Background: The potato tuber moth (PTM), Phthorimaea operculella (Zeller), is a worldwide pest that feeds on both the leaves and tubers of potato plants. PTM larvae can digest leaves, or tubers, resulting in serious damage to potato plants in the field and potato tubers in storage. To understand how midgut bacterial diversity is influenced by the consumption of these two tissue types, the symbiotic bacteria in the potato-feeding PTM midgut and the endophytic bacteria of potato tissues were analyzed. Results: At the genus level, the bacterial community composition in the PTM midgut was influenced by the tissues consumed, owing to their different nutrient contents. Escherichia_Shigella and Enterobacter were the most dominant genera in the midgut of leaf-feeding and tuber-feeding PTMs, respectively. Interestingly, even though only present in low abundance in leaves and tubers, Escherichia_Shigella were dominantly distributed only in the midgut of leaffeeding PTMs, indicating that specific accumulation of these genera have occurred by feeding on leaves. Moreover, Enterobacter, the most dominant genus in the midgut of tuber-feeding PTMs, was undetectable in all potato tissues, indicating it is gut-specific origin and tuber feeding-specific accumulation. Both Escherichia_Shigella and Enterobacter abundances were positively correlated with the dominant contents of potato leaves and tubers, respectively. Conclusions: Enrichment of specific PTM midgut bacterial communities was related to different nutrient levels in different tissues consumed by the insect, which in turn influenced host utilization. We provide evidence that a portion of the intestinal microbes of PTMs may be derived from potato endophytic bacteria and improve the understanding of the relationship between potato endophytic bacteria and the gut microbiota of PTMs, which may offer support for integrated management of this worldwide pest.
BACKGROUND The potato tuber moth (PTM), Phthorimaea operculella (Zeller) (Lepidoptera: Gelechiidae), is a destructive pest of Solanaceae crops worldwide. α‐solanine and α‐chaconine are toxic steroidal glycoalkaloids (SGAs) in Solanaceae crops and are most abundant in potatoes (Solanum tuberosum L.), accounting for more than 95% of the total SGAs. PTM grows on potatoes with a higher concentration of SGAs. Gut bacteria play an important role in the physiology and behavior of insects. To understand the role of gut bacteria of PTM in host adaptability, we isolated and identified major SGA (α‐chaconine and α‐solanine)‐degrading gut bacteria in the gut of PTM by a selective medium and analyzed their degradability and degradation mechanism. RESULTS The gut Glutamicibacter halophytocola S2 of PTM with high degradation capacity to α‐solanine and α‐chaconine were detected by liquid chromatography mass spectrometry (LC–MS) and identified by morphological and 16S rRNA gene sequence analysis. A gene cluster involving α‐rhamnosidases, β‐glucosidases, and β‐galactosidases was identified by whole‐genome sequencing of G. halophytocola S2. These genes had higher expression on the α‐solanine medium. PTM inoculated with the isolated G. halophytocola S2 obtained higher fitness than antibiotic‐treated PTM. CONCLUSION The G. halophytocola S2 in the gut of PTM could degrade the major toxic α‐solanine and α‐chaconine in potatoes. This enhances the fitness of PTM feeding on potatoes with high SGA contents. The results provide a theoretical foundation for the integrated pest management of PTM and provide an effective strain for the treatment of α‐solanine and α‐chaconine in potato food. © 2022 Society of Chemical Industry.
Spodoptera frugiperda is one of the most destructive crop pests in the world. Metarhizium rileyi is an entomopathogenic fungus specific for noctuid pests and is a very promising prospect in biological control against S. frugiperda. Two M. rileyi strains (XSBN200920 and HNQLZ200714) isolated from infected S. frugiperda were used to evaluate the virulence and biocontrol potential to different stages and instars of S. frugiperda. The results showed that XSBN200920 was significantly more virulent than HNQLZ200714 to eggs, larvae, pupae, and adults of S. frugiperda. In the larvae infected with the two M. rileyi strains, the activity of three protective enzymes (including peroxidase (POD), superoxide dismutase (SOD), catalase (CAT)) and two detoxifying enzymes (including glutathione-S transferase (GST) and carboxylesterase (CarE)) increased firstly and then decreased. The expression levels of protective enzymes and detoxification enzymes in larvae treated with XSBN200920 were greater than with HNQLZ200714. Furthermore, antioxidant stress-related gene (MrSOD and MrCAT family genes) expression in the two strains was measured by RT-qPCR (real-time quantitative PCR). The expression of these genes was significantly higher in the XSBN200920 strain compared to HNQLZ200714. There were also significant differences in the sensitivity of the two strains to the growth of different carbon and nitrogen sources and oxidative stress agents. In addition, the activity expression of antioxidant enzymes on the third day of culturing in XSBN200920 was significantly higher than with HNQLZ200714. In summary, the high virulence of M. rileyi XSBN200920 was not only determined by the expression levels of protective and detoxifying enzymes of the host but also regulated by the growth of entomogenic fungi and the resistance to the oxidative stress against S. frugiperda at different stages and instars. This study provides a theoretical fundament for the systematic control of Spodoptera frugiperda using Metarhizium rileyi.
Spodoptera frugiperda (Lepidoptera: Noctuidae) is a major pest of maize worldwide. This pest colonized maize in Shizong, Qujing, Yunnan, China in 2019. To explore the temporal and spatial distribution of S. frugiperda in local fields, “W” type 5-point sampling was performed from 2020 to 2021. The spatial distribution was analyzed using the aggregation index, Iwao’s regression, and Taylor’s power law. The temporal distribution showed two peaks for both 2020 and 2021 when the density of eggs, larvae, and adults was high throughout the maize growth period. Additionally, 1st and 3rd instar larvae were higher in number during the maize seedling, jointing, and spinning stages. Fourth to 6th instar larvae were higher in number after the tasseling stage. Additionally, the spatial distribution results showed that 1st to 3rd instar larvae were aggregated, while 4th to 6th instar larvae were uniformly distributed in mountain maize fields. This study provides monitoring data for S. frugiperda and clarifies the temporal and spatial distribution characteristics for larvae in mountain maize fields. Further, it also provides guidance for investigation into population dynamics and the development of predictive models for integrated S. frugiperda management.
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