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Abba, S.

Publications and source records attributed to Abba, S..

2 recordsLinked to original sources

Infection with non-retroviral RNA viruses produces virus-derived DNA across diverse insect species

Growing evidence shows that eukaryotic genomes contain DNA sequences of non-retroviral RNA virus origin, yet the mechanisms underlying the generation of this virus-derived complementary DNA (vDNA) remain poorly understood, particularly in insects. Here, we demonstrate that infection with diverse non-retroviral RNA viruses induces the production of reverse-transcribed vDNA across multiple lepidopteran and hemipteran species. We further show that a Drosophila melanogaster-derived cell line actively secretes reverse-transcribed vDNA associated with extracellular vesicles (EVs), widely conserved nanoscale mediators of intercellular communication. Together, these findings reveal that infection-induced vDNA formation is a widespread phenomenon in insects and suggest that EVs may facilitate the systemic dissemination of vDNA.

biochemistry↗

Silencing of ATP synthase β reduces phytoplasma multiplication in the leafhopper vector Euscelidius variegatus

The leafhopper Euscelidius variegatus is a natural vector of the chrysanthemum yellows phytoplasma (CYp) and a laboratory vector of the Flavescence doree phytoplasma (FDp). Previous studies indicated a crucial role for insect ATP synthase and {beta} subunits during phytoplasma infection of the vector species. Gene silencing of ATP synthase {beta} was obtained by injection of specific dsRNAs in E. variegatus. Here we present the systemic and long-lasting nature of such silencing, its effects on the small RNA profile, the significant reduction of the corresponding protein expression, and the impact on phytoplasma acquisition capability. The specific transcript expression was silenced at least up to 37 days post injection with an average reduction of 100 times in insects injected with dsRNAs targeting ATP synthase {beta} (dsATP) compared with those injected with dsRNAs targeting green fluorescent protein (dsGFP), used as negative controls. Insects injected either with dsATP or dsGFP successfully acquired CYp and FDp during feeding on infected plants. However, the average phytoplasma amount in dsATP insects was significantly lower than that measured in dsGFP specimens, indicating a probable reduction of the pathogen multiplication rate when ATP synthase {beta} was silenced. The role of the insect ATP synthase {beta} during phytoplasma infection process is discussed.

microbiology↗