Phytopathology. 2005 Sep;95(9):1037-42. doi: 10.1094/PHYTO-95-1037.
ABSTRACT A strain of Bean common mosaic necrosis virus (BCMNV) from Idaho was identified by enzyme-linked immunosorbent assay using monoclonal antibodies and determined to be similar to the NL-3 D strain (of Drifjhout) by reaction of differential bean cultivars. However, this BCMNV strain (designated NL-3 K) caused earlier and more severe symptoms on bean plants representing host groups 0, 4, and 5. The nucleotide sequence encoding the predicted polyprotein of NL-3 K was 9,893 nucleotides (nt) in length, yielding a peptide with a molecular size of 362.1 kDa compared with a 9,626-nt, 350.9-kDa polyprotein for NL-3 D. Sequence analysis of the putative P1 protein suggests that the NL-3 K strain is a recombinant between NL-3 D and the Russian strain (RU1) of Bean common mosaic virus. The P1 protein of NL-3 K consisted of 415 amino acids compared with 317 for NL-3 D. The first 114 predicted amino acids of the NL-3 K P1 region were 98% identical with RU1. The remaining 301 amino acids of the protein shared only 34% identity with RU1 but were 98% identical with NL-3 D. Primers were designed that flanked the recombination point in the P1 coding sequence of NL-3 K. An amplicon of the expected size was produced by reverse-transcriptase polymerase chain reaction of total nucleic acid extracts of bean plants inoculated with NL-3 K, but not from those with NL-3 D or RU1. The increased symptom severity on selected common bean lines induced by NL-3 K suggests that the P1 gene may play a significant role in pathogenicity and virulence.
摘要 一种从爱达荷州分离的菜豆普通花叶坏死病毒(BCMNV),通过单克隆抗体酶联免疫吸附试验鉴定,并通过差异菜豆品种的反应确定与 NL-3 D 株(来自 Drifjhout)相似。然而,这种 BCMNV 株(命名为 NL-3 K)在代表寄主组 0、4 和 5 的菜豆植物上引起更早和更严重的症状。NL-3 K 的预测多蛋白的核苷酸序列长 9893 个核苷酸(nt),与 NL-3 D 的 9626-nt、350.9-kDa 多蛋白相比,产生一个 362.1kDa 的肽。对假定的 P1 蛋白的序列分析表明,NL-3 K 株是 NL-3 D 和俄罗斯株(RU1)菜豆花叶病毒之间的重组体。NL-3 K 的 P1 蛋白由 415 个氨基酸组成,而 NL-3 D 由 317 个氨基酸组成。NL-3 K P1 区的前 114 个预测氨基酸与 RU1 有 98%的同一性。该蛋白的其余 301 个氨基酸与 RU1 只有 34%的同一性,但与 NL-3 D 有 98%的同一性。设计了引物,它们侧翼包围 NL-3 K P1 编码序列中的重组点。用 NL-3 K 接种的菜豆总核酸提取物进行逆转录-聚合酶链反应,产生了预期大小的扩增子,但 NL-3 D 或 RU1 则没有。NL-3 K 对选定的普通菜豆品系引起的症状严重程度增加表明,P1 基因可能在致病性和毒力方面发挥重要作用。