Section of Phytopathology, Department of Plant Protection, Ferdowsi University of Mashhad, Iran; Section of Microbiology, Department of Biology, University of Copenhagen, Copenhagen, Denmark.
Agricultural Research, Education and Extension Organization (AREEO), Agricultural Biotechnology Research Institute of Iran-North branch (ABRII), Rasht, Iran.
Int J Biol Macromol. 2024 Nov;281(Pt 2):136402. doi: 10.1016/j.ijbiomac.2024.136402. Epub 2024 Oct 9.
Fire blight, caused by Erwinia amylovora, is a destructive bacterial disease affecting pear and apple trees. The biocontrol ability of Pseudomonas fluorescens EK007 suppresses E. amylovora through competitive exclusion. In this study, EK007 was isolated from the pear phylloplane and characterized as an effective biological agent through antibacterial compounds. To identify the mechanisms underlying EK007's biocontrol activity, physiological tests, transposon insertion mutant libraries, allelic exchange, and whole-genome sequencing were performed. A transposon mutation in the massC homolog gene, part of the massetolide A lipopeptide biosynthesis cluster, reduced the biocontrol efficiency. Allelic exchange confirmed cyclic lipopeptide (CLP) as part of the mechanism. Additionally, a gacA mutant isolated by transposon mutagenesis showed deficient inhibition activity. Culture conditions and nutritional sources clearly influenced EK007's antimicrobial activity against E. amylovora. Growth yield generally correlated with antibiotic production, with amino acids and iron affecting production. Asparagine and aspartate shut down biocontrol activity. This study presents preliminary findings on a novel CLP that may contribute to EK007's antibacterial activity against E. amylovora. While EK007 shows promise as a biocontrol candidate compared to related strains, these results are based solely on in vitro studies, highlighting the need for further investigations to evaluate its efficacy in natural environments.
火疫病由丁香假单胞菌引起,是一种破坏性的细菌性疾病,影响梨树和苹果树。荧光假单胞菌 EK007 的生物防治能力通过竞争排斥抑制丁香假单胞菌。在这项研究中,EK007 从梨叶面上分离出来,并通过抗菌化合物被鉴定为一种有效的生物制剂。为了确定 EK007 生物防治活性的机制,进行了生理测试、转座子插入突变文库、等位基因交换和全基因组测序。在 massC 同源基因的转座子突变中,该基因是 massetolide A 脂肽生物合成簇的一部分,降低了生物防治效率。等位基因交换证实了环状脂肽 (CLP) 是该机制的一部分。此外,通过转座子诱变分离的 gacA 突变体显示出抑制活性不足。培养条件和营养来源明显影响 EK007 对丁香假单胞菌的抗菌活性。生长产量通常与抗生素的产生相关,氨基酸和铁影响生产。天冬酰胺和天冬氨酸抑制生物防治活性。本研究初步发现了一种可能有助于 EK007 对丁香假单胞菌抗菌活性的新型 CLP。虽然 EK007 与相关菌株相比作为生物防治候选物显示出前景,但这些结果仅基于体外研究,突出了需要进一步研究以评估其在自然环境中的功效。