Evidence map›Paper›PMID 41417353›Full record

ArticleMemorias do Instituto Oswaldo Cruz2025

Breaking the ice - simplified freeze-fracture of parasitic protists: a cost-effective approach without highly specialised equipment.

Marcia Attias, Luis Otávio da Silva Pacheco, Sharmila Fiama das Neves Ortiz, Raphael Verdan, Kildare Miranda, Ana Paula Gadelha, Wanderley de Souza, Marlene Benchimol

Abstract read
In one paragraph

Article in Memorias do Instituto Oswaldo Cruz, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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.

Marcia AttiasUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Luis Otávio da Silva PachecoUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Sharmila Fiama das Neves OrtizUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Raphael VerdanUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Kildare MirandaUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Ana Paula GadelhaInstituto Nacional de Metrologia, Qualidade e Tecnologia, Diretoria de Metrologia Científica, Laboratório de Biologia de Células Eucariontes, Duque de Caxias, RJ, Brasil.
Wanderley de SouzaUniversidade Federal do Rio de Janeiro, Centro de Pesquisa em Medicina de Precisão, Instituto de Biofísica Carlos Chagas Filho, Laboratório de Ultraestrutura Celular Hertha Meyer, Rio de Janeiro, RJ, Brasil.
Marlene BenchimolUniversidade Federal do Rio de Janeiro, Centro Nacional de Biologia Estrutural e Bioimagem, Instituto Nacional de Ciência e Tecnologia em Biologia Estrutural e Bioimagem, Rio de Janeiro, RJ, Brasil.ORCID http://orcid.org/0000-0002-4957-8538

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe present a simplified freeze-fracture method to reveal the internal structure of protozoan parasites and their host cells, without the need for costly transmission electron microscopy (TEM) equipment. In a traditional procedure, the four key steps in making a freeze-fracture replica are (1) freezing, (2) fracturing, (3) replication, and (4) replica cleaning. In conventional protocols, visualisation is performed using a TEM.

objectivesThis study aimed to adapt the traditional freeze-fracture protocol to a more accessible method, eliminating the need for vacuum equipment and TEM, while preserving the capacity to visualise cellular structures.

methodsIn our adapted method, vacuum equipment was not required for sample fracturing, shadowing, or replica preparation. Cells were fixed with glutaraldehyde, embedded in a gelatin-chitosan matrix, cryoprotected with dimethyl sulfoxide (DMSO), and subsequently frozen in Freon, followed by immersion in liquid nitrogen. We manually break the cells with a previously frozen razor blade and macerate them with osmium tetroxide (OsO4). The samples are visualised using scanning electron microscopy (SEM).

findingsWe present various structures of Toxoplasma gondii, Trypanosoma cruzi, Trichomonas vaginalis, Giardia intestinalis, and cultured cells observed using our adapted freeze-fracture method. MAIN

conclusionsThis is a rapid and low-cost technique that reveals cell structures comparable to those observed using traditional freeze-fracture methods, although with reduced resolution.

Indexed as

Freeze FracturingGiardiaToxoplasmaTrichomonas vaginalisTrypanosoma cruziAnimalsCost-Benefit AnalysisMicroscopy, Electron, ScanningMicroscopy, Electron, Transmission

Identifiers

PMID41417353
PMCPMC12711207

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LicenceCC BY
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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.