Evidence map›Paper›PMID 36604333›Full record

ArticleParasitology research2023

Differentiating paramphistome species in cattle using DNA barcoding coupled with high-resolution melting analysis (Bar-HRM).

Kittisak Buddhachat, Sirikhwan Sriuan, Sirapat Nak-On, Thapana Chontananarth

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Article in Parasitology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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3citing papers in PubMed
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1 · What the graph read from it

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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.

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Amphistomes.Advances in experimental medicine and biology · 2024
    Review
  3. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kittisak BuddhachatDepartment of Biology, Faculty of Science, Naresuan University, Phitsanulok, 65000, Thailand.ORCID http://orcid.org/0000-0003-4746-9861
Sirikhwan SriuanDepartment of Biology, Faculty of Science, Naresuan University, Phitsanulok, 65000, Thailand.
Sirapat Nak-OnApplied Parasitology Research Laboratory, Department of Biology, Faculty of Science, Srinakharinwirot University, Bangkok, 10110, Thailand.
Thapana ChontananarthApplied Parasitology Research Laboratory, Department of Biology, Faculty of Science, Srinakharinwirot University, Bangkok, 10110, Thailand. thapana@g.swu.ac.th.ORCID http://orcid.org/0000-0002-4241-6966

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paramphistomosis is caused by paramphistome or amphistome parasites, including Fischoederius elongatus, Gastrothylax crumenifer, Orthocoelium parvipapillatum, and Paramphistomum epiclitum. The control and prevention of these parasite outbreaks are difficult because of the wide occurrence of these species. Besides, the clinical manifestations and their egg characteristics are similar to those of other intestinal flukes in the paramphistome group, leading to misdiagnosis. Here, we employed DNA barcoding using NADH dehydrogenase (ubiquinone, alpha 1) (ND1) and cytochrome c oxidase subunit I (COI), coupled with high-resolution melting analysis (Bar-HRM), for species differentiation. As a result, ParND1_3 and ParCOI4 resulted in positive amplification in the paramphistomes and Fasciola gigantica, with significantly different melting curves for each species. The melting temperatures of each species obtained clearly differed. Regarding sensitivity, the limit of detection (LoD) for all species of paramphistomes was 1 pg/µl. Our findings suggest that Bar-HRM using ParND1_3 is highly suitable for the differentiation of paramphistome species. This approach can be used in parasite detection and epidemiological studies in cattle.

Indexed as

Cattle DiseasesFasciolaParamphistomatidaeTrematode InfectionsAnimalsCattleDNA Barcoding, TaxonomicPolymerase Chain ReactionCattleCytochrome c oxidase subunit I (COI)NADH dehydrogenase 1 (ND1)ParamphistomeRumen fluke

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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.