpartum,and was highest 7 weeks postpartum.The expression level at 5 weeks postpartum was main-tained during 13 to 57 weeks postpartum.The Cymgl expression level in the testes over different develop-mental stages correlates with the mouse spermatogenesis and sexual maturation process.All these indicatethat Cymgl might play an important role in mouse spermatogenesis and sexual maturation. Cystatins are cysteine proteinase inhibitors,We found two expression sequence tags(ESTs),CA463109 and AV042522,from a mouse testis library using Digital differential display (DDD).By electricalhybridization,a novel gene,Cymgl(GenBank accession No.AY600990),which has a full length of 0.78 kb,and contains four exons and three introns,was cloned from a mouse testis eDNA library.The gene is locatedin the 2G3 area of chromosome 2.The full eDNA encompasses the entire open reading frame,encoding 141amino acid residues.The protein has a cysteine protease inhibitor domain that is related to the family 2cystatins but lacks critical consensus sites important for cysteine protease inhibition.These characteristicsare seen in the CRES subfamily,which are related to the family 2 cystatins and are expressed specifically inthe male reproductive tract.CYMG1 has a 44%(48/108)identity with mouse CRES and 30%(42/140)identity with mouse cystatin C.Northern blot analysis showed that the Cymgl is specifically expressed inadult mouse testes.Cell location studies showed that the GFP-tagged CYMG 1 protein was localized in thecytoplasm of HeLa cells,lmmunohistochemistry revealed that the CYMG1 protein was expressed in mousetestes spermatogonium,spermatocytes,round spermatids,elongating spermatids and spermatozoa.RT-PCRresults also showed that Cymgl was expressed in mouse testes and spermatogonium.The Cymgl expressionlevel varied in different developmental stages:it was low 1 week postpartum,steadily increased 2 to 5 weekspostpartum,and was highest 7 weeks postpartum.The expression level at 5 weeks postpartum was main-tained during 13 to 57 weeks postpartum.The Cymgl expression level in the testes over different develop-mental stages correlates with the mouse spermatogenesis and sexual maturation process.All these indicatethat Cymgl might play an important role in mouse spermatogenesis and sexual maturation.     

云南省甲属披膜病毒的分离和鉴定

从采自云南省的6种蚊子和1份发热病人血清分离到披膜病毒11株,电镜检查该病毒为球形有囊膜颗粒,直径为56.10±1.38nm,病毒抵抗5-IdU,对酸、热、醚均敏感,在pH5.5～6.4间能凝集鹅血球,乳鼠皮下或脑内注射均能稳定致死,酶免疫法鉴定表明这11株病毒与甲属披膜病毒(MAY、RR、WEE、EEE)抗体有反应,尤与MAY反应最强,与我国分离的M1、M4病毒抗体也有反应,但空斑抑制中和试验显示,云南甲病毒和MAY病毒间没有交叉中和反应,在以上性状方面蚊体和人体分离的病毒间未见明显差异,对云南甲属病毒的分类学地位及我国甲属披膜病毒分布和意义进行了讨论。     

桔小实蝇在中国云南省的分布(英文)

在云南 1 2个县的诱捕试验表明 ,桔小实蝇在云南的分布可以划分为 3个区域。广南、元江和瑞丽以南的地区为该虫常年发生区。在该区域内 ,桔小实蝇年发生 4- 5代 ,可对瓜果形成周年危害。位于六库、大姚和曲靖以北的地区为该虫的非分布区。本试验未能在该地区诱捕到桔小实蝇或桔小实蝇受害果。位于上述两区域之间的区域为桔小实蝇季节性分布区。桔小实蝇在该地区年发生 2 - 3代 ,出现于 5- 1 1月。桔小实蝇在分布区内不同地区的发生高峰期 ,由南向北逐渐推移 ,如在景洪为 6月而在姚安为 1 0月。在地理垂直分布上 ,该虫主要分布于海拔 50 0 - 2 30 0m范围内 ,而其在 50 0 - 1 0 0 0m范围内发生量最大。研究认为 ,桔小实蝇在上述经度和海拔范围的发生与分布 ,主要与当地气候条件与寄主植物有关。     

禄丰蜥龙动物群的组成及初步分析

本文在对禄丰蜥龙动物群的组成进行分析的同时,修正了部分化石产出层位.分层列出了迄今报道过的采自禄丰盆地下禄丰组的脊椎动物化石名单;并以此为依据,倾向于下禄丰组深红层,更确切地说是表4的第"8"层中所含化石,代表里阿斯期.