中国农业科学 ›› 2026, Vol. 59 ›› Issue (5): 996-1007.doi: 10.3864/j.issn.0578-1752.2026.05.006

• 植物保护 • 上一篇    下一篇

解淀粉欧文氏菌新质粒pEA60通过调节毒力因子的合成增强菌株的致病力

董钰(), 吴千, 冯萱, 郑银英, 崔百明()   

  1. 石河子大学生命科学学院,新疆石河子 832003
  • 收稿日期:2025-11-10 接受日期:2025-12-21 出版日期:2026-03-01 发布日期:2026-03-06
  • 通信作者:
    崔百明,E-mail:
  • 联系方式: 董钰,E-mail:dongyu2589@163.com。
  • 基金资助:
    兵团科技攻关计划(2023AB004-03)

A Novel Plasmid pEA60 of Erwinia amylovora Enhances the Pathogenicity of Strains by Regulating the Synthesis of Virulence Factors

DONG Yu(), WU Qian, FENG Xuan, ZHENG YinYing, CUI BaiMing()   

  1. College of Life Sciences, Shihezi University, Shihezi 832003, Xinjiang
  • Received:2025-11-10 Accepted:2025-12-21 Published:2026-03-01 Online:2026-03-06

摘要:

【背景】 火疫病严重威胁新疆库尔勒香梨产业发展,其病原菌解淀粉欧文氏菌(Erwinia amylovora)常携带多样化的质粒,是导致菌株表型(如致病力、抗生素抗性)差异的关键。近期,从解淀粉欧文氏菌的新疆库尔勒香梨分离株Ea102中鉴定出一个新质粒pEA60。【目的】 探究解淀粉欧文氏菌pEA60质粒的起源、功能及其对病原菌致病力的影响。【方法】 采用PacBio和Illumina进行解淀粉欧文氏菌Ea102基因组测序,利用SPAdes进行基因组组装,通过PAGP等工具进行功能注释,使用BLASTN比较基因组,MLST分类质粒;利用质粒不相容性鉴定其复制区,并构建pEA60质粒消除突变体;利用接合转移试验评估其自主转移能力。在功能验证方面,通过胞外多糖定量测定以及香梨未成熟果实和离体枝条试验,系统评估该质粒对菌株致病力的影响。【结果】 pEA60是可接合转移的质粒,大小为61 198 bp,共有65个预测的CDS,主要涉及复制与稳定、菌毛形成及接合转移三大功能模块。未鉴定到已知的抗生素耐药性基因或毒力相关基因。比较分析结果表明,pEA60的菌毛形成和接合转移功能区与解淀粉欧文氏菌质粒pEA68高度相似(平均核苷酸一致性为97.04%),而其质粒复制和稳定性的区域与蚜虫欧文氏菌(Erwinia aphidicola)质粒p1B06c相似,提示pEA60起源于某个重组事件。pEA60属IncFII型质粒,其包含复制蛋白基因和复制起始点的2 610 bp片段足以维持质粒生存。pEA60质粒影响解淀粉欧文氏菌胞外多糖的合成和病原菌的致病力,消除pEA60质粒导致菌株的梨火疫病菌素含量和果聚糖蔗糖合成酶活性下降,纤维素含量增加,在香梨枝条和未成熟果实上引发的病症减轻。【结论】 pEA60是一种新的解淀粉欧文氏菌质粒,属IncFII型质粒,具有接合转移能力;pEA60影响解淀粉欧文氏菌胞外多糖的合成,提高宿主菌的致病力。研究结果可为深入解析解淀粉欧文氏菌的致病机制及质粒介导的毒力进化提供新线索。

关键词: 解淀粉欧文氏菌, 库尔勒香梨, 火疫病, pEA60质粒, 胞外多糖, 致病力

Abstract:

【Background】 Fire blight poses a serious threat to the development of the Korla fragrant pear industry in Xinjiang. Its pathogen, Erwinia amylovora, often carries diverse plasmids, which are key factors leading to phenotypic differences among strains, such as pathogenicity and antibiotic resistance. Recently, a novel plasmid pEA60 was identified from the E. amylovora strain Ea102 which was isolated from Xinjiang Korla fragrant pear.【Objective】 The objective of this study is to investigate the origin, function of E. amylovora plasmid pEA60 and its impact on pathogenicity of the pathogen.【Method】 The genome of Ea102 was sequenced using PacBio and Illumina and assembled with SPAdes. Functional annotation was performed using tools such as PAGP, while BLASTN was used for comparative genomic analysis, and MLST for plasmid typing. The replication region was identified using plasmid incompatibility, and a pEA60-cured mutant was constructed. Conjugation experiments were conducted to assess its self-transfer capability. In terms of functional verification, the effect of the plasmid on bacterial pathogenicity was systematically evaluated by quantitative determination of exopolysaccharide production and immature fruit and in vitro shoots test of pear.【Result】 pEA60 is a conjugative plasmid with a size of 61 198 bp, containing 65 predicted CDSs primarily involved in three functional modules: replication and stability, pilus formation, and conjugation. No known antibiotic resistance genes or virulence-related genes were identified. Comparative analysis revealed that the pilus formation and conjugation functional regions of pEA60 are highly similar to those of the E. amylovora plasmid pEA68 (average nucleotide identity: 97.04%), while its replication and stability regions resemble those of the Erwinia aphidicola plasmid p1B06c, suggesting that pEA60 likely originated from a recombination event. pEA60 is an IncFII-type plasmid, and its 2 610 bp fragment harboring the replication protein gene and the origin of replication is sufficient to maintain plasmid viability. The plasmid influenced exopolysaccharide synthesis and pathogenicity in E. amylovora. Curing of pEA60 resulted in reduced amylovoran production and levansucrase activity, increased cellulose production, and attenuated symptoms on both pear shoots and immature fruits.【Conclusion】 pEA60 is a novel, conjugative IncFII plasmid in E. amylovora. It affects exopolysaccharide synthesis and enhances the pathogenicity of its host strain. This study provides new insights into the pathogenic mechanisms of E. amylovora and plasmid-mediated evolution of virulence.

Key words: Erwinia amylovora, Korla fragrant pear, fire blight, pEA60 plasmid, exopolysaccharide, pathogenicity