Evidence map›Paper›PMID 40448150›Full record

ArticleParasites & vectors2025

Molecular detection and identification of Trichobilharzia: development of a LAMP, qPCR, and multiplex PCR toolkit.

Jan Procházka, Zikmund Bartoníček, Roman Leontovyč, Petr Horák, Tomáš Macháček

Abstract read
In one paragraph

Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. The avian schistosomeFood and waterborne parasitology · 2025
    Article
  3. Article
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

5 authors.

Jan ProcházkaCharles University, Prague, Czechia. prochazkajan1@natur.cuni.cz.ORCID http://orcid.org/0009-0004-6190-8722
Zikmund BartoníčekCharles University, Prague, Czechia.ORCID http://orcid.org/0000-0002-5093-8123
Roman LeontovyčCharles University, Prague, Czechia.ORCID http://orcid.org/0000-0002-0035-949X
Petr HorákCharles University, Prague, Czechia.ORCID http://orcid.org/0000-0001-9820-5044
Tomáš MacháčekCharles University, Prague, Czechia. tomas.machacek@natur.cuni.cz.ORCID http://orcid.org/0000-0002-6310-4099

Funding

Charles University institutional funding SVV 260678/2023Charles University institutional funding UNCE24/SCI/011Grantová Agentura České Republiky GA24-11031S
6 · The paper itself

Abstract

backgroundCercarial dermatitis (CD), or swimmer's itch, is a water-borne allergic skin reaction caused by the penetration of the larval stages of bird schistosomes (cercariae) into the skin. Members of the genus Trichobilharzia are the primary causative agents of CD worldwide. Due to the increasing number of cases, CD is regarded as a (re)emerging disease. Outbreaks in recreational waters can significantly impact public health and local economies. Environmental monitoring of Trichobilharzia is crucial for outbreak prediction and public health management. However, conventional methods, such as cercarial shedding and snail dissections, are labour-intensive and lack sensitivity. To overcome these limitations, we present a molecular toolkit that combines loop-mediated isothermal amplification (LAMP), quantitative polymerase chain reaction (qPCR), and multiplex PCR for rapid, sensitive, and accurate detection and identification of Trichobilharzia spp. from various biological samples.

methodsTricho-LAMP and Tricho-qPCR were designed and optimised for Trichobilharzia DNA detection. A multiplex PCR assay was also developed and optimised to identify the three main species causing CD in Europe (Trichobilharzia franki, T. szidati, and T. regenti).

resultsTricho-LAMP specifically detected T. regenti and T. franki at 10

conclusionsWe provide a molecular toolkit consisting of LAMP, qPCR, and multiplex PCR. By exhibiting high sensitivity, Tricho-LAMP and Tricho-qPCR assays are potentially suitable for environmental DNA (eDNA)-based environmental monitoring of bird schistosomes, by both researchers and public health authorities. Multiplex PCR can be used for species determination without the need for further sequencing.

Indexed as

Molecular Diagnostic TechniquesMultiplex Polymerase Chain ReactionNucleic Acid Amplification TechniquesReal-Time Polymerase Chain ReactionSchistosomatidaeTrematode InfectionsAnimalsBirdsDNA, HelminthSensitivity and SpecificitySnailsDNA, HelminthBird schistosomesCercarial dermatitisDetectionLAMPMonitoringMultiplex PCRqPCRTrichobilharzia

Identifiers

PMID40448150
PMCPMC12124058

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.