植物病理学报
植物病理學報
식물병이학보
ACTA PHYTOPATHOLOGICA SINICA
2009年
6期
630-637
,共8页
崔晓岚%孟庆晓%毕扬%吴鹏飞%刘西莉
崔曉嵐%孟慶曉%畢颺%吳鵬飛%劉西莉
최효람%맹경효%필양%오붕비%류서리
辣椒疫霉%烯酰吗啉%敏感性基线%抗药突变体
辣椒疫黴%烯酰嗎啉%敏感性基線%抗藥突變體
랄초역매%희선마람%민감성기선%항약돌변체
Phytophthora capsici%dimethomorph%baseline sensitivity%resistant-mutant
采用菌丝生长速率法测定了125株采自河北、内蒙古、陕西、安徽和北京等地区的辣椒疫霉病菌对烯酰吗啉的敏感性,结果表明,其EC_(50)值分布于0.126~0.318 μg/mL之间,最不敏感菌株是最敏感菌株的2.5倍,平均EC_(50)=(0.218±0.0368)μg/mL.125个菌株对烯酰吗啉的敏感性分布呈单峰曲线,未出现抗性的病原菌亚群体,可将该单峰曲线作为辣椒疫霉对烯酰吗啉的敏感性基线,将烯酰吗啉对该病原群体的平均EC_(50)值作为田间抗药性监测的参考标准.通过紫外诱变敏感菌株N-7的菌丝获得了12株抗烯酰吗啉的突变体,抗性指数在16.38~132.15之间;通过紫外诱变敏感菌株DZ-16的游动孢子获得1株抗性指数为680倍的高抗药水平的突变体.突变体的部分生物学性状研究表明,其致病力与敏感菌株相当;大部分突变体产生孢子囊的能力与亲本菌株相比均有不同程度的提高;离体条件下,突变体和亲本菌株释放游动孢子的能力相当;突变体的菌丝生长速率与亲本菌株相比具有不同程度的差异.测定了敏感亲本菌株和突变体的交配型,均为A_1型菌株,经紫外诱变后交配型没有发生改变.综合分析表明,抗性突变体的产生有利于抗药性群体的发展.为避免和延缓抗药性的产生,生产上应将烯酰吗啉与其它无交互抗药性的杀菌剂交替使用.
採用菌絲生長速率法測定瞭125株採自河北、內矇古、陝西、安徽和北京等地區的辣椒疫黴病菌對烯酰嗎啉的敏感性,結果錶明,其EC_(50)值分佈于0.126~0.318 μg/mL之間,最不敏感菌株是最敏感菌株的2.5倍,平均EC_(50)=(0.218±0.0368)μg/mL.125箇菌株對烯酰嗎啉的敏感性分佈呈單峰麯線,未齣現抗性的病原菌亞群體,可將該單峰麯線作為辣椒疫黴對烯酰嗎啉的敏感性基線,將烯酰嗎啉對該病原群體的平均EC_(50)值作為田間抗藥性鑑測的參攷標準.通過紫外誘變敏感菌株N-7的菌絲穫得瞭12株抗烯酰嗎啉的突變體,抗性指數在16.38~132.15之間;通過紫外誘變敏感菌株DZ-16的遊動孢子穫得1株抗性指數為680倍的高抗藥水平的突變體.突變體的部分生物學性狀研究錶明,其緻病力與敏感菌株相噹;大部分突變體產生孢子囊的能力與親本菌株相比均有不同程度的提高;離體條件下,突變體和親本菌株釋放遊動孢子的能力相噹;突變體的菌絲生長速率與親本菌株相比具有不同程度的差異.測定瞭敏感親本菌株和突變體的交配型,均為A_1型菌株,經紫外誘變後交配型沒有髮生改變.綜閤分析錶明,抗性突變體的產生有利于抗藥性群體的髮展.為避免和延緩抗藥性的產生,生產上應將烯酰嗎啉與其它無交互抗藥性的殺菌劑交替使用.
채용균사생장속솔법측정료125주채자하북、내몽고、협서、안휘화북경등지구적랄초역매병균대희선마람적민감성,결과표명,기EC_(50)치분포우0.126~0.318 μg/mL지간,최불민감균주시최민감균주적2.5배,평균EC_(50)=(0.218±0.0368)μg/mL.125개균주대희선마람적민감성분포정단봉곡선,미출현항성적병원균아군체,가장해단봉곡선작위랄초역매대희선마람적민감성기선,장희선마람대해병원군체적평균EC_(50)치작위전간항약성감측적삼고표준.통과자외유변민감균주N-7적균사획득료12주항희선마람적돌변체,항성지수재16.38~132.15지간;통과자외유변민감균주DZ-16적유동포자획득1주항성지수위680배적고항약수평적돌변체.돌변체적부분생물학성상연구표명,기치병력여민감균주상당;대부분돌변체산생포자낭적능력여친본균주상비균유불동정도적제고;리체조건하,돌변체화친본균주석방유동포자적능력상당;돌변체적균사생장속솔여친본균주상비구유불동정도적차이.측정료민감친본균주화돌변체적교배형,균위A_1형균주,경자외유변후교배형몰유발생개변.종합분석표명,항성돌변체적산생유리우항약성군체적발전.위피면화연완항약성적산생,생산상응장희선마람여기타무교호항약성적살균제교체사용.
The sensitivity to dimethomorph of 125 Phytophthora capsici strains collected from Hebei, Mongolia, Shannxi, Anhui and Beijing were determined by mycelia growth inhibition method. The results showed that EC_(50) values ranged from 0.126 -0.318 μg/mL. EC_(50) of the most insensitive strains was 2. 5 folds of the most sensitive ones with a mean of 0.218 0.0368 μg/mL . The sensitivity frequency of P. capsici to dimethomorph distributed as a unimodel curve, which showed there was no resistant subpopulation among these isolates , so this sensitivity baseline was suitable for resistance monitoring of P. capsici to dimethomorph. 12 resistant mutants to dimethomorph were obtained from N-7 parental strain in vitro by UV- irradiating,and the resistant factors ranged from 16.38-132.15 folds. One very high resistant mutant with 680 folds resistance factor was also selected from DZ-16 strain. The parental strains and their mutants were investigated for mating type. Some biological characteristics of mutants were studied in laboratory. The results indicated that the mutants possessed consistent pathogenicity with their parental strains. As compared to their original strain, sporulation ability of resistant mutants were increased in vivo, the quantity of asexual spores corresponded to that of sensitive strains in vitro and the resistant mutants exhibited diversity in mycelial growth rate. All the strains were A_1 mating type. Based on the above, the resistant mutants would favor the development of dimethomorph resistant population. It was suggested that the dimethomorph should be used alternately with other no cross-resistant fungicides to avoid or delay the development of resistance.