Juncong Liu, Yuge He, Zongbo Qiu, Shah Fahad, Sujing Zhao, Mo 墨 Zhu 朱
{"title":"Erysiphe russellii 在华中地区牛膝草上引起白粉病。","authors":"Juncong Liu, Yuge He, Zongbo Qiu, Shah Fahad, Sujing Zhao, Mo 墨 Zhu 朱","doi":"10.1094/PDIS-10-24-2249-PDN","DOIUrl":null,"url":null,"abstract":"<p><p>Oxalis corniculata L. (Creeping woodsorrel) is a perennial plant of the genus Oxalis in Oxalidaceae family, which has the high ornamental and medicinal value. Extracts of creeping woodsorrel are used as antioxidants and cholinesterase inhibitors and for anti-inflammatory, antiseptic, analgesic, antirheumatic ache, and antimicrobial purposes (Leporatti et al. 2003). In June 2024, powdery mildew was found on the leaves of Creeping woodsorrel in Xinxiang City, Henan Province, China (113.925°E, 35.294°N). About 100 plants were examined and 80 % were infected with disease symptoms, i.e. curling and senescence. The white masses were on the both sides of plant leaves covering up to 90% of the leaves area. The slightly or straight curved conidiophores (n = 50) were 68 to 99× 6 to 12 μm in size and consisted of foot cells, shorter cells and singly conidia. The ellipsoidal to oval conidia (n =50), were 26 to 10 ×11 to 5 μm in size and had a length/width ratio of 1.6 to 2.2. These morphological characteristics were similar to the previously reported Creeping woodsorrel powdery mildew fungus, Erysiphe russellii (Thuong et al. 2017; Takamatsu et al. 2015). Following previously described methods (White et al. 1990; Bradshaw et al. 2022; Zhu et al. 2022), the ITS (ribosomal transcribed spacer), GAPDH (glyceraldehyde-3-phosphate dehydrogenase), RPB2 (RNA polymerase II), GS (glutamine synthetase) and CAM (calmodulin) gene regions of three isolates were amplified with specific primers ITS1/ITS4 (ITS1 5'-TCCGTAGGTGAACCTGCGG-3'; ITS4 5'-TCCTCCGCTTATTGATATGC-3'), PMGAPDH1/PMGAPDH3R (PMGAPDH1 5'-GGAATGGCTATGCGTGTACC-3'; PMGAPDH3R 5'-CCCCATTCGTTGTCGTACCATG-3'), CAM1/CAM4R (CAM1 5'-CTTTGCATCATGAGTTGGAC-3'; CAM4R 5'-GGCTCGAAAAATGAAAGATACCG-3'), Rpb2_4/Rpb2_6R (Rpb2_4 5'-GCAAGCTCAACTGCTGGTG-3'; Rpb2_6R 5'-TCCAGCGATGTGCTGTTGG-3'), GSPM2/GSPM3R (GSPM2 5'-CCAATCAGTTACTGTTTGTTCCC-3'; GSPM3R 5'-GGACTTCCTGATATTATGCC3'). Sanger sequencing results showed that each sequence of the three isolates were the same. Then sequences of one isolate were uploaded in GenBank (Accession No. PQ044579, PQ149219, PQ149220, PQ149221and PQ149222, respectively). The sequences were 100% identical to those of a previously reported E russellii on O. corniculata (Thuong et al. 2017; Takamatsu et al. 2015). The pathogen and the previously reported E russellii are clustered in the same branch in the phylogenetic tree (Thuong et al. 2017; Takamatsu et al. 2015). The pathogenicity was tested according to the method previously described (Zhu et al. 2021). By blowing conidia on infected leaves with pressurized air, the fungus was inoculated onto the leaves of three healthy plants (three-month-old), with three uninoculated plants (three-month-old) treated as controls. The infected plants and the control plants were placed in the culture room with the temperature 23 °C, humidity 50% and light/Dark 16/8 h, respectively. 10-12 days post inoculation, the leaves of the inoculated plants showed signs and symptoms of powdery mildew, while the control group was unaffected. The pathogen of the infected plant disease was re-examined by morphological characteristics and was similar to the original fungus. The pathogenicity tests were repeated three times and same results were obtained. Therefore, the pathogen was identified and confirmed as E russellii (isolate ER-ZM2024). Previously, E russellii was reported on Oxalis corniculata L. in Japan and Korea (Thuong et al. 2017; Takamatsu et al. 2015). To the best our knowledge, this is the first report of powdery mildew caused by E russellii on O. corniculata L. in central China. This identification of E russellii on O. corniculata L. provides a new perspective for the study of the disease. The results of this study provide the sequences of E russellii for further phylogenetic analysis.</p>","PeriodicalId":20063,"journal":{"name":"Plant disease","volume":" ","pages":""},"PeriodicalIF":4.4000,"publicationDate":"2024-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Erysiphe russellii</i> Causing Powdery Mildew on <i>Oxalis corniculata</i> L. in Central China.\",\"authors\":\"Juncong Liu, Yuge He, Zongbo Qiu, Shah Fahad, Sujing Zhao, Mo 墨 Zhu 朱\",\"doi\":\"10.1094/PDIS-10-24-2249-PDN\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Oxalis corniculata L. (Creeping woodsorrel) is a perennial plant of the genus Oxalis in Oxalidaceae family, which has the high ornamental and medicinal value. Extracts of creeping woodsorrel are used as antioxidants and cholinesterase inhibitors and for anti-inflammatory, antiseptic, analgesic, antirheumatic ache, and antimicrobial purposes (Leporatti et al. 2003). In June 2024, powdery mildew was found on the leaves of Creeping woodsorrel in Xinxiang City, Henan Province, China (113.925°E, 35.294°N). About 100 plants were examined and 80 % were infected with disease symptoms, i.e. curling and senescence. The white masses were on the both sides of plant leaves covering up to 90% of the leaves area. The slightly or straight curved conidiophores (n = 50) were 68 to 99× 6 to 12 μm in size and consisted of foot cells, shorter cells and singly conidia. The ellipsoidal to oval conidia (n =50), were 26 to 10 ×11 to 5 μm in size and had a length/width ratio of 1.6 to 2.2. These morphological characteristics were similar to the previously reported Creeping woodsorrel powdery mildew fungus, Erysiphe russellii (Thuong et al. 2017; Takamatsu et al. 2015). Following previously described methods (White et al. 1990; Bradshaw et al. 2022; Zhu et al. 2022), the ITS (ribosomal transcribed spacer), GAPDH (glyceraldehyde-3-phosphate dehydrogenase), RPB2 (RNA polymerase II), GS (glutamine synthetase) and CAM (calmodulin) gene regions of three isolates were amplified with specific primers ITS1/ITS4 (ITS1 5'-TCCGTAGGTGAACCTGCGG-3'; ITS4 5'-TCCTCCGCTTATTGATATGC-3'), PMGAPDH1/PMGAPDH3R (PMGAPDH1 5'-GGAATGGCTATGCGTGTACC-3'; PMGAPDH3R 5'-CCCCATTCGTTGTCGTACCATG-3'), CAM1/CAM4R (CAM1 5'-CTTTGCATCATGAGTTGGAC-3'; CAM4R 5'-GGCTCGAAAAATGAAAGATACCG-3'), Rpb2_4/Rpb2_6R (Rpb2_4 5'-GCAAGCTCAACTGCTGGTG-3'; Rpb2_6R 5'-TCCAGCGATGTGCTGTTGG-3'), GSPM2/GSPM3R (GSPM2 5'-CCAATCAGTTACTGTTTGTTCCC-3'; GSPM3R 5'-GGACTTCCTGATATTATGCC3'). Sanger sequencing results showed that each sequence of the three isolates were the same. Then sequences of one isolate were uploaded in GenBank (Accession No. PQ044579, PQ149219, PQ149220, PQ149221and PQ149222, respectively). The sequences were 100% identical to those of a previously reported E russellii on O. corniculata (Thuong et al. 2017; Takamatsu et al. 2015). The pathogen and the previously reported E russellii are clustered in the same branch in the phylogenetic tree (Thuong et al. 2017; Takamatsu et al. 2015). The pathogenicity was tested according to the method previously described (Zhu et al. 2021). By blowing conidia on infected leaves with pressurized air, the fungus was inoculated onto the leaves of three healthy plants (three-month-old), with three uninoculated plants (three-month-old) treated as controls. The infected plants and the control plants were placed in the culture room with the temperature 23 °C, humidity 50% and light/Dark 16/8 h, respectively. 10-12 days post inoculation, the leaves of the inoculated plants showed signs and symptoms of powdery mildew, while the control group was unaffected. The pathogen of the infected plant disease was re-examined by morphological characteristics and was similar to the original fungus. The pathogenicity tests were repeated three times and same results were obtained. Therefore, the pathogen was identified and confirmed as E russellii (isolate ER-ZM2024). Previously, E russellii was reported on Oxalis corniculata L. in Japan and Korea (Thuong et al. 2017; Takamatsu et al. 2015). To the best our knowledge, this is the first report of powdery mildew caused by E russellii on O. corniculata L. in central China. This identification of E russellii on O. corniculata L. provides a new perspective for the study of the disease. The results of this study provide the sequences of E russellii for further phylogenetic analysis.</p>\",\"PeriodicalId\":20063,\"journal\":{\"name\":\"Plant disease\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-12-14\",\"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-10-24-2249-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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant disease","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1094/PDIS-10-24-2249-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
摘要
酢浆草(Oxalis corniculata L.)是酢浆草科酢浆草属的多年生植物,具有很高的观赏和药用价值。爬草的提取物被用作抗氧化剂和胆碱酯酶抑制剂,并用于抗炎、防腐、镇痛、抗风湿疼痛和抗菌目的(Leporatti等人,2003)。2024年6月,在河南省新乡市(113.925°E, 35.294°N)发现匍匐木参叶上有白粉病。对约100株植株进行了检测,80%的植株出现卷曲和衰老等病征。白色团块分布在植物叶片两侧,占叶片面积的90%。微弯或直弯的分生孢子体(n = 50)大小为68 ~ 99× 6 ~ 12 μm,由足细胞、短细胞和单个分生孢子组成。50个分生孢子大小为26 ~ 10 ×11 ~ 5 μm,长/宽比为1.6 ~ 2.2。这些形态特征与先前报道的爬行木酢白粉病真菌Erysiphe russellii (thong et al. 2017;Takamatsu et al. 2015)。遵循先前描述的方法(White et al. 1990;Bradshaw et al. 2022;Zhu et al. 2022),利用特异性引物ITS1/ITS4 (ITS1 5′-TCCGTAGGTGAACCTGCGG-3′;Its4 5'- tcctgcttattgatatgc -3'), pmgapdh1 / pmgapdh3r (pmgapdh1 5' -ggaatggctatgcgtgtacc-3 ';cam1 / cam4r (cam1 5'- ctttgcatgagttggac -3';CAM4R 5′-GGCTCGAAAAATGAAAGATACCG-3′),Rpb2_4/Rpb2_6R (Rpb2_4 5′-GCAAGCTCAACTGCTGGTG-3′;Rpb2_6R 5'-TCCAGCGATGTGCTGTTGG-3'), GSPM2/GSPM3R (GSPM2 5'- ccaatcagttactgtttgttcc -3';GSPM3R 5“-GGACTTCCTGATATTATGCC3”)。Sanger测序结果显示,三个分离株的各序列相同。将其中一个分离物的序列上传到GenBank(登录号:;PQ044579, PQ149219, PQ149220, pq149221和PQ149222)。该序列与先前报道的O. corniculata上的russellii的序列100%相同(thong et al. 2017;Takamatsu et al. 2015)。该病原体和先前报道的罗素氏肠杆菌在系统发育树上聚集在同一分支上(thong et al. 2017;Takamatsu et al. 2015)。按照先前描述的方法检测致病性(Zhu et al. 2021)。用加压空气吹灭病叶上的分生孢子,将真菌接种到3株健康植株(3月龄)的叶片上,以3株未接种植株(3月龄)作为对照。将感染植株和对照植株分别置于温度23℃、湿度50%、光/暗16/8 h的培养室内。接种后10 ~ 12天,接种植株的叶片出现白粉病的体征和症状,而对照组则不受影响。对侵染植物的病原菌进行了形态特征鉴定,发现病原菌与原真菌相似。致病性试验重复3次,结果一致。因此,病原鉴定为罗素氏肠杆菌(分离物ER-ZM2024)。此前,日本和韩国的Oxalis corniculata L.上有E russellii的报道(Thuong et al. 2017;Takamatsu et al. 2015)。据我们所知,这是华中地区首次报道由russellii对O. corniculata L.造成的白粉病。该鉴定结果为该病的研究提供了新的视角。本研究结果为进一步的系统发育分析提供了依据。
Erysiphe russellii Causing Powdery Mildew on Oxalis corniculata L. in Central China.
Oxalis corniculata L. (Creeping woodsorrel) is a perennial plant of the genus Oxalis in Oxalidaceae family, which has the high ornamental and medicinal value. Extracts of creeping woodsorrel are used as antioxidants and cholinesterase inhibitors and for anti-inflammatory, antiseptic, analgesic, antirheumatic ache, and antimicrobial purposes (Leporatti et al. 2003). In June 2024, powdery mildew was found on the leaves of Creeping woodsorrel in Xinxiang City, Henan Province, China (113.925°E, 35.294°N). About 100 plants were examined and 80 % were infected with disease symptoms, i.e. curling and senescence. The white masses were on the both sides of plant leaves covering up to 90% of the leaves area. The slightly or straight curved conidiophores (n = 50) were 68 to 99× 6 to 12 μm in size and consisted of foot cells, shorter cells and singly conidia. The ellipsoidal to oval conidia (n =50), were 26 to 10 ×11 to 5 μm in size and had a length/width ratio of 1.6 to 2.2. These morphological characteristics were similar to the previously reported Creeping woodsorrel powdery mildew fungus, Erysiphe russellii (Thuong et al. 2017; Takamatsu et al. 2015). Following previously described methods (White et al. 1990; Bradshaw et al. 2022; Zhu et al. 2022), the ITS (ribosomal transcribed spacer), GAPDH (glyceraldehyde-3-phosphate dehydrogenase), RPB2 (RNA polymerase II), GS (glutamine synthetase) and CAM (calmodulin) gene regions of three isolates were amplified with specific primers ITS1/ITS4 (ITS1 5'-TCCGTAGGTGAACCTGCGG-3'; ITS4 5'-TCCTCCGCTTATTGATATGC-3'), PMGAPDH1/PMGAPDH3R (PMGAPDH1 5'-GGAATGGCTATGCGTGTACC-3'; PMGAPDH3R 5'-CCCCATTCGTTGTCGTACCATG-3'), CAM1/CAM4R (CAM1 5'-CTTTGCATCATGAGTTGGAC-3'; CAM4R 5'-GGCTCGAAAAATGAAAGATACCG-3'), Rpb2_4/Rpb2_6R (Rpb2_4 5'-GCAAGCTCAACTGCTGGTG-3'; Rpb2_6R 5'-TCCAGCGATGTGCTGTTGG-3'), GSPM2/GSPM3R (GSPM2 5'-CCAATCAGTTACTGTTTGTTCCC-3'; GSPM3R 5'-GGACTTCCTGATATTATGCC3'). Sanger sequencing results showed that each sequence of the three isolates were the same. Then sequences of one isolate were uploaded in GenBank (Accession No. PQ044579, PQ149219, PQ149220, PQ149221and PQ149222, respectively). The sequences were 100% identical to those of a previously reported E russellii on O. corniculata (Thuong et al. 2017; Takamatsu et al. 2015). The pathogen and the previously reported E russellii are clustered in the same branch in the phylogenetic tree (Thuong et al. 2017; Takamatsu et al. 2015). The pathogenicity was tested according to the method previously described (Zhu et al. 2021). By blowing conidia on infected leaves with pressurized air, the fungus was inoculated onto the leaves of three healthy plants (three-month-old), with three uninoculated plants (three-month-old) treated as controls. The infected plants and the control plants were placed in the culture room with the temperature 23 °C, humidity 50% and light/Dark 16/8 h, respectively. 10-12 days post inoculation, the leaves of the inoculated plants showed signs and symptoms of powdery mildew, while the control group was unaffected. The pathogen of the infected plant disease was re-examined by morphological characteristics and was similar to the original fungus. The pathogenicity tests were repeated three times and same results were obtained. Therefore, the pathogen was identified and confirmed as E russellii (isolate ER-ZM2024). Previously, E russellii was reported on Oxalis corniculata L. in Japan and Korea (Thuong et al. 2017; Takamatsu et al. 2015). To the best our knowledge, this is the first report of powdery mildew caused by E russellii on O. corniculata L. in central China. This identification of E russellii on O. corniculata L. provides a new perspective for the study of the disease. The results of this study provide the sequences of E russellii for further phylogenetic analysis.
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.