Evidence map›Paper›PMID 41042807›Full record

ArticlePLoS neglected tropical diseases2025

Temporal and spatial profiling of Aedes albopictus immune responses to chikungunya virus infection.

Maria Greta Dipaola, Claudia Fortuna, Francesco Severini, Giulia Bevivino, Marco Di Luca, Tony Nolan, Marco Salvemini, Bruno Arcà, Fabrizio Lombardo

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Maria Greta DipaolaParasitology Unit, Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Claudia FortunaDepartment of Infectious Diseases, National Institute of Health, Rome, Italy.
Francesco SeveriniDepartment of Infectious Diseases, National Institute of Health, Rome, Italy.
Giulia BevivinoParasitology Unit, Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Marco Di LucaDepartment of Infectious Diseases, National Institute of Health, Rome, Italy.
Tony NolanDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Marco SalveminiDepartment of Biology, University of Naples Federico II, Naples, Italy.
Bruno ArcàParasitology Unit, Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
Fabrizio LombardoParasitology Unit, Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.ORCID 0000-0002-8563-0612

Funding

European Union Horizon 2020Sapienza University of Rome
6 · The paper itself

Abstract

The global expansion of Aedes albopictus from Southeast Asia to various regions worldwide poses a significant public health concern due to its role as a vector for several pathogens, including chikungunya virus (CHIKV), which infects over one million people annually. In this study, aimed at understanding the molecular interactions between Ae. albopictus and CHIKV, we analyzed by RNA sequencing CHIKV-infected and uninfected control mosquitoes. We focused our attention on key mosquito organs at one- and five-days post-blood meal ingestion, which correspond to viral entry and dissemination, and found specific transcriptional changes involving various pathways during the CHIKV lifecycle. The mosquito midgut plays a crucial role in the early stages, when the virus enters along with human blood components, encounters the resident microbiota, interacts with the developing peritrophic matrix, and counteracts the mosquito's digestive enzymes. We found that RNA interference (RNAi) was predominantly activated in the midgut during the initial virus invasion. Additionally, several key enzymes involved in autophagy and ubiquitination were also more abundant in infected midguts compared to controls. At later time points, after viral dissemination into the hemocoel, key immune responses are triggered in the hemolymph and, accordingly, immune mechanisms such as the activation of leucine-rich repeats (LRRs) proteins, secretion of antimicrobial peptides (e.g., holotricin), and melanization (mediated by phenoloxidase, PO) were the most prominent. RNA-seq results were validated by RT-qPCR on selected candidates in different tissues and a catalogue of Ae. albopictus immune genes (891 contigs) grouped into 24 different immune and immune-related families was compiled. This study explores the molecular interactions between Ae. albopictus and CHIKV across developmental stages, providing key insights into arbovirus transmission dynamics and mosquito vector competence.

Indexed as

AedesChikungunya FeverChikungunya virusMosquito VectorsAnimalsFemaleInsect ProteinsRNA InterferenceInsect Proteins

Identifiers

PMID41042807
PMCPMC12510663

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.