First report of target spot caused by Corynespora cassiicola on cotton in North Carolina.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Marcela Vasquez-Mayorga, Maria Fernanda Lainfiesta Palomo, Daisy Ahumada
{"title":"First report of target spot caused by <i>Corynespora cassiicola</i> on cotton in North Carolina.","authors":"Marcela Vasquez-Mayorga, Maria Fernanda Lainfiesta Palomo, Daisy Ahumada","doi":"10.1094/PDIS-05-25-1059-PDN","DOIUrl":null,"url":null,"abstract":"<p><p>On August 13, 2024, during a routine insect scouting walkthrough, symptomatic cotton leaves were collected from a field in Washington County, North Carolina (NC), and submitted to the Plant Pathology Laboratory of the corresponding author at North Carolina State University for diagnosis. The samples exhibited circular lesions with yellow halos and concentric circles in brown to reddish hues, characteristic of target spot caused by Corynespora cassiicola. Leaf tissue from lesion margins, was surface sterilized and plated on acidified potato dextrose agar (A-PDA). Plates were incubated at 28°C in the dark for seven days. Emerging fungal colonies were subcultured to obtain pure cultures. The isolates showed dark mycelial growth with a surrounding white halo and produced conidia measuring 60 µm to 120 µm long, on average, with cylindrical to obclavate morphology. Two isolates were recovered. Mycelial fragments from a pure culture were grown in malt extract broth for 48 hours before genomic DNA extraction, PCR, and sequencing. The internal transcribed spacer (ITS) region was amplified using primers ITS4 (5' TCCTCCGCTTATTGATATGC 3') and ITS5 (5' GGAAGTAAAAGTCGTAACAAGG 3') (White et al., 1990). Sequencing showed 100% nucleotide identity with Corynespora cassiicola (GenBank accession MF428364.1). To confirm pathogenicity, Koch's postulates were completed under greenhouse conditions. Cotton seedlings (DP2127 B3XF) were grown for 24 days. A 12-day-old quarter-strength PDA culture of the isolate was covered with 0.01% Tween solution and filtered through four layers of cheesecloth. The resulting spore suspension was adjusted to 4 x 104 spores/ml (Moore et al. 2021). Nine cotton plants were inoculated by pipetting 500 ul of the conidial suspension onto true leaves. Nine control plants received 0.01% Tween solution only. Leaves were covered with Kimwipes, misted with water, and enclosed in plastic bags for 48 hours. Plants were maintained at 81°F with 51.6% relative humidity. At seven days post-inoculation, inoculated plants developed characteristic C. casiicola lesions with concentric rings. The pathogen was successfully reisolated and confirmed by PCR and ITS sequencing, again showing 100% identity to C. casiicola (MF428364.1). This constitutes the first confirmed report of C. casiicola causing target spot in cotton fields in NC. The pathogen has previously been reported in Georgia (Fulmer et al., 2012), Alabama (Conner et al. 2013), Louisiana (Price et al. 2015) and Tennessee (Butler et al. 2016). In 2024, target spot was also observed and diagnosed by the Plant Disease and Insect Clinic (PDIC) in a separate cotton field in Edgecombe County, NC, with 15% incidence on variety 'DP2127 B3XF.' However, isolates from that location did not survive. The Washington County field from which Koch's postulates were completed is the same site where target spot symptoms were informally reported in 2012 with 10% incidence on an unknown variety. Also in 2012, the PDIC confirmed C. cassiicola in variety 'PHY 499 WRF' in Chowan County, with 50% field incidence. This current confirmation supports improved monitoring and management of this emerging disease.</p>","PeriodicalId":20063,"journal":{"name":"Plant disease","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant disease","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PDIS-05-25-1059-PDN","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

On August 13, 2024, during a routine insect scouting walkthrough, symptomatic cotton leaves were collected from a field in Washington County, North Carolina (NC), and submitted to the Plant Pathology Laboratory of the corresponding author at North Carolina State University for diagnosis. The samples exhibited circular lesions with yellow halos and concentric circles in brown to reddish hues, characteristic of target spot caused by Corynespora cassiicola. Leaf tissue from lesion margins, was surface sterilized and plated on acidified potato dextrose agar (A-PDA). Plates were incubated at 28°C in the dark for seven days. Emerging fungal colonies were subcultured to obtain pure cultures. The isolates showed dark mycelial growth with a surrounding white halo and produced conidia measuring 60 µm to 120 µm long, on average, with cylindrical to obclavate morphology. Two isolates were recovered. Mycelial fragments from a pure culture were grown in malt extract broth for 48 hours before genomic DNA extraction, PCR, and sequencing. The internal transcribed spacer (ITS) region was amplified using primers ITS4 (5' TCCTCCGCTTATTGATATGC 3') and ITS5 (5' GGAAGTAAAAGTCGTAACAAGG 3') (White et al., 1990). Sequencing showed 100% nucleotide identity with Corynespora cassiicola (GenBank accession MF428364.1). To confirm pathogenicity, Koch's postulates were completed under greenhouse conditions. Cotton seedlings (DP2127 B3XF) were grown for 24 days. A 12-day-old quarter-strength PDA culture of the isolate was covered with 0.01% Tween solution and filtered through four layers of cheesecloth. The resulting spore suspension was adjusted to 4 x 104 spores/ml (Moore et al. 2021). Nine cotton plants were inoculated by pipetting 500 ul of the conidial suspension onto true leaves. Nine control plants received 0.01% Tween solution only. Leaves were covered with Kimwipes, misted with water, and enclosed in plastic bags for 48 hours. Plants were maintained at 81°F with 51.6% relative humidity. At seven days post-inoculation, inoculated plants developed characteristic C. casiicola lesions with concentric rings. The pathogen was successfully reisolated and confirmed by PCR and ITS sequencing, again showing 100% identity to C. casiicola (MF428364.1). This constitutes the first confirmed report of C. casiicola causing target spot in cotton fields in NC. The pathogen has previously been reported in Georgia (Fulmer et al., 2012), Alabama (Conner et al. 2013), Louisiana (Price et al. 2015) and Tennessee (Butler et al. 2016). In 2024, target spot was also observed and diagnosed by the Plant Disease and Insect Clinic (PDIC) in a separate cotton field in Edgecombe County, NC, with 15% incidence on variety 'DP2127 B3XF.' However, isolates from that location did not survive. The Washington County field from which Koch's postulates were completed is the same site where target spot symptoms were informally reported in 2012 with 10% incidence on an unknown variety. Also in 2012, the PDIC confirmed C. cassiicola in variety 'PHY 499 WRF' in Chowan County, with 50% field incidence. This current confirmation supports improved monitoring and management of this emerging disease.

北卡罗莱纳棉花枯斑病的首次报道。
2024年8月13日,在美国北卡罗来纳州华盛顿县(NC)的一处田间采集了有症状的棉花叶片,并将其提交给通讯作者北卡罗来纳州立大学植物病理学实验室进行诊断。样品呈圆形病变,带有黄色晕和褐色至红色的同心圆,这是由cassiicola引起的目标斑点的特征。对病变边缘的叶片组织进行表面灭菌,并涂于酸化马铃薯葡萄糖琼脂(A-PDA)上。28℃黑暗孵育7天。继代培养新出现的真菌菌落以获得纯培养物。分离菌株菌丝生长呈黑色,周围有白色的光晕,分生孢子平均长60µm ~ 120µm,形态为圆柱形到倒棒状。分离得到2株。在基因组DNA提取、PCR和测序之前,将纯培养的菌丝片段在麦芽提取物肉汤中培养48小时。利用引物ITS4 (5' tcctccgcttattgatatggc 3‘)和ITS5 (5’ GGAAGTAAAAGTCGTAACAAGG 3')扩增内部转录间隔区(White et al., 1990)。测序结果显示与cassiicola Corynespora 100%核苷酸同源(GenBank登录MF428364.1)。为了确认致病性,在温室条件下完成了Koch的假设。棉花幼苗(DP2127 B3XF)生长24 d。培养12天的四分之一强度PDA培养物用0.01% Tween溶液覆盖,并通过四层粗棉布过滤。将得到的孢子悬浮液调整为4 × 104孢子/ml (Moore et al. 2021)。将500 ul分生孢子悬浮液移栽到棉花真叶上,接种9株棉花植株。9个对照植物只接受0.01%的Tween溶液。用湿纸巾覆盖叶子,用水湿润,然后用塑料袋密封48小时。植物保持在81°F,相对湿度为51.6%。接种后第7天,接种植株出现了具有同心圆环的特征性卡西菌病损。重新分离得到病原菌,经PCR和ITS测序证实,病原菌100%为卡西菌(C. casiicola, MF428364.1)。这是北卡罗莱纳州棉田首次确认卡西柯拉菌引起靶斑的报告。此前在佐治亚州(Fulmer等人,2012年)、阿拉巴马州(Conner等人,2013年)、路易斯安那州(Price等人,2015年)和田纳西州(Butler等人,2016年)均报道过该病原体。2024年,在北卡罗莱纳州Edgecombe县另一块棉花田,通过植物病虫诊所(PDIC)观察和诊断靶斑,发病品种为DP2127 B3XF,发生率为15%。然而,来自该地点的分离株没有存活下来。完成Koch假设的华盛顿县田间是2012年非正式报告目标斑点症状的同一地点,其中未知品种的发生率为10%。同样在2012年,PDIC在Chowan县确认了“PHY 499 WRF”品种的cassiicola,田间发病率为50%。目前的这一确认支持改进对这一新发疾病的监测和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信