Evidence map›Paper›PMID 42087076›Full record

ArticleBMC microbiology2026

Helicoverpa armigera (Lepidoptera, Noctuidae) as a reservoir of potential polystyrene-degrading fungi.

Gabrieli Seiscentos Cardenas, Eduardo Pereira de Souza, Yan Eiji Matuhara, Célio Dias Santos-Júnior, Thais Fernanda-Carlos, Milene Ferro, Silvia Helena Prado Bettini, Flávio Henrique-Silva

Abstract read
In one paragraph

Article in BMC microbiology, 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

8 authors.

Gabrieli Seiscentos Cardenas *Laboratory of Molecular Biology, Department of Genetics and Evolution, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Eduardo Pereira de Souza *Laboratory of Molecular Biology, Department of Genetics and Evolution, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Yan Eiji MatuharaLaboratory of Molecular Biology, Department of Genetics and Evolution, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Célio Dias Santos-JúniorDepartment of Hydrobiology, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Thais Fernanda-CarlosLaboratory of Molecular Biology, Department of Genetics and Evolution, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Milene FerroDepartment of General and Applied Biology, Institute of Biosciences, São Paulo State University (UNESP), Rio Claro, 01049-010, SP, Brazil.
Silvia Helena Prado BettiniDepartment of Materials Engineering, Center for Exact Sciences and Technology, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil.
Flávio Henrique-SilvaLaboratory of Molecular Biology, Department of Genetics and Evolution, Federal University of São Carlos (UFSCar), Rodovia Washington Luís, km 235, São Carlos, 13565-905, SP, Brazil. dfhs@ufscar.br.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 315618/2021-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2022/04312-6Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/02321-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/11974-8
6 · The paper itself

Abstract

backgroundA substantial portion of plastic waste is composed of polystyrene (PS). The polymer's end-of-life disposal is a concern due to its recalcitrant structure, which makes biodegradation difficult. Studies have shown that certain insect larvae are capable of ingesting, degrading, and mineralizing this material. This process is actively mediated by the intestinal larval microbiota, which comprises bacteria and fungi. The role of fungi is scarcely investigated, despite the extensive research conducted on the involvement of bacteria in the process.

resultsThe cotton bollworm (Helicoverpa armigera) was fed with expanded polystyrene (EPS), and the changes in the gut mycobiota were investigated. The ITS metabarcoding revealed that the yeast Diutina sp. was the most representative taxon in the samples, surpassing other taxa. Conversely, the feeding with EPS resulted in a decrease in the presence of Diutina sp. Additionally, four cultivable fungi (i.e., Aspergillus sp., Talaromyces sp., and two Penicillium species) isolated from the larvae's intestine were evaluated for their capacity to degrade PS. The fungi were cultured in low-carbon PDA and then covered with a PS film for 60 days. Scanning electron microscopy (SEM) analysis revealed that the fungi interacted with and altered the polymer's surface, resulting in the formation of cavities within the PS film.

conclusionsThese findings indicate that Helicoverpa armigera has the potential to serve as a reservoir for polystyrene-degrading fungi.

Indexed as

FungiHelicoverpa armigeraPolystyrenesAnimalsBiodegradation, EnvironmentalGastrointestinal MicrobiomeLarvaMicroscopy, Electron, ScanningPhylogenyPolystyrenesInsect gut microbiotaMetabarcodingPlastic degradation

Identifiers

PMID42087076
PMCPMC13312719

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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.