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Social wasps are invasive in many regions around the world. In their new communities, introduced predators such as these wasps may be beneficial as consumers of exotic pests, but they will also consume native species. Here, we examined the diet of the exotic European paper wasp (Polistes dominula) and the closely related congener, Polistes chinensis, in a region of New Zealand where they co-occur. DNA barcoding was used to analyse their diet. The diet of both wasp species was largely Lepidopteran but other orders such as Hemiptera, Diptera and Coleoptera were also represented. Our analysis showed substantial site-to-site variation in diet. The two wasps differed significantly in their prey, although these differences appear to be driven by taxa identified from a small number of DNA reads in a small number of samples. Native and introduced fauna were represented in the diets of both wasps and included important agricultural pests. Of the 92 prey taxa able to be identified to species level, 81 were identified as exotic or introduced to New Zealand. The remaining 11 were species native to New Zealand. However, our estimates suggest over 50% of the prey DNA in the wasp diet is derived from native species. These wasps are abundant in some coastal and urban habitats, where they are likely to consume pest species as well as native species of conservation importance. The ecosystem services or costs and benefits provided by these invasive species are likely to be contingent on the prey communities and habitats they occupy.

The most devastating pest to honey bees (Apis mellifera) worldwide is the parasitic miteVarroa destructor. The development of miticide-resistant mite populations has been a major driver of colony loss in many countries. We investigated the threat Varroa poses to honey bee populations in New Zealand and tested the effectiveness of the two most popular chemical treatments used by beekeepers. Colony losses reported by New Zealand beekeepers have risen over five consecutive years from 2017 to 2021, as have the proportion of losses attributed to Varroa, with this parasite found to be the main driver of colony loss in 2021. Varroa resistance to miticide treatments flumethrin and amitraz was tested. The concentration of flumethrin required to kill 50% of the mites (LC50) was 156 μg/g, 13 times greater than the adjusted LC50value of 12 μg/g observed in a trial also conducted in New Zealand in 2003, thus indicating evidence of developing mite resistance to flumethrin in New Zealand. Molecular analyses searching for mutations in the Varroa genome known to be associated with flumethrin resistance found no evidence of such mutations, suggesting that any extant resistance to flumethrin has evolved independently in New Zealand. No evidence of resistance to amitraz was found, as the LC50value of 12 μg/g was lower than what was observed in the 2003 trial (110 μg/g). Further development of integrated pest management, such as gene-silencing RNA interference (RNAi) and selective breeding of Varroa-resistant bees, is needed to effectively manage a parasite that threatens global agriculture.

Pest control methods that can target pest species with limited environmental impacts are a conservation and economic priority. Species-specific pest control using RNA interference is a challenging but promising avenue in developing the next generation of pest management. We investigate the feasibility of manipulating a biological invader's immune system using double-stranded RNA (dsRNA) in order to increase susceptibility to naturally occurring pathogens. We used the invasive Argentine ant as a model, targeting the immunity-associated genes Spaetzle and Dicer-1 with dsRNA. We show that feeding of Spaetzle dsRNA can result in partial target gene silencing for up to 28 days in the laboratory and 5 days in the field. Dicer-1 dsRNA only resulted in partial gene knockdown after 2 days in the laboratory. Double-stranded RNA treatments were associated with significant gene expression disruptions across immune pathways in the laboratory and to a lower extent in the field. Twelve viruses and four bacteria were found in these ant populations. Some changes in viral loads in dsRNA-treated groups were observed. For example, Linepithema humile Polycipivirus 2 (LhuPCV2) loads increased after 2 days of treatment with Spaetzle and Dicer-1 dsRNA treatments in the laboratory. After treatment with the dsRNA in the field, after 5 days the virus Linepithema humile toti-like virus 1 (LhuTLV1) was significantly more abundant. However, immune pathways disruption did not result in consistent increase in microbial infections, nor did they alter ant abundance in the field. Some viruses even declined in abundance after dsRNA treatment. Our study explores the feasibility of lowering a pest's immunity as a control tool. We demonstrate that it is possible to alter immune gene expression of pest species and pathogen loads, though in our specific system the affected pathogens did not appear to influence pest abundance. We provide suggestions on future directions for dsRNA-mediated immune disruption in pest species, including potential avenues to improve dsRNA delivery as well as the importance of the pest and pathogen biology. Double-stranded RNA targeting immune function might be especially useful for pest control in systems where viruses or other microorganisms are prevalent and have the potential to be pathogenic. This article is protected by copyright. All rights reserved.

The parasitic mite Varroa destructor is a leading cause of mortality for Western honey bee (Apis mellifera) colonies around the globe. We sought to confirm the presence and likely introduction of only one V. destructor haplotype in New Zealand, and describe the viral community within both V. destructor mites and the bees that they parasitise. A 1232 bp fragment from mitochondrial gene regions suggests the likely introduction of only one V. destructor haplotype to New Zealand. Seventeen viruses were found in bees. The most prevalent and abundant was the Deformed wing virus A (DWV-A) strain, which explained 95.0% of the variation in the viral community of bees. Black queen cell virus, Sacbrood virus, and Varroa destructor virus 2 (VDV-2) played secondary roles. DWV-B and the Israeli acute paralysis virus appeared absent from New Zealand. Ten viruses were observed in V. destructor, with > 99.9% of viral reads from DWV-A and VDV-2. Substantially more variation in viral loads was observed in bees compared to mites. Where high levels of VDV-2 occurred in mites, reduced DWV-A occurred in both the mites and the bees co-occurring within the same hive. Where there were high loads of DWV-A in mites, there were typically high viral loads in bees.