作 者:
王美玉;冀志蕊;王娜;迟福梅;周宗山;张俊祥
单 位:
中国农业科学院果树研究所;中国农业科学院果树研究所农业部园艺作物种质资源利用重点实验室
关键词:
苹果炭疽叶枯病菌;甲基硫菌灵;戊唑醇;咪鲜胺;β-tubulin基因;敏感性
摘 要:
【目的】了解我国苹果主产区苹果炭疽叶枯病菌(Colletotrichum gloeosporioides)对苯并咪唑类、甾醇脱甲基抑制剂类和咪唑类杀菌剂敏感性的现状,旨为苹果炭疽叶枯病的科学防治提供参考,以及为苹果炭疽叶枯病菌抗药分子机制研究提供理论依据。【方法】采用区分剂量法和菌丝生长速率法,对采自于我国苹果主产区的117个苹果炭疽叶枯病菌菌株进行甲基硫菌灵、戊唑醇、咪鲜胺的敏感性测定,并对随机抽测的28个菌株的β-微管蛋白基因(β-tubulin)进行序列分析。【结果】117个供试菌株对甲基硫菌灵的抗药性频率为100%,均为高水平抗性菌株(HR)。随机抽测24个菌株的β-tubulin基因,其中23个菌株的β-tubulin蛋白第198位氨基酸从谷氨酸(Glu)突变为丙氨酸(Ala),另外1个菌株ZG4-7的第200位氨基酸从苯丙氨酸(Phe)突变成酪氨酸(Tyr)。苹果炭疽叶枯病菌对戊唑醇的敏感性检测结果表明,戊唑醇对供试菌株的EC_(50)值(ρ,后同)为0~0.843 0 mg·L~(-1),平均EC_(50)值为0.155 5 mg·L~(-1),75.21%的菌株对戊唑醇表现出低水平抗药性,设置质量浓度为5 mg·L~(-1)时,对供试群体的平均抑制率为92.72%。苹果炭疽叶枯病菌供试群体对咪鲜胺的敏感性较强,平均EC_(50)值为0.011 9 mg·L~(-1),设置质量浓度为0.5 mg·L~(-1)时,咪鲜胺对供试群体的平均抑制率为95.02%。【结论】苹果炭疽叶枯病菌对苯并咪唑类杀菌剂甲基硫菌灵表现出高抗性;对DMIs类杀菌剂戊唑醇表现出低水平抗性,但已产生高水平抗性菌株;对咪唑类药剂咪鲜胺敏感性较强。
译 名:
Detection of the sensitivity of Colletotrichum gloeosporioides to three fungicides
作 者:
WANG Meiyu;JI Zhirui;WANG Na;CHI Fumei;ZHOU Zongshan;ZHANG Junxiang;Research Institute of Pomology, Chinese Academy of Agricultural Sciences;Key Laboratory of Biology and Genetic Improvement of Horticultural Crops(Germplasm Resources Utilization), Ministry of Agriculture;
关键词:
Glomerella leaf spot of apple;;Thiophanate-methyl;;Tebuconazole;;Prochloraz;;β-tubulin gene;;Sensitivity
摘 要:
【Objective】Colletotrichum gloeosporioides(anamorph of Glomerella cingulata), a ubiquitous fungal pathogen, is the agent causing Glomerella leaf spot(GLS) on apples. Under favorable conditions, GLS can result in seventy-five percent defoliation by harvest, weakening trees and reducing yield.In recent years, an epidemic of GLSA broke out in most apple planting areas in China, because of an indefinite occurrence period and resulitn in a severe impairment. The disease is initiated when conidia attaches to the plants surfaces via wind or rain splash dispersal, where trhe conidia germinates and differentiates into a specialized infection structure called appressorium. After invasion, C. gloeosporioides grows biotrophically, proliferates into neighboring cells, turns into a necrotrophic development and eventually results in lesions on the plants. Planting a resistance cultivar is considered to be a key strategy and one of the most efficient methods of controlling plant diseases. Many quality cultivars derived from the"Delicious"group, including'Gala''Gold Delicious', were widely planted. Some biocontrol products are applied to plants for protection and achieve good benefits of social and economic, but the commercial biocontrol product showed no effect on GLS in leaves and fruits. Therefore, this disease is primarily managed with chemical controls, such as benzimidazole fungicides, sterol demethylation in-hibitors(DMI) and imidazole. The severity of GLS can be reduced in the orchard by applying some fungicides beginning about 6 weeks after petal fall and continuing every 2 weeks until 2 to 3 weeks before harvest. Combinations of chelated zinc materials and dithiocarbamate fungicides improve control. However, while frequent applications are effective, they also increase production costs and can have damaging effects on the environment and human health. Moreover, plant pathogens can become resistant to fungicides and it can then fail as a control. For investigating the sensitivity of C. gloeosporioides to benzimidazole, DMI and imidazole, diseased leaves were collected from different apple gardens, and the obtained pathogen isolates were tested to see if they were resistance to benzimidazole, DMI and imidazole. This study could provide a theoretical basis for effective scientific controlling of GLSA.【Methods】One hundred and seventeen C. gloeosporioides strains were isolated from their diseased leaves, which were collected from different apple cultivars including'Gala''Golden Delicious' 'Jonagold''Jinxiuhong''Jinhong'and'K12'in different apple growing areas, such as Anyang, Henan; Zhengzhou,Henan; Zhaoyuan, Shandong; Qufu, Shandong; Yixian, Hebei; Xianyang, Shanxi and Dangshan, Anhui.The obtained isolates were separated using the single-spore method. The cultural characteristics of all the different isolates were studied on 6 cm diameter PLA plates. The morphology of the colony and conidia were studied after the plates were incubated for 10 days at 25 ℃ under a light microscope. For infection assays, a droplet(2 μL) of freshly harvested conidial suspensions was placed onto the obverse of the apple leaves('Gold Delicious'), while 2 μL conidial suspensions were also inoculated into the wounded leaves by stabbing with a toothpick. Inoculated leaves were placed on plates containing water agar(12%). Disease lesions were examined at 4 days postinoculation. Each test was repeated three times with three repetitions for each time. In all, we obtained one hundred and seventeen C. gloeosporioides strains from five hundred and thirty-five isolates tested. To evaluate the resistance of C. gloeosporioides against thiophanate-methyl, prochloraz and tebuconazole, we tested the pathogen growth by using distinguishing dosages and the hyphae growth inhibition method. C. gloeosporioides strains were cultured on the PDA plates for seven days in the dark, then transferred into fresh PDA plates with different dosages,and the diameter of the colony was investigated on the seventh day. The effective inhibiting concentration(EC_(50)) and resistance frequency were calculated by using the DPS software. For investigating the mechanism of C. gloeosporioides resistance against thiophanate-methyl, β-tubulin gene sequences of 28 strains were amplified and sequenced. The fungal genomic DNA of the twenty-eight strains was isolated from the fungal vegetative hyphae using the cetyltrimethylammonium bromide(CTAB) procedure combined with RNase A and proteinase K treatment. PCR was conducted with pfu DNA polymerase, and PCR products were purified and sequenced by a bio-company. The partial amino acid sequences of β-tubulin proteins were aligned and analyzed by using the Bioedit software.【Results】The resistance frequency of the 117 isolates to thiophanate-methyl was 100%, which can be attributed to high level resistance. The β-tubulin gene sequence alignment of 27 of the selected 28 isolates indicated that GAA at codon 198 mutated into GCA, which resulted in a substitution of glutamic acid for alanine at codon 198. In addition, phenylalanine acid of the isolate Dj1-1-6 mutated into tyrosine acid at codon 200. The effective inhibiting concentrations(EC_(50)) of hyphen radial growth on tebuconazole ranged from 0 to 0.843 0 mg·L~(-1) with a mean value of 0.155 5 mg · L~(-1). The sensitive assay showed that 75.21% of the 117 isolates had a low resistance to tebuconazole, and the hyphen inhibition rate was 92.72% at 5 mg · L~(-1). All 117 isolates were highly sensitive to prochloraz with a mean value of 0.011 9 mg · L~(-1), and the average inhibition rate of the colony growth was 95.02% at 0.5 mg · L~(-1).【Conclution】This study shows that C. gloeosporioides has a high resistance to thiophanate-methyl, a low resistance to tebuconazole and a high sensitivity to prochloraz.