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

Author:

He Rong1,Liu Pu1,Jia Bing1,Xue Shizhou1,Wang Xiaojie1,Hu Jiayong1,Al Shoffe Yosef2,Gallipoli Lorenzo3,Mazzaglia Angelo3,Balestra Giorgio M.3,Zhu Liwu12ORCID

Affiliation:

1. Key Lab of Pomology, School of Horticulture, Anhui Agricultural University, West Changjiang Road 130, Hefei 230036, Anhui Province, P.R. China;

2. Section of Horticulture, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY 14853, USA; and

3. Department of Science and Technologies for Agriculture, Forestry, Nature and Energy, University of Tuscia, Via S. Camillo de Lellis 01100, Viterbo, Italy

Abstract

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.

Funder

National Natural Science Foundation of China

Anhui Provincial Annual Key Project Foundation

Anhui Provincial Natural Science Foundation

Discipline Capacity Promotion at Anhui Agricultural University, China

Foreign Visiting Scholars of Anhui Higher Education Revitalization

Publisher

Scientific Societies

Subject

Plant Science,Agronomy and Crop Science

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