Eight novel diagnostic markers differentiate lineages of the highly invasive myrtle rust pathogen Austropuccinia psidii.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Zhenyan Luo, Jinghang Feng, Austin Bird, Mareike Moeller, Rita Tam, Luc Shepherd, Lydia Murphy, Lavi Singh, Abigail Graetz, Lilian Amorim, Nelson Sidnei Massola Júnior, M Asaduzzaman Prodhan, Louise S Shuey, Douglas Beattie, Alejandro Trujillo Gonzalez, Peri Tobias, Amanda Padovan, Rohan Benjamin Essex Kimber, A R McTaggart, Monica Kehoe, Benjamin Schwessinger, Thais Regina Boufleur
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引用次数: 0

Abstract

Austropuccinia psidii is the causal agent of myrtle rust in over 480 species within the family Myrtaceae. Lineages of A. psidii are structured by their hosts in the native range, and some have success in infecting newly encountered hosts. For example, the pandemic biotype has spread beyond South America, and proliferation of other lineages is an additional risk to biodiversity and industries. Efforts to manage A. psidii incursions, including lineage differentiation, relies on variable microsatellite markers. Testing these markers is time-consuming, complex, and requires reference material that is not always readily available. We designed a novel diagnostic approach targeting eight selectively chosen loci including the fungal mating-type HD (homeodomain) transcription factor locus. The HD locus (bW1/2-HD1 and bE1/2-HD2) is highly polymorphic, facilitating clear biological predictions about its inheritance from founding populations. To be considered as potentially derived from the same lineage, all four HD alleles must be identical. If all four HD alleles are identical six additional markers can further differentiate lineage identity. Our lineage diagnostics relies on PCR amplification of eight loci in different genotypes of A. psidii followed by amplicon sequencing using Oxford Nanopore Technologies (ONT) and comparative analysis. The lineage-specific assay was validated on four isolates with existing genomes, uncharacterized isolates, and directly from infected leaf material. We reconstructed alleles from amplicons and confirmed their sequence identity relative to their reference. Genealogies of alleles confirmed the variations at the loci among lineages/isolates. Our study establishes a robust diagnostic tool for differentiating known lineages of A. psidii based on biological predictions and available nucleotide sequences. This tool is suited to detecting the origin of new pathogen incursions.

八种新型诊断标记可区分高侵染性桃金娘锈病病原体Austropuccinia psidii的品系。
桃金娘锈菌(Austropuccinia psidii)是桃金娘科 480 多个物种桃金娘锈病的病原菌。A.psidii的品系由其在原产地的寄主构成,有些品系能成功感染新遇到的寄主。例如,大流行生物型已扩散到南美洲以外,其他品系的扩散对生物多样性和产业造成了额外的风险。管理 A. psidii 入侵(包括品系区分)的工作依赖于可变的微卫星标记。对这些标记进行测试既费时又复杂,而且需要参考材料,而这些材料并不总能轻易获得。我们设计了一种新的诊断方法,针对八个选择性位点,包括真菌交配型 HD(homeodomain)转录因子位点。HD 基因座(bW1/2-HD1 和 bE1/2-HD2)具有高度多态性,有助于从生物学角度明确预测其在原生种群中的遗传性。要想被视为可能来自同一血统,所有四个 HD 等位基因必须完全相同。如果所有四个 HD 等位基因都相同,则六个附加标记可进一步区分血统身份。我们的品系诊断依赖于对不同基因型 A. psidii 的八个位点进行 PCR 扩增,然后使用牛津纳米孔技术(ONT)进行扩增片段测序和比较分析。我们在四个已有基因组的分离株、未定性的分离株以及直接从感染叶片材料中提取的分离株上验证了该品系特异性检测方法。我们从扩增子中重建了等位基因,并确认了它们相对于参照物的序列同一性。等位基因谱系证实了不同品系/分离株之间基因位点的变异。我们的研究为根据生物学预测和现有核苷酸序列区分 A. psidii 的已知品系提供了一种可靠的诊断工具。该工具适用于检测新病原体入侵的起源。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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