Evidence map›Paper›PMID 42090697›Full record

ArticleMemorias do Instituto Oswaldo Cruz2026

Aedes aegypti salivary gland extract enhances Zika virus replication through immune modulation.

Gabriel Hilario, Gilson Pires Dorneles, Deise Nascimento de Freitas, Onilda Santos da Silva, Josiane Somariva Prophiro, Tiago Fazolo, Rafael Rahal Guaragna Machado, Cristina Bonorino, Danielle Bruna Leal Oliveira, Simone Gonçalves da Fonseca and 2 more

Abstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2026. 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

12 authors.

Gabriel HilarioUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.
Gilson Pires DornelesUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Ciências da Saúde, Porto Alegre, RS, Brasil.
Deise Nascimento de FreitasUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.
Onilda Santos da SilvaUniversidade Federal do Rio Grande do Sul, Programa de Pós-Graduação em Microbiologia Agrícola e do Ambiente, Porto Alegre, RS, Brasil.
Josiane Somariva ProphiroUniversidade do Sul de Santa Catarina, Programa de Pós-Graduação em Ciências da Saúde, Tubarão, SC, Brasil.
Tiago FazoloUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.
Rafael Rahal Guaragna MachadoUniversidade de São Paulo, Instituto de Ciências Biomédicas, Laboratório de Virologia Clínica e Molecular, São Paulo, SP, Brasil.
Cristina BonorinoUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.
Danielle Bruna Leal OliveiraUniversidade de São Paulo, Instituto de Ciências Biomédicas, Laboratório de Virologia Clínica e Molecular, São Paulo, SP, Brasil.
Simone Gonçalves da FonsecaUniversidade Federal de Goiás, Instituto de Patologia Tropical e Saúde Pública, Goiânia, GO, Brasil.
Pedro Roosevelt Torres RomãoUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.ORCID http://orcid.org/0000-0002-1039-2509
Luiz Carlos RodriguesUniversidade Federal de Ciências da Saúde de Porto Alegre, Programa de Pós-Graduação em Biociências, Porto Alegre, RS, Brasil.ORCID http://orcid.org/0000-0002-5380-8930

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMosquito saliva contains bioactive molecules that modulate host immunity and may influence arboviral infection. The contribution of Aedes aegypti salivary gland extract (SGE) to viral replication and immune regulation during Zika virus (ZIKV) infection remains poorly understood.

objectivesTo investigate the immunomodulatory effects of Ae. aegypti SGE during ZIKV infection.

methodsPeripheral blood mononuclear cells (PBMCs) and murine antigen-presenting cell lines were exposed to ZIKV with or without SGE. Viral replication was measured by quantitative polymerase chain reaction (qPCR), cell death and immune subsets by flow cytometry, oxidative stress markers by biochemical assays, and cytokine production by enzyme-linked immunosorbent assay (ELISA).

findingsSGE enhanced ZIKV replication, particularly in PBMCs, with increased RNA copies (median Δ = +1,779), reduced late apoptosis of CD4⁺ T cells (p = 0.0055), dendritic cell death (p < 0.01), and impaired T-cell proliferation. SGE attenuated ZIKV-induced oxidative damage by restoring glutathione levels, reducing lipid and protein oxidation (p < 0.001), and increasing nitric oxide (NO) production. Cytokine profiling revealed suppression of interferon-y (IFN-γ) (p < 0.001) and induction of interleukin-4 (IL-4) (p < 0.0001), indicating a Th2-skewed response. Murine cell lines confirmed SGE-driven cytokine modulation. MAIN

conclusionsAe. aegypti SGE alters host immune homeostasis, favouring ZIKV infection by weakening antiviral defences and redirecting immune and redox pathways, thereby facilitating viral expansion.

Indexed as

AedesLeukocytes, MononuclearSalivary GlandsTissue ExtractsVirus ReplicationZika VirusAnimalsCell LineCytokinesEnzyme-Linked Immunosorbent AssayFlow CytometryHumansMiceOxidative StressCytokinesTissue Extracts

Identifiers

PMID42090697
PMCPMC13143171

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Registered trials

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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.