FUNGAL PATHOGENIC COMPLEX OF THE ROOT ZONE OF CULTIVATED SOYBEAN PLANTS

H. Tsekhmister, Y. Kopylov, A. Kyslynska
{"title":"FUNGAL PATHOGENIC COMPLEX OF THE ROOT ZONE OF CULTIVATED SOYBEAN PLANTS","authors":"H. Tsekhmister, Y. Kopylov, A. Kyslynska","doi":"10.35868/1997-3004.35.73-81","DOIUrl":null,"url":null,"abstract":"Objective. To characterize the fungal pathogenic complex of the root zone of cultivated soybean plants grown on sod-medium podzolic soil, to identify the most harmful pathogens of root diseases. Methods. Phytopathogenic micromycetes were isolated from affected soybean plants. For this, segments of plant material (roots, seeds, leaf blade) (3–5 mm) were thoroughly washed for 15 min under running water, their surface was sterilized with 96 % ethyl alcohol for 1 min, washed twice with sterile water and placed in Petri dishes on 4 % wort agar with 250 ppm streptomycin and placed in a thermostat (26 °C). At Day 4, isolates were obtained on wort agar and grown for 14 days at 26 °C. Confirmation of the pathogenicity of the selected isolates was carried out in a sterile vegetative experiment on Strive variety soybean plants. To do this, 1 dm3 glasses were filled with a substrate containing 50 g of consolidated vermiculite and 200 g of water and sterilized for 1 hour at 1.5 atm. Healthy soybean seeds were pre-selected, thoroughly washed under running water and sprouted in a humid chamber for 2 days so that the seedlings had a root length of 1–2 cm and carefully washed in sterile tap water. Ten soybean sprouts were placed in each glass and 3 mL of an aqueous spore-mycelial mixture of selected isolates (experiment) or 3 mL of sterile water (control) were added. At Day 14, the plants were removed, thoroughly and carefully washed, the number of affected plants was counted (% prevalence) and the dry matter of roots and shoots was measured. Results. A total of 16 strains of fungi, the causative agents of root diseases, were isolated in pure culture from roots, seeds and leaf plates of affected soybean plants. The isolated pathogens belonged to the genera Fusarium Link:Fr, Alternaria (Fr.) Keissler, Verticillium Nees. The phytopathogenic effect of fungi of the genus Verticillium isolated from the washed roots of soybean plants was insignificant. Fusarium was represented by F. oxysporum, F. solani, F. moniliforme var. lactis, F. gibbosum, among which F. gibbosum exerted the greatest phytopathogenic effect. The isolated F. gibbosum C4 affects seedlings first. The roots of the affected plants develop poorly, the plants are easily pulled out and lag behind in growth and development. Among the selected Alternaria strains, A. consortiale C8 which was characterized by rapid growth, turned out to be the most harmful. A. consortiale C8 first affects seedlings, then appears on other parts of plants: roots, stems, leaves. On soybean leaves, the first sign of alternaria leaf spots is dark brown spots of various sizes and shapes, the leaves wither and die. Affected plants lag behind in growth. Infection of soybean plants by phytopathogenic fungi leads to a decrease in the content of dry matter both in the roots and in the aboveground mass of the plants. In the case of F. gibbosum C4 infection, the content of dry matter in the roots decreased by 27 %, in the aboveground mass of plants — by 19 %. Infection with A. consortiale C8 led to a decrease in dry matter by 29 % and 27 %, respectively. Conclusion. The fungal pathogenic complex in soybean crops consisted of representatives of the Objective. To characterize the fungal pathogenic complex of the root zone of cultivated soybean plants grown on sod-medium podzolic soil, to identify the most harmful pathogens of root diseases. Methods. Phytopathogenic micromycetes were isolated from affected soybean plants. For this, segments of plant material (roots, seeds, leaf blade) (3–5 mm) were thoroughly washed for 15 min under running water, their surface was sterilized with 96 % ethyl alcohol for 1 min, washed twice with sterile water and placed in Petri dishes on 4 % wort agar with 250 ppm streptomycin and placed in a thermostat (26 °C). At Day 4, isolates were obtained on wort agar and grown for 14 days at 26 °C. Confirmation of the pathogenicity of the selected isolates was carried out in a sterile vegetative experiment on Strive variety soybean plants. To do this, 1 dm3 glasses were filled with a substrate containing 50 g of consolidated vermiculite and 200 g of water and sterilized for 1 hour at 1.5 atm. Healthy soybean seeds were pre-selected, thoroughly washed under running water and sprouted in a humid chamber for 2 days so that the seedlings had a root length of 1–2 cm and carefully washed in sterile tap water. Ten soybean sprouts were placed in each glass and 3 mL of an aqueous spore-mycelial mixture of selected isolates (experiment) or 3 mL of sterile water (control) were added. At Day 14, the plants were removed, thoroughly and carefully washed, the number of affected plants was counted (% prevalence) and the dry matter of roots and shoots was measured. Results. A total of 16 strains of fungi, the causative agents of root diseases, were isolated in pure culture from roots, seeds and leaf plates of affected soybean plants. The isolated pathogens belonged to the genera Fusarium Link:Fr, Alternaria (Fr.) Keissler, Verticillium Nees. The phytopathogenic effect of fungi of the genus Verticillium isolated from the washed roots of soybean plants was insignificant. Fusarium was represented by F. oxysporum, F. solani, F. moniliforme var. lactis, F. gibbosum, among which F. gibbosum exerted the greatest phytopathogenic effect. The isolated F. gibbosum C4 affects seedlings first. The roots of the affected plants develop poorly, the plants are easily pulled out and lag behind in growth and development. Among the selected Alternaria strains, A. consortiale C8 which was characterized by rapid growth, turned out to be the most harmful. A. consortiale C8 first affects seedlings, then appears on other parts of plants: roots, stems, leaves. On soybean leaves, the first sign of alternaria leaf spots is dark brown spots of various sizes and shapes, the leaves wither and die. Affected plants lag behind in growth. Infection of soybean plants by phytopathogenic fungi leads to a decrease in the content of dry matter both in the roots and in the aboveground mass of the plants. In the case of F. gibbosum C4 infection, the content of dry matter in the roots decreased by 27 %, in the aboveground mass of plants — by 19 %. Infection with A. consortiale C8 led to a decrease in dry matter by 29 % and 27 %, respectively. Conclusion. The fungal pathogenic complex in soybean crops consisted of representatives of the","PeriodicalId":135696,"journal":{"name":"Agriciltural microbiology","volume":"41 33-34 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Agriciltural microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35868/1997-3004.35.73-81","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective. To characterize the fungal pathogenic complex of the root zone of cultivated soybean plants grown on sod-medium podzolic soil, to identify the most harmful pathogens of root diseases. Methods. Phytopathogenic micromycetes were isolated from affected soybean plants. For this, segments of plant material (roots, seeds, leaf blade) (3–5 mm) were thoroughly washed for 15 min under running water, their surface was sterilized with 96 % ethyl alcohol for 1 min, washed twice with sterile water and placed in Petri dishes on 4 % wort agar with 250 ppm streptomycin and placed in a thermostat (26 °C). At Day 4, isolates were obtained on wort agar and grown for 14 days at 26 °C. Confirmation of the pathogenicity of the selected isolates was carried out in a sterile vegetative experiment on Strive variety soybean plants. To do this, 1 dm3 glasses were filled with a substrate containing 50 g of consolidated vermiculite and 200 g of water and sterilized for 1 hour at 1.5 atm. Healthy soybean seeds were pre-selected, thoroughly washed under running water and sprouted in a humid chamber for 2 days so that the seedlings had a root length of 1–2 cm and carefully washed in sterile tap water. Ten soybean sprouts were placed in each glass and 3 mL of an aqueous spore-mycelial mixture of selected isolates (experiment) or 3 mL of sterile water (control) were added. At Day 14, the plants were removed, thoroughly and carefully washed, the number of affected plants was counted (% prevalence) and the dry matter of roots and shoots was measured. Results. A total of 16 strains of fungi, the causative agents of root diseases, were isolated in pure culture from roots, seeds and leaf plates of affected soybean plants. The isolated pathogens belonged to the genera Fusarium Link:Fr, Alternaria (Fr.) Keissler, Verticillium Nees. The phytopathogenic effect of fungi of the genus Verticillium isolated from the washed roots of soybean plants was insignificant. Fusarium was represented by F. oxysporum, F. solani, F. moniliforme var. lactis, F. gibbosum, among which F. gibbosum exerted the greatest phytopathogenic effect. The isolated F. gibbosum C4 affects seedlings first. The roots of the affected plants develop poorly, the plants are easily pulled out and lag behind in growth and development. Among the selected Alternaria strains, A. consortiale C8 which was characterized by rapid growth, turned out to be the most harmful. A. consortiale C8 first affects seedlings, then appears on other parts of plants: roots, stems, leaves. On soybean leaves, the first sign of alternaria leaf spots is dark brown spots of various sizes and shapes, the leaves wither and die. Affected plants lag behind in growth. Infection of soybean plants by phytopathogenic fungi leads to a decrease in the content of dry matter both in the roots and in the aboveground mass of the plants. In the case of F. gibbosum C4 infection, the content of dry matter in the roots decreased by 27 %, in the aboveground mass of plants — by 19 %. Infection with A. consortiale C8 led to a decrease in dry matter by 29 % and 27 %, respectively. Conclusion. The fungal pathogenic complex in soybean crops consisted of representatives of the Objective. To characterize the fungal pathogenic complex of the root zone of cultivated soybean plants grown on sod-medium podzolic soil, to identify the most harmful pathogens of root diseases. Methods. Phytopathogenic micromycetes were isolated from affected soybean plants. For this, segments of plant material (roots, seeds, leaf blade) (3–5 mm) were thoroughly washed for 15 min under running water, their surface was sterilized with 96 % ethyl alcohol for 1 min, washed twice with sterile water and placed in Petri dishes on 4 % wort agar with 250 ppm streptomycin and placed in a thermostat (26 °C). At Day 4, isolates were obtained on wort agar and grown for 14 days at 26 °C. Confirmation of the pathogenicity of the selected isolates was carried out in a sterile vegetative experiment on Strive variety soybean plants. To do this, 1 dm3 glasses were filled with a substrate containing 50 g of consolidated vermiculite and 200 g of water and sterilized for 1 hour at 1.5 atm. Healthy soybean seeds were pre-selected, thoroughly washed under running water and sprouted in a humid chamber for 2 days so that the seedlings had a root length of 1–2 cm and carefully washed in sterile tap water. Ten soybean sprouts were placed in each glass and 3 mL of an aqueous spore-mycelial mixture of selected isolates (experiment) or 3 mL of sterile water (control) were added. At Day 14, the plants were removed, thoroughly and carefully washed, the number of affected plants was counted (% prevalence) and the dry matter of roots and shoots was measured. Results. A total of 16 strains of fungi, the causative agents of root diseases, were isolated in pure culture from roots, seeds and leaf plates of affected soybean plants. The isolated pathogens belonged to the genera Fusarium Link:Fr, Alternaria (Fr.) Keissler, Verticillium Nees. The phytopathogenic effect of fungi of the genus Verticillium isolated from the washed roots of soybean plants was insignificant. Fusarium was represented by F. oxysporum, F. solani, F. moniliforme var. lactis, F. gibbosum, among which F. gibbosum exerted the greatest phytopathogenic effect. The isolated F. gibbosum C4 affects seedlings first. The roots of the affected plants develop poorly, the plants are easily pulled out and lag behind in growth and development. Among the selected Alternaria strains, A. consortiale C8 which was characterized by rapid growth, turned out to be the most harmful. A. consortiale C8 first affects seedlings, then appears on other parts of plants: roots, stems, leaves. On soybean leaves, the first sign of alternaria leaf spots is dark brown spots of various sizes and shapes, the leaves wither and die. Affected plants lag behind in growth. Infection of soybean plants by phytopathogenic fungi leads to a decrease in the content of dry matter both in the roots and in the aboveground mass of the plants. In the case of F. gibbosum C4 infection, the content of dry matter in the roots decreased by 27 %, in the aboveground mass of plants — by 19 %. Infection with A. consortiale C8 led to a decrease in dry matter by 29 % and 27 %, respectively. Conclusion. The fungal pathogenic complex in soybean crops consisted of representatives of the
栽培大豆根区真菌致病复合体
目标。研究在草质-灰化土中栽培大豆根系区真菌致病复合体的特征,鉴定根系病害的最有害病原体。方法。从受影响的大豆植株中分离出植物致病微菌。为此,植物材料片段(根、种子、叶片)(3-5 mm)在自来水下彻底清洗15分钟,其表面用96%乙醇消毒1分钟,用无菌水清洗两次,并放置在含有250 ppm链霉素的4%麦汁琼脂的培养皿中,放置在恒温器(26°C)中。第4天,在麦汁琼脂上获得分离株,在26°C下培养14天。对所选菌株的致病性进行了无菌性营养试验。为此,将1 dm3的玻璃杯装满含有50 g固化剂蛭石和200 g水的底物,并在1.5 atm下消毒1小时。预先选择健康的大豆种子,在流水下彻底清洗,在潮湿的室内发芽2天,使幼苗的根长为1-2厘米,并在无菌自来水中仔细清洗。每个玻璃杯中放入10个豆芽,加入3ml选定分离株的孢子-菌丝混合液(实验)或3ml无菌水(对照)。在第14天,将植株取出,彻底仔细清洗,计算受影响植株的数量(患病率%),并测量根和芽的干物质。结果。从染病大豆植株的根、种子和叶片中分离到16株病原菌。分离的病原菌属镰刀菌属(Fusarium Link:Fr)、Alternaria (Fr.) Keissler、Verticillium Nees。从大豆洗涤根中分离得到的黄萎病菌属真菌的植物致病作用不显著。镰刀菌以尖孢镰刀菌、番茄镰刀菌、乳酸菌镰刀菌和赤霉病镰刀菌为代表,其中赤霉病镰刀菌的植物致病作用最大。分离的赤霉素C4首先影响幼苗。患病植株根系发育不良,植株易拔除,生长发育滞后。在所选的交替孢菌中,以生长速度快的联合孢杆菌C8危害最大。A.联合体C8首先影响幼苗,然后出现在植物的其他部分:根、茎、叶。在大豆叶片上,互交菌叶斑病的第一个迹象是大小形状各异的深棕色斑点,叶片枯萎死亡。受影响的植物生长滞后。植物病原真菌侵染大豆植株后,导致植株根部和地上部干物质含量下降。在赤霉素C4侵染的情况下,根系干物质含量下降了27%,植株地上质量下降了19%。C8侵染导致干物质分别减少29%和27%。结论。大豆作物的真菌致病复合体是目标的代表。研究在草质-灰化土中栽培大豆根系区真菌致病复合体的特征,鉴定根系病害的最有害病原体。方法。从受影响的大豆植株中分离出植物致病微菌。为此,植物材料片段(根、种子、叶片)(3-5 mm)在自来水下彻底清洗15分钟,其表面用96%乙醇消毒1分钟,用无菌水清洗两次,并放置在含有250 ppm链霉素的4%麦汁琼脂的培养皿中,放置在恒温器(26°C)中。第4天,在麦汁琼脂上获得分离株,在26°C下培养14天。对所选菌株的致病性进行了无菌性营养试验。为此,将1 dm3的玻璃杯装满含有50 g固化剂蛭石和200 g水的底物,并在1.5 atm下消毒1小时。预先选择健康的大豆种子,在流水下彻底清洗,在潮湿的室内发芽2天,使幼苗的根长为1-2厘米,并在无菌自来水中仔细清洗。每个玻璃杯中放入10个豆芽,加入3ml选定分离株的孢子-菌丝混合液(实验)或3ml无菌水(对照)。在第14天,将植株取出,彻底仔细清洗,计算受影响植株的数量(患病率%),并测量根和芽的干物质。结果。从染病大豆植株的根、种子和叶片中分离到16株病原菌。 分离的病原菌属镰刀菌属(Fusarium Link:Fr)、Alternaria (Fr.) Keissler、Verticillium Nees。从大豆洗涤根中分离得到的黄萎病菌属真菌的植物致病作用不显著。镰刀菌以尖孢镰刀菌、番茄镰刀菌、乳酸菌镰刀菌和赤霉病镰刀菌为代表,其中赤霉病镰刀菌的植物致病作用最大。分离的赤霉素C4首先影响幼苗。患病植株根系发育不良,植株易拔除,生长发育滞后。在所选的交替孢菌中,以生长速度快的联合孢杆菌C8危害最大。A.联合体C8首先影响幼苗,然后出现在植物的其他部分:根、茎、叶。在大豆叶片上,互交菌叶斑病的第一个迹象是大小形状各异的深棕色斑点,叶片枯萎死亡。受影响的植物生长滞后。植物病原真菌侵染大豆植株后,导致植株根部和地上部干物质含量下降。在赤霉素C4侵染的情况下,根系干物质含量下降了27%,植株地上质量下降了19%。C8侵染导致干物质分别减少29%和27%。结论。大豆作物的真菌致病复合体由几种真菌的代表组成
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信