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. 2005 May;4(5):937–947. doi: 10.1128/EC.4.5.937-947.2005

TABLE 2.

Effects of locust organic extracts on spore adhesion (A), germination (G), and appressorium differentiation (D)

Treatmenta % Change
15 h
24 h
A G D A G D
YE 95 39 0 100 79 0
Dichloromethane 40 28 3 97 81 9
Dichloromethane + YE 100 87 9 100 >99 66
Dichloromethane + YE + H89 (5 μM) 84 61 0 100 87 0
Dichloromethane + YE + PD98059 (10 nM) 80 22 0 95 65 0
Hexane 0 0 0 50 10 0
Hexane + YE 95 55 0 100 80 0
Methanol 100 91 3 98 >99 47
Methanol + YE 100 93 53 100 >99 63
LPL (1 mg/ml) 95 67 0 100 >99 13
LPL (2 mg/ml) 100 94 4 100 >99 17
LPL (4 mg/ml) 100 95 0 100 >99 0
LPL (1 mg/ml) + YE 95 85 3 100 >99 8
a

Ethanol containing 1 mg of locust dichloromethane, hexane, or methanol extract was evaporated on coverslips that were placed in 5.5-cm petri dishes containing 2 ml of water or 0.0125% yeast extract (YE) and 10,000 conidia of M. anisopliae var. acridum ARSEF 324. The effects of YE alone and the water-soluble fraction of the methanol extract (locust polar lipid [LPL]) were tested using ethanol-washed cover slips. Percent germination and differentiation frequencies were determined from counts on the petri dish surface overlaid by the coverslip. Adhesion was determined on separate petri dishes not containing coverslips.