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Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)

A probe-hybridization quantitative polymerase chain reaction assay specific for Cryptosporidium serpentis (qPCR) has been developed and shown to be extremely sensitive in the laboratory, but clinical sensitivity and specificity for this test are lacking. To approximate the sensitivity and specificit...

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Autores principales: Bogan, James E., Wellehan, James F. X., Garner, Michael M., Childress, April L., Jackson, Bethany
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653349/
https://www.ncbi.nlm.nih.gov/pubmed/36171408
http://dx.doi.org/10.1007/s00436-022-07676-4
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author Bogan, James E.
Wellehan, James F. X.
Garner, Michael M.
Childress, April L.
Jackson, Bethany
author_facet Bogan, James E.
Wellehan, James F. X.
Garner, Michael M.
Childress, April L.
Jackson, Bethany
author_sort Bogan, James E.
collection PubMed
description A probe-hybridization quantitative polymerase chain reaction assay specific for Cryptosporidium serpentis (qPCR) has been developed and shown to be extremely sensitive in the laboratory, but clinical sensitivity and specificity for this test are lacking. To approximate the sensitivity and specificity of the C. serpentis qPCR, the medical records from a captive snake colony were reviewed, and between November 2015 and June 2021, 63 eastern indigo snakes (Drymarchon couperi) were necropsied. Of these 63 snakes, 11 had qPCR performed on gastric biopsies collected at the time of necropsy, 8 had qPCR performed on samples collected by gastric swab within 35 days of necropsy, and 34 had qPCR performed on samples collected by cloacal swab within 84 days of necropsy. The qPCR results were then compared to the post-mortem histological findings, where all three sampling techniques had a 100% specificity. The sensitivity was highest in samples collected at necropsy (100%, CI: 63.06 – 100%) followed by the ante-mortem testing: gastric swab (87.50%, CI: 42.13 – 99.64%) and cloacal swab (66.67%, CI: 44.68 – 84.37%).
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spelling pubmed-96533492022-11-15 Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi) Bogan, James E. Wellehan, James F. X. Garner, Michael M. Childress, April L. Jackson, Bethany Parasitol Res Research A probe-hybridization quantitative polymerase chain reaction assay specific for Cryptosporidium serpentis (qPCR) has been developed and shown to be extremely sensitive in the laboratory, but clinical sensitivity and specificity for this test are lacking. To approximate the sensitivity and specificity of the C. serpentis qPCR, the medical records from a captive snake colony were reviewed, and between November 2015 and June 2021, 63 eastern indigo snakes (Drymarchon couperi) were necropsied. Of these 63 snakes, 11 had qPCR performed on gastric biopsies collected at the time of necropsy, 8 had qPCR performed on samples collected by gastric swab within 35 days of necropsy, and 34 had qPCR performed on samples collected by cloacal swab within 84 days of necropsy. The qPCR results were then compared to the post-mortem histological findings, where all three sampling techniques had a 100% specificity. The sensitivity was highest in samples collected at necropsy (100%, CI: 63.06 – 100%) followed by the ante-mortem testing: gastric swab (87.50%, CI: 42.13 – 99.64%) and cloacal swab (66.67%, CI: 44.68 – 84.37%). Springer Berlin Heidelberg 2022-09-29 2022 /pmc/articles/PMC9653349/ /pubmed/36171408 http://dx.doi.org/10.1007/s00436-022-07676-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Bogan, James E.
Wellehan, James F. X.
Garner, Michael M.
Childress, April L.
Jackson, Bethany
Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title_full Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title_fullStr Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title_full_unstemmed Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title_short Evaluation of a probe hybridization quantitative polymerase chain reaction assay for Cryptosporidium serpentis in eastern indigo snakes (Drymarchon couperi)
title_sort evaluation of a probe hybridization quantitative polymerase chain reaction assay for cryptosporidium serpentis in eastern indigo snakes (drymarchon couperi)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9653349/
https://www.ncbi.nlm.nih.gov/pubmed/36171408
http://dx.doi.org/10.1007/s00436-022-07676-4
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