Ou Kangmiao, He Xiangyi, Cai Ke, Zhao Weirong, Jiang Xiaoxun, Ai Wenfeng, Ding Yue, Cao Yuanyuan
School of Life Sciences, Anhui Agricultural University, Hefei, China.
Anhui Province Key Laboratory of Farmland Ecological Conservation and Pollution Prevention, Anhui Agricultural University, Hefei, China.
Front Microbiol. 2022 Jun 30;13:927889. doi: 10.3389/fmicb.2022.927889. eCollection 2022.
Rhizosphere colonization is a pre-requisite for the favorable application of plant growth-promoting rhizobacteria (PGPR). Exchange and mutual recognition of signaling molecules occur frequently between plants and microbes. Here, the luciferase AB gene was electrotransformed into the phosphate-solubilizing strain sp. WS32, a type of plant growth-promoting rhizobacterium with specific affinity for wheat. A labeled WS32 strain (WS32-L) was applied to determine the temporal and spatial traits of colonization within the wheat rhizosphere using rhizoboxes experimentation under natural condition. The effects of colonization on wheat root development and seedling growth were evaluated, and RNA sequencing (RNA-seq) was performed to explore the transcriptional changes that occur in wheat roots under WS32 colonization. The results showed that WS32-L could survive in the wheat rhizosphere for long periods and could expand into new zones following wheat root extension. Significant increases in seedling fresh and dry weight, root fresh and dry weight, root surface area, number of root tips, and phosphorus accumulation in the wheat leaves occurred in response to WS32 rhizosphere colonization. RNA-seq analysis showed that a total of 1485 genes in wheat roots were differentially expressed between the inoculated conditions and the uninoculated conditions. Most of the transcriptional changes occurred for genes annotated to the following functional categories: "phosphorus and other nutrient transport," "hormone metabolism and organic acid secretion," "flavonoid signal recognition," "membrane transport," and "transcription factor regulation." These results are therefore valuable to future studies focused on the molecular mechanisms underlying the growth-promoting activities of PGPR on their host plants.
根际定殖是促进植物生长的根际细菌(PGPR)良好应用的先决条件。植物和微生物之间频繁发生信号分子的交换和相互识别。在此,将荧光素酶AB基因电转化到解磷菌株sp. WS32中,WS32是一种对小麦具有特异性亲和力的促进植物生长的根际细菌。使用标记的WS32菌株(WS32-L),通过根箱试验在自然条件下确定其在小麦根际定殖的时空特性。评估了定殖对小麦根系发育和幼苗生长的影响,并进行了RNA测序(RNA-seq)以探索WS32定殖下小麦根中发生的转录变化。结果表明,WS32-L能够在小麦根际长期存活,并能随着小麦根的延伸扩展到新的区域。响应于WS32根际定殖,小麦幼苗的鲜重和干重、根的鲜重和干重、根表面积、根尖数量以及小麦叶片中的磷积累均显著增加。RNA-seq分析表明,接种条件和未接种条件下小麦根中共有1485个基因差异表达。大多数转录变化发生在注释为以下功能类别的基因上:“磷和其他养分转运”、“激素代谢和有机酸分泌”、“类黄酮信号识别”、“膜转运”和“转录因子调控”。因此,这些结果对于未来关注PGPR对其寄主植物促生长活性分子机制的研究具有重要价值。