Whole genome analysis of the koa wilt pathogen (Fusarium oxysporum f. sp. koae) and the development of molecular tools for early detection and monitoring

被引:12
作者
Dobbs, John T. [1 ]
Kim, Mee-Sook [2 ]
Dudley, Nicklos S. [3 ]
Klopfenstein, Ned B. [4 ]
Yeh, Aileen [3 ]
Hauff, Robert D. [5 ]
Jones, Tyler C. [3 ]
Dumroese, R. Kasten [4 ]
Cannon, Philip G. [6 ]
Stewart, Jane E. [1 ]
机构
[1] Colorado State Univ, Dept Agr Biol, 1177 Campus Delivery, Ft Collins, CO 80523 USA
[2] US Forest Serv, USDA, Pacific Northwest Res Stn, 3200 SW Jefferson Way, Corvallis, OR 97331 USA
[3] Hawaii Agr Res Ctr, Maunawili Res Stn, Oahu, HI USA
[4] US Forest Serv, USDA, Rocky Mt Res Stn, 1221 South Main St, Moscow, ID 83843 USA
[5] Dept Land & Nat Resources, Div Forestry & Wildlife, 1151 Punchbowl St,Room 325, Honolulu, HI 96813 USA
[6] US Forest Serv, USDA, Forest Hlth Protect, 1323 Club Dr, Vallejo, CA 94592 USA
关键词
Fusarium oxysporum; Lineage-specific DNA; Virulence genes; PCR primer; Haplotypes; Acacia koa; ACACIA-KOA; GENETIC DIVERSITY; VASCULAR WILT; PCR; VIRULENCE; ALGORITHM; EFFECTOR; CONGLUTINANS; CHROMOSOMES; PHYLOGENIES;
D O I
10.1186/s12864-020-07156-y
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundDevelopment and application of DNA-based methods to distinguish highly virulent isolates of Fusarium oxysporum f. sp. koae [Fo koae; cause of koa wilt disease on Acacia koa (koa)] will help disease management through early detection, enhanced monitoring, and improved disease resistance-breeding programs.ResultsThis study presents whole genome analyses of one highly virulent Fo koae isolate and one non-pathogenic F. oxysporum (Fo) isolate. These analyses allowed for the identification of putative lineage-specific DNA and predicted genes necessary for disease development on koa. Using putative chromosomes and predicted gene comparisons, Fo koae-exclusive, virulence genes were identified. The putative lineage-specific DNA included identified genes encoding products secreted in xylem (e. g., SIX1 and SIX6) that may be necessary for disease development on koa. Unique genes from Fo koae were used to develop pathogen-specific PCR primers. These diagnostic primers allowed target amplification in the characterized highly virulent Fo koae isolates but did not allow product amplification in low-virulence or non-pathogenic isolates of Fo. Thus, primers developed in this study will be useful for early detection and monitoring of highly virulent strains of Fo koae. Isolate verification is also important for disease resistance-breeding programs that require a diverse set of highly virulent Fo koae isolates for their disease-screening assays to develop disease-resistant koa.ConclusionsThese results provide the framework for understanding the pathogen genes necessary for koa wilt disease and the genetic variation of Fo koae populations across the Hawaiian Islands.
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页数:15
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