Baseline Susceptibility of Tobacco Hornworms (Lepidoptera: Sphingidae) to Acephate, Methomyl and Spinosad in Georgia

2002 ◽  
Vol 37 (1) ◽  
pp. 94-100 ◽  
Author(s):  
Gary A. Herzog ◽  
Robert M. McPherson ◽  
David C. Jones ◽  
Russell J. Ottens

The tobacco hornworm, Manduca sexta (L.), is a serious defoliating pest of flue-cured tobacco in Georgia. Isolated producer reports of increased difficulty in controlling this pest with standard insecticides have created concern. Therefore, a topical application technique was used to determine the dosage-mortality responses of M. sexta to three commonly-used insecticides for Georgia tobacco: acephate, methomyl and spinosad. Larvae, 4 to 5 days old (second instar) and weighing 20 to 40 mg, were collected from tobacco plants. Serial concentrations of selected insecticides were applied topically to the larvae. The larvae were subsequently examined for mortality up to 72 h after exposure. Hornworm larvae were highly susceptible to spinosad, with LD50's of 0.059, 0.002, and 0.0004 μg/larva at 24, 48, and 72 h, respectively. Susceptibility to methomyl was intermediate, ranging from 0.123 to 0.176 μg/larva at 72 h, and acephate was the least toxic, with an LD50 of approximately 1.0 μg/larva. The LD50 values for methomyl and acephate remained constant from 24 to 72 h exposure. Location of the hornworm population within the state (south-central, eastern, and southeastern) did not appear to influence the overall susceptibility of the larvae. Baseline data are now established for the three commonly used insecticides for hornworm control, and can be used to document insecticide resistance if it occurs.

2003 ◽  
Vol 38 (2) ◽  
pp. 262-268 ◽  
Author(s):  
Robert M. McPherson ◽  
Michael P. Seagraves ◽  
Russell J. Ottens ◽  
C. Scott Bundy

The tobacco hornworm, Manduca sexta (L.), is an annual economic pest of flue-cured tobacco in Georgia and throughout the southeastern U.S. Recent concerns about controlling hornworms with standard insecticides have been reported by producers and the Cooperative Extension Service. Therefore, a tobacco leaf dip assay was developed to determine the dosage-mortality responses of tobacco hornworms to three standard tobacco insecticides: acephate, methomyl, and spinosad. Larvae, 4 to 5 days old (second instar) and weighing 20 to 40 mg, were reared from eggs collected on field-grown tobacco. Serial concentrations of selected insecticides were prepared in 3.8-L containers, and untreated tobacco leaves were immersed in the solution for 5 s, then air dried. Larvae were placed directly on the treated foliage and examined for mortality after 24, 48 and 72 h of exposure. Hornworm larvae were highly susceptible to foliage dipped in spinosad, with LC50's of 4.3 × 10−4 at 24 h, 1.0 × 10−6 at 48 h, and 5.7 × 10−7 at 72 h (ml/ml). Hornworms were moderately susceptible to both methomyl and acephate, with 72 h LC50's of 1.0 × 10−4 (ml/ml) and 1.2 × 10−4 (mg/ml), respectively. Although the LC50's for spinosad continued to drop from 24 to 72 h, the LC50's for methomyl and acephate remained relatively constant from 24 to 72 h. Hornworm larval feeding was disrupted within 1 h of exposure to the higher concentrations of spinosad and methomyl, with cessation of feeding accompanied by larvae moving off the treated foliage. Feeding disruption on acephate foliage was not as evident during the initial 4 h of exposure. Baseline results from leaf dip assays are now established for three commonly used tobacco hornworm controls and can be used to document insecticide resistance.


1993 ◽  
Vol 28 (3) ◽  
pp. 308-314
Author(s):  
K. Panchapakesan ◽  
R. M. Roe ◽  
Emmett P. Lampert

Studies were conducted to determine the effect of pigmentation on the field survivorship of larvae of the tobacco hornworm, Manduca sexta (L.). Larvae of the white-mutant tobacco hornworm were found to have a lower mean survival rate as compared with black-mutant and wild-type strains. Tests in the greenhouse demonstrated the larvae of the white-mutant were able to establish on the tobacco plants as well as the black-mutant and wild-type strains. Differential predation seems to be an important factor in the low recovery of the white tobacco hornworm in the field. Parasitism rates by Cotesia congregata (Say) were low for all three strains.


Plants ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 963
Author(s):  
Maria C. Holeva ◽  
Athanasios Sklavounos ◽  
Rajendran Rajeswaran ◽  
Mikhail M. Pooggin ◽  
Andreas E. Voloudakis

Cucumber mosaic virus (CMV) is a destructive plant virus with worldwide distribution and the broadest host range of any known plant virus, as well as a model plant virus for understanding plant–virus interactions. Since the discovery of RNA interference (RNAi) as a major antiviral defense, RNAi-based technologies have been developed for plant protection against viral diseases. In plants and animals, a key trigger of RNAi is double-stranded RNA (dsRNA) processed by Dicer and Dicer-like (DCL) family proteins in small interfering RNAs (siRNAs). In the present study, dsRNAs for coat protein (CP) and 2b genes of CMV were produced in vitro and in vivo and applied onto tobacco plants representing a systemic solanaceous host as well as on a local host plant Chenopodium quinoa. Both dsRNA treatments protected plants from local and systemic infection with CMV, but not against infection with unrelated viruses, confirming sequence specificity of antiviral RNAi. Antiviral RNAi was effective when dsRNAs were applied simultaneously with or four days prior to CMV inoculation, but not four days post inoculation. In vivo-produced dsRNAs were more effective than the in vitro-produced; in treatments with in vivo dsRNAs, dsRNA-CP was more effective than dsRNA-2b, while the effects were opposite with in vitro dsRNAs. Illumina sequencing of small RNAs from in vivo dsRNA-CP treated and non-treated tobacco plants revealed that interference with CMV infection in systemic leaves coincides with strongly reduced accumulation of virus-derived 21- and 22-nucleotide (nt) siRNAs, likely generated by tobacco DCL4 and DCL2, respectively. While the 21-nt class of viral siRNAs was predominant in non-treated plants, 21-nt and 22-nt classes accumulated at almost equal (but low) levels in dsRNA treated plants, suggesting that dsRNA treatment may boost DCL2 activity. Taken together, our findings confirm the efficacy of topical application of dsRNA for plant protection against viruses and shed more light on the mechanism of antiviral RNAi.


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