Evidence map›Paper›PMID 42198581›Full record

ArticlePathogens (Basel, Switzerland)2026

Clinical, Virological, and Pathological Outcomes Associated with Viral Dose in AG129 Mice Infected with Chikungunya Virus: An In Vivo Model to Study Viral Pathogenesis and Antiviral Preclinical Evaluation.

Marília Mazzi Moraes, Natália de Godoy, Eduardo Maffud Cilli, Paulo Ricardo da Silva Sanches

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 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

4 authors.

Marília Mazzi MoraesInstitute of Chemistry, São Paulo State University (UNESP), Araraquara 14800-060, SP, Brazil.ORCID 0000-0002-3545-8551
Natália de GodoySchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara 14800-903, SP, Brazil.ORCID 0009-0009-9465-8471
Eduardo Maffud CilliInstitute of Chemistry, São Paulo State University (UNESP), Araraquara 14800-060, SP, Brazil.ORCID 0000-0002-4767-0904
Paulo Ricardo da Silva SanchesSchool of Pharmaceutical Sciences, São Paulo State University (UNESP), Araraquara 14800-903, SP, Brazil.ORCID 0000-0002-2898-8191

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/05411-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/02956-6Fundação de Amparo à Pesquisa do Estado de São Paulo 2024/02000-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2024/02577-8Fundação de Amparo à Pesquisa do Estado de São Paulo 2025/07072-4
6 · The paper itself

Abstract

Chikungunya virus (CHIKV) infection presents a wide spectrum of clinical outcomes, ranging from mild self-limiting disease to severe and fatal manifestations, which are influenced by both host and viral factors. Animal models are essential for elucidating CHIKV pathogenesis and for preclinical evaluation of antiviral strategies; however, a well-characterized model evaluating the effect of different viral doses in AG129 mice remains limited. In this study, we investigated the clinical, virological, and pathological outcomes of CHIKV infection in male AG129 mice inoculated intraperitoneally with different viral doses (10, 100, and 1000 PFU/mL) of a Brazilian strain belonging to the East/Central/South African (ECSA) lineage. Lower-dose inoculation (10 PFU/mL) resulted in a milder disease course, characterized by transient viremia, limited tissue viral dissemination, minimal histopathological alterations, partial survival, and viral clearance. In contrast, higher doses (≥100 PFU/mL) led to rapid systemic viral dissemination, severe histopathological damage in the spleen, liver, and kidneys, and uniform lethality. Viral RNA was detected in serum and multiple organs in a time-dependent manner, with limited differences among inoculum doses in most tissues. Notably, dose-related differences were observed in specific compartments and time points, particularly in hind-limb muscles at early time points and in serum at later stages.

Indexed as

Antiviral AgentsChikungunya FeverChikungunya virusAnimalsDisease Models, AnimalMaleMiceRNA, ViralViral LoadAntiviral AgentsRNA, ViralAG129 miceanimal modelChikungunya virusviral kinetics

Identifiers

PMID42198581
PMCPMC13209420

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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.