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Application of a universal parasite diagnostic test to biological specimens collected from animals

A previously described universal parasite diagnostic (nUPDx) based on PCR amplification of the 18S rDNA and deep-amplicon sequencing, can detect human blood parasites with a sensitivity comparable to real-time PCR. To date, the efficacy of this assay has only been assessed on human blood. This study...

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Autores principales: Lane, Meredith, Kashani, Mitra, Barratt, Joel LN., Qvarnstrom, Yvonne, Yabsley, Michael J., Garrett, Kayla B., Bradbury, Richard S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803608/
https://www.ncbi.nlm.nih.gov/pubmed/36593876
http://dx.doi.org/10.1016/j.ijppaw.2022.12.003
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author Lane, Meredith
Kashani, Mitra
Barratt, Joel LN.
Qvarnstrom, Yvonne
Yabsley, Michael J.
Garrett, Kayla B.
Bradbury, Richard S.
author_facet Lane, Meredith
Kashani, Mitra
Barratt, Joel LN.
Qvarnstrom, Yvonne
Yabsley, Michael J.
Garrett, Kayla B.
Bradbury, Richard S.
author_sort Lane, Meredith
collection PubMed
description A previously described universal parasite diagnostic (nUPDx) based on PCR amplification of the 18S rDNA and deep-amplicon sequencing, can detect human blood parasites with a sensitivity comparable to real-time PCR. To date, the efficacy of this assay has only been assessed on human blood. This study assessed the utility of nUPDx for the detection of parasitic infections in animals using blood, tissues, and other biological sample types from mammals, birds, and reptiles, known to be infected with helminth, apicomplexan, or pentastomid parasites (confirmed by microscopy or PCR), as well as negative samples. nUPDx confirmed apicomplexan and/or nematode infections in 24 of 32 parasite-positive mammals, while also identifying several undetected coinfections. nUPDx detected infections in 6 of 13 positive bird and 1 of 2 positive reptile samples. When applied to 10 whole parasite specimens (worms and arthropods), nUPDx identified all to the genus or family level, and detected one incorrect identification made by morphology. Babesia sp. infections were detected in 5 of the 13 samples that were negative by other diagnostic approaches. While nUPDx did not detect PCR/microscopy-confirmed trichomonads or amoebae in cloacal swabs/tissue from 8 birds and 2 reptiles due to primer template mismatches, 4 previously undetected apicomplexans were detected in these samples. Future efforts to improve the utility of the assay should focus on validation against a larger panel of tissue types and animal species. Overall, nUPDx shows promise for use in both veterinary diagnostics and wildlife surveillance, especially because species-specific PCRs can miss unknown or unexpected pathogens.
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spelling pubmed-98036082023-01-01 Application of a universal parasite diagnostic test to biological specimens collected from animals Lane, Meredith Kashani, Mitra Barratt, Joel LN. Qvarnstrom, Yvonne Yabsley, Michael J. Garrett, Kayla B. Bradbury, Richard S. Int J Parasitol Parasites Wildl Article A previously described universal parasite diagnostic (nUPDx) based on PCR amplification of the 18S rDNA and deep-amplicon sequencing, can detect human blood parasites with a sensitivity comparable to real-time PCR. To date, the efficacy of this assay has only been assessed on human blood. This study assessed the utility of nUPDx for the detection of parasitic infections in animals using blood, tissues, and other biological sample types from mammals, birds, and reptiles, known to be infected with helminth, apicomplexan, or pentastomid parasites (confirmed by microscopy or PCR), as well as negative samples. nUPDx confirmed apicomplexan and/or nematode infections in 24 of 32 parasite-positive mammals, while also identifying several undetected coinfections. nUPDx detected infections in 6 of 13 positive bird and 1 of 2 positive reptile samples. When applied to 10 whole parasite specimens (worms and arthropods), nUPDx identified all to the genus or family level, and detected one incorrect identification made by morphology. Babesia sp. infections were detected in 5 of the 13 samples that were negative by other diagnostic approaches. While nUPDx did not detect PCR/microscopy-confirmed trichomonads or amoebae in cloacal swabs/tissue from 8 birds and 2 reptiles due to primer template mismatches, 4 previously undetected apicomplexans were detected in these samples. Future efforts to improve the utility of the assay should focus on validation against a larger panel of tissue types and animal species. Overall, nUPDx shows promise for use in both veterinary diagnostics and wildlife surveillance, especially because species-specific PCRs can miss unknown or unexpected pathogens. Elsevier 2022-12-22 /pmc/articles/PMC9803608/ /pubmed/36593876 http://dx.doi.org/10.1016/j.ijppaw.2022.12.003 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lane, Meredith
Kashani, Mitra
Barratt, Joel LN.
Qvarnstrom, Yvonne
Yabsley, Michael J.
Garrett, Kayla B.
Bradbury, Richard S.
Application of a universal parasite diagnostic test to biological specimens collected from animals
title Application of a universal parasite diagnostic test to biological specimens collected from animals
title_full Application of a universal parasite diagnostic test to biological specimens collected from animals
title_fullStr Application of a universal parasite diagnostic test to biological specimens collected from animals
title_full_unstemmed Application of a universal parasite diagnostic test to biological specimens collected from animals
title_short Application of a universal parasite diagnostic test to biological specimens collected from animals
title_sort application of a universal parasite diagnostic test to biological specimens collected from animals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9803608/
https://www.ncbi.nlm.nih.gov/pubmed/36593876
http://dx.doi.org/10.1016/j.ijppaw.2022.12.003
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