ABSTRACT
Maize lethal necrosis is one of the most devastating diseases of maize causing yield losses reaching up to 90% in sub-Saharan Africa. The disease is caused by a combination of maize chlorotic mottle virus (MCMV) and any one of cereal viruses in the Potyviridae group such as sugarcane mosaic virus. MCMV has been reported to be transmitted mainly by maize thrips (Frankliniella williamsi) and onion thrips (Thrips tabaci). To better understand the role of thrips vectors in the epidemiology of the disease, we investigated behavioral responses of F. williamsi and T. tabaci, to volatiles collected from maize seedlings infected with MCMV in a four-arm olfactometer bioassay. Volatile profiles from MCMV-infected and healthy maize plants were compared by gas chromatography (GC) and GC coupled mass spectrometry analyses. In the bioassays, both sexes of F. williamsi and male T. tabaci were significantly attracted to volatiles from maize plants infected with MCMV compared to healthy plants and solvent controls. Moreover, volatile analysis revealed strong induction of (E)-4,8-dimethyl-1,3,7-nonatriene, methyl salicylate and (E,E)-4,8,12-trimethyltrideca-1,3,7,11-tetraene in MCMV-infected maize seedlings. Our findings demonstrate MCMV induces changes in volatile profiles of host plants to elicit attraction of thrips vectors. The increased vector contact rates with MCMV-infected host plants could enhance virus transmission if thrips feed on the infected plants and acquire the pathogen prior to dispersal. Uncovering the mechanisms mediating interactions between vectors, host plants and pathogens provides useful insights for understanding the vector ecology and disease epidemiology, which in turn may contribute in designing integrated vector management strategies.
Subject(s)
Gammaherpesvirinae/physiology , Host-Pathogen Interactions , Plant Diseases/virology , Volatile Organic Compounds/metabolism , Zea mays/virology , Animals , Female , Gas Chromatography-Mass Spectrometry , Insect Vectors/virology , Male , Seedlings/chemistry , Seedlings/physiology , Seedlings/virology , Thysanoptera/virology , Volatile Organic Compounds/analysis , Zea mays/chemistry , Zea mays/physiologyABSTRACT
The false codling moth (FCM), Thaumatotibia leucotreta, is a major quarantine pest native to Africa. Physical postharvest phytosanitary measures such as cold and heat treatments are championed to control its spread to new regions. However, the molecular changes that T. leucotreta undergoes as it attempts to adjust to its surroundings during the treatments and withstand the extreme temperatures remain largely unknown. The current study employs RNA-seq using the next-generation Illumina HiSeq platform to produce transcriptome profiles for differential gene expression analysis of T. leucotreta larvae under thermal stress. The transcriptome assembly analysis revealed 226,067 transcripts, clustering into 127,018 unigenes. In comparison to the 25 °C treated group, 874, 91, 159, and 754 individual differentially expressed genes (DEGs) co-regulated at -10, 0, 40, and 50 °C, respectively were discovered. Annotation of the DEGs by gene ontology (GO) revealed several genes, previously implicated in low and high-temperature stresses, including heat shock proteins, cytochrome P450, cuticle proteins, odorant binding proteins, and immune system genes. Kyoto Encyclopedia of Genes and Genomics (KEGG) classification analysis revealed that substantive DEGs were those involved in metabolic pathways such as thiamine, purine, folate, and glycerolipid metabolism pathways. The RT-qPCR validation of several significantly up- and down-regulated DEGs showed congruence between RNA-seq and qPCR data. This baseline study lays a foundation for future research into the molecular mechanisms underlying T. leucotreta's cold/heat tolerance by providing a thorough differential gene expression analysis that has identified multiple genes that may be associated with the insect's ability to withstand cold and heat.
Subject(s)
Gene Expression Profiling , Moths , Transcriptome , Animals , Moths/genetics , Cold Temperature , Insect Proteins/genetics , Hot Temperature , Larva/genetics , Larva/growth & developmentABSTRACT
BACKGROUND: The western flower thrips, Frankliniella occidentalis, is a quarantine pest of French beans that requires phytosanitary treatment to meet quarantine requirements for strict lucrative markets. In this study, the efficacy of hot water treatment against F. occidentalis eggs and its effects on the postharvest physicochemical quality parameters of French beans was evaluated. RESULTS: The immersion time of 8.01 min (95% critical limits CL 7.77-8.24) was predicted by the probit model as the minimum time required to achieve a 99.9968% control level. Confirmatory tests with a large number of F. occidentalis eggs were performed to validate the estimated time to achieve probit-9 control level, and there were no survivors from the 50 103 eggs treated. Likewise, none of the 55 364 eggs exposed to 45 ± 0.2 °C for 7 min (observational time) survived. The effect of the treatment schedule on French beans quality parameters was assessed and there were no differences in weight loss, moisture content, total soluble solids, titratable acidity, pH, and reducing sugars between treated and untreated samples. CONCLUSION: Our results indicate that hot water treatment (at 45 ± 0.2 °C for a duration of 8.01 min is an effective phytosanitary treatment for the control of Frankliniella occidentalis on French beans, with no significant impact on pods quality. © 2022 Society of Chemical Industry.
Subject(s)
Phaseolus , Thysanoptera , Water Purification , Animals , FlowersABSTRACT
Mango production and trade in sub-Saharan Africa is hampered by direct damage and the high quarantine status of B. dorsalis and the paucity of effective post-harvest phytosanitary treatments. The current study reports the development of a quarantine treatment protocol using hot water to disinfest B. dorsalis and assess its effect on cv. Tommy Atkins mango quality. We first determined the development of the eggs and all larval stages of B. dorsalis in cv. Tommy Atkins mango and used the information to establish a time-mortality relationship of the immature stages after subjecting infested fruits to a regimen of eight, time instances of hot water at 46.1 °C. Using probit analysis, we estimated the minimum time required to achieve 99.9968% mortality of each stage. Our results indicate that the egg was the least heat tolerant, followed by the first, second, and third instar. The time required to achieve 99.9968% control of the third instar in cv. Tommy Atkins mango (400-600 g) was determined to be 72.63 min (95% Cl: 70.32-74.95). In the confirmatory trials, the hot water treatment schedule of 46.1 °C/72.63 min was validated, and none of the 59,120 most heat-tolerant individuals treated survived. Further, there were no significant differences between hot water-treated and untreated mangoes recorded in weight loss, fruit firmness, pH, total soluble solids, moisture content, and titratable acidity eleven days post-treatment. These findings demonstrate an effectively optimum post-harvest disinfestation treatment against B. dorsalis in cv. Tommy Atkins mango that should be adopted commercially to facilitate access to profitable but strict export markets globally.