Shifts in the ecological niche of Lutzomyia peruensis under climate change scenarios in Peru

The Peruvian Andes presents a climate suitable for many species of sandfly that are known vectors of leishmaniasis or bartonellosis, including Lutzomyia peruensis (Diptera: Psychodidae), among others. In the present study, occurrences data for Lu. peruensis were compiled from several items in the scientific literature from Peru published between 1927 and 2015. Based on these data, ecological niche models were constructed to predict spatial distributions using three algorithms [Support vector machine (SVM), the Genetic Algorithm for Rule‐set Prediction (GARP) and Maximum Entropy (MaxEnt)]. In addition, the environmental requirements of Lu. peruensis and three niche characteristics were modelled in the context of future climate change scenarios: (a) potential changes in niche breadth; (b) shifts in the direction and magnitude of niche centroids, and (c) shifts in elevation range. The model identified areas that included environments suitable for Lu. peruensis in most regions of Peru (45.77%) and an average altitude of 3289 m a.s.l. Under climate change scenarios, a decrease in the distribution areas of Lu. peruensis was observed for all representative concentration pathways. However, the centroid of the species' ecological niche showed a northwest direction in all climate change scenarios. The information generated in this study may help health authorities responsible for the supervision of strategies to control leishmaniasis to coordinate, plan and implement appropriate strategies for each area of risk, taking into account the geographic distribution and potential dispersal of Lu. peruensis.     

18 例维吾尔族膀胱阴道瘘临床分析

目的:探讨维吾尔族膀胱阴道瘘的病因、诊断及治疗措施。方法:对2006年6月～2011年6月新疆自治区人民医院泌尿外科经美兰试验和膀胱镜检查确诊的18例维吾尔族膀胱阴道瘘患者的病历资料进行回顾性的临床分析。17例患者行瘘修补术,其中12例(70.59%)经腹修补,5例(29.41%)经阴道修补。1例患者行双侧输尿管经皮造瘘术。结果:18例患者中,16例1次修补成功,1例2次修补后成功。术后随访1至12个月无复发。结论:阴道分娩难产在维吾尔族膀胱阴道瘘患者中最为多见,根据患者全身情况、瘘道大小及位置选择合适的手术路径,术前充分准备,术后严格管理,大大提高手术成功率。     

Carboxyl terminal of rhodopsin kinase is required for the phosphorylation of photo—activated rhodopsin

Human rhodopsin kinase (RK) and a carboxyl terminus-truncated mutant RK lacking the last 59 amino acids (RKC) were expressed in human embryonic kidney 293 cells to investigate the role of the carboxyl terminus of RK in recognition and phosphorylation of rhodopsin.RKC,like the wild-type RK,was detected in both plasma membranes and cytosolic fractions.The Cterminal truncated rhodopsin kinase was unable to phosphorylate photo-activated rhodopsin,but possesses kinase activity similar to the wild-type RK in phosphorylation of small peptide substrate.It suggests that the truncation did not disturb the gross structures of RK catalytic domain.Our results also show that RKC failed to translocate to photo-activated rod out segments.Taken together,our study demonstrate the carboxyl terminus of RK is required for phosphorylation of photo-activated rhodopsin and strongly indicate that carboxyl-terminus of RK may be involved in interaction with photo-activated rhodopsin.     

护理士官分子生物学常用实验技术备课体会

目的：通过精心备课,以提高分子生物学教学中护理士官学员的学习效果。方法：在护理士官分子生物学常用实验技术理论教学中,从备学员、备目的要求、备内容、备方法和备小结几方面做好充分准备。结果：教学准备充分,学员学习兴趣浓,热情高。结论：结合护理士官特点备课,可以提高学员学习效果。     

能在肝癌细胞特异表达的自主复制型肝导向基因转移系统

构建了以人甲胎蛋白基因上游调控序列控制外源基因的表达的自主复制型EB病毒复制子载体pEBAF.该载体与半乳糖基化组蛋白结合组成了一种能为肝细胞表面特异受体识别并内在化的核酸蛋白复合物,能通过肝细胞受体介导的内吞作用以非病毒感染的形式,将外源基因导入细胞内自主复制并仅在产甲胎蛋白的肝癌细胞特异表达.这种新型的基因转移系统,具有比直接使用重组病毒颗粒感染细胞更高的安全性,有应用于原发性肝癌的基因治疗的前景     

一个含端粒序列的水稻BAC克隆的分析和定位

对一个含 (TTTAGGG) _n 同源序列的水稻BAC克隆 (BAC2 )进行了分析 ,揭示出水稻近端区DNA的组成 .BAC2的插入片段中除含有大量的以串联形式存在的称之为TA35 2序列的卫星DNA外 ,还含有TTTAGGG或其变体组成的简单重复 .荧光原位杂交 (FISH)将含 (TTTAGGG) _n 序列的 0 .8kbPstⅠ片段定位在至少 5对染色体的端粒区 .通过对BAC2中低拷贝序列的RFLP分析 ,BAC2被定位在水稻第 6号染色体端部 .这些结果说明水稻的端粒序列可能也是TTTAGGG或其变体构成的简单重复 ,而与其相连的卫星DNATA35 2则属于端粒相关序列 .     

A Pin gene families encoding components of auxin efflux carriers in Brassica juncea

Based on the sequence information of Arabidopsis PIN1, two cDNAs encoding PIN homologues fromBrassica juncea, Bjpin2 and Bjpin3, were isolated through cDNA library screening. Bjpin2 and Bjpin3encoded proteins containing 640 and 635 amino acid residues, respectively, which shared 97.5% identities witheach other and were highly homologous to Arabidopsis PIN1, PIN2 and other putative PIN proteins. BjPIN2and BjPIN3 had similar structures as AtPIN proteins. Northern blot analysis indicated that Bjpin2 wasexpressed in stem, leaf and floral tissues, while Bjpin3 was expressed predominantly in stem and hypocotyls.Two promoter fragments of pin genes, Bjpin-X and Bjpin-Z, were isolated by ‘genome walking‘ techniqueusing primers at 5‘-end of pin cDNA. Promoter-gus fusion studies revealed the GUS activities driven byBjpin-X were at internal side of xylem and petal; while those driven by Bjpin-Z were detected at leaf vein,epidermal cell and cortex of stem, vascular tissues and anther. Results of the pin genes with differentexpression patterns in B. juncea suggested the presence of a gene family.     

红火蚁三龄、四龄幼虫肠道菌菌群多样性分析

昆虫体内细菌的多样性对昆虫的消化、营养的吸收、生长发育繁殖具有至关重要的作用.本研究利用16S rRNA基因序列,构建内生菌16S rRNA克隆文库,探明红火蚁3龄幼虫和4龄幼虫种群体内微生物菌群结构并加以对比,采用Miseq高通量测序的方法揭示红火蚁3龄幼虫与4龄幼虫肠道菌的相似性和差异性.结果表明:红火蚁高龄幼虫的...     

宏基因组来源耐Mn2+、热稳定细菌漆酶的分子克隆及酶学特性

【背景】漆酶和锰过氧化物酶(Manganese peroxidase,Mnp)是木质素降解的主要酶,二者有协同效应。Mnp活性依赖于Mn~(2+),而Mn~(2+)是大多数漆酶的抑制剂。【目的】获得耐Mn~(2+)的细菌漆酶用于木质素降解。【方法】构建许昌市某污水河污泥宏基因组文库,通过活性筛选获得细菌漆酶基因lac1542。使用大肠杆菌异源表达Lac1542,研究纯化后的重组蛋白酶学性质并进一步检测了含Lac1542复合酶系降解木质素能力。【结果】测序结果显示lac1542编码一个含513个氨基酸的蛋白。以ABTS为底物Lac1542最适反应pH为4.0,在pH 3.0-6.5范围内酶活性稳定。最适反应温度是75°C,在70°C以下酶活性稳定;100 mmol/L的Mn~(2+)仍能提高酶的活性。动力学参数研究发现,该酶的最适底物顺序为:ABTS丁香醛联氮儿茶酚2,6-DMP愈创木酚。Lac1542/Mnp复合酶系对木质素降解率为47.8%,比单独使用Mnp木质素降解率(22.4%)提高25.4%。Lac1542/Mnp/灰盖鬼伞过氧化物酶(Coprinus cinereus Peroxidase,CIP)复合酶系木质素降解高达71.5%,比Mnp/CIP酶系木质素降解率(48.9%)提高22.6%,加入Lac1542后的复合酶系能明显提高木质素的降解率。【结论】Lac1542的可溶性表达、耐受高浓度Mn~(2+)、热稳定性使得Lac1542可以替代一些经典的真菌漆酶应用于制浆、造纸、纤维素乙醇生产、染料脱色等工业。     

胆汁三烯结合蛋白在大肠杆菌中的表达、复性与纯化

目的：合成胆汁三烯结合蛋白（BBP）基因并在大肠杆菌中表达,获得重组BBP纯化制品。方法：根据天然BBP的基因序列和大肠杆菌偏好密码子设计并合成BBP基因的引物,PCR扩增优化的BBP基因序列,克隆至载体pEasy-T3;测序正确后,将该序列克隆至表达载体pET-32a上,构建表达质粒,转化至大肠杆菌BL21（DE3）pLysS,在IPTG诱导下表达融合蛋白;采用Ni柱纯化融合蛋白。结果：PCR扩增获得了优化后的BBP基因序列,构建了表达载体pET-32a-BBP;SDS-PAGE分析表明表达的融合蛋白相对分子质量为20×10^3,以包涵体形式存在,占全菌蛋白的40%以上;变性、复性后经Ni2＋柱纯化,获得纯度达98%以上的重组蛋白。结论：优化并合成了BBP全基因序列,获得了高纯度重组融合蛋白,为进一步鉴定其生物活性及筛选小分子的研究奠定了基础。