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. 2005 Aug;71(8):4254–4262. doi: 10.1128/AEM.71.8.4254-4262.2005

TABLE 3.

Logit regression analysis of insect mortality following 11 SfMNPV treatments including wild-type SfNIC, five pure genotypes, and five co-occluded genotype mixtures, in second-instar Spodoptera frugiperda following per os inoculationa

Inoculum LC50 (OB/ml) 95% Confidence limits
Intercept + SE Relative potency P Reference
Low High
Wild-type SfNIC 5.47 × 104 3.82 × 104 7.84 × 104 −6.734 + 0.2602 1 This study
Genotype A 2.38 × 105 1.64 × 105 3.48 × 105 −7.643 + 0.2785 0.23 <0.001 This study
Genotype B 1.93 × 105 1.33 × 105 2.82 × 105 −7.515 + 0.2752 0.28 <0.001 This study
Genotype C This study
Genotype D This study
Genotype F 1.53 × 105 1.06 × 105 2.22 × 105 −7.369 + 0.2731 0.36 <0.001 This study
Genotype G 34
Genotype H 2.45 × 105 1.89 × 105 3.21 × 105 −7.392 + 0.2000 0.22 <0.001 34
Genotype I 1.66 × 105 1.29 × 105 2.15 × 105 −7.160 + 0.1963 0.33 <0.001 34
75% B + 25% A 1.08 × 105 7.53 × 104 1.56 × 105 −7.156 + 0.2679 0.51 0.014 This study
75% B + 25% D 5.05 × 104 3.09 × 104 8.24 × 104 −4.431 + 0.5141 1.09 N.S. This study
75% B + 25% F 2.33 × 105 1.59 × 105 3.41 × 105 −7.630 + 0.2787 0.24 <0.001 This study
75% A + 25% C 2.18 × 105 1.50 × 105 3.18 × 105 −7.588 + 0.2766 0.25 <0.001 This study
75% F + 25% C 1.69 × 105 1.17 × 105 2.45 × 105 −7.432 + 0.2735 0.32 <0.001 This study
a

Logit regression of number of responding insects against loge(virus concentration) given in terms of loge odds ratio: loge(p/q) = a + bx. Regressions were fitted in GLIM with a common slope of 0.6173+0.0216(standard error) for all the virus inocula except the B + D mixture, which was fitted separately with a slope of 0.4090+0.0467, and the variants described in a previous study(31), H and I, with a slope of 0.5813+0.034. A test for nonparallelism was not significant for those virus inocula (χ2 = 4.18, d.f. = 24, P > 0.05). P values were calculated by t test of the differences between regression intercepts compared to that of the wild-type SfNIC isolate. Relative potencies were calculated as the ratio of effective concentrations relative to SfNIC except in the case of the B + D mixture, for which this represents the ratio of LC50 values and is not significant (N.S.) based on overlap of 95% confidence limits (26). As such, relative potencies indicate the relative pathogenicity of each genotype or mixtures of genotypes compared with that of the wild-type isolate. All bioassays were performed in second-instar S. frugiperda (∼25 insects/concentration, three replicates) using the droplet feeding method. OBs containing co-occluded genotype mixtures were produced by injecting S. frugiperda with mixtures of occlusion-devired virions (B+A, B+D, B+F, A+C, and F+C) in a ratio of 3:1. The proportion of each genotype was confirmed by densitometric analysis from semiquantitative PCR amplification (Fig. 3).