Clonal integration affects allocation in the perennial herb <Emphasis Type="Italic">Alternanthera philoxeroides</Emphasis> in N-limited homogeneous environments

Most work on clonal growth in plants has focused on the advantages of clonality in heterogeneous habitats. We hypothesized (1) that physiological integration of connected ramets within a clone can also increase plant performance in homogeneous environments, (2) that this effect depends on whether ramets differ in ability to take up resources, and (3) that only ramets with relatively low uptake ability benefit. We tested these hypotheses using the perennial amphibious herb Alternanthera philoxeroides. We grew clonal fragments and varied numbers of rooted versus unrooted ramets, connection between the apical and basal parts of fragments, and availability of nitrogen. Patterns of final size and mass of fragments did not support these hypotheses. By some measures, severance did reduce the growth of more apical ramets and increase the growth of less apical ones, consistent with net apical transfer of resources. Rooting of individual ramets strongly influenced their growth: second and third most apical ramets each grew most when they were the most apical rooted ramet, and this pattern was more pronounced under higher nitrogen levels. This adds to the evidence that signalling between ramets is an important aspect of clonal integration. Overall, the results indicate that physiological integration between ramets within clones in homogeneous environments can alter the allocation of resources between connected ramets even when it does not affect the total growth of clonal fragments.     

A panel of IgG1 b12 variants with selectively diminished or enhanced affinity for Fcγ receptors to define the role of effector functions in protection against HIV

Passive transfer of neutralizing antibodies is effective in protecting rhesus macaques against simian/human immunodeficiency virus (SHIV) challenge. In addition to neutralization, effector functions of the crystallizable fragment (Fc) of antibodies are involved in antibody-mediated protection against a number of viruses. We recently showed that interaction between the Fc fragment of the broadly neutralizing antibody IgG1 b12 and cellular Fcγ receptors (FcγRs) plays an important role in protection against SHIV infection in rhesus macaques. The specific nature of this Fc-dependent protection is largely unknown. To investigate, we generated a panel of 11 IgG1 b12 antibody variants with selectively diminished or enhanced affinity for the two main activating FcγRs, FcγRIIa and FcγRIIIa. All 11 antibody variants bind gp120 and neutralize virus as effectively as does wild-type b12. Binding studies using monomeric (enzyme-linked immunosorbent assay [ELISA] and surface plasmon resonance [SPR]) and cellularly expressed Fcγ receptors show decreased (up to 5-fold) and increased (up to 90-fold) binding to FcγRIIa and FcγRIIIa with this newly generated panel of antibodies. In addition, there was generally a good correlation between b12 variant affinity for Fcγ receptor and variant function in antibody-dependent cell-mediated virus inhibition (ADCVI), phagocytosis, NK cell activation assays, and antibody-dependent cellular cytotoxicity (ADCC) assays. In future studies, these b12 variants will enable the investigation of the protective role of individual FcγRs in HIV infection.     

高灵敏焦测序结合生物发光分析仪检测甲型H1N1流感病毒

目的:建立基于核酸序列分析的快速、准确、低成本的甲型H1N1流感病毒检测方法。方法:通过优化焦测序反应体系中ATP硫酸化酶和荧光素酶的浓度,建立高灵敏的焦测序反应体系;将该体系应用于低成本、小型化的便携式生物发光分析仪,焦测序分析流感病毒M、NP、HA基因片段的核酸序列。结果:优化后的焦测序反应体系可检测低至10 fmol的DNA样本,检测灵敏度较传统焦测序提高了10倍以上。对两例样本进行检测,根据所测得的M、NP、HA基因特异性片段序列,可以确认其均为甲型H1N1感染;另外,对M2蛋白阻断剂耐药性标志位点(S31N突变)的测定结果显示该病毒存在S31N突变,为M2蛋白阻断剂耐药型。结论:高灵敏焦测序体系结合便携式生物发光分析仪成功实现了对甲型H1N1流感病毒快速、准确的低成本检测。     

G蛋白偶联受体与G蛋白相互作用的最新研究进展

传统观念认为,在激动剂作用下,G蛋白偶联受体(GPCRs)能够激活G蛋白的α亚基,从而使Gα亚基与Gβγ亚基分离,被激活的Gα亚基通过信号转导进一步参与细胞的生理过程。但是,最新研究发现GPCRs和G蛋白存在多种偶联关系,GPCRs不仅能够激活Gα亚基,还可以与Gβγ亚基相互靠近,甚至会使G蛋白亚基构象发生重排而不分离,这对于疾病发病机制的研究及新的药物靶点的发现具有重要意义。就GPCRs与G蛋白之间的相互作用以及最新研究技术作一简要综述。     

医院感染多重耐药革兰阴性杆菌耐消毒剂基因的检测分析

目的研究医院感染多重耐药革兰阴性杆菌耐消毒剂基因qac E△1-sul1存在情况。方法采用聚合酶链反应(PCR)技术检测qac E△1-sul1基因。结果 201株多重耐药革兰阴性杆菌对阿莫西林和头孢类等抗菌药物多数耐药率均达到50%以上,但对碳青霉烯类仍高度敏感。qac E△1-sul1基因的总检出率为40.80%,其中产超广谱β-内酰胺酶(ESBLs)大肠埃希菌、产ESBLs肺炎克雷伯菌、多重耐药鲍曼不动杆菌、多重耐药的铜绿假单胞菌qac E△1-sul1检出率分别为34.78%、44.23%、58.91%和31.25%。结论医院感染患者临床分离多重耐药革兰阴性杆菌耐消毒剂基因qac E△1-sul1携带率较高,加强多重耐药革兰阴性杆菌对消毒剂耐药性的监测,对临床合理使用消毒剂具有重要意义。     

登革病毒NS3全基因的扩增与克隆

登革热(DF)、登革出血热及登革休克综合征(DHF/DSS)是由登革病毒所致的两种不同临床类型的急性传染病,广泛流行于全球热带及亚热带地区.DHF/DSS以高热、出血、休克、高病死率为主要特征,近年来其发病率有迅速增加的趋势,已成为严重影响人类健康的公共卫生问题.     

不同方式处理牛粪对大豆生长和品质的影响

大型养殖场粪便堆积造成严重的环境污染,对这类废弃物开展资源化利用研究具有重要生态学和经济学意义。以不施肥料处理(CK)为对照,研究了生态养殖场牛粪经腐熟(DD)和蚯蚓处理(RD)后对大豆生长与品质的影响。研究表明:生态养殖场牛粪经过两种处理后,在一定施用量范围(DD≤30 t/hm2,RD≤45 t/hm2)内,可显著增加大豆株高、分株数、干物质积累,促进植株生长,增加单株荚数、籽粒数、籽粒重,提高大豆产量(P<0.01)。施入腐熟牛粪30 t/hm2株高和单株结荚数比CK分别增加24.2 cm、63%;经蚯蚓处理后,可以提高牛粪施用量的上限,施入蚯蚓处理过的牛粪45 t/hm2时产量最高、单株结荚数最多,比CK分别增加72%和75%(P<0.01);施入蚯蚓处理过的牛粪15 t/hm2时,粗蛋白含量、蛋脂总量最高,比CK分别增加7%和6%(P<0.01)。本研究可为大型养殖场牛粪资源化利用提供科学依据。     

SRAP、ISSR技术的优化及在甘蓝类植物种子鉴别中的应用

将SRAP与ISSR 2种分子标记技术应用于8种甘蓝类植物（Brassica oleracea L.）的种子鉴别中。先以甘蓝（Brassica oleracea var. capitata）基因组DNA为模板,通过对SRAP、ISSR反应体系中各影响因素的逐一筛选,优化了甘蓝类植物SRAP、ISSR反应体系。进而采用30个SRAP引物组合和15个ISSR引物对白甘蓝、皱叶甘蓝、红甘蓝、羽衣甘蓝、花椰菜、青花菜、抱子甘蓝、球茎甘蓝的基因组DNA进行了PCR扩增,结果表明：M3E5与M4E5两个SRAP引物组合可以在8种甘蓝类植物之间显示较高的多态性;844和888两个ISSR引物也可在8种甘蓝类植物之间产生很好的多态,特别是844引物单独应用即可区分所有材料。     

中国森林生态资产价值评估

森林资源是支撑人类社会发展的重要生态资产,探索森林生态资产价值的评估方法,对合理利用和有效保护森林资源具有重要意义。运用净现值法计算了中国森林生态资产总价值为698.5万亿元,其中直接价值为7.5万亿元,包括林木价值4.5万亿元和林下产品价值3.0万亿元;间接价值为691万亿元,其中,气候调节价值量最高,占间接价值的48%;水源涵养价值量次之,占间接价值的27%。从森林生态资产总价值的分布来看,广西省、广东省和云南省位于全国前列,分别占森林生态资产总价值的10%、9%和9%。单位面积森林生态资产价值表现为海南省、浙江省和广东省较高,分别为954万元/hm2,915万元/hm2和888万元/hm2。森林生态资产价值研究为我国编制自然资源资产负债表提供理论依据,因此全面的估算中国森林生态资产价值很有意义。