Mail: 320 Morrill Hall, 505 S. Goodwin Ave, Urbana, IL 61801
African American Studies
PhD Entomology, Auburn University
Broadly interested in understanding the multifaceted uses of chemical signals (both volatile and non-volatile) by herbivores, natural enemies, plants and their associated microorganisms and insects. Moreover, my research on beneficial soil microbes seeks to find microbial-based solutions for improving crop production, alleviating drought stress in crop plants and sustainable pest management. We use a comparative approach with model tritrophic systems and employ several chemical ecology tools.
Natural, healthy, and functioning ecosystems comprise plants, plant-associated mutualists, insect herbivores, parasitoids and a complex network of microorganisms. Chemical signals (both volatile and nonvolatile) and chemical-mediated communication play central roles in almost every possible interaction in multitrophic communities. Volatile organic compounds (VOCs), in particular, that provide species-specific and highly reliable information mediate many conversations among plant-plant, plant-herbivore, plant-herbivore-natural enemy, beneficial soil microbe-plant-herbivore-natural enemy, and insect-insect participants. Through volatiles and volatile signaling, plants, insects, and the complex network of microorganisms with which they associate can advertise their physiological and ecological states. Importantly, these signals can broadcast the presence of insect pests and other abiotic stressors such as drought, which are among the most serious constraints to crop production and food security worldwide. These complex chemical-mediated communications are poorly understood, but once deciphered, they potentially could provide novel opportunities for manipulating beneficial microbe-plant-insect-natural enemy interactions to promote crop yields and food security.
Research in my lab is aimed at understanding the multifaceted uses of chemical signals (both volatile and non-volatile) by herbivores, natural enemies, plants and their associated microorganisms and insects. The overarching goals are to decipher many of these complex chemical-mediated conversations, whose outcomes are important with relevance to agriculture, insect pest management and the functioning of ecosystems. Results obtained from my research can open avenues for integrated management of pests and disease vectors and for the rapid detection of plant stress.
Volatile cues for recruitment of mutualists to help plants to tolerate biotic and abiotic stress Conversations in the dark: Who is listening?
In nature, plants are part of complex communities. Plants grow in soil and living in the soil are complex communities that include beneficial soil microorganisms such as plant growth-promoting rhizobacteria (PGPR) and mycorryhizal fungi (AMF). Both PGPR and AMF form symbioses with diverse groups of plants; among these are agricultural crops such as corn, cotton, tomato and soybeans. These microbes confer beneficial effects such as increased plant growth and enhanced tolerance to biotic and abiotic stress. Our research is unravelling the systemic effects of mycorrhizal fungal mutualisms on the chemical phenotype of tomato plants.
Volatile cues for monitoring abiotic plant stress intensity Stressed plants: Who is listening? Plants are continuously exposed to multiple abiotic stressors, including drought and soil pollution. With the ongoing global climate change scenario, the severity, frequency and duration of drought in the North American corn and soybean belt areas such as Illinois and other agriculturally relevant areas around the world is predicted to continue to increase in the future. We are investigating the dynamic changes in identities and quantities of volatile emission by drought stressed plants and the consequences for plant-insect interactions.
Joseph, D.O., Zebelo, S., Ngumbi, E. and Fadamiro, H.Y. (2017). cis-Jasmone primes defense pathways in tomato via emission of volatile organic compounds and regulation of genes with consequences for Spodoptera exigua oviposition. Journal -Arthropod-Plant Interactions. DOI: 10.1007/s11829-017-9503-y
Ngumbi E. and Kloepper, J.W. (2016). Bacterial-mediated drought tolerance: Current and future prospects. Applied Soil Ecology. 105: 109-125.
Ngumbi, E. and Fadamiro, H.Y. (2014). Comparative responses of four Pseudacteon phorid fly species to host fire ant alarm pheromone and analogs. Chemoecology. 25: 85-92.
Sims, S.R., Balusu, R.R., Ngumbi, E.N. and Appel, A.G. (2014). Topical and vapor toxicity of saturated fatty acids to the german cockroach (Dictyoptera: Blattellidae) - Journal of Economic Entomology 107: 758-763.
Ngumbi, E. and Fadamiro, H.Y. (2012). Species and sexual differences in behavioural responses of a specialist and generalist parasitoid species to host-related volatiles -Bulletin of Entomological Research. 102: 710-718.
Ngumbi, E., Jordan, M., and Fadamiro, H.Y. (2012). Comparison of associative learning of host-related plant volatiles in two parasitoids with different degrees of host specificity, Cotesia marginiventris and Microplitis croceipes. Chemoecology. 22: 207-215.
Ngumbi, E., Chen, L. and Fadamiro, H.Y. (2010). Electroantennogram (EAG) responses of Microplitis croceipes and Cotesia marginiventris and their lepidopteran hosts to a wide array of odor stimuli: Correlation between EAG response and degree of host specificity? Journal of Insect Physiology. 56: 1260–1268.
Ngumbi, E., Chen, L. and Fadamiro, H.Y. (2009). Comparative GC-EAD responses of a specialist (Microplitis croceipes) and a generalist (Cotesia marginiventris) parasitoid to cotton volatiles induced by two caterpillar species. Journal of Chemical Ecology. 35: 1009-1020.
Medina-Ortega, K.N., Bosque-Perez, N.A., Ngumbi, E., Jimenez-Martinez, E.S. and Eigenbrode, S.D. (2009). Rhopalosiphum padi (Hemiptera: Aphididae) responses to volatile cues from Barley yellow dwarf virus-infected wheat. Environmental Entomology. 38: 836-845.
Ngumbi, E., Eigenbrode, S.D., Bosque-Perèz, N.A., Ding, H. and Rodriguez, A. (2007). Myzus persicae is arrested more by blends than by individual compounds elevated in headspace of PLRV-infected potato. Journal of Chemical Ecology. 33: 1733-1747.
Ngumbi, E.N., Ngi-Song, A.J., Njagi, E.N., Torto, R., Wadhams, L.J., Birkett, M.A., Pickett, J.A., Overholt, W.A. and Torto, B. (2005). Responses of the stem borer larval endoparasitoid Cotesia flavipes (Hymenoptera: Braconidae) to plant derived synomones: laboratory and field cage experiments. Biocontrol Science and Technology Journal. 15: 271-279.