Hao Guixia, Zhang Hongsheng, Zheng Desen, Burr Thomas J
Department of Plant Pathology, NYSAES, Cornell University, Geneva, NY 14456, USA.
J Bacteriol. 2005 Jan;187(1):185-92. doi: 10.1128/JB.187.1.185-192.2005.
The luxR homolog aviR in Agrobacterium vitis strain F2/5 was recently shown to be associated with induction of a hypersensitive response (HR) on tobacco and necrosis on grape plants, indicating that the responses are regulated by quorum sensing. We now report a second luxR homolog, avhR, whose disruption (mutant M1320) results in HR-negative and reduced grape necrosis phenotypes. The deduced AvhR protein has characteristic autoinducer binding and DNA binding domains and is unique among reported functional LuxR homologs in having substitutions at highly conserved Asp70, Trp57, and Trp85 residues, which are predicted to play important roles in autoinducer binding in TraR. M1320 was fully complemented with cloned avhR. The same array of N-acylhomoserine lactones (AHL) from F2/5, M1320, and complemented M1320 were observed; however, the signal strength from extracts of 6-day-old M1320 cultures was stronger than that of F2/5. Cultures of F2/5 amended with AHL extracts from overnight and 6-day cultures of F2/5 and M1320 were not affected in ability to cause HR or necrosis. A region of about 14 kb flanking avhR was sequenced and compared with homologous regions of A. tumefaciens C58 and Sinorhizobium meliloti Rm1021 genomes. Gene order and homology are conserved between the species. A site-directed mutation in a putative gene that resides downstream of avhR and that has homology to genes belonging to the ATP-binding cassette transporter family did not affect HR or necrosis phenotypes. It was determined that avhR and aviR are expressed independently and that neither regulates the expression of a clpA homolog in F2/5.
最近研究表明,葡萄土壤杆菌F2/5菌株中的luxR同源基因aviR与烟草上的过敏反应(HR)诱导以及葡萄植株上的坏死有关,这表明这些反应受群体感应调节。我们现在报道第二个luxR同源基因avhR,其缺失(突变体M1320)导致HR阴性和葡萄坏死表型减弱。推导的AvhR蛋白具有特征性的自诱导物结合和DNA结合结构域,在已报道的功能性LuxR同源物中是独特的,其在高度保守的Asp70、Trp57和Trp85残基处有替换,预计这些残基在TraR的自诱导物结合中起重要作用。M1320用克隆的avhR完全互补。观察到来自F2/5、M1320和互补M1320的相同系列的N-酰基高丝氨酸内酯(AHL);然而,6日龄M1320培养物提取物的信号强度比F2/5的更强。用来自F2/5和M1320过夜及6日培养物的AHL提取物处理的F2/5培养物,其引起HR或坏死的能力没有受到影响。对avhR侧翼约14 kb的区域进行了测序,并与根癌土壤杆菌C58和苜蓿中华根瘤菌Rm1021基因组的同源区域进行了比较。物种间的基因顺序和同源性是保守的。位于avhR下游且与ATP结合盒转运蛋白家族基因同源的一个假定基因中的定点突变不影响HR或坏死表型。已确定avhR和aviR独立表达,且二者均不调节F2/5中clpA同源物的表达。