Direct and Indirect Infection Effects of Four Potent Fungal Isolates on the Survival and Performance of Fall Armyworm Larval Parasitoid Cotesia icipe

Author:

Chepkemoi Junitor12,Fening Ken Okwae2ORCID,Ambele Felicitas Chaba3,Munywoki Joseph1ORCID,Akutse Komivi Senyo1ORCID

Affiliation:

1. International Centre of Insect Physiology and Ecology (icipe), Nairobi P.O. Box 30772-00100, Kenya

2. African Regional Postgraduate Programme in Insect Science (ARPPIS), University of Ghana, Legon, Accra P.O. Box LG 68, Ghana

3. Department of Zoology, University of Bamenda, Bambili P.O. Box 39, Cameroon

Abstract

Fall armyworm (FAW), Spodoptera frugiperda, has recently invaded Africa where it is seriously threatening food security. Current management methods rely heavily on synthetic insecticides which are harmful to humans, the environment, and non-target beneficial insects. Cotesia icipe was recently identified as a major FAW-associated indigenous parasitoid causing a high parasitism rate on the pest in Kenya. Previous studies have demonstrated the efficacy of Metarhizium anisopliae ICIPE 7, ICIPE 41, ICIPE 78, and Beauveria bassiana ICIPE 621 against FAW. However, limited information is available on the interactions between these potent isolates and C. icipe. This study therefore assessed direct and indirect infection effects of these fungal isolates on C. icipe, induced 2nd instar FAW mortality, and parasitism rates of the infected C. icipe. Results showed that when C. icipe were directly exposed to dry conidia of the fungal isolates, ICIPE 7 and ICIPE 41 caused the highest (100%) C. icipe adult mortality seven days post-exposure. Both isolates also induced the highest FAW larval mortality of 55% and 53%, respectively. ICIPE 78 recorded the highest parasitism rates after direct infection. In the indirect exposure (fungal-infected FAW larvae exposed to the parasitoid), 1 × 109 conidia mL−1 recorded high C. icipe adult and FAW 2nd instar mortalities for all fungal isolates. This study provides an important baseline for effective fungal-based biopesticides development that could also be used in augmentative biological control. However, further studies are warranted to assess the performance of C. icipe in combination with these potent biopesticides in the field.

Funder

UK’s Foreign, Commonwealth and Development Office

International Centre of Insect Physiology and Ecology

Publisher

MDPI AG

Subject

Management, Monitoring, Policy and Law,Renewable Energy, Sustainability and the Environment,Geography, Planning and Development,Building and Construction

Reference37 articles.

1. Food security and the 2015–2030 sustainable development goals: From human to planetary health: Perspectives and opinions;Curr. Dev. Nutr.,2017

2. Fall armyworm: Impacts and implications for Africa;Day;Outlooks Pest Manag.,2017

3. Goergen, G., Lava, K.P., Sankung, S.B., Togola, A., and Tamò, M. (2016). First Report of Outbreaks of the Fall Armyworm, Spodoptera frugiperda (J E Smith) (Lepidoptera, Noctuidae): A New Alien Invasive Pest in West and Central Africa. PLoS ONE, 11.

4. First report of the fall army worm, Spodoptera frugiperda (Lepidoptera, Noctuidae) in Cameroon;Tindo;Cameroon J. Biol. Biochem. Sci.,2017

5. FAO (Food and Agriculture Organization of the United Nations) (2017). Sustainable Management of the Fall Armyworm in Africa, FAO. Available online: http://www.fao.org/3/a-bt417e.pdf.

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