Jackson R W, Mansfield J W, Arnold D L, Sesma A, Paynter C D, Murillo J, Taylor J D, Vivian A
Centre for Research in Plant Science, Faculty of Applied Sciences, University of the West of England, Coldharbour Lane, Bristol BS16 1QY, UK.
Mol Microbiol. 2000 Oct;38(2):186-97. doi: 10.1046/j.1365-2958.2000.02133.x.
Pseudomonas syringae pv. phaseolicola (Pph) race 4 strain 1302A carries avirulence gene avrPphB. Strain RJ3, a sectoral variant from a 1302A culture, exhibited an extended host range in cultivars of bean and soybean resulting from the absence of avrPphB from the RJ3 chromosome. Complementation of RJ3 with avrPphB restored the race 4 phenotype. Both strains showed similar in planta growth in susceptible bean cultivars. Analysis of RJ3 indicated loss of > 40 kb of DNA surrounding avrPphB. Collinearity of the two genomes was determined for the left and right junctions of the deleted avrPphB region; the left junction is approximately 19 kb and the right junction > 20 kb from avrPphB in 1302A. Sequencing revealed that the region containing avrPphB was inserted into a tRNALYS gene, which was re-formed at the right junction in strain 1302A. A putative lysine tRNA pseudogene (PsitRNALYS) was found at the left junction of the insertion. All tRNA genes were in identical orientation in the chromosome. Genes near the left junction exhibited predicted protein homologies with gene products associated with a virulence locus of the periodontal pathogen Actinobacillus actinomycetemcomitans. Specific oligonucleotide primers that differentiate 1302A from RJ3 were designed and used to demonstrate that avrPphB was located in different regions of the chromosome in other strains of Pph. Deletion of a large region of the chromosome containing an avirulence gene represents a new route to race change in Pph.
丁香假单胞菌菜豆致病变种(Pph)4号小种1302A菌株携带无毒基因avrPphB。RJ3菌株是1302A培养物的一个扇形变体,由于RJ3染色体上不存在avrPphB,其在菜豆和大豆品种中表现出扩大的寄主范围。用avrPphB对RJ3进行互补恢复了4号小种的表型。两种菌株在感病菜豆品种中的体内生长情况相似。对RJ3的分析表明,avrPphB周围有超过40 kb的DNA缺失。确定了缺失的avrPphB区域左右连接处两个基因组的共线性;在1302A中,左连接处距avrPphB约19 kb,右连接处距avrPphB大于20 kb。测序显示,含有avrPphB的区域插入到一个tRNALYS基因中,该基因在1302A菌株的右连接处重新形成。在插入的左连接处发现了一个假定的赖氨酸tRNA假基因(PsitRNALYS)。所有tRNA基因在染色体上的方向相同。左连接处附近的基因与牙周病原体伴放线放线杆菌毒力位点相关的基因产物表现出预测的蛋白质同源性。设计了区分1302A和RJ3的特异性寡核苷酸引物,并用于证明avrPphB位于其他Pph菌株染色体的不同区域。包含无毒基因的染色体大片段缺失代表了Pph小种变化的一条新途径。