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nosema apis
相关语句
  蜜蜂微孢子
     The inhibition of EM on germination of Nosema apis in vitro was very strong,and the higher the concentration of EM the better effect of the inhibition.
     第四部分探索了EM对蜜蜂微孢子体外发芽抑制作用,试验证明EM对蜜蜂微孢子体外发芽有较强的抑制的作用,浓度越高,抑制效果越好。
短句来源
     Inhibition of Microbial Ecological Agents on Germination of Nosema apis in Vitro
     微生态制剂EM对蜜蜂微孢子体外发芽抑制实验
短句来源
  “nosema apis”译为未确定词的双语例句
     (2)The spore from A. c. cerena was 4.68±0.60×2.19±0.35μm,significantly shorter and slimmer than spore of Nosema apis from A.
     (2)来自中蜂的微孢子虫孢子大小为(4.68±0.60×2.19±0.35)μm,很可能就是中蜂微孢子虫;
短句来源
     Changes in content of hemolymph protein in the honeybee (Apis mellifera L.) workers infected by Nosema apis and Varroa destructor respectively
     微孢子虫和狄斯瓦螨分别侵染后的意蜂血淋巴蛋白质含量变化
短句来源
     The honey bee worker's hemolymph protein was investigaged in the situation of Nosema apis infection or Varroa destructor infection. Newly emerged worker honeybees were fed Nosema spores for 21 days running.
     利用自制微孢子虫(Nosema apis)悬液(5.5×10~7个孢子/毫升)与50%的白糖水1:1混合,以每次20毫升剂量对幼年健康意蜂(Apis mellifera)进行感染,每日一次,连续21次,制作动态病理模型。
短句来源
     The ITS region (internal transcribed spacer), positioned between the ssu and LSUrRNA genes,was found to be 41bp in length. The LSUrDNA 580r region of MPr is 470bp,longer than 437bp of Nosema apis, 447bp of Nosema algerae.
     与SSUrRNA基因核心序列拼接后SSUrRNA全基因长为 1 2 4 5bp ,rRNA基因内转录间隔区为 41bp及核糖体大亚单位RNA(LSUr RNA)编码基因 580R区为 470bp。
短句来源
     The changes in content of hemolymph protein in the honeybee (Apis mellifera L.) workers infected by spores of Nosema apis and the mite Varroa destructor (Acari: Varroidae) respectively were assayed.
     微孢子虫Nosemaapis和狄斯瓦螨Varroadestructor (Acari:Varroidae)均为危害意蜂Apismellifera的重要寄生虫 ,该文对其危害后意蜂血淋巴蛋白质含量的变化进行了研究。
短句来源
  相似匹配句对
     apis.
     apis有差异。
短句来源
     apis.
     apis属于不同种类。
短句来源
     Inhibition of Microbial Ecological Agents on Germination of Nosema apis in Vitro
     微生态制剂EM对蜜蜂微孢子体外发芽抑制实验
短句来源
     Changes in content of hemolymph protein in the honeybee (Apis mellifera L.) workers infected by Nosema apis and Varroa destructor respectively
     微孢子虫和狄斯瓦螨分别侵染后的意蜂血淋巴蛋白质含量变化
短句来源
     IMAGEANALYSIS FOR NOSEMA BOMBYCIS MICROSPORIDIA
     家蚕微粒子病病原图象分析
短句来源
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  nosema apis
Nosema apis (Microsporidia) und die Aminos?uren der Honigbiene (Apis mellifica L.)
      
Endoplasmic reticulum is the most prominent cytoplasmic organelle in the developing stages of Nosema apis.
      
Fine structure of the developing spore of Nosema apis zander
      
Ultrastructural changes in Nosema apis in the midgut of the honeybee treated with thimerosal in vitro
      
Neue Erkenntnisse über die Biologie des Bienenparasiten Nosema apis (Zander)
      
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It is indicated that chimozine is relative to the forming of peritrophic membrane (PMb) and the den-sity of PMb determined whether Nosema Apis Zander can inject in the ventriculus epithelium. The vitality of chimozine was measured using Apis mellifera ligustica,which shows that the vitality of chimozine is relative negatively to the rate of Nosema disease and changes with seasons.

蜜蜂中肠酪素酶与蜜蜂中肠围食膜的形成有关,而围食膜的致密度又决定了蜜蜂微孢子虫能否侵入蜜蜂中肠上皮细胞。取蜜蜂中肠测定其酪素酶的活力,得知对意大利蜂而言,酶的活力越高,孢子虫病发病率越低;反之,则发病率高,且酶活力随季节变化。

Nuclotide sequence (1205bp) of small subunit ribosomal RNA (SSUrDNA) of a microsporidium isolated from Pieris rapae L.(abbr:MPr) was specifically amplified by polymerase chain reaction (PCR).Another fragment of 657bp downstream of MPr SSUrDNA 3′end was amplified with two other primers.Within this 657bp fragment,the putative 3′terminus of MPr SSUrDNA and the extreme 5′ of large subunit ribosomal RNA gene (LSUrDNA) were identified,which situated at base 145,146~186 and 187,respectively.Then the full sequence...

Nuclotide sequence (1205bp) of small subunit ribosomal RNA (SSUrDNA) of a microsporidium isolated from Pieris rapae L.(abbr:MPr) was specifically amplified by polymerase chain reaction (PCR).Another fragment of 657bp downstream of MPr SSUrDNA 3′end was amplified with two other primers.Within this 657bp fragment,the putative 3′terminus of MPr SSUrDNA and the extreme 5′ of large subunit ribosomal RNA gene (LSUrDNA) were identified,which situated at base 145,146~186 and 187,respectively.Then the full sequence of MPr ssurDNA is 1245bp.Its GC content was also nearly 34%.The ITS region (internal transcribed spacer), positioned between the ssu and LSUrRNA genes,was found to be 41bp in length.The LSUrDNA 580r region of MPr is 470bp,longer than 437bp of Nosema apis, 447bp of Nosema algerae. The secondary structure of MPr SSUrRNA was constructed.These analyses of MPr rRNA gene contributed to the somewhat limited microsporidian taxonomic classification based on morphology.

用PCR方法扩增、克隆了菜粉蝶微孢子虫核糖体小亚单位RNA(SSUrRNA)编码基因的核心序列 1 2 0 5bp后 ,进一步克隆到菜粉蝶微孢子虫SSUrRNA基因 3′端至LSUrRNA基因 5′端 (580R区 ) 657bp长的序列。与GenBank中对应序列比较后 ,在 657bp这段序列鉴定出菜粉蝶微孢子虫SSUrRNA基因 3′末端、rRNA基因内转录间隔区 (ITS)及LSUrRNA基因 5′端 (580R区 ) ,它们分别位于该序列中 1 45位、1 46 1 86位及 1 87位。与SSUrRNA基因核心序列拼接后SSUrRNA全基因长为 1 2 4 5bp ,rRNA基因内转录间隔区为 41bp及核糖体大亚单位RNA(LSUr RNA)编码基因 580R区为 470bp。同时还构建了菜粉蝶微孢子虫SSUrRNA的完整二级结构。关于微孢子虫rRNA基因的克隆及SSUrRNA的二级结构在国内尚属首次报道 ,它为进一步利用核糖体RNA编码基因及SSUrRNA的二级结构对不同微孢子虫的分类及亲缘关系的确定奠定了基础

The changes in content of hemolymph protein in the honeybee (Apis mellifera L.) workers infected by spores of Nosema apis and the mite Varroa destructor (Acari: Varroidae) respectively were assayed. The content of hemolymph protein was detected using Bradford method. The component difference of hemolymph proteins between the healthy (CK) and the infected bees were analyzed using high voltage isoelectric focusing electrophoresis (IEF). The results showed that the content of hemolymph protein of the...

The changes in content of hemolymph protein in the honeybee (Apis mellifera L.) workers infected by spores of Nosema apis and the mite Varroa destructor (Acari: Varroidae) respectively were assayed. The content of hemolymph protein was detected using Bradford method. The component difference of hemolymph proteins between the healthy (CK) and the infected bees were analyzed using high voltage isoelectric focusing electrophoresis (IEF). The results showed that the content of hemolymph protein of the bees tended to rise progressively within 10 days after being infected by Nosema spores, and then decreased gradually, till reaching a level below the content before being infected in 12-27 days after infection. The content of hemolymph protein of the bees infected by V. destructor was significantly higher than that of the control, and the components of hemolymph proteins were also different between the healthy and infected bees as indicated by IEF results. The results suggested the honey bees developed immunological reaction in some degree to N. apis or V. destructor after their infection.

微孢子虫Nosemaapis和狄斯瓦螨Varroadestructor (Acari:Varroidae)均为危害意蜂Apismellifera的重要寄生虫 ,该文对其危害后意蜂血淋巴蛋白质含量的变化进行了研究。用考马斯亮蓝法测定了意蜂受侵染后血淋巴的蛋白质总量 ,并用高压超薄层等电点聚焦法进行血淋巴蛋白质分类。结果显示 ,病蜂血淋巴蛋白质总量 ,在人工感染微孢子虫后 1~ 10天呈上升趋势 ,然后逐渐下降 ,感染后 12~ 2 7天保持在感染前意蜂血淋巴总蛋白质含量水平以下。螨侵染后意蜂血淋巴蛋白质含量明显增高 ,与健康意蜂相比差异极显著。高压超薄层等电点聚焦分析表明 :狄斯瓦螨自然侵染意蜂后 ,意蜂血淋巴蛋白质组分与健康对照组相比发生了明显改变。这些结果提示 ,意蜂对于微孢子虫或狄斯瓦螨的侵染产生了一定的免疫反应

 
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