通过比较分析黄单胞菌 III 型分泌效应器基因组发现的宿主驱动选择揭示了新型识别效应器。

IF 2.6 2区 农林科学 Q2 PLANT SCIENCES Phytopathology Pub Date : 2024-10-16 DOI:10.1094/PHYTO-04-24-0147-R
Yao Xiao, Shatrupa Ray, Saul Burdman, Doron Teper
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引用次数: 0

摘要

黄单胞菌是专门的植物病原体,通常寄主范围很窄。它们依靠通过 III 型分泌系统转运效应蛋白来定植于各自的寄主。黄单胞菌属的效应蛋白库各不相同,通常具有物种特异性。这种物种特异性效应物组成统称为效应物组,被认为会影响宿主的特化。我们测定了 300 多个与茄科或十字花科寄主相关的黄单胞菌物种基因组的植物寄主衍生效应器组。比较分析发现了明显的物种特异性效应基因组特征。但是,没有发现茄科或十字花科寄主相关的效应基因组特征。不过,在存在或不存在特定效应物类别的情况下,也观察到了宿主的偏差。为了评估宿主相关效应物的缺失是否源于选择压力,我们向野油菜黄单胞菌(Xcc)引入了茄科病原体特有的效应物,向黄单胞菌(Xeue)引入了十字花科病原体特有的效应物,并评估了这些引入是否阻碍了它们在各自宿主上的毒力。在 Xcc 中引入效应子 XopI 会降低其在白甘蓝叶片上的毒力,但不会影响局部或系统定殖。将 XopAC 或 XopJ5 效应体引入 Xeue 会降低对番茄的毒力和定殖,但不会影响对辣椒的毒力和定殖。此外,XopAC 和 XopJ5 通过 Xeue 或农杆菌介导的瞬时表达在番茄叶片上诱导超敏反应,证实了在番茄上的识别能力。这项研究证明了宿主衍生选择在建立物种特异性效应子群中的作用,确定了 XopAC 和 XopJ5 是番茄中的识别效应子。
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Host-Driven Selection, Revealed by Comparative Analysis of Xanthomonas Type III Secretion Effectoromes, Unveils Novel Recognized Effectors.

Xanthomonas species are specialized plant pathogens, often exhibiting a narrow host range. They rely on the translocation of effector proteins through the type III secretion system to colonize their respective hosts. The effector arsenal varies among Xanthomonas spp., typically displaying species-specific compositions. This species-specific effector composition, collectively termed the effectorome, is thought to influence host specialization. We determined the plant host-derived effectoromes of more than 300 deposited genomes of Xanthomonas species associated with either Solanaceae or Brassicaceae hosts. Comparative analyses revealed clear species-specific effectorome signatures. However, Solanaceae or Brassicaceae host-associated effectorome signatures were not detected. Nevertheless, host biases in the presence or absence of specific effector classes were observed. To assess whether host-associated effector absence results from selective pressures, we introduced effectors unique to Solanaceae pathogens to X. campestris pv. campestris and effectors unique to Brassicaceae pathogens to X. euvesicatoria pv. euvesicatoria (Xeue) and evaluated if these introductions hindered virulence on their respective hosts. Introducing the effector XopI into X. campestris pv. campestris reduced virulence on white cabbage leaves without affecting localized or systemic colonization. Introducing the XopAC or XopJ5 effectors into Xeue reduced virulence and colonization on tomato but not on pepper. Additionally, XopAC and XopJ5 induced a hypersensitive response on tomato leaves when delivered by Xeue or through Agrobacterium-mediated transient expression, confirming recognition in tomato. This study demonstrates the role of host-derived selection in establishing species-specific effectoromes, identifying XopAC and XopJ5 as recognized effectors in tomato.

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来源期刊
Phytopathology
Phytopathology 生物-植物科学
CiteScore
5.90
自引率
9.40%
发文量
505
审稿时长
4-8 weeks
期刊介绍: Phytopathology publishes articles on fundamental research that advances understanding of the nature of plant diseases, the agents that cause them, their spread, the losses they cause, and measures that can be used to control them. Phytopathology considers manuscripts covering all aspects of plant diseases including bacteriology, host-parasite biochemistry and cell biology, biological control, disease control and pest management, description of new pathogen species description of new pathogen species, ecology and population biology, epidemiology, disease etiology, host genetics and resistance, mycology, nematology, plant stress and abiotic disorders, postharvest pathology and mycotoxins, and virology. Papers dealing mainly with taxonomy, such as descriptions of new plant pathogen taxa are acceptable if they include plant disease research results such as pathogenicity, host range, etc. Taxonomic papers that focus on classification, identification, and nomenclature below the subspecies level may also be submitted to Phytopathology.
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