Serra P, Gago S, Duran-Vila N
Centro de Protección Vegetal y Biotecnología, Instituto Valenciano de Investigaciones Agrarias, Apartado Oficial, 46113 Moncada, Valencia, Spain.
Virus Res. 2008 Dec;138(1-2):130-4. doi: 10.1016/j.virusres.2008.08.003. Epub 2008 Sep 26.
Cachexia disease of citrus is caused by Hop stunt viroid (HSVd). In citrus, pathogenic and non-pathogenic strains differ by a "cachexia expression motif" of five to six nucleotides located in the variable domain of the proposed rod-like secondary structure. Here, site-directed mutants were generated to investigate if all these nucleotides were required for infectivity and/or symptom expression. Specifically an artificial cachexia inducing mutant M0 was generated by introducing the six nucleotides changes of the "cachexia expression motif" into a non-pathogenic sequence variant and M0 was used as a template to systematically restore some of the introduced changes. The resulting mutants in which specific changes introduced to generate M0, were restored presented a variety of responses: (i) M1, obtained by introducing two insertions forming a base-pair, was infectious but non-pathogenic; (ii) M2, obtained by introducing an insertion and restoring a substitution, presented low infectivity and the resulting progeny reverted to M0; (iii) M3, obtained by restoring a single substitution in the lower strand of the viroid secondary structure, was infectious but induced only mild cachexia symptoms; (iv) M4, obtained by restoring a single substitution in the upper strand of the viroid secondary structure, was non-infectious. These results confirm that the "cachexia expression motif" plays a major role in inciting cachexia symptoms, and that subtle changes within this motif affect symptom severity and may even suppress symptom expression.
柑橘的衰退病是由柑橘速衰类病毒(HSVd)引起的。在柑橘中,致病菌株和非致病菌株的区别在于,在所提出的棒状二级结构可变区中一个由五到六个核苷酸组成的“衰退病表达基序”。在此,通过定点突变来研究是否所有这些核苷酸对于感染性和/或症状表达都是必需的。具体而言,通过将“衰退病表达基序”的六个核苷酸变化引入一个非致病序列变体中,构建了一个人工衰退病诱导突变体M0,并将M0用作模板来系统地恢复一些引入的变化。对因恢复了为构建M0而引入的特定变化所产生的突变体进行研究,得到了多种反应:(i)通过引入两个形成碱基对的插入而获得的M1具有感染性但无致病性;(ii)通过引入一个插入并恢复一个替换而获得的M2具有低感染性,其产生的子代又回复为M0;(iii)通过恢复类病毒二级结构下链中的一个单一替换而获得的M3具有感染性,但仅诱导轻度的衰退病症状;(iv)通过恢复类病毒二级结构上链中的一个单一替换而获得的M4无感染性。这些结果证实,“衰退病表达基序”在引发衰退病症状方面起主要作用,并且该基序内的细微变化会影响症状严重程度,甚至可能抑制症状表达。