TABLE 2.
Effect of P. luminescens HGB008 phenotypic variation on ADF activity at California test sites
Test conditiona | Strainb | Form | ADF activityc |
---|---|---|---|
Field in vitro | E. coli | NAg | 0.95 ± 0.11 Ad |
HGB008 | 1° | 0.08 ± 0.01 Bd | |
HGB159 | 2° | 0.08 ± 0.02 Bd | |
Laboratory in vitro | E. coli | NA | 1 Ae |
HGB008 | 1° | 0.05 ± 0.01 Be | |
HGB159 | 2° | 0.05 ± 0.01 Be | |
Field in vivo | Control | NA | 0.51 ± 0.08 Af |
HGB008 | 1° | 0.019 ± 0.002 Bf | |
HGB159 | 2° | 0.47 ± 0.05 Af |
See Materials and Methods for detailed explanation of test conditions.
See Table 1 for details on the strains. E. coli, E. coli (Migula). Control, freeze-killed insects used for in vivo experiments.
For in vitro assays, values are the proportion of volume (in microliters) removed from wells. For in vivo studies, values are the mean proportion of ants visiting. Different letters after values indicate significant difference within an experiment (P < 0.05 by Duncan's new multiple-range test).
There was a significant difference between the number of field ants visiting the E. coli control versus the bacterial treatments (F = 34.93, df = 2, 32; P < 0.05).
Significantly more suspension remained in the wells of 1°- or 2°-form bacterial treatments than that for the E. coli control treatment (F = 4697.98, df = 2, 32; P < 0.001).
There was a significant difference between the treatments of 1°- and 2°-form bacteria or freeze-killed control (F = 67.5, df = 2, 67; P < 0.0001).
NA, not applicable.