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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51076
Title: Diagnosis of feline filariasis assisted by a novel semi-automated microfluidic device in combination with high resolution melting real-time PCR
Authors: Achinya Phuakrod
Witsaroot Sripumkhai
Wutthinan Jeamsaksiri
Pattaraluck Pattamang
Ekachai Juntasaro
Therdthai Thienthong
Suporn Foongladda
Paul J. Brindley
Sirichit Wongkamchai
King Mongkut's University of Technology North Bangkok
Thailand National Electronics and Computer Technology Center
Faculty of Medicine, Siriraj Hospital, Mahidol University
The George Washington University
Keywords: Immunology and Microbiology;Medicine
Issue Date: 8-Apr-2019
Citation: Parasites and Vectors. Vol.12, No.1 (2019)
Abstract: © 2019 The Author(s). Background: The diagnosis of filariasis traditionally relies on the detection of circulating microfilariae (mf) using Giemsa-stained thick blood smears. This approach has several limitations. We developed a semi-automated microfluidic device to improve and simplify the detection of filarial nematodes. Methods: The efficiency and repeatability of the microfluidic device was evaluated. Human EDTA blood samples were 'spiked' with B. malayi mf at high, moderate, and low levels, and subsequently tested 10 times. The device was also used for a field survey of feline filariasis in 383 domesticated cats in an area of Narathiwat Province, Thailand, the endemic area of Brugia malayi infection. Results: In the control blood arbitrarily spiked with mf, the high level, moderate level and low level mf-positive controls yielded coefficient variation (CV) values of 4.44, 4.16 and 4.66%, respectively, at the optimized flow rate of 6 μl/min. During the field survey of feline filariasis in Narathiwat Province, the device detected mf in the blood of 34 of 383 cats (8.9%) whereas mf were detected in 28 (7.3%) cats using the blood smear test. Genomic DNA was extracted from mf trapped in the device after which high-resolution melting (HRM) real-time PCR assay was carried out, which enabled the simultaneous diagnosis of filarial species. Among the 34 mf-positive samples, 12 were identified as B. malayi, 15 as Dirofilaria immitis and 7 as| D. repens. Conclusions: We developed a semi-automated microfluidic device to detect mf of filarial parasites that could be used to diagnose lymphatic filariasis in human populations. This novel device facilitates rapid, higher-throughput detection and identification of infection with filariae in blood samples.
URI: http://repository.li.mahidol.ac.th/dspace/handle/123456789/51076
metadata.dc.identifier.url: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064118299&origin=inward
ISSN: 17563305
Appears in Collections:Scopus 2019

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