Molecular Marker Development for the Rapid Differentiation of Black Rot Causing Xanthomonas campestris pv. campestris Race 7

被引:2
作者
Kim, Yeo-Hyeon [1 ]
Mao, Sopheap [1 ]
Sahu, Nihar [1 ]
Somaddar, Uzzal [1 ,2 ]
Kim, Hoy-Taek [1 ]
Watanabe, Masao [3 ]
Park, Jong-In [1 ,2 ,3 ]
机构
[1] Sunchon Natl Univ, Dept Hort, Sunchon 57922, South Korea
[2] Sunchon Natl Univ, Interdisciplinary Program IT Bio Convergence Syst, Sunchon 57922, South Korea
[3] Tohoku Univ, Grad Sch Life Sci, Sendai 9808577, Japan
关键词
Brassicaceae; black rot; marker; PCR; Xanthomonas campestris pv. campestris; TIME PCR ASSAY; REP-PCR; BRASSICA; RACES; IDENTIFICATION; RESISTANCE; PATHOGEN; CRUCIFERS; DIVERSITY; PATHOVARS;
D O I
10.5423/PPJ.OA.07.2023.0102
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Xanthomonas campestris pv. campestris (Xcc) is a plant pathogen of Brassica crops that causes black rot disease throughout the world. At present, 11 physiological races of Xcc (races 1-11) have been reported. The conventional method of using differential cultivars for Xcc race detection is not accurate and it is laborious and time-consuming. Therefore, the development of specific molecular markers has been used as a substitute tool because it offers an accurate and reliable result, particularly a quick diagnosis of Xcc races. Previously, our laboratory has successfully developed race-specific molecular markers for Xcc races 1-6. In this study, specific molecular markers to identify Xcc race 7 have been developed. In the course of study, whole genome sequences of several Xcc races, X. campestris pv. incanae, X. campestris pv. raphani, and X. campestris pv. vesicatoria were aligned to identify variable regions like sequence-characterized amplified regions and insertions and deletions specific to race 7. Primer pairs were designed targeting these regions and validated against 22 samples. The polymerase chain reaction analysis re vealed that three primer pairs specifically amplified the DNA fragment corresponding to race 7. The obtained finding clearly demonstrates the efficiency of the newly developed markers in accurately detecting Xcc race 7 among the other races. These results indicated that the newly developed marker can successfully and rapidly detect Xcc race 7 from other races. This study represents the first report on the successful development of specific molecular markers for Xcc race 7.
引用
收藏
页码:494 / 503
页数:10
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