Harley V R, Hudson P J, Coupar B E, Selleck P W, Westbury H, Boyle D B
St. Vincent's Institute of Medical Research, Fitzroy, Australia.
Arch Virol. 1990;113(1-2):133-41. doi: 10.1007/BF01318362.
The nucleoprotein (NP) gene from avian influenza strain A/Shearwater/Aust/1/72 (H6N5) was cloned, sequenced, and expressed in vaccinia virus for the production of potent sera in immunised rabbits. The NP gene is 1565 bp and shares greater than 95% amino acid sequence identity with other NPs of the avian subtype. The recombinant NP expressed by vaccinia virus comigrated with endogenous A/Shearwater/Aust/1/72 NP by Western blot analysis. Polyclonal rabbit sera raised against recombinant NP was evaluated in an antigen capture ELISA system as a potential diagnostic tool for the detection of avian influenza. All type A strains, comprising several HA and NA subtypes, but not type B nor other avian viruses, were detected.
克隆、测序了来自禽流感病毒A/Shearwater/Aust/1/72(H6N5)株的核蛋白(NP)基因,并在痘苗病毒中表达,以在免疫兔中产生高效价血清。NP基因长度为1565 bp,与禽亚型的其他NP具有大于95%的氨基酸序列同一性。通过蛋白质印迹分析,痘苗病毒表达的重组NP与内源性A/Shearwater/Aust/1/72 NP迁移情况相同。在抗原捕获ELISA系统中评估了针对重组NP产生的兔多克隆血清作为检测禽流感的潜在诊断工具。检测到了所有A型毒株,包括几种HA和NA亚型,但未检测到B型毒株或其他禽病毒。