Next Article in Journal
Transcriptional Profiling Reveals Key Regulatory Roles of the WUSCHEL-Related Homeobox Gene Family in Yellowhorn (Xanthoceras sorbifolia Bunge)
Previous Article in Journal
Predicting Individual Tree Mortality of Larix gmelinii var. Principis-rupprechtii in Temperate Forests Using Machine Learning Methods
Previous Article in Special Issue
Infestation by Ips amitinus (Eichhoff, 1872), Its Associated Fungi, and Butt Rots in Stands of Pinus sibirica in South-Western Siberia
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti

by
Roberto Faedda
1,* and
Gabriela B. Silva
2
1
Department of Agriculture, Food and Environment, University of Catania, 95123 Catania, Italy
2
Amarelo Agroflorestal Ltda., Porto Alegre 90020180, Brazil
*
Author to whom correspondence should be addressed.
Forests 2024, 15(2), 375; https://doi.org/10.3390/f15020375
Submission received: 4 January 2024 / Revised: 26 January 2024 / Accepted: 16 February 2024 / Published: 17 February 2024

Abstract

Quambalaria eucalypti is a fungal pathogen that causes leaf spot, shoot blight, and stem canker on Eucalyptus spp. Early diagnosis of the disease is difficult, although the symptoms are clear in its advanced phase. To enable a rapid and sensitive screening of asymptomatic or latently infected plant material for Q. eucalypti, a SYBR green-based real-time PCR assay targeting the partial histone-H3 region was developed. The assay demonstrated specificity for Q. eucalypti, not showing cross-reactivity with other Quambalaria species or the other eucalyptus fungal pathogens tested. The primers developed in this study ensured high analytical sensitivity, allowing the detection of Q. eucalypti DNA concentrations as low as 10 fg DNA from asymptomatic plants. The robustness and efficacy of the assay was demonstrated by interlaboratory comparisons with similar results. This newly developed quantitative PCR assay can be used for more comprehensive epidemiological investigations, testing the plant material in known Q. eucalypti distribution areas for early management strategies, or collecting data for resistance breeding programs.
Keywords: Quambalaria eucalypti; Quambalaria shoot blight; qPCR; diagnostics; molecular detection; Eucalyptus Quambalaria eucalypti; Quambalaria shoot blight; qPCR; diagnostics; molecular detection; Eucalyptus

Share and Cite

MDPI and ACS Style

Faedda, R.; Silva, G.B. Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti. Forests 2024, 15, 375. https://doi.org/10.3390/f15020375

AMA Style

Faedda R, Silva GB. Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti. Forests. 2024; 15(2):375. https://doi.org/10.3390/f15020375

Chicago/Turabian Style

Faedda, Roberto, and Gabriela B. Silva. 2024. "Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti" Forests 15, no. 2: 375. https://doi.org/10.3390/f15020375

APA Style

Faedda, R., & Silva, G. B. (2024). Development of a Real-Time PCR Assay for the Early Detection of the Eucalyptus Pathogen Quambalaria eucalypti. Forests, 15(2), 375. https://doi.org/10.3390/f15020375

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop