Genetic Diversity of Pseudomonas syringae pv. actinidiae Strains from Different Geographic Regions in China

被引:6
|
作者
He, Rong [1 ]
Liu, Pu [1 ]
Jia, Bing [1 ]
Xue, Shizhou [1 ]
Wang, Xiaojie [1 ]
Hu, Jiayong [1 ]
Al Shoffe, Yosef [2 ]
Gallipoli, Lorenzo [3 ]
Mazzaglia, Angelo [3 ]
Balestra, Giorgio M. [3 ]
Zhu, Liwu [1 ,2 ]
机构
[1] Anhui Agr Univ, Sch Hort, Key Lab Pomol, West Changjiang Rd 130, Hefei 230036, Anhui, Peoples R China
[2] Cornell Univ, Coll Agr & Life Sci, Hort Sect, Ithaca, NY 14853 USA
[3] Univ Tuscia, Dept Sci & Technol Agr Forestry Nat & Energy, Via S Camillo de Lellis, I-01100 Viterbo, Italy
基金
中国国家自然科学基金;
关键词
BACTERIAL CANKER; CAUSAL AGENT; KIWIFRUIT; IDENTIFICATION; CHINENSIS; PATHOVARS; EVOLUTION; ACTINIDIFOLIORUM; OUTBREAK; ORIGIN;
D O I
10.1094/PHYTO-06-18-0188-R
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Pseudomonas syringae pv. actinidiae causes kiwifruit bacterial canker, with severe infection of the kiwifruit plant resulting in heavy economic losses. Little is known regarding the biodiversity and genetic variation of populations of P. syringae pv. actinidiae in China. A collection of 269 strains of P. syringae pv. actinidiae was identified from 300 isolates obtained from eight sampling sites in five provinces in China. The profiles of 50 strains of P. syringae pv. actinidiae and one strain of P. syringae pv. actinidifoliorum were characterized by Rep-, insertion sequences 50, and randomly amplified polymorphic DNA polymerase chain reaction (PCR). Discriminant analysis of principal coordinates, principal component analysis, and hierarchical cluster analysis were used to analyze the combined fingerprints of the different PCR assays. The results revealed that all isolates belonged to the Psa3 group, that strains of P. syringae pv. actinidiae from China have broad genetic variability that was related to source geographic region, and that Chinese strains can be readily differentiated from strains from France but are very similar to those from Italy. Multilocus sequence typing of 24 representative isolates using the concatenated sequences of five housekeeping genes (cts, gapA, gyrB, pfk, and rpoD) demonstrated that strain Jzhy2 from China formed an independent clade compared with the other biovars, which possessed the hopH1 effector gene but lacked the hopA1 effector gene. A constellation analysis based on the presence or absence of the four loci coding for phytotoxins and a cluster analysis based on the 11 effector genes showed that strains from China formed two distinct clades. All of the strains, including K3 isolated in 1997 from Jeju, Korea, lacked the cfl gene coding for coronatine. In contrast, the tox-argK gene cluster coding for phaseolotoxin was detected in K3 and in the biovar 1 strains (K3, Kw30, and Psa92), and produced a false-positive amplicon for the hopAM1-like gene in this study. To date, only one biovar (biovar 3) is represented by the strains of P. syringae pv. actinidiae from China, despite China being the center of origin for kiwifruit.
引用
收藏
页码:347 / 357
页数:11
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