嗜碱放线菌生理学特性的初步研究*

对从新疆、青海采集的盐碱土样中分离获得的29株嗜碱放线菌(AlkAlipbilic actinomyeetes)及1株模式菌株Nocardiopsis prasina的pH实验,不同碱性物质KOH、K2CO3、NaOH、Na2CO3对生长的影响,及对NaCl、KCl耐受性进行了研究。结果发现,少数嗜碱放线菌对Na^ 有一定的依赖性,对K^ 碱性物质敏感;一些嗜碱放线菌对CO3^2-敏感,NaCl、KCl对一些嗜碱放线菌的生长有抑制作用;4种碱性物质对Nocardiopsis菌株生长无影响,且它们可耐受高浓度NaCl、KCl。因此提出高碱性环境中是否存在K^ 、CO3^2-专一性依赖的嗜碱放线菌的推测。     

盐胁迫下刺槐无性系生长和矿质营养平衡研究

以一年生盆栽刺槐无性系BH327和B56为材料,对盐胁迫下刺槐无性系生长和矿质营养平衡进行了研究。结果表明：盐胁迫下BH56生长受抑不明显,组织水平上K^＋、Ca^2＋、Mg^2＋保持较高水平,尤其是在高盐下上部叶片足Ca^2＋、Mg^2＋的选择性吸收增强;而BH327,的生长受盐胁迫明显的抑制,组织水平上K^＋、Ca^2＋、Mg^2-水平相对较低,在高盐下上部叶片对Ca^2-、Mg^2＋的选择性吸收能力低于BH56。同时,从体内离子分配及选择性运输角度讨论了各无性系盐伤害或耐盐的原因。     

Na+和Ca2+对拟南芥根原生质体质膜内向K+通道电流的影响

以拟南芥(Arabidopsis thaliana Columbia)根为材料,利用膜片钳技术测定其根细胞原生质体质膜内向K^ 电流,并对Na^ 对其K^ 电流的影响进行了初步研究,发现Na^2 可明显抑制拟南芥根细胞原生质体的内向K^ 电流,外施Ca^2 可缓解Na^ 对内向K^ 电流的抑制．说明Ca^2 参与了质膜上K^ 通道对K^ ／Na^ 的选择性吸收的调节,从而使植物适应盐胁迫．     

盐胁迫下氯丙嗪和LaCl3对稻苗K^＋、Na^＋、Cl^—吸收转运的影响

研究了氯丙嗪（CPZ）和LaCl3预处理阻碍Ca^2 。CaM信使系统传导后,盐胁迫下稻苗体内Na^ 、K^ 和Cl^-含量及吸收转运的变化。结果表明：CPZ和LaCl3预处理后,盐胁迫下稻苗对K^ /Na^ 的选择性吸收下降,致使稻苗K^ 含量减少、Na^ 含量增加,Na^ /K^ 比值显著增加;并且稻苗地上部Cl^-含量也显著增加,盐胁迫处理稻苗2d后解除盐胁迫,改用蒸馏水培养,在蒸馏水中加入CPZ或LaCl3时,稻苗中含有较高的Na^ ,即CPZ和LaCl3抑制稻苗将体内Na^ 排出体外的能力,上述结果表明,盐胁迫下,Ca^2 .CaM信使系统可能参与稻苗对K^ 、Na^ 和Cl^-的吸收转运以适应盐胁迫。     

罗布麻对不同浓度盐胁迫的生理响应

利用网室盆栽实验,研究不同浓度的NaCl（100-400mmol·L^-1）胁迫对罗布麻（Apocynum venetum）生长及生理特性的影响。结果表明,100mmol·L^-1NaCl处理显著降低了罗布麻植株的鲜重,但对其干重影响不大;随着盐浓度继续增加,罗布麻鲜重和干重显著下降。在盐胁迫下,罗布麻叶片内的丙二醛含量、电解质渗漏率、根部和地上部Na^＋的含量明显增加,K^＋的含量随着盐离子浓度的增加而降低。盐胁迫显著降低了地上部Ca^2＋的含量,而对根部Ca^2＋的含量没有影响。植株K^＋/Na^＋和Ca^2＋/Na^＋比值随着盐胁迫强度的增加而降低。盐胁迫显著促进了罗布麻根部对K^＋和Ca^2＋的选择性吸收及对K^＋的选择性运输。当NaCl浓度小于或等于200mmol·L^-1时,随着盐离子浓度的增加,罗布麻叶片内的脯氨酸和可溶性糖积累显著增加,而当NaCl浓度大于200mmol·L^-1时,这2种有机溶质含量显著下降。总体上,罗布麻通过积累无机离子、合成有机溶质及维持较高的K^＋、Ca^2＋选择性吸收和运输来适应一定浓度（≤200mmol·L^-1NaCl）的盐胁迫。     

盐胁迫下柚和橘幼苗体内矿质元素变化的比较研究

采用沙培法,对盐胁迫下坪山柚和福橘幼苗体内矿质元素的变化进行了研究。结果表明,随着NaCl浓度的增加,坪山柚和福橘幼苗根部及地上部Na^＋、Cl-含量增加,且相同浓度下,福橘比坪山柚高。40mmol／L NaCI胁迫下,坪山柚和福橘幼苗地上部的K^＋、Fe含量,根部的Ca^2＋、Mg^2＋、Zn含量显著下降,而根部Fe含量及地上部Zn含量显著增加。随NaCl浓度增大,坪山柚根部K^＋含量,地上部Ca^2＋、Mg^2＋含量变化不明显,而福橘根部、地上部上述离子含量在NaCl浓度≥160mmol／L时均显著下降。因此,根部K^＋含量,地上部Ca^2＋、Mg^2＋含量存在品种问差异,或许可作为耐盐性鉴定指标。NaCl胁迫降低坪山柚和福橘幼苗根部及地上部P、Mn含量,而Cu含量在较高浓度NaCl胁迫下显著增加。NaCl胁迫明显降低坪山柚和福橘幼苗地上部K^＋／Na^＋、Ca^2＋／Na^＋和Mg^2＋／Na^＋值,其中K^＋／Na^＋值的变化可考虑作为柑橘耐盐性鉴定的指标。     

盐胁迫下水稻叶绿体中Na+、Cl-积累导致叶片净光合速率下降

研究了0-200mmol/L的NaCl胁迫下耐盐性不同的水稻品种Pokkali(耐盐）和Peta(盐敏感）根系,叶片和叶绿体中Na^ ,K^ 和Cl^-含量的变化及其与叶片光合作用的关系。结果表明：随着NaCl胁迫时间和浓度的增加,供试2个品种在根,叶片和叶绿体中Na^ ,Cl^－含量增加,K^ 含量下降。耐盐品种体内Na^ ,Cl^－含量增加或K^ 含量减少的幅度小于盐敏感品种。在200mmol/L的NaCl胁迫下盐敏感品种根,叶片和叶绿体中的Na^ /K^ 分别是耐盐品种的208％,308％和297％。与Na^ 相比,耐盐品种根系对K^ 吸收和向叶片运输的选择性（SK,Na)较强。但在经过0,100和200mmol/L的NaCl处理后2个品种叶绿体中的Na^ /K^ 均高于叶片（SK,Na均小于1）。盐胁迫下水稻叶绿体中Na^ ,Cl^-含量和Na^ /K^ 与叶片净光合速度呈极显著负相关。     

盐胁迫对高羊茅(Festuca arundinacea)幼苗生长和离子分布的影响

盐胁迫环境抑制植物的生长，影响植物组织的离子分布，不同的盐分组成对植物的抑制伤害存在差异，为了研究上海市临港新城滨海盐渍土的生态恢复和重建，模拟该地区的盐分组成，进行了高羊茅（Festuca arundinacea）幼苗的盐胁迫试验。高羊茅种子在非盐胁迫条件下萌发，出苗5d后，进行了不同浓度NaCl：0、50、100、150、200、300、400mmol／L处理，15d后测定生长情况、组织含水量和Na^＋、K^＋、Ca^2＋、Mg^2＋等离子含量。研究结果表明：盐分对高羊茅幼苗的抑制作用随NaCl浓度增加而加剧，低盐胁迫环境下，幼苗地上部分和根系的鲜重、干重和含水量都与对照没有显著性差异，但是高盐环境严重影响了高羊茅幼苗的生长，而且对地上部分的抑制作用大于根部；盐胁迫影响植物组织的离子分布，Na^＋浓度持续增加，Ca^2＋和K^＋浓度下降，Mg^2＋含量的影响不大；各组织中K／Na、Ca／Na和Mg／Na随盐胁迫增加而下降。     

盐胁迫下盐地碱蓬体内无机离子含量分布特点的研究

用不同浓度NaCl溶液处理盐地碱蓬（Suaeda salsa)植株后,测定并比较老叶、幼叶及根部的无机离子含量和对K的选择性,叶片及根部的Na^ 、Cl^-含量随盐度的增加而升高,且累积趋势相似,盐胁迫下根部Na^ 、Cl^-及总离子含量（K^ 、Na^ 、Ca^2 ,NO3^-,Cl^-)明显低于叶片,说明盐地碱蓬地盐胁迫下,以叶片优先积累大量离子（如Na^ ,Cl^-) 为其适应特征。NaCl处理下,叶片的K^ ,Ca^2 含量低于对照,但随盐度的增加保持相对稳定,而根部K^ 含量,K/Na比、对K的选择性则高于叶片,这对盐胁迫下地上部的K^ 亏缺有一定补偿作用。低盐度处理（100mmol/LNaCl)促进NO3^-的吸收,另外随盐度的增加,叶片渗透势下降,渗透调节能力增强,幼叶渗透势低于老叶,但渗透调节能力相同。     

江苏野生大豆的耐盐性和离子在体内的分布及选择性运输

以相对发芽率和出苗率为指标比较了3个野生大豆(Glycine soja)种群的耐盐性,测定了NaCl胁迫下2个耐盐性不同的野生大豆种群(江苏野生大豆,JWS,耐盐;N23232,盐敏感)植株根、茎和叶片中Na^+、K^+和Cl^-含量的变化。结果表明,JWS的耐盐性最强,盐胁迫抑制野生大豆幼苗生长,使其干物质积累量减少,根冠比上升,对耐盐性弱的N23232抑制作用大于耐盐性强的JWS,不同器官离子含量测定结果表明,盐胁迫下野生大豆茎部Na^+含量最高,耐盐的JWS根系具有积累Na^+和Cl^-的能力,叶片Na^+、Cl含量较低,而盐敏感种群N23232根系中：Na^+、Cl^-含量低于耐盐种群JWS,叶片中Na^+、Cl^-含量则高于JWS,JWS根系对K^+、Na^+吸收的选择性(selectivity ratio,SK,Na)和N23232没有明显差异;但叶片和茎运输的SK,Na明显高于N23232,使地上部K^+／Na^+较高,因此认为野生大豆根系对Na^+、Cl^-的积累及K^+向地上部运输的选择性高是其耐盐性强的主要原因。     

Entwicklungsgeschichte und Ultrastruktur von Pollenkitt und Exine bei nahe verwandten entomophilen und anemophilen Angiospermensippen derAlismataceae,Liliaceae, Juncaceae,Cyperaceae, Poaceae undAraceae

Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.

     

Identification and Characterization of the First Equine Parainfluenza Virus 5

正Dear Editor,Parainfluenza virus 5 (PIV5), known as canine parainfluenza virus in the veterinary field, is a negative-sense,nonsegmented, single-stranded RNA virus belonging to the Paramyxoviridae family (Chen 2018). The virus was first reported in primary monkey kidney cells in 1954 (Hsiung1972), then it has been frequently discovered in various     

Pathogenic Characterization and Full Length Genome Sequence of a Reassortant Infectious Bursal Disease Virus Newly Isolated in Pakistan

<正>Dear Editor,Infectious bursal disease (IBD) is one of the most important diseases of the poultry. The IBD virus (IBDV), a nonenveloped virus belonging to the Birnaviridae family with a genome consisting of two segments of double-stranded RNA (segments A and B), targets B lymphocytes of bursa of Fabricious leading to immunosuppression. In Pakistan,poultry farming is the second biggest industry and IBD is the second biggest disease threating the poultry sector.However, there is limited genome information of IBDV     

Mink Circovirus Can Infect Minks,Foxes and Raccoon Dogs

正Dear Editor,Mink circovirus (MiCV), which is clustered in the genus Circovirus of the family Circoviridae, was first described in minks from farms in Dalian, China in 2013 (Lian et al.2014). The complete single-stranded circular genome of the virus is 1,753 nucleotides long and contains two major open reading frames (ORFs), designated ORF1 (Rep gene)and ORF2 (Cap gene)(Lian et al. 2014; Ge et al. 2018).Sequence analysis has shown that MiCV is most closely     

CypA Regulates AIP4-Mediated M1 Ubiquitination of Influenza A Virus

Cyclophilin A (CypA) is a peptidyl-prolyl cis/trans isomerase that interacts with the matrix protein (M1) of influenza A virus (IAV) and restricts virus replication by regulating the ubiquitin–proteasome-mediated degradation of M1. However,the mechanism by which CypA regulates M1 ubiquitination remains unknown. In this study, we reported that E3 ubiquitin ligase AIP4 promoted K48-linked ubiquitination of M1 at K102 and K104, and accelerated ubiquitin–proteasome-mediated degradation of M1. The recombinant IAV with mutant M1 (K102 R/K104 R) could not be rescued, suggesting that the ubiquitination of M1 at K102/K104 was essential for IAV replication. Furthermore, CypA inhibited AIP4-mediated M1 ubiquitination by impairing the interaction between AIP4 and M1. More importantly, both the mutations of M1 (K102 R/K104 R) and CypA inhibited the nuclear export of M1, indicating that CypA regulates the cellular localization of M1 via inhibition of AIP4-mediated M1 ubiquitination at K102 and K104, which results in the reduced replication of IAV.Collectively, our findings reveal a novel ubiquitination-based mechanism by which CypA regulates the replication of IAV.