Yang Bing, Sugio Akiko, White Frank F
Department of Plant Pathology, Kansas State University, Manhattan, KS 66502, USA.
Mol Plant Microbe Interact. 2005 Feb;18(2):142-9. doi: 10.1094/MPMI-18-0142.
avrXa7 is a member of the avrBs3/pthA gene family. The gene is a critical type III effector in several strains of Xanthomonas oryzae pv. oryzae (virulence activity), and in the presence of the Xa7 host gene for resistance, controls the elicitation of resistance in rice (avirulence activity). The ability of strains containing avrXa7 to adapt to the presence of Xa7 in the host population is dependent, in part, on the genetic plasticity of avrXa7. The potential for the conversion of avrXa7 to a virulence effector without Xa7-dependent elicitor activity was examined. Internal reorganization of avrXa7 by artificially deleting a portion of the central repetitive region resulted in gene pthXo4, which retained virulence activity and lost Xa7-dependent avirulence activity. Similarly, spontaneous rearrangements between repetitive regions of avrXa7 during bacterial culture gave rise to gene pthXo5, which also had virulence activity without Xa7-dependent avirulence activity. pthXo5 appeared to be the result of recombination between avrXa7 and a related gene in the genome. Loss of avirulence activity and retention of virulence activity also resulted from replacement of a portion of the C-terminal coding region of avrXa7 with the corresponding sequence from avrBs3. The results demonstrated the potential for a critical virulence effector to lose avirulence activity while retaining effector function. The results also demonstrated that features of both repetitive and nonrepetitive C-terminal regions of AvrXa7 are involved in avirulence specificity.
avrXa7是avrBs3/pthA基因家族的成员。该基因是水稻白叶枯病菌(致病活性)多个菌株中的关键III型效应子,在存在抗性宿主基因Xa7的情况下,控制水稻中的抗性诱导(无毒活性)。含有avrXa7的菌株适应宿主群体中Xa7存在的能力部分取决于avrXa7的遗传可塑性。研究了avrXa7转化为无Xa7依赖性激发子活性的致病效应子的可能性。通过人工删除中央重复区域的一部分对avrXa7进行内部重组,产生了基因pthXo4,该基因保留了致病活性并丧失了Xa7依赖性无毒活性。同样,在细菌培养过程中,avrXa7重复区域之间的自发重排产生了基因pthXo5,该基因也具有致病活性且无Xa7依赖性无毒活性。pthXo5似乎是avrXa7与基因组中一个相关基因之间重组的结果。用avrBs3的相应序列替换avrXa7 C末端编码区域的一部分也导致无毒活性丧失和致病活性保留。结果表明,关键致病效应子有可能在保留效应子功能的同时丧失无毒活性。结果还表明,AvrXa7重复和非重复C末端区域的特征都参与无毒特异性。