Adhesins of uropathogenic bacteria: Properties,identification and use for new antibacterial strategies

Adherence is a major virulence factor in the complex pathogenesis of urinary tract infections (UTI). Colonization of the urinary tract and subsequent spread of infection ascending to the kidneys depends not only on the expression of adhesins by bacteria but also on the presence of host factors which may either contribute to or inhibit infection. The presence of certain types of adhesins expressed by the bacteria and their interactions with epithelial cells play a role in determining where bacteria localize in the urinary tract, the kind and severity of symptoms and how the disease progresses. The knowledge of the molecular mechanisms underlying adherence may be useful for epidemiological research in the pathogenesis of UTI, for the diagnosis of different types of UTI and, in some cases, for prognosis. Furthermore, attachment to epithelia is a promising target for developing new methods in prophylaxis and therapy.     

家族性腺瘤性息肉病伴发硬纤维瘤的诊断和治疗

目的探讨家族性腺瘤性息肉病伴发硬纤维瘤的诊断和治疗.方法回顾性分析1995年1月至2005年1月收治的6例家族性腺瘤性息肉病并发硬纤维瘤患者的手术史、临床表现、治疗方法和随访结果,分析总结诊疗经验.结果5例患者发生硬纤维瘤前有大肠手术史,1例无腹部手术史.腹部无痛性肿块是最常见的临床表现,6例均通过影像学检查确诊.手术治疗4例,术后2例继续服用药物治疗,期待治疗1例.术后复发2例,1例出现短肠综合征.6例患者均存活.结论FAP患者伴发硬纤维瘤并不罕见,应提高警惕,及时发现并治疗.需根据患者全身情况和肿瘤部位,选择合理的治疗方式.     

消毒剂敌菲特的研究

经全面考察研究,敌菲特缓释消毒灭菌剂具有良好的消毒灭菌效果,对细菌繁殖体、病毒和细菌芽孢均可完全灭活;即使在—20℃低温条件下,对枯黑变种芽孢仍具很好的杀灭效果。此外,该消毒剂基本克服了氯制剂对金属腐蚀性的缺陷;原药性能基本稳定。     

人PD-L2基因克隆及其在大肠杆菌中的表达

目的 克隆人PD-L2基因并构建PD-L2胞外区的原核表达载体，在大肠杆菌中进行表达。方法 以RT-PCR方法从活化的人外周血单个核细胞总RNA中克隆PD-L2基因的cDNA，构建PD-L2胞外区的原核表达载体，在大肠杆菌BL21(ED3)中进行表达并鉴定。结果 克隆到PD-L2基因cDNA编码区全长序列，经DNA测序证明其与已报道的序列一致。进而构建了PD-L2胞外区的原核表达载体，并在大肠杆菌表达，免疫印迹分析表明在IPTG诱导后表达PD-L2胞外区蛋白，相对分子质量Mr为22000，与理论值大小相符。结论 成功克隆PD-L2基因，其胞外区蛋白在大肠杆菌中获得表达，为进一步研究PD-L2功能提供了条件。     

Selection of an Escherichia coli O157:H7 bacteriophage for persistence in the circulatory system of mice infected experimentally

A bacteriophage lytic for Escherichia coli O157:H7 was isolated from bovine manure. Following in-vivo selection, the phage acquired the capacity to persist in the circulatory system of mice for at least 38 days. When mice were infected experimentally with E. coli O157:H7 (10(7) CFU/mouse), simultaneous injection of the mice with phage (10(8) PFU/mouse) cleared E. coli O157:H7 from the mice within 48 h.     

Adhesion inhibitory activity of β-lactoglobulin isolated from infant formulae

β-Lactoglobulin was isolated from infant formulae that were ultra high temperature (UHT) -treated, sterilized or spray-dried. The effect of the isolated β-lactoglobulin on SfaII-fimbriae-mediated adhesion of Escherichia coli to human ileostomy glycoproteins was studied in vitro. β-Lactoglobulin isolated from sterilized formulae was found to perform significantly less well than preparations from spray-dried formulae (p = 0:05). Great heterogeneity was observed in the adhesion inhibitory capacity of β-lactoglobulin isolated from UHT-treated formulae. Therefore, no significant difference was observed between UHT-treated and sterilized formulae or spray-dried formulae (p < 0:10). It can be hypothesized that β-lactoglobulin from spray-dried and some UHT-treated infant formulae may affect the colonization of mucous membranes by E. coli strains causing neonatal septicaemia and meningitis.     

纳米抗菌剂抑菌杀菌性能研究

目的：检测纳米抗菌剂对标准菌株的杀菌、抑菌性能和高温对其抑菌效果的影响。方法：目标菌为大肠杆菌、金黄色葡萄球菌和白色念珠菌，通过悬液定量杀灭试验和抑菌环试验检测纳米抗菌剂的杀菌、抑菌能力。结果：水溶性纳米抗菌膜溶于5ml灭菌水中作用l0min可杀灭95．39％的金黄色葡萄球菌和93．28％的白色念珠菌，复合了纳米银的抗菌医用棉条、烧烫伤贴、创伤贴对大肠杆菌和金黄色葡萄球菌的抑菌环直径大于l0mm，对白色念珠菌的抑菌环直径大于7mm。结论：纳米抗菌剂对细菌繁殖体和白色念珠菌具有良好的抑菌、杀菌作用，高压灭菌处理对纳米银抗菌剂抑菌效果影响不大，但织物构造对其抑菌效果有影响。     

利用T7和PR双启动子的新型表达载体的构建及其应用

构建具有λＰＲ与Ｔ７双启动动子的新型原核表达载体ｐＤＯＧ，以便使用同一载体研究不同诱导条件下，重组蛋白在大肠杆菌中表达，降解以及折叠的情况，从而选择最佳的诱导条件。方法采用ｐＢＶ２２０与ＰＥＴ－３表达载体作为原始材料，将ＰＥＴ－３上包括Ｔ７启动子与Ｔ７ｇ－１０释译起始序列的一段序列克隆到     

表达屋尘螨Ⅰ类变应原Der p 1的基因工程菌的发酵条件探讨

目的 探讨发酵条件对大肠杆菌工程菌表达重组屋尘螨Ⅰ类变应原(Der p 1)的影响.方法 应用摇瓶发酵试验观察不同诱导时间和不同诱导时机对Der p 1表达量的影响.结果 (1)Der p 1基因在E.coli BL21(pBVDP8)菌密度A600 nm0.6左右时,42℃最佳诱导时间为4 h.(2)工程菌E.coli BL21(pBVDP8)在30℃培养至A600 nm为0.5～0.7时,42℃诱导4 h Der p 1表达量最高.结论 确定了最适诱导时间和诱导时机,初步形成了一套高表达Der p 1的发酵技术.