Eight Novel Diagnostic Markers Differentiate Lineages of the Highly Invasive Myrtle Rust Pathogen <i>Austropuccinia psidii</i>

<i>Austropuccinia psidii</i> is the causal agent of myrtle rust in more than 480 species within the family Myrtaceae. Lineages of <i>A. psidii</i> 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 <i>A. psidii</i> incursions, including lineage differentiation, rely on variable microsatellite markers. Testing these markers is time-consuming and 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 <i>HD</i> (homeodomain) transcription factor locus. The <i>HD</i> locus (<i>bW1/2-HD1</i> and <i>bE1/2-HD2)</i> 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 <i>HD</i> alleles must be identical. If all four <i>HD</i> 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 <i>A. psidii</i> followed by amplicon sequencing using Oxford Nanopore Technologies and comparative analysis. The lineage-specific assay was validated on four isolates with existing genomes, on 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 <i>A. psidii</i> based on biological predictions and available nucleotide sequences. This tool is suited to detecting the origin of new pathogen incursions.

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Publication Details

Journal
Plant Disease
Published
2024-10-17
DOI
https://doi.org/10.1094/pdis-10-24-2111-sr
Citations
3
Primary Topic
Yeasts and Rust Fungi Studies
Type
article
Field-Weighted Citation Impact
0.70
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article

Eight Novel Diagnostic Markers Differentiate Lineages of the Highly Invasive Myrtle Rust Pathogen Austropuccinia psidii

Peri A. Tobias, Amanda Padovan, Mareike Moeller, Thaís Regina Boufleur et al.
3 citations
Plant Disease
Yeasts and Rust Fungi Studies
0.70
article

Eight Novel Diagnostic Markers Differentiate Lineages of the Highly Invasive Myrtle Rust Pathogen Austropuccinia psidii

Peri A. Tobias, Amanda Padovan, Mareike Moeller, Thaís Regina Boufleur, Rita Tam, Rohan B. E. Kimber, Nelson Sidnei Massola Júnior, Alejandro Trujillo González, Abigail Graetz, M. Asaduzzaman Prodhan, Monica Kehoe, Zhenyan Luo, Louise S. Shuey, Benjamin Schwessinger, Lydia Murphy, Alistair R. McTaggart, Douglas Beattie, Lílian Amorim, Jinghang Feng, Austin Bird, Luc Shepherd, Lavi Singh
article en
3 citations

Abstract

<i>Austropuccinia psidii</i> is the causal agent of myrtle rust in more than 480 species within the family Myrtaceae. Lineages of <i>A. psidii</i> 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 <i>A. psidii</i> incursions, including lineage differentiation, rely on variable microsatellite markers. Testing these markers is time-consuming and 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 <i>HD</i> (homeodomain) transcription factor locus. The <i>HD</i> locus (<i>bW1/2-HD1</i> and <i>bE1/2-HD2)</i> 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 <i>HD</i> alleles must be identical. If all four <i>HD</i> 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 <i>A. psidii</i> followed by amplicon sequencing using Oxford Nanopore Technologies and comparative analysis. The lineage-specific assay was validated on four isolates with existing genomes, on 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 <i>A. psidii</i> based on biological predictions and available nucleotide sequences. This tool is suited to detecting the origin of new pathogen incursions.

Plant DiseaseVol. 109(4)
Australian National University (AU), The University of Sydney (AU), The University of Queensland (AU), Universidade de São Paulo (BR), University of Canberra (AU), South Australian Research and Development Institute (AU), Australian Government (AU), Department of Health and Aged Care (AU), Department of Primary Industries and Regional Development (AU), Agriculture and Food (AU), CSIRO Health and Biosecurity (AU), ARC Centre of Excellence for Plant Success in Nature and Agriculture (AU), Department of Primary Industries (AU), ACT Government (AU)
Life in Land
Openalex Percentile: Top 29%
Yeasts and Rust Fungi Studies
0.70
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