LIU Xin, LIU Sheng-wang, KONG Xian-gang, ZHANG Qing-xia, RONG Jun-gong, HAN Zong-xi and SHAO Yu-hao. Characterization of Spike Gene of Infectious Bronchitis Coronavirus CK/CH/ LDL97Ⅰ/97 Isolated in China[J]. Virologica Sinica, 2006, 21(1): 68-70.
Citation: LIU Xin, LIU Sheng-wang, KONG Xian-gang, ZHANG Qing-xia, RONG Jun-gong, HAN Zong-xi, SHAO Yu-hao. Characterization of Spike Gene of Infectious Bronchitis Coronavirus CK/CH/ LDL97Ⅰ/97 Isolated in China .VIROLOGICA SINICA, 2006, 21(1) : 68-70.

鸡传染性支气管炎病毒CK/CH/LDL97Ⅰ/97株S基因特征

  • 通讯作者: 刘胜旺, 

Characterization of Spike Gene of Infectious Bronchitis Coronavirus CK/CH/ LDL97Ⅰ/97 Isolated in China

  • Corresponding author: LIU Sheng-wang, 
  • The spike gene (S) of Infectious bronchitis virus (IBV) CK/CH/LDL97Ⅰ/97 isolate was amplified,cloned, sequenced and analyzed. Results showed that the S gene was 3501 bp encoding a polypeptide of 1167 amino acids. The precursor of the S protein was cleaved into S1 and S2 fragments, which comprised 541 and 626 amino acid residues, respectively. The cleavage site sequence was RRTGR. The homologies of nucleotide and amino acid sequences of S1 gene between CK/CH/LDL97Ⅰ/97 and 27 reference IBV strains ranged from 60.6% to 99.6%, and 50.5% to 99.1%, respectively. The CK/CH/LDL97Ⅰ/97 S1 was most similar to that of three proventriculus IBV isolates, Q1(99.1%), J2(98.9%), T3 (98.9%), which were isolated in China. Phylogenetic analysis of S1 proteins indicated that CK/CH/LDL97Ⅰ/97, Q1, J2 and T3 formed a separated cluster, which might belong to a novel genotype of IBV.

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    Characterization of Spike Gene of Infectious Bronchitis Coronavirus CK/CH/ LDL97Ⅰ/97 Isolated in China

      Corresponding author: LIU Sheng-wang,
    • 1. 1. National Key Laboratory of Veterinary Biotechnology, Institute of Harbin Veterinary Medicine, CAAS, Harbin 150001, China
    • 2. College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China

    Abstract: The spike gene (S) of Infectious bronchitis virus (IBV) CK/CH/LDL97Ⅰ/97 isolate was amplified,cloned, sequenced and analyzed. Results showed that the S gene was 3501 bp encoding a polypeptide of 1167 amino acids. The precursor of the S protein was cleaved into S1 and S2 fragments, which comprised 541 and 626 amino acid residues, respectively. The cleavage site sequence was RRTGR. The homologies of nucleotide and amino acid sequences of S1 gene between CK/CH/LDL97Ⅰ/97 and 27 reference IBV strains ranged from 60.6% to 99.6%, and 50.5% to 99.1%, respectively. The CK/CH/LDL97Ⅰ/97 S1 was most similar to that of three proventriculus IBV isolates, Q1(99.1%), J2(98.9%), T3 (98.9%), which were isolated in China. Phylogenetic analysis of S1 proteins indicated that CK/CH/LDL97Ⅰ/97, Q1, J2 and T3 formed a separated cluster, which might belong to a novel genotype of IBV.

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