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Aguiar, E. R. G. R.

Publications and source records attributed to Aguiar, E. R. G. R..

5 recordsLinked to original sources

The Initial Detection of a Diversity of Viruses Associated with Ladybirds and Other Biocontrol Agents Prompts Interesting Ecological Insights

Predatory insects such as ladybirds, green lacewings, and an aphid-feeding gall midge have been commercialized and deployed worldwide to deal with the challenge of pest control. However, no information is available on their viruses which could interfere with the efficiency of biocontrol. To start filling this gap, this study employed an integrative bioinformatics approach starting from 21 publicly available RNA-seq libraries from 6 countries of 8 natural enemy species used to control aphids. A total of 41 putative novel viruses were identified and classified into 16 families and 1 genus. In addition, 13 known viruses were detected, including aphid and phytopathogenic viruses, and a virus from the invasive harlequin ladybird. The Aphid lethal paralysis virus was detected in several species at different trophic levels, including plants, aphid vectors, predatory insects, and insectivorous vertebrates. Thus, an ecosystem perspective on viruses across trophic levels is proposed because feeding may facilitate the spread of viruses between distant taxonomic species, such as invertebrate and vertebrate insectivorous predators. In conclusion, a simple assessment of the viral diversity in eight predatory insects of agricultural relevance, using a bioinformatics approach, has revealed a potential interspecies viral flux that deserves research attention. Further studies on viruses circulating in agricultural insect species are essential to improve biological control strategies based on trophic interactions, to conserve biodiversity, and to develop knowledge on the evolution of viral entities and their role as members of an agroecological system.

microbiology↗

ViralQuest: A user-friendly interactive pipeline for viral-sequences analysis and curation

BackgroundHigh-throughput sequencing (HTS) has become an essential, unbiased tool in virology for identifying known and novel viruses. However, analyzing the large and complex datasets generated by HTS presents significant bioinformatics challenges. The process of accurately identifying and characterizing viral sequences from assembled contigs remains a bottleneck, often requiring specialized expertise and involving non-standardized parameters. There is a pressing need for robust, user-friendly, and reproducible pipelines to streamline this post-assembly analysis. ResultsTo address these challenges, we developed ViralQuest, a bioinformatics tool that automates the in-depth characterization of viral sequences from pre-assembled contigs. The pipeline integrates multiple lines of evidence for robust identification, using Diamond BLASTx against the Viral RefSeq database and pyHMMER searches against the RVDB, Vfam, and eggNOG profile HMM databases. For detailed characterization, ViralQuest performs taxonomic classification based on the ICTV nomenclature and functional annotation via Pfam domain analysis. Novel features of ViralQuest include an AI-powered summarization module that uses a Large Language Model (LLM) to generate contextual narratives for key viral findings and a comprehensive confidence score to rank putative viral contigs. All results are consolidated into a single, interactive HTML report that includes dynamic visualizations of contigs, ORFs, and protein domains, alongside detailed data tables that are exportable in TSV and SVG formats. ConclusionViralQuest provides an accessible and comprehensive solution for the post-assembly analysis of viral metagenomic data. By combining rigorous bioinformatics methods with novel AI-driven features and an intuitive reporting interface, it streamlines the complex process of viral identification and characterization. The tool enhances the interpretability and reliability of results, making in-depth virome analysis more accessible to the broader research community. ViralQuest is available on GitHub at https://github.com/gabrielvpina/viralquest/.

bioinformatics↗

The virome of the invasive Asian bush mosquito Aedes japonicus in Europe

BackgroundThe Asian bush mosquito Aedes japonicus is rapidly invading North America and Europe. Due to its potential to transmit multiple pathogenic arthropod-borne (arbo)viruses including Zika virus, West Nile virus and chikungunya virus, it is important to understand the biology of this vector mosquito in more detail. In addition to arboviruses, mosquitoes can also carry insect-specific viruses that receive increasing attention due to their potential effects on host physiology and arbovirus transmission. In this study, we characterized the collection of viruses, referred to as the virome, circulating in Ae. japonicus populations in the Netherlands and France. ResultsApplying a small RNA-based metagenomic approach to Ae. japonicus, we uncovered a distinct group of viruses present in samples from both the Netherlands and France. These included one known virus, Ae. japonicus narnavirus 1 (AejapNV1), and three new virus species that we named Ae. japonicus totivirus 1 (AejapTV1), Ae. japonicus anphevirus 1 (AejapAV1) and Ae. japonicus bunyavirus 1 (AejapBV1). We also discovered sequences that were presumably derived from two additional novel viruses: Ae. japonicus bunyavirus 2 (AejapBV2) and Ae. japonicus rhabdovirus 1 (AejapRV1). All six viruses induced strong RNA interference responses, including the production of 21 nucleotide sized small interfering RNAs, a signature of active replication in the host. Notably, AejapBV1 and AejapBV2 belong to different viral families, however, no RNA-dependent RNA polymerase sequence has been found for AejapBV2. Intriguingly, our small RNA-based approach identified a [~]1 kb long ambigrammatic RNA that is associated with AejapNV1 as a secondary segment but showed no similarity to any sequence in public databases. We confirmed the presence of AejapNV1 primary and secondary segments, AejapTV1, AejapAV1 and AejapBV1 by reverse-transcriptase PCR in wild-caught Ae. japonicus mosquitoes. AejapNV1 and AejapTV1 were found at high prevalence (87-100%) in adult females, adult males and larvae. ConclusionsUsing a small RNA-based, sequence-independent metagenomic strategy, we uncovered a conserved and prevalent virome among Ae. japonicus mosquito populations. The high prevalence of AejapNV1 and AejapTV1 across all tested mosquito life stages suggests that these viruses are intimately associated with Ae. japonicus and may affect different aspects of the physiology of this vector mosquito.

microbiology↗

Genomic Analysis of Two Phlebotomine Sand Fly Vectors of Leishmania from the New and Old World

Phlebotomine sand flies are of global significance as important vectors of human disease, transmitting bacterial, viral, and protozoan pathogens, including the devastating kinetoplastid parasites of the genus Leishmania, the causative agents of diseases collectively termed leishmaniasis. More than 40 pathogenic Leishmania species are transmitted to humans by approximately 35 sand fly species in 98 countries with hundreds of millions of people at risk around the world. As no approved efficacious vaccine exists, available drugs are expensive and/or toxic, and resistance is emerging, management of sand fly populations to break transmission is currently the most effective disease control strategy. To better understand the biology of sand flies, including the mechanisms involved in their vectorial capacity, insecticide resistance, and population structures we sequenced the genomes of two of the most important sand fly species: Phlebotomus papatasi, a cutaneous leishmaniasis vector, (distributed in the Middle East and North Africa) and Lutzomyia longipalpis, a visceral leishmaniasis vector (distributed across Central and South America). We categorized and curated genes involved in processes important to their roles as disease vectors, including chemosensation, blood feeding, circadian rhythm, immunity, and detoxification, as well as mobile genetic elements. We also defined gene orthology and observed micro-synteny among the genomes. Finally, we present the genetic diversity and population structure of these species in their respective geographical areas. These genomes will be a foundation on which to base future efforts to prevent vector-borne transmission of Leishmania parasites. Author SummaryThe leishmaniases are a group of neglected tropical diseases caused by protist parasites from the Genus Leishmania. Different Leishmania species present a wide clinical profile, ranging from mild, often self-resolving cutaneous lesions that can lead to protective immunity, to severe metastatic mucosal disease, to visceral disease that is ultimately fatal. Leishmania parasites are transmitted by the bites of sand flies, and as no approved vaccine exists, available drugs are toxic and/or expensive and resistance is emerging, new dual control strategies to combat these diseases must be developed, combining interventions on human infections and integrated sand fly population management. Effective vector control requires a good understanding of the biology of sand flies. To this end, we sequenced and annotated the genomes of two sand fly species that are important leishmaniasis vectors from the Old and New Worlds. These genomes allow us to better understand, at the genetic level, processes important in the vector biology of these species, such as finding hosts, blood-feeding, immunity, and detoxification. These genomic resources highlight the driving forces of evolution of two major Leishmania vectors and provide foundations for future research on how to better prevent leishmaniasis by control of the sand fly vectors.

genomics↗

Insect-specific viruses regulate vector competence in Aedes aegypti mosquitoes via expression of histone H4

Aedes aegypti and Aedes albopictus are major mosquito vectors for arthropod-borne viruses (arboviruses) such as dengue (DENV) and Zika (ZIKV) viruses. Mosquitoes also carry insect-specific viruses (ISVs) that may affect the transmission of arboviruses. Here, we analyzed the global virome in urban Aedes mosquitoes and observed that two insect-specific viruses, Phasi Charoen-like virus (PCLV) and Humaita Tubiacanga virus (HTV), were the most prevalent in A. aegypti worldwide except for African cities, where transmission of arboviruses is low. Spatiotemporal analysis revealed that presence of HTV and PCLV led to a 200% increase in the chances of having DENV in wild mosquitoes. In the laboratory, we showed that HTV and PCLV prevented downregulation of histone H4, a previously unrecognized proviral host factor, and rendered mosquitoes more susceptible to DENV and ZIKV. Altogether, our data reveals a molecular basis for the regulation of A. aegypti vector competence by highly prevalent ISVs that may impact how we analyze the risk of arbovirus outbreaks.

microbiology↗