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Biological control of the soft rot bacterium Pectobacterium carotovorum by Bacillus amyloliquefaciens strain Ar10 producing glycolipid-like compounds.

Authors :
Azaiez, Sana
Ben Slimene, Imen
Karkouch, Ines
Essid, Rym
Jallouli, Selim
Djebali, Naceur
Elkahoui, Salem
Limam, Ferid
Tabbene, Olfa
Source :
Microbiological Research. Dec2018, Vol. 217, p23-33. 11p.
Publication Year :
2018

Abstract

Abstract Four hundred and fifty bacteria were evaluated for antagonistic activity against bacterial soft rot of potato caused by Pectobacterium carotovorum sp strain II16. A strain Ar10 exhibiting potent antagonist activity has been identified as Bacillus amyloliquefaciens on the basis of biochemical and molecular characterization. Cell free supernatant showed a broad spectrum of antibacterial activity against human and phytopathogenic bacteria in the range of 10-60 AU/mL. Incubation of P. carotovorum cells with increasing concentrations of the antibacterial compound showed a killing rate of 94.8 and 96% at MIC and 2xMIC respectively. In addition, the antibacterial agent did not exert haemolytic activity at the active concentration and has been preliminary characterized by TLC and GC–MS as a glycolipid compound. Treatment of potato tubers with strain Ar10 for 72 h significantly reduced the severity of disease symptoms (100 and 85.05% reduction of necrosis deep / area and weight loss respectively). The same levels in disease symptoms severity was also recorded following treatment of potato tubers with cell free supernatant for 1 h. Data suggest that protection against potato soft rot disease may be related to glycolipid production by strain Ar10. The present study affords new alternatives for anti- Pectobacterium carotovorum bioactive compounds against the soft rot disease of potato. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09445013
Volume :
217
Database :
Academic Search Index
Journal :
Microbiological Research
Publication Type :
Academic Journal
Accession number :
132690307
Full Text :
https://doi.org/10.1016/j.micres.2018.08.013