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解淀粉欧文氏菌argD基因的突变导致精氨酸营养缺陷型、对苹果无致病性以及对梨的毒力降低。

Mutation of the Erwinia amylovora argD gene causes arginine auxotrophy, nonpathogenicity in apples, and reduced virulence in pears.

作者信息

Ramos Laura S, Lehman Brian L, Peter Kari A, McNellis Timothy W

机构信息

Department of Plant Pathology and Environmental Microbiology, The Pennsylvania State University, University Park, Pennsylvania, USA Graduate Degree Program in Plant Pathology, Department of Plant Pathology and Environmental Microbiology, The Pennsylvania State University, University Park, Pennsylvania, USA.

The Pennsylvania State University Fruit Research and Extension Center, Biglerville, Pennsylvania, USA.

出版信息

Appl Environ Microbiol. 2014 Nov;80(21):6739-49. doi: 10.1128/AEM.02404-14. Epub 2014 Aug 29.

Abstract

Fire blight is caused by Erwinia amylovora and is the most destructive bacterial disease of apples and pears worldwide. In this study, we found that E. amylovora argD(1000)::Tn5, an argD Tn5 transposon mutant that has the Tn5 transposon inserted after nucleotide 999 in the argD gene-coding region, was an arginine auxotroph that did not cause fire blight in apple and had reduced virulence in immature pear fruits. The E. amylovora argD gene encodes a predicted N-acetylornithine aminotransferase enzyme, which is involved in the production of the amino acid arginine. A plasmid-borne copy of the wild-type argD gene complemented both the nonpathogenic and the arginine auxotrophic phenotypes of the argD(1000)::Tn5 mutant. However, even when mixed with virulent E. amylovora cells and inoculated onto immature apple fruit, the argD(1000)::Tn5 mutant still failed to grow, while the virulent strain grew and caused disease. Furthermore, the pCR2.1-argD complementation plasmid was stably maintained in the argD(1000)::Tn5 mutant growing in host tissues without any antibiotic selection. Therefore, the pCR2.1-argD complementation plasmid could be useful for the expression of genes, markers, and reporters in E. amylovora growing in planta, without concern about losing the plasmid over time. The ArgD protein cannot be considered an E. amylovora virulence factor because the argD(1000)::Tn5 mutant was auxotrophic and had a primary metabolism defect. Nevertheless, these results are informative about the parasitic nature of the fire blight disease interaction, since they indicate that E. amylovora cannot obtain sufficient arginine from apple and pear fruit tissues or from apple vegetative tissues, either at the beginning of the infection process or after the infection has progressed to an advanced state.

摘要

火疫病由解淀粉欧文氏菌引起,是全球苹果和梨最具毁灭性的细菌性病害。在本研究中,我们发现解淀粉欧文氏菌argD(1000)::Tn5(一种argD Tn5转座子突变体,其Tn5转座子插入在argD基因编码区第999位核苷酸之后)是一种精氨酸营养缺陷型菌株,在苹果上不引发火疫病,且在未成熟梨果实中的毒力降低。解淀粉欧文氏菌argD基因编码一种预测的N - 乙酰鸟氨酸转氨酶,该酶参与氨基酸精氨酸的合成。野生型argD基因的质粒携带拷贝互补了argD(1000)::Tn5突变体的非致病性和精氨酸营养缺陷型表型。然而,即使与有毒力的解淀粉欧文氏菌细胞混合并接种到未成熟苹果果实上,argD(1000)::Tn5突变体仍无法生长,而有毒力的菌株则生长并引发病害。此外,pCR2.1 - argD互补质粒在宿主组织中生长的argD(1000)::Tn5突变体中能稳定维持,无需任何抗生素选择。因此,pCR2.1 - argD互补质粒可用于在植物体内生长的解淀粉欧文氏菌中表达基因、标记物和报告基因,而无需担心随时间丢失质粒。ArgD蛋白不能被视为解淀粉欧文氏菌的毒力因子,因为argD(1000)::Tn5突变体是营养缺陷型且存在初级代谢缺陷。尽管如此,这些结果为火疫病病害相互作用的寄生性质提供了信息,因为它们表明解淀粉欧文氏菌在感染过程开始时或感染进展到晚期后,无法从苹果和梨果实组织或苹果营养组织中获取足够的精氨酸。

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