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Factors affecting the virulence of Ralstonia solanacearum and its colonization on tobacco roots
Author(s) -
Li X.,
Liu Y.,
Cai L.,
Zhang H.,
Shi J.,
Yuan Y.
Publication year - 2017
Publication title -
plant pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.928
H-Index - 85
eISSN - 1365-3059
pISSN - 0032-0862
DOI - 10.1111/ppa.12675
Subject(s) - ralstonia solanacearum , bacterial wilt , biology , rhizosphere , colonization , population , virulence , transplanting , nicotiana tabacum , horticulture , pathogen , agronomy , microbiology and biotechnology , botany , bacteria , gene , sowing , biochemistry , genetics , demography , sociology
Tobacco bacterial wilt caused by Ralstonia solanacearum is a serious disease affecting tobacco cultivation in southwest China. The response surface methodology was employed to evaluate the optimal conditions of tobacco bacterial wilt, and green fluorescent protein gene ( gfp ) labelling was applied to monitor the location and survival dynamics of R. solanacearum (Rs:: gfp ) on tobacco roots and in soil under these optimal conditions. The results showed that the highest wilt incidence was 91.13%, which occurred when the population reached 6.6 × 10 6 CFU /g soil, the temperature was 30.55 °C, and the humidity was >81.42%. The Rs:: gfp densely colonized the root tips and root hairs, and cells of Rs:: gfp were observed intermittently in the elongation zone or at the point of the emerging lateral roots. The Rs:: gfp number in the rhizosphere soil was 10.75‐, 73.13‐ and 74.86‐times higher than that in the bulk soil at 10, 15 and 20 days after transplantation, respectively. Increased colonization by Rs:: gfp was related to the population of the pathogen, the environmental temperature and the humidity in the soil. These three conditions determined whether R. solanacearum would induce tobacco wilt. This is the first study to investigate factors affecting the virulence of a tobacco wilt bacterial pathogen, which is important for conducting field diagnosis and biocontrol of tobacco bacterial wilt.