Key Laboratory of South China Agricultural Plant Molecular Analysis and Genetic Improvement, Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, 510650, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
BMC Plant Biol. 2020 Jul 3;20(1):313. doi: 10.1186/s12870-020-02524-y.
Bacterial blight of rice, caused by Xanthomonas oryzae pv. oryzae (Xoo), is a devastating rice disease in Southeast Asia and West Africa. OsSWEET14, encoding a sugar transporter, is known to be a major susceptible gene of bacterial blight targeted by four different transcription activator-like (TAL) effectors from either Asian or African Xoo strains. However, the OsSWEET14 single knockout or promoter mutants in the Kitaake background are moderately resistant or even susceptible to African Xoo strains. Therefore, in this study, we knocked out OsSWEET14 in rice cv. Zhonghua 11 background for disease assessment.
In this study, CRISPR/Cas9 was utilized to disrupt the function of OsSWEET14 by modifying its corresponding coding region in the genome of rice cv. Zhonghua 11 (CR-S14). In total, we obtained nine different OsSWEET14-mutant alleles. Besides conferring broad-spectrum resistance to Asian Xoo strains, tested mutant alleles also showed strong resistance to African Xoo strain AXO1947. Moreover, the expression of OsSWEET14 was detected in vascular tissues, including the stem, leaf sheath, leaf blade and root. The disruption of OsSWEET14 led to increased plant height without a reduction in yield.
Disruption of OsSWEET14 in the Zhonghua 11 background is able to confer strong resistance to African Xoo strain AXO1947 and Asian Xoo strain PXO86. CR-S14 has normal reproductive growth and enhanced plant height under normal growth conditions. These results imply that CR-S14 may serve as a better tester line than sweet14 single-knockout mutant in the Kitaake background for the diagnostic kit for rice blight resistance. The genetic background and increased plant height need to be taken into consideration when utilizing OsSWEET14 for resistant rice breeding.
稻细菌性条斑病由稻黄单胞菌稻致病变种(Xoo)引起,是东南亚和西非地区破坏性极大的水稻病害。蔗糖转运蛋白 OsSWEET14 是已知的细菌性条斑病主要感病基因,受来自亚洲或非洲 Xoo 菌株的四个不同转录激活因子样(TAL)效应物靶向。然而,Kitaake 背景下 OsSWEET14 的单敲除或启动子突变体对非洲 Xoo 菌株表现为中度抗性甚至易感性。因此,在本研究中,我们在水稻品种 Zhonghua 11 背景下敲除 OsSWEET14 以进行病害评估。
本研究利用 CRISPR/Cas9 技术通过修饰水稻 cv. Zhonghua 11 基因组中 OsSWEET14 的相应编码区来破坏其功能(CR-S14)。共获得了九个不同的 OsSWEET14 突变等位基因。除了赋予对亚洲 Xoo 菌株的广谱抗性外,测试的突变等位基因还对非洲 Xoo 菌株 AXO1947 表现出强烈的抗性。此外,在包括茎、叶鞘、叶片和根在内的维管束组织中检测到 OsSWEET14 的表达。OsSWEET14 的破坏导致株高增加而不降低产量。
在 Zhonghua 11 背景下敲除 OsSWEET14 能够赋予对非洲 Xoo 菌株 AXO1947 和亚洲 Xoo 菌株 PXO86 的强抗性。CR-S14 在正常生长条件下具有正常的生殖生长和增加的株高。这些结果表明,与 Kitaake 背景下的 sweet14 单敲除突变体相比,CR-S14 可能成为水稻条斑病抗性诊断试剂盒的更好测试系。在利用 OsSWEET14 进行抗性水稻育种时,需要考虑遗传背景和增加的株高。