2017
DOI: 10.1016/j.aspen.2017.08.001
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Photorhabdus luminescens subsp. akhurstii SL0708 pathogenicity in Spodoptera frugiperda (Lepidoptera: Noctuidae) and Galleria mellonella (Lepidoptera: Pyralidae)

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Cited by 14 publications
(10 citation statements)
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“…The crude extract from the strain ETL had higher fungal MIC properties (≤1 mg/mL of MIC) against A. flavus and A. niger than a crude extract from another reported EPNB (4 mg/mL ant 5 mg/mL for A. flavus and A. niger, respectively) [35], although a pur-antifungal compound (cyclo(l-Prod-Leu)) isolated from it showed greater MIC values of 0.008 mg/mL and 0.032 mg/mL against A. flavus and A. niger, respectively [35]. Members of the Photorhabdus produce numerous SMs with various antimicrobial activities [5,12] to suit the entomopathogenic lifestyle with their nematode vectors and to contribute to the symbiotic association with the nematode host by providing a monoxenic growth environment while killing off competitive microbes and insect larvae, and providing nutrients for both the nematodes and bacteria [4,[36][37][38][39]. This could justify the notable inhibitory activity found in this study.…”
Section: Minimum Inhibitory Concentration (Mic)mentioning
confidence: 99%
“…The crude extract from the strain ETL had higher fungal MIC properties (≤1 mg/mL of MIC) against A. flavus and A. niger than a crude extract from another reported EPNB (4 mg/mL ant 5 mg/mL for A. flavus and A. niger, respectively) [35], although a pur-antifungal compound (cyclo(l-Prod-Leu)) isolated from it showed greater MIC values of 0.008 mg/mL and 0.032 mg/mL against A. flavus and A. niger, respectively [35]. Members of the Photorhabdus produce numerous SMs with various antimicrobial activities [5,12] to suit the entomopathogenic lifestyle with their nematode vectors and to contribute to the symbiotic association with the nematode host by providing a monoxenic growth environment while killing off competitive microbes and insect larvae, and providing nutrients for both the nematodes and bacteria [4,[36][37][38][39]. This could justify the notable inhibitory activity found in this study.…”
Section: Minimum Inhibitory Concentration (Mic)mentioning
confidence: 99%
“…Bacterium metabolic phase I is required for EPN production, particularly due to four metabolic characteristics: (1) capacity to degrade media into compounds that can be assimilated and necessary for IJs, distinctively sterols by lytic enzymes; (2) secretion of "feeding signals" to induce development and production of new IJs generations; (3) capacity to establish symbiosis or re-associate/adherence to the nematode's intestines; and (4) secretion of antibiotic substances, avoiding contamination in the media (Ehlers 2001;Salazar-Gutiérrez et al 2017). Consequently, it is most important to maintain phase I during in vitro EPNs production to increase recovery percentage and to obtain high IJ yield during the production process (Stock et al 2017).…”
Section: Resultsmentioning
confidence: 99%
“…After approximately 24 h, IJs which are suspended in an enriched nutrient broth are inoculated into the bacterial culture. To check the entompathogenicity, the greater wax moth, Galleria mellonella Linnaeus (Lepidoptera: Pyralidae), was infected by the nematodes along with its symbiont, and its death occurs within 48 h, and the insect pathogenicity of the H. indica-P. luminescens combination is confirmed (Salazar-Gutiérrez et al 2017).…”
Section: Introductionmentioning
confidence: 99%
“…The LC 50 dose of the strain K-1 was 1010 cells per S. litura sixth-instar larvae in 48 h [ 53 ]. A 100% mortality of both the fall armyworms, Spodoptera frugiperda and G. mellonella , was also attained after 48 h of treatment with the strain P. luminescens akhurstii SL0708 at 1 × 10 3 –1 × 10 4 CFU/larva [ 66 ]. On the other hand, P. temperata showed oral toxicity to the olive moth, Prays oleae , with an LC 50 of 58.1 × 10 6 cells/mL [ 67 ].…”
Section: Pathogenicity Of Photorhabdus Sppmentioning
confidence: 99%
“…For instance, a cumulative percent mortality of 63% and 100% for G. mellonella, but 10% and 93% for S. frugiperda, was achieved after 72 h of injecting intra- or extra-cellular extracts of the strain P. luminescens akhurstii SL0708, respectively. These differences also indicate the impact of extracellular factors in pathogenicity [ 66 ]. Those authors detected proteases, esterases, ureases, hemolysins and siderophores as responsible for the high pathogenicity/extra-cellular activities.…”
Section: Pathogenicity Of Photorhabdus Sppmentioning
confidence: 99%