Vernon Jacobs, Francois Halleen Elodie Stempien, Lizel Mostert
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The qPCR primers were specific for <i>D. seriata</i> (Cq ≤ 35 and Tm = 85<span>\\(\\:\\pm\\:\\)</span>0.17 °C) when compared with DNA from nineteen other fungal taxa associated with canker or wood rot of apple trees tested, excluding <i>Botryosphaeria dothidea</i> (Cq = 38 and Tm = 85.25 °C). The qPCR assay was sensitive and had a limit of quantification of 2859 fg/µl and limit of detection of 571 fg/µl. Wood chips were collected at two time periods (from heaps and 6 months after it was spread in tree rows) in three apple orchards in the Western Cape of South Africa. DNA was extracted from water-washes of 120 wood piece samples and <i>D</i>. <i>seriata</i> was detected from 101 of these samples. This study showed that the newly developed primers was able to successfully detect <i>D. seriata</i> from mulched apple wood. The presence of <i>D. seriata</i> on apple tree wood chips indicates that there is a risk involved in using wood chips made from old apple trees.</p></div>","PeriodicalId":8598,"journal":{"name":"Australasian Plant Pathology","volume":"53 5","pages":"413 - 418"},"PeriodicalIF":0.9000,"publicationDate":"2024-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s13313-024-00991-7.pdf","citationCount":"0","resultStr":"{\"title\":\"Development of a qPCR assay to detect Diplodia seriata on chipped apple wood\",\"authors\":\"Vernon Jacobs, Francois Halleen Elodie Stempien, Lizel Mostert\",\"doi\":\"10.1007/s13313-024-00991-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In the deciduous fruit industry, orchards are often excavated and trees chipped. The organic material is then used as mulch for soil conservation, a practice that form part of sustainable agricultural. The presence and possible transmission of plant pathogens are not considered when trees are removed, chipped and used for mulch. Young apple trees can develop cankers due to <i>Diplodia seriata</i> of which the inoculum source might come from fruiting structures present on apple wood mulch. Therefore, the presence of <i>D. seriata</i>, on chipped apple tree wood pieces used for mulch in younger orchards was investigated. To be able to detect <i>D. seriata</i>, qPCR primers were designed from a previously identified unique sequence characterised amplified region (SCAR). The qPCR primers were specific for <i>D. seriata</i> (Cq ≤ 35 and Tm = 85<span>\\\\(\\\\:\\\\pm\\\\:\\\\)</span>0.17 °C) when compared with DNA from nineteen other fungal taxa associated with canker or wood rot of apple trees tested, excluding <i>Botryosphaeria dothidea</i> (Cq = 38 and Tm = 85.25 °C). The qPCR assay was sensitive and had a limit of quantification of 2859 fg/µl and limit of detection of 571 fg/µl. 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引用次数: 0
摘要
在落叶水果业中,果园经常被挖掘,树木被切碎。然后将有机物用作土壤保持的覆盖物,这种做法是可持续农业的一部分。在移除树木、切碎并用作覆盖物时,并没有考虑到植物病原体的存在和可能的传播。苹果幼树可能会因 D. seriata 而产生溃疡,其接种源可能来自苹果木覆盖物上的果实结构。因此,我们调查了幼年果园中用于覆盖物的削片苹果树木片上是否存在 D. seriata。为了检测 D. seriata,我们根据之前确定的独特序列特征扩增区域 (SCAR) 设计了 qPCR 引物。与测试的与苹果树腐烂病或木腐病相关的 19 个其他真菌类群的 DNA 相比,qPCR 引物对 D. seriata 具有特异性(Cq ≤ 35,Tm = 85\(\:\:\)0.17 °C),但不包括 Botryosphaeria dothidea(Cq = 38,Tm = 85.25 °C)。qPCR 检测灵敏度高,定量限为 2859 fg/µl,检测限为 571 fg/µl。在南非西开普省的三个苹果园收集了两个时期的木屑(从堆中收集和在树行中铺开 6 个月后)。从 120 个木片样本的水洗液中提取了 DNA,并从其中 101 个样本中检测到了 D. seriata。这项研究表明,新开发的引物能够成功地从覆膜苹果木材中检测出 D. seriata。苹果树木片上出现 D. seriata 表明,使用由老苹果树制成的木片存在风险。
Development of a qPCR assay to detect Diplodia seriata on chipped apple wood
In the deciduous fruit industry, orchards are often excavated and trees chipped. The organic material is then used as mulch for soil conservation, a practice that form part of sustainable agricultural. The presence and possible transmission of plant pathogens are not considered when trees are removed, chipped and used for mulch. Young apple trees can develop cankers due to Diplodia seriata of which the inoculum source might come from fruiting structures present on apple wood mulch. Therefore, the presence of D. seriata, on chipped apple tree wood pieces used for mulch in younger orchards was investigated. To be able to detect D. seriata, qPCR primers were designed from a previously identified unique sequence characterised amplified region (SCAR). The qPCR primers were specific for D. seriata (Cq ≤ 35 and Tm = 85\(\:\pm\:\)0.17 °C) when compared with DNA from nineteen other fungal taxa associated with canker or wood rot of apple trees tested, excluding Botryosphaeria dothidea (Cq = 38 and Tm = 85.25 °C). The qPCR assay was sensitive and had a limit of quantification of 2859 fg/µl and limit of detection of 571 fg/µl. Wood chips were collected at two time periods (from heaps and 6 months after it was spread in tree rows) in three apple orchards in the Western Cape of South Africa. DNA was extracted from water-washes of 120 wood piece samples and D. seriata was detected from 101 of these samples. This study showed that the newly developed primers was able to successfully detect D. seriata from mulched apple wood. The presence of D. seriata on apple tree wood chips indicates that there is a risk involved in using wood chips made from old apple trees.
期刊介绍:
Australasian Plant Pathology presents new and significant research in all facets of the field of plant pathology. Dedicated to a worldwide readership, the journal focuses on research in the Australasian region, including Australia, New Zealand and Papua New Guinea, as well as the Indian, Pacific regions.
Australasian Plant Pathology is the official journal of the Australasian Plant Pathology Society.