# Assessing whole-host homogenisation as a new tool for parasite detection and identification

**Authors:** Kamil Hupało, Celine Sassor, Mia Merle Fuhren, Dominik Buchner, Daniel Grabner, Bernd Sures

PMC · DOI: 10.1016/j.crpvbd.2026.100348 · Current Research in Parasitology & Vector-borne Diseases · 2026-01-01

## TL;DR

This paper introduces a new method for detecting and identifying parasites by homogenizing whole hosts and using DNA-based techniques, which could be faster and require less expertise than traditional methods.

## Contribution

The study introduces whole-host homogenisation as a novel, time-efficient method for parasite detection and identification.

## Key findings

- The method successfully detected all parasite taxa identified through morphology, including some not previously detected.
- Acanthocephalans showed low molecular detection, indicating a limitation of the method.
- The approach has high potential for efficient and accurate parasite detection, sometimes surpassing traditional methods.

## Abstract

Despite their importance in ecosystem functioning, parasites remain the most neglected components of biodiversity monitoring. This neglect is partly due to the methodological challenges associated with their detection and identification. Current traditional morphological and molecular approaches are time-consuming, labour-intensive, and require specialised expertise. Here, we explore a novel approach of deriving parasite information through whole-host homogenisation followed by DNA-based identification of its parasite biota. Our goal was to validate whether the approach is feasible and if it could become a complementary method for studying parasites, providing a time-efficient solution allowing for a holistic parasite scan with limited taxonomic expertise. To test the method’s efficiency, we analysed five specimens of European eel as model hosts. Their parasites were identified morphologically, and then all the parasites and the entire host tissue were homogenised together using a commercial blender. Molecular identification of the morphologically detected parasites was conducted using DNA barcoding with parasite-specific primers. Following homogenisation and DNA-based identification, we successfully detected all parasite taxa identified during morphological analyses, even including instances where they had not been detected morphologically. A notable exception were acanthocephalans, which showed low levels of molecular detection. Despite certain limitations, the detection of parasites directly from the whole-host homogenate shows high potential for efficient and accurate parasite detection, in some cases even surpassing morphological identification. The further development of the method, particularly through exploration of DNA metabarcoding, could improve the reliability of parasite assessments and facilitate parasite detection, which could aid in proper parasite recognition.

Image 1

•A new approach for DNA-based parasite detection using whole-host homogenisation.•The new approach showed high congruence with parasite identification based on morphology.•The new approach at times outperformed the morphological methods.•When optimised, the new approach can allow for a holistic parasite scan with DNA metabarcoding.•The new approach can significantly reduce dependence on taxonomic expertise.

A new approach for DNA-based parasite detection using whole-host homogenisation.

The new approach showed high congruence with parasite identification based on morphology.

The new approach at times outperformed the morphological methods.

When optimised, the new approach can allow for a holistic parasite scan with DNA metabarcoding.

The new approach can significantly reduce dependence on taxonomic expertise.

## Full-text entities

- **Diseases:** parasite (MESH:D010272), infection (MESH:D007239)
- **Chemicals:** Alconox (-), sodium bicarbonate (MESH:D017693), ethanol (MESH:D000431), NaOH (MESH:D012972)
- **Species:** Schyzocotyle acheilognathi (species) [taxon 135513], Proteocephalus sp. (species) [taxon 109197], Ixodida (ticks, order) [taxon 6935], Pomphorhynchus bosniacus (species) [taxon 2487691], Homo sapiens (human, species) [taxon 9606], Anguilla anguilla (European eel, species) [taxon 7936], Senga ophiocephalina (species) [taxon 1981834], Pseudodactylogyrus bini (species) [taxon 165850], Bothriocephalus claviceps (species) [taxon 56209], Anguillicola crassus (species) [taxon 620897]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12818088/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12818088/full.md

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Source: https://tomesphere.com/paper/PMC12818088