江西农业大学学报
江西農業大學學報
강서농업대학학보
ACTA AGRICULTURAE UNIVERSITATIS JIANGXIENSIS
2014年
5期
1127-1131
,共5页
赵永坡%初雷霞%岳开华%李振方%林文雄
趙永坡%初雷霞%嶽開華%李振方%林文雄
조영파%초뢰하%악개화%리진방%림문웅
太子参%连作障碍%根际微生态%尖孢镰刀菌%qRT-PCR
太子參%連作障礙%根際微生態%尖孢鐮刀菌%qRT-PCR
태자삼%련작장애%근제미생태%첨포렴도균%qRT-PCR
Pseudostellaria heterophylla%successive cropping obstacle%rhizosphere microecology%Fusari-um oxysporum%qRT-PCR
根据太子参尖孢镰刀菌的测序结果,用设计的一对特异性引物,构建其分子定量检测方法,并进行不同连作年限太子参根际土壤中该尖孢镰刀菌的菌群定量分析,研究结果表明,结果表明:(1)扩增的阳性条带106 bp,特异性、敏感性结果显示,该PCR方法对太子参镰刀菌DNA的最低检测量为0.000012 ng/μL,而禾谷镰刀菌、茄病镰刀菌、黄曲霉和解淀粉芽孢杆菌的扩增结果均为阴性。(2)运用此方法对该太子参镰刀菌的定量结果表明,尖孢镰刀菌随太子参连作年限的增加而逐年增多。该检测方法具有快速、准确、灵敏度高、易于操作等优点,并且实现了由定性向定量的跨越,可以为太子参根际微生态中该种病原菌的动态变化研究提供方法及依据,也为阐释太子参重茬连作时伴随爆发大规模病害提供了参考。
根據太子參尖孢鐮刀菌的測序結果,用設計的一對特異性引物,構建其分子定量檢測方法,併進行不同連作年限太子參根際土壤中該尖孢鐮刀菌的菌群定量分析,研究結果錶明,結果錶明:(1)擴增的暘性條帶106 bp,特異性、敏感性結果顯示,該PCR方法對太子參鐮刀菌DNA的最低檢測量為0.000012 ng/μL,而禾穀鐮刀菌、茄病鐮刀菌、黃麯黴和解澱粉芽孢桿菌的擴增結果均為陰性。(2)運用此方法對該太子參鐮刀菌的定量結果錶明,尖孢鐮刀菌隨太子參連作年限的增加而逐年增多。該檢測方法具有快速、準確、靈敏度高、易于操作等優點,併且實現瞭由定性嚮定量的跨越,可以為太子參根際微生態中該種病原菌的動態變化研究提供方法及依據,也為闡釋太子參重茬連作時伴隨爆髮大規模病害提供瞭參攷。
근거태자삼첨포렴도균적측서결과,용설계적일대특이성인물,구건기분자정량검측방법,병진행불동련작년한태자삼근제토양중해첨포렴도균적균군정량분석,연구결과표명,결과표명:(1)확증적양성조대106 bp,특이성、민감성결과현시,해PCR방법대태자삼렴도균DNA적최저검측량위0.000012 ng/μL,이화곡렴도균、가병렴도균、황곡매화해정분아포간균적확증결과균위음성。(2)운용차방법대해태자삼렴도균적정량결과표명,첨포렴도균수태자삼련작년한적증가이축년증다。해검측방법구유쾌속、준학、령민도고、역우조작등우점,병차실현료유정성향정량적과월,가이위태자삼근제미생태중해충병원균적동태변화연구제공방법급의거,야위천석태자삼중치련작시반수폭발대규모병해제공료삼고。
The specific primers of Fusarium oxysporum f.sp.were designed and the molecular quantitative detection method was built to be used to quantify and analyze the Fusarium oxysporum f.sp.in rhizosphere soil under monoculturally cropped Pseudostellaria heterophylla for different years.The results showed that ( 1 ) the amplified positive strip was 106 bp;the minimum detectable amount of Fusarium oxysporum f.sp.DNA was 0.000 012 ng/μL with this method and the amplification results of Fusarium graminearum,Fusarium solani,Aspergillus flavus,bacillus amyloliquefaciens were all negative,(2) the quantifying results of Fusarium oxyspo-rum f.sp.with this method suggested that the number of Fusarium oxysporum f.sp.increased with the monocul-ture years.This detecting method is of accuracy,high sensitivity and easy accessibility,which realizs the leap from qualitative to quantitative.It offers the methods and foundation for analysis of this pathogen in the rhizo-sphere micro ecology of Pseudostellaria heterophylla,and illuminates the reason for large-scale occurrence of the disease in successively cropped Pseudostellaria heterophylla.