鵝細小病毒 的英文怎麼說

中文拼音 [éxiǎobìng]
鵝細小病毒 英文
goose parvovirus
  • : 名詞goose
  • : 形容詞1 (條狀物橫剖面小) thin; slender 2 (顆粒小) in small particles; fine 3 (音量小) thin ...
  • : Ⅰ形容詞1 (體積、面積、數量、強度等不大) small; little; petty; minor 2 (年紀小的; 年幼的) youn...
  • : Ⅰ名詞1 (疾病; 失去健康的狀態) illness; sickness; disease; malum; nosema; malady; morbus; vitium...
  • : Ⅰ名詞1 (對生物體有害的性質或物質; 毒物) poison; toxin 2 (毒品) drug; narcotics 3 (姓氏) a s...
  • 細小 : very small; tiny; trivial; micr-; micro-; -ling
  • 病毒 : [醫學] virus; inframicrobe (濾過性)
  1. Goose parvovirus ( gpv ) is the pathogen of goslings plague

    鵝細小病毒( gooseparvovirus , gpv )為瘟的原體。
  2. Goose provirus ( gpv ) is the pathogen of highly contagious and fatal infectious diseases of goslings and muscovy ducklings

    鵝細小病毒( gooseprovirus , gpv )可引起雛、雛番鴨高度致死性傳染?瘟。
  3. Goose parvovirus is the causitive agent of goose plague. which is also named as derzsy ' s disease. it is one of highly fatal diseases of goslings and muscovy ducklings

    鵝細小病毒( gooseparvovirus , gpv )主要引起雛、雛番鴨的高致死性疾,稱為瘟或derzsy ' s
  4. The pathogen of goose plaque, goose parvovirus ( gpv ), can cause acute infectious disease characterized by acute intestitis and inflammation of liver, kidney and heart in goslings and muscovy duckings under 1 month of age, which threaten the goose industry

    鵝細小病毒( gooseparvovirus , gpv )為瘟的原體。瘟主要發生於1月齡內雛和雛番鴨,是以急性腸炎及肝、腎、心實質臟器炎癥為特徵的烈性傳染,對養業發展造成很大威脅。
  5. Gpv ( goose parvovrius ) has been classified by its morphological, biochemical, and clut - ure characteristics as a member of the parvovirus genus of the parvoviridae. lt is a highly fatal disease of gos1ings and muscovy ducklings, the typical pathological lesions was found in digest tract, specially in small intestine

    Gpv ( gooseparvovirus )依據其形態、生化及培養特性被劃歸為屬成員,引起雛和雛番鴨高度致死性疾,主要以消化道,尤其是腸部位的典型變為特徵。
  6. In this study, the recombinant fowl - poxvirus was transfected into expressing the vp3 gene of isolated gpv h1 strain into the cef cells with fpv - 017 by liposome, which have the lacz reporter gene, earlier / latter promoters lp2ep2 of fpv, promoters p7. 5 and p7. 1 of vaccinia virus, replication unnecessary region of fpv - 017. following 6 cycles screenings, clonings, purification of blue plaques, detection of pcr and dot - elisa, which verified the genetic stable vp3 - fowlpox virus recombinant constructed successfully. this study provided the theoretical and practical foundation for development of gpv recombinant fowl - poxvirus genetic engineering vaccine, as well as provided substance preparatory for prevention the high mortality gpv

    本研究採用脂質體轉染方法,將含有完整gpvh1分離株vp3基因、報告基因lacz 、禽痘早晚期啟動子lp2ep2 、痘苗啟動子p7 . 5 、 p11和fpv - 017復制非必須區的轉移載體質粒psy681vp3lacz與fpv - 017共轉染雞胚成纖維胞,經6輪蝕斑克隆、篩選、表達, pcr鑒定和dot - elisa檢測,證明該重組已構建成功,並獲得了遺傳性狀穩定的鵝細小病毒vp3基因的重組禽痘
  7. This study provides the basis evidence for the research of nucleotide sequence evolution relationship between domestic and exterior countries. it also establishes foundation for further research about developing gpv molecular diagnostic reagent and genetic engineering vaccine

    本研究為了解國內外鵝細小病毒核苷酸序列演化上的關系,為開發研製新型分子診斷試劑和抗鵝細小病毒感染的基因工程疫苗提供了理論依據。
  8. Vp2 is one of viral structural proteins on the surface of provirus. its neutralizing antigenicity has been proved. in this study

    Vp2是鵝細小病毒結構蛋白之一,是gpv的重要保護性抗原,在體內誘導的抗體具有中和作用。
  9. The recombinant plasmid was identit1ed with restriction endonuclease, pcr, then sequenced. the resuit of sequence analysis showed that the vp3 gene is 1605bp and inc1uds a complete open reading frame encoding a protein of 534 amino acids. the hl isolate shares 98. 5 % and 98. 3 % identity with b isolate at nucieotide and amino acid levels respectively

    結果表明:鵝細小病毒h1分離株vp3基因全長1605bp ,編碼534個氨基酸,只有一個完整的開放閱讀框架,與國外已發表的鵝細小病毒b株核苷酸序列同源性為98 . 5 ,氨基酸序列同源性為98 . 3 ,表明這二個株親緣關系相近。
  10. The close genetic relationship of goose parvoviruse and aav allows the examination of the molecular biological properties of the nonstructural proteins of gpv. after the gpv infected the cell the viral life cycle was regulated by the nonstructural proteins encoded by the virus. according to the published of gpv b strain genome nucleotide sequences in genbank and a pair of specific primers were disigned with oligo4. 1

    本研究根據genbank發表的gpvb株全基因序列,藉助oligo4 . 1軟體設計一對引物,採用pcr技術擴增gpvh1株非結構蛋白ns2基因,並與pmd18 - t載體連接后測序,結果表明:鵝細小病毒h1株ns2基因核苷酸全長1356bp ,編碼451個氨基酸殘基,與gpvb株的ns2基因相比,核苷酸數目相同,有17個堿基、 6個氨基酸的差異;同源性分析表明:二者核苷酸序列同源性為98 . 75 ,推導氨基酸序列同源性為98 . 67 。
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