4.5 Article

The low-temperature-induced viable-but-nonculturable state affects the virulence of Ralstonia solanacearum biovar 2

Journal

PHYTOPATHOLOGY
Volume 94, Issue 5, Pages 463-469

Publisher

AMER PHYTOPATHOLOGICAL SOC
DOI: 10.1094/PHYTO.2004.94.5.463

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van Overbeek. L. S.. Bergervoet. J. H. W.. Jacobs, F. H. H.. and van Elsas. J. D. 2004. The low-ternperature-induced viable-but-nonculturable state 2. Phytopathology affects the virulence of Ralstonia solanacearum biovar 94:463-469. The physiology and virulence of Ralstonia solanacerum biovar 2 strain 1609. kept in water at 4 and 20degreesC, were studied. At 20degreesC. total cell and plate count (colony forming units: CFU) numbers were similar, between log 5.03 and log 5.55 CFU,and log 5.03 and log 5.51 cells per ml. at days 0 and 132. respectively. However, CFU in the Cultures kept at 4degreesC dropped from log 6.78 CFU/ml at day 0 to below detection after 84 days. The presence of catalase in the agar resulted in higher CFU. and at day 84. log, 1.95 CFU/ml still was detectable. No colonies were observed at day 125. The presence of viable-but-nonculturable (VBNC) cells in the 4degreesC Cultures was confirmed using SYTO9 viability staining. Viable Cell numbers were log 1.77 higher than CFU on plates with catalase. At day 84 and after 125 days, log 3.70 viable cells per ml still were I present. Shifts in subpopulations differing in viability were found by flow cytometric sorting of 4degreesC-treated cells stained with SYTO9 (healthy) and propidium iodide (PI, compromised). The SYTO9-stained cell fractions dropped from 99 to 39%, and the PI-stained fractions increased from 0.7 to 33.3% between days 0 and 125. At 20degreesC. the SYTO9-stained fraction remained stable at 99% until day 132, SYTO9-stained cells sorted from 4degreesC Cultures at day 100 were injected into tomato plants. Upon incubation for 30 days, these plants did not show wilting. However. more than log 4.19 CFU and log 8.17 cells were recovered from these plants. Cells from colonies isolated from the nonwilted plants did not regain their virulence as demonstrated by Subsequent injection into several mew, sets of tomato plants. Cells from 4degreesC cultures injected at day 125 were not able to cause wilting of, or proliferate in, tomato plants. The threat posed by VBNC R. solanacearum cells upon incubation at 4degreesC was thus ephemeral because cells lost their capacity to cause disease after 125 days.

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