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Efficacy of the newly discovered entomopathogenic nematode Steinernema adamsi against Helicoverpa zea: life stage susceptibility, UV tolerance, and field performance Cover

Efficacy of the newly discovered entomopathogenic nematode Steinernema adamsi against Helicoverpa zea: life stage susceptibility, UV tolerance, and field performance

Open Access
|Apr 2025

Figures & Tables

Figure 1:

Stages of S. adamsi Infection in H. zea Larvae. (A) Second instar Helicoverpa zea larva showing a positive infection of Steinernema adamsi through the anus. (B) Fourth instar H. zea larva with a large EPN mat covering most of its body, indicating advanced nematode infection. The upper right inset image shows a H. zea larva with a severe infection of the head capsule by S. adamsi.
Stages of S. adamsi Infection in H. zea Larvae. (A) Second instar Helicoverpa zea larva showing a positive infection of Steinernema adamsi through the anus. (B) Fourth instar H. zea larva with a large EPN mat covering most of its body, indicating advanced nematode infection. The upper right inset image shows a H. zea larva with a severe infection of the head capsule by S. adamsi.

Figure 2:

Application of Alginate/Congo Red Encapsulated S. adamsi Nematodes on H. zea larvae in Cotton Blooms. (A) Three-day-old Helicoverpa zea larva inside a cotton bloom, demonstrating infestation conditions. (B) Detailed view of an alginate/Congo red treatment droplet applied to the dorsal surface of the larva. (C) Magnified image showing encapsulated Steinernema adamsi nematodes within the alginate/Congo red droplet.
Application of Alginate/Congo Red Encapsulated S. adamsi Nematodes on H. zea larvae in Cotton Blooms. (A) Three-day-old Helicoverpa zea larva inside a cotton bloom, demonstrating infestation conditions. (B) Detailed view of an alginate/Congo red treatment droplet applied to the dorsal surface of the larva. (C) Magnified image showing encapsulated Steinernema adamsi nematodes within the alginate/Congo red droplet.

Figure 3:

Mortality (% ± SEM) of 2nd instars of Helicoverpa. zea caused by Steinernema adamsi exposed to ultraviolet radiation in the laboratory (27°C, 75% RH).
Means with different letters are significantly different via Tukey’s HSD test after a significant ANOVA, p = 0.05).
Mortality (% ± SEM) of 2nd instars of Helicoverpa. zea caused by Steinernema adamsi exposed to ultraviolet radiation in the laboratory (27°C, 75% RH). Means with different letters are significantly different via Tukey’s HSD test after a significant ANOVA, p = 0.05).

Figure 4:

Effect of Steinernema adamsi formulations from field experiments A and B on 1st instars of Helicoverpa zea in cotton (2024, Leland, Mississippi). Field experiment A (Initial efficacy test) was conducted on August 29, 2024, with an average 33°C, 62%RH and under full sun (9495/29) (U.V. AB/C) using water as the carrier agent at 10 IJs/cm2. Field experiment B (Encapsulation and UV degradation test) was conducted on September 4, 2024, with an average 34°C, 55%RH, and full sun (9289/33) (U.V. AB/C) using alginate (0.05%, w/v) and Congo red (0.02%, w/v) formulations at 50 IJs/cm2.
Means with different letters are significantly different via Tukey’s HSD test after a significant ANOVA, p = 0.05).
Effect of Steinernema adamsi formulations from field experiments A and B on 1st instars of Helicoverpa zea in cotton (2024, Leland, Mississippi). Field experiment A (Initial efficacy test) was conducted on August 29, 2024, with an average 33°C, 62%RH and under full sun (9495/29) (U.V. AB/C) using water as the carrier agent at 10 IJs/cm2. Field experiment B (Encapsulation and UV degradation test) was conducted on September 4, 2024, with an average 34°C, 55%RH, and full sun (9289/33) (U.V. AB/C) using alginate (0.05%, w/v) and Congo red (0.02%, w/v) formulations at 50 IJs/cm2. Means with different letters are significantly different via Tukey’s HSD test after a significant ANOVA, p = 0.05).

Mortality (% ± SEM) of 2nd instars of Helicoverpa_ zea caused by Steinernema adamsi mutualistic bacteria Xenorhabdus hemocoel injections and oral toxicity in the laboratory (27°C, 75% RH)_

Exposure method% Mortality ± SEM
Hemocoel injections Water5th instar
100a
0b
F(1, 4) = 69.45
P < 0.0001
Oral toxicity Water2nd instar
35.93 ± 1.5a
2.83 ± 0.87b
F(1, 4) = 35.04
P < 0.0274

Mortality (% ± SEM) of 1st-5th instars, and pupae of Helicoverpa_ zea caused by Steinernema adamsi entomopathogenic nematode strain in the laboratory (27°C, 75% RH)_ Mean values within a column followed by the same letter are not significantly different at P < 0_05 (Tukey’s HSD test)_

EPN strainH. zea

1st instar2nd instar3rd instar4th instar5th instarsPupae
S. adamsi75.83 ± 4.7a74.21 ± 1.6a79.16 ± 2.3a100b10 ± 1.2d36.66 ± 3.6c0d
Water0d0d0d 0d0d
F-Value(1, 7)353.7662.57166.201019.9787.96-
P-Value<.0001<.00020.0001<.0001<.0001-
DOI: https://doi.org/10.2478/jofnem-2025-0012 | Journal eISSN: 2640-396X | Journal ISSN: 0022-300X
Language: English
Submitted on: Nov 12, 2024
Published on: Apr 24, 2025
Published by: Society of Nematologists, Inc.
In partnership with: Paradigm Publishing Services
Publication frequency: 1 times per year

© 2025 James Paul Glover, Nathan Spaulding, Justin George, Maribel Portilla, Gadi V.P. Reddy, Adler Dillman, published by Society of Nematologists, Inc.
This work is licensed under the Creative Commons Attribution 4.0 License.