Sequence Analysis of the Full‐Length Cloned DNA of a Chicken Anaemia Virus (CAV) Strain from Bangladesh: Evidence for Genetic Grouping of CAV Strains Based on the Deduced VP1 Amino Acid Sequences

生物 放大器 传染性法氏囊病 氨基酸 拉伤 病毒 遗传学 病毒学 基因组 核酸序列 全基因组测序 谱系(遗传) 序列分析 DNA测序 遗传分析 肽序列 DNA 基因 聚合酶链反应 毒力 解剖
作者
MR Islam,Reimar Johne,R. Raue,D. Todd,H. Müller
出处
期刊:Journal of Veterinary Medicine Series B-infectious Diseases and Veterinary Public Health [Wiley]
卷期号:49 (7): 332-337 被引量:57
标识
DOI:10.1046/j.1439-0450.2002.00581.x
摘要

Summary Chicken anaemia virus (CAV) was detected in the bursa of Fabricius of a 4‐week‐old chicken obtained from an outbreak of acute infectious bursal disease in Bangladesh. Repeated attempts to grow this virus in MDCC‐MSB1 cells were not successful. A full‐length PCR amplicon of the genome of this strain, designated as BD‐3 CAV, was cloned and sequenced. The complete nucleotide sequence and the deduced amino acid sequence were compared with those of 12 other CAV strains. The genetic analysis of the amino acid sequences of VP1 indicated the possible existence of genetic groups among CAV strains, as BD‐3 CAV along with four other strains (CIA‐1, L‐028, Isolate 704 and TR‐20) formed a distinct lineage. These strains have four signatory amino acids in VP1, such as 75 I/T, 97 L, 139 Q and 144 Q, out of which the latter two are located in a small hydrophilic peak.
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