Key Laboratory for Northern Urban Agriculture of Ministry of Agriculture and Rural Affairs, Beijing University of Agriculture, Beijing, 102206, China.
State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing, China.
Appl Microbiol Biotechnol. 2020 Nov;104(21):9251-9265. doi: 10.1007/s00253-020-10915-2. Epub 2020 Sep 24.
Bacillus cereus 905, one of the plant growth-promoting rhizobacteria (PGPRs), is capable of colonizing wheat roots in a large population size. From previous studies, we learned that the sodA2-encoding manganese-containing superoxide dismutase (MnSOD2) is important for B. cereus 905 to survive in wheat rhizosphere. In this investigation, we demonstrated that deletion of the recA gene, which codes for the recombinase A, significantly reduced MnSOD2 expression at both the mRNA and the protein levels. Through comparison with the wild-type, the ∆recA showed a dramatic decrease in cell survival after exposure to 50 μM paraquat or 15 mM HO. Evidence indicated that the recA gene of B. cereus 905 also notably regulated nutrition utilization efficiency, biofilm formation, and swarming motility. The root colonization examination showed that the ∆recA had a 1000- to 2500-fold reduction in colonization on wheat roots, suggesting that RecA plays an indispensable role in effective colonization on wheat roots by B. cereus 905. Taken together, the recA gene positively regulates MnSOD2 production and nutrition utilization and protects B. cereus 905 cells against paraquat and HO. Besides, biofilm formation and swarming motility of B. cereus 905 are promoted by RecA. Finally, RecA significantly contributes to wheat root colonization of B. cereus 905. Our results showed the important role of RecA during physiological processes in B. cereus 905, especially for colonization on wheat roots. Our findings will point out a research direction to study the colonization mechanisms of B. cereus 905 in the future and provide potential effective strategy to enhance the biocontrol efficacy of PGPR strains. KEY POINTS : • RecA plays an indispensable role in root colonization of B. cereus.
蜡状芽孢杆菌 905 是一种植物促生根际细菌(PGPR),能够在小麦根系中大量定殖。从先前的研究中,我们了解到 sodA2 编码的锰结合超氧化物歧化酶(MnSOD2)对蜡状芽孢杆菌 905 在小麦根际中存活至关重要。在这项研究中,我们证明了删除编码重组酶 A 的 recA 基因会显著降低 MnSOD2 在 mRNA 和蛋白质水平上的表达。与野生型相比,ΔrecA 在暴露于 50 μM 百草枯或 15 mM HO 后,细胞存活率明显下降。有证据表明,蜡状芽孢杆菌 905 的 recA 基因还显著调节营养利用效率、生物膜形成和群集运动。根定植试验表明,ΔrecA 在小麦根上的定植减少了 1000 至 2500 倍,这表明 RecA 在蜡状芽孢杆菌 905 有效定植于小麦根上发挥了不可或缺的作用。总的来说,recA 基因正向调节 MnSOD2 的产生和营养利用,并保护蜡状芽孢杆菌 905 细胞免受百草枯和 HO 的侵害。此外,RecA 促进了蜡状芽孢杆菌 905 的生物膜形成和群集运动。最后,RecA 显著促进了蜡状芽孢杆菌 905 对小麦根的定殖。我们的结果表明,RecA 在蜡状芽孢杆菌 905 的生理过程中起着重要作用,特别是在小麦根定殖方面。我们的发现将为未来研究蜡状芽孢杆菌 905 的定植机制指明一个研究方向,并为提高 PGPR 菌株的生物防治效果提供潜在的有效策略。要点:• RecA 在蜡状芽孢杆菌的根定植中起着不可或缺的作用。