Evidence map›Paper›PMID 41810631›Full record

ArticleJournal of applied oral science : revista FOB2026

Effects of highly leukotoxic Aggregatibacter actinomycetemcomitans associated with ligature-induced periodontitis on oral and gut tissues in male rats.

Gabriela Furian Trama Ferraz, Camila Philipe de Araujo Camilo, Ana Luisa Palhares de Miranda, Mariana Alves Soares, Carmelo Sansone, Ricardo Tadeu Lopes, Aline Correa Abrahão, Ana Paula Vieira Colombo, Carina Maciel Silva-Boghossian

Abstract readEvaluation Study
In one paragraph

Article in Journal of applied oral science : revista FOB, 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

9 authors.

Gabriela Furian Trama FerrazUniversidade Federal do Rio de Janeiro, Faculdade de Odontologia, Departamento de Clínica Odontológica, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-9475-2830
Camila Philipe de Araujo CamiloUniversidade Federal do Rio de Janeiro, Faculdade de Odontologia, Departamento de Clínica Odontológica, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-9778-5849
Ana Luisa Palhares de MirandaUniversidade Federal do Rio de Janeiro, Faculdade de Farmácia, Departamento de Biotecnologia Farmacêutica, Laboratório de Estudos em Farmacologia Experimental (LEFEx), Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-4410-9521
Mariana Alves SoaresUniversidade Federal do Rio de Janeiro, Faculdade de Farmácia, Departamento de Biotecnologia Farmacêutica, Laboratório de Estudos em Farmacologia Experimental (LEFEx), Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0003-3279-6050
Carmelo SansoneUniversidade Federal do Rio de Janeiro, Faculdade de Odontologia, Departamento de Clínica Odontológica, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-0293-5147
Ricardo Tadeu LopesUniversidade Federal do Rio de Janeiro, Instituto Alberto Luiz de Coimbra de Pós-graduação e Pesquisa de Engenharia, Programa de Engenharia Nuclear, Laboratório de Instrumentação Nuclear, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0001-7250-824X
Aline Correa AbrahãoUniversidade Federal do Rio de Janeiro, Faculdade de Odontologia, Departamento de Patologia Oral, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-3397-3234
Ana Paula Vieira ColomboUniversidade Federal do Rio de Janeiro, Instituto de Microbiologia, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-2061-1840
Carina Maciel Silva-BoghossianUniversidade Federal do Rio de Janeiro, Faculdade de Odontologia, Departamento de Clínica Odontológica, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-4500-4350

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the effects of gastric administration of the highly leukotoxic Aggregatibacter actinomycetemcomitans JP2 strain (Aa JP2), with or without ligature-induced periodontitis, on periodontal and small intestinal tissues in a rat model. METHODOLOGY: Forty-eight-week-old male Wistar rats were divided into four groups (n=10/group): Control (CG), Periodontitis (PG), Periodontitis and Aa JP2 (PAaG), and Aa JP2 only (AaG). Ligatures were placed in PG and PAaG on day one and maintained for 42 days. After six weeks of twice-weekly gastric Aa JP2 inoculation, mandibles and small intestines were analyzed using stereomicroscopy, micro-computed tomography (CT), and histopathology to assess alveolar bone loss, trabecular architecture, inflammatory infiltrate, vascular congestion, goblet cell density, and villus morphology. Statistical analyses included the Kruskal-Wallis, Mann-Whitney, and Chi-square tests for group comparisons (p<0.05), as well as Spearman's correlation test.

resultsPG and PAaG exhibited significantly greater bone loss compared to CG and AaG (p<0.05). Micro-CT analysis revealed reduced trabecular thickness in AaG (342.4±23.1µm) compared to PG (378.2±28.1µm) and PAaG (385.5±45.1µm) (p<0.05). PAaG and AaG presented higher inflammatory infiltrate scores (>751 inflammatory cells) compared to CG and/or PG (p<0.05). Elevated vascular congestion and/or goblet cell hyperplasia in the jejunum and ileum were observed in PAaG and AaG compared to CG and PG (p<0.05). Villus height (duodenum/ileum) and villus width (jejunum/ileum) differed significantly among groups (p<0.0001). Significant correlations were identified: the alveolar bone volume/total volume ratio was positively associated with duodenal vascular congestion (rho=0.738; p=0.037); the periodontal inflammatory infiltrate was positively associated with jejunal goblet cell counts (rho=0.704; p=0.007); alveolar bone loss was positively associated with both duodenal and jejunal villus height (rho≥0.762; p<0.05); and bone volume was negatively associated with both jejunal vascular congestion (rho=-0.696; p=0.003) and jejunal goblet cell counts (rho=-0.617; p=0.011).

conclusionsGastric inoculation with Aa JP2 exacerbates ligature-induced periodontitis and independently induces intestinal morphological changes.

Indexed as

Aggregatibacter actinomycetemcomitansAlveolar Bone LossIntestine, SmallPeriodontitisAnimalsDisease Models, AnimalLigationMaleMandibleRandom AllocationRatsRats, WistarReference ValuesReproducibility of ResultsStatistics, NonparametricTime Factors

Identifiers

PMID41810631
PMCPMC13123778

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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.