Prasannath Kandeeparoopan, Galea Victor J, Akinsanmi Olufemi A
The University of Queensland, Queensland Alliance for Agriculture & Food Innovation, Centre for Horticultural Science, Dutton Park, QLD 4102, Australia.
The University of Queensland, School of Agriculture & Food Sciences, Gatton, QLD 4343, Australia.
Phytopathology. 2022 Oct;112(10):2151-2158. doi: 10.1094/PHYTO-08-21-0365-R. Epub 2022 Sep 19.
Dry flower disease caused by spp., green mold caused by spp., and gray mold caused by spp., collectively known as flower blight cause significant yield losses in macadamia. Potential sources of inoculum of the various pathogens in macadamia tree canopy were examined using pathogenicity tests and a multiplex quantitative PCR (qPCR) assay developed in this study. The qPCR assay detected and quantified the relative abundance of the inoculum of flower blight pathogens. The assay revealed that remnant racemes contributed a high amount of inoculum of all the three groups of flower blight pathogens, while the yellow halo leaf spot contributed only species. The amount of conidia per gram of remnant racemes ranged from 7 × 10 to 2 × 10 for dry flower disease, 3 × 10 to 1 × 10 for green mold, and 5 to 8 × 10 for gray mold pathogens. Conidia of species quantified from leaf spots varied from 1 × 10 to 1 × 10 per cm. Pathogenicity tests performed on developing racemes under field conditions, using conidial suspensions from both sources of inoculum (remnant racemes and yellow halo leaf spot), resulted in severe flower bight symptoms. Disease severity was not significantly different ( > 0.05) when remnant racemes were incubated directly with the developing racemes compared with inoculation with conidial suspension from the material. This suggests that racemes from preceding seasons that remain in the tree canopy carryover inoculum between seasons and should be removed as a control option for flower blights in macadamia orchards.
由……属引起的干花病、由……属引起的绿霉病和由……属引起的灰霉病,统称为花疫病,会给澳洲坚果造成重大产量损失。本研究通过致病性测试和开发的多重定量聚合酶链反应(qPCR)分析,检测了澳洲坚果树冠中各种病原体的潜在接种源。qPCR分析检测并量化了花疫病病原体接种体的相对丰度。该分析表明,残留总状花序是所有三组花疫病病原体接种体的大量来源,而黄晕叶斑仅产生……属的接种体。每克残留总状花序的分生孢子数量,干花病为7×10至2×10,绿霉病为3×10至1×10,灰霉病病原体为5至8×10。从叶斑中量化的……属分生孢子数量为每平方厘米1×10至1×10。在田间条件下,对发育中的总状花序进行致病性测试,使用来自两种接种源(残留总状花序和黄晕叶斑)的分生孢子悬浮液,均导致严重的花疫病症状。与用来自该材料的分生孢子悬浮液接种相比,将残留总状花序直接与发育中的总状花序一起培养时,病害严重程度无显著差异(P>0.05)。这表明,前一季留在树冠中的总状花序会在季节间携带接种体,应将其去除作为澳洲坚果果园花疫病的一种防治措施。