Please use this identifier to cite or link to this item:
https://ir.swu.ac.th/jspui/handle/123456789/29379
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Panich W. | |
dc.contributor.author | Tejangkura T. | |
dc.contributor.author | Chontananarth T. | |
dc.contributor.other | Srinakharinwirot University | |
dc.date.accessioned | 2023-11-15T02:08:27Z | - |
dc.date.available | 2023-11-15T02:08:27Z | - |
dc.date.issued | 2023 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85153226323&doi=10.1080%2f03079457.2023.2196251&partnerID=40&md5=d904e1193749f8d3f32def2b2314061c | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/29379 | - |
dc.description.abstract | Ascaridia galli is an important nematode that causes ascaridiasis in free-range and indoor system chicken farms. Infection with A. galli may damage the intestinal mucosa and inhibit nutrient absorption, leading to a reduced growth rate, weight loss and a decreased egg production. Consequently, A. galli infection is a significant health problem in chickens. In this study, we developed a loop-mediated isothermal amplification coupled with a lateral flow dipstick (LAMP-LFD) assay for the visual detection of A. galli eggs in faecal samples. The LAMP-LFD assay consists of six primers and one DNA probe that recognize the internal transcribed spacer 2 (ITS2) region; it can be performed within 70 min and the results can be interpreted with the naked eye. Using the LAMP-LFD assay developed in this study, A. galli DNA was specifically amplified without any cross-reactions with other related parasites (Heterakis gallinarum, Raillietina echinobothrida, R. tetragona, R. cesticillus, Cotugnia sp., Echinostoma miyagawai) and definitive hosts (Gallus gallus domesticus, Anas platyrhynchos domesticus). The minimum detectable DNA concentration was 5 pg/μl, and the detectable egg count was 50 eggs per reaction. The assay can be performed in a water bath, without the need for post-mortem morphological investigations and laboratory instruments. It is therefore a viable alternative for the detection of A. galli in chicken faeces and can replace classical methods in field screening for epidemiological investigations, veterinary health and poultry farming management. RESEARCH HIGHLIGHTS This is the first study using the LAMP-LFD assay for Ascaridia galli detection. The results can be observed by the naked eye. The developed assay can be used to detect Ascaridia galli eggs in faecal samples. © 2023 Houghton Trust Ltd. | |
dc.publisher | Taylor and Francis Ltd. | |
dc.subject | Ascaridia galli | |
dc.subject | chicken | |
dc.subject | DNA biosensor | |
dc.subject | lateral flow dipstick | |
dc.subject | loop-mediated isothermal amplification | |
dc.subject | visual interpretation | |
dc.title | Feasibility of a DNA biosensor assay based on loop-mediated isothermal amplification combined with a lateral flow dipstick assay for the visual detection of Ascaridia galli eggs in faecal samples | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | Avian Pathology. Vol 52, No.3 (2023), p.209-218 | |
dc.identifier.doi | 10.1080/03079457.2023.2196251 | |
Appears in Collections: | Scopus 2023 |
Files in This Item:
There are no files associated with this item.
Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.