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A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors

The ocular onchocercosis is caused by the zoonotic parasite Onchocerca lupi (Spirurida: Onchocercidae). A major hindrance to scientific progress is the absence of a reliable diagnostic test in affected individuals. Microscopic examination of skin snip sediments and the identification of adults embed...

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Autores principales: Latrofa, Maria Stefania, Annoscia, Giada, Colella, Vito, Cavalera, Maria Alfonsa, Maia, Carla, Martin, Coralie, Šlapeta, Jan, Otranto, Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902036/
https://www.ncbi.nlm.nih.gov/pubmed/29617361
http://dx.doi.org/10.1371/journal.pntd.0006402
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author Latrofa, Maria Stefania
Annoscia, Giada
Colella, Vito
Cavalera, Maria Alfonsa
Maia, Carla
Martin, Coralie
Šlapeta, Jan
Otranto, Domenico
author_facet Latrofa, Maria Stefania
Annoscia, Giada
Colella, Vito
Cavalera, Maria Alfonsa
Maia, Carla
Martin, Coralie
Šlapeta, Jan
Otranto, Domenico
author_sort Latrofa, Maria Stefania
collection PubMed
description The ocular onchocercosis is caused by the zoonotic parasite Onchocerca lupi (Spirurida: Onchocercidae). A major hindrance to scientific progress is the absence of a reliable diagnostic test in affected individuals. Microscopic examination of skin snip sediments and the identification of adults embedded in ocular nodules are seldom performed and labour-intensive. A quantitative real-time PCR (qPCR) assay was herein standardized for the detection of O. lupi DNA and the results compared with microscopic examination and conventional PCR (cPCR). The specificity of qPCR and cPCR was assessed by processing the most common filarial nematodes infecting dogs, skin samples from O. lupi infected (n = 35 dogs) or uninfected animals (n = 21 dogs; n = 152 cats) and specimens of potential insect vector (n = 93 blackflies; n = 59 mosquitoes/midges). The analytical sensitivity of both assays was assessed using 10-fold serial dilutions of DNA from adult specimen and from a pool of microfilariae. The qPCR on skin samples revealed an analytical specificity of 100% and a sensitivity up to 8 x 10(−1) fg/2μl O. lupi adult-DNA and up to 3.6 x 10(−1) pg/2μl of mfs-DNA (corresponding to 1 x 10(−2) mfs/2μl). Only 9.5% O. lupi-infected skin samples were positive for cPCR with a sensitivity of 8 x 10(−1) pg/2μl of DNA. Out of 152 blackflies and mosquitoes/midges, eight specimens experimentally infected (n = 1 S. erythrocephalum; n = 1 S. ornatum; n = 6 Simulium sp.) were positive by qPCR. The qPCR assay herein standardized represents an important step forward in the diagnosis of zoonotic onchocercosis caused by O. lupi, especially for the detection and quantification of low number of mfs. This assay provides a fundamental contribution for the establishment of surveillance strategies aiming at assessing the presence of O. lupi in carnivores and in insect species acting as potential intermediate hosts. The O. lupi qPCR assay will enable disease progress monitoring as well as the diagnosis of apparently clinical healthy dogs and cats.
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spelling pubmed-59020362018-05-04 A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors Latrofa, Maria Stefania Annoscia, Giada Colella, Vito Cavalera, Maria Alfonsa Maia, Carla Martin, Coralie Šlapeta, Jan Otranto, Domenico PLoS Negl Trop Dis Research Article The ocular onchocercosis is caused by the zoonotic parasite Onchocerca lupi (Spirurida: Onchocercidae). A major hindrance to scientific progress is the absence of a reliable diagnostic test in affected individuals. Microscopic examination of skin snip sediments and the identification of adults embedded in ocular nodules are seldom performed and labour-intensive. A quantitative real-time PCR (qPCR) assay was herein standardized for the detection of O. lupi DNA and the results compared with microscopic examination and conventional PCR (cPCR). The specificity of qPCR and cPCR was assessed by processing the most common filarial nematodes infecting dogs, skin samples from O. lupi infected (n = 35 dogs) or uninfected animals (n = 21 dogs; n = 152 cats) and specimens of potential insect vector (n = 93 blackflies; n = 59 mosquitoes/midges). The analytical sensitivity of both assays was assessed using 10-fold serial dilutions of DNA from adult specimen and from a pool of microfilariae. The qPCR on skin samples revealed an analytical specificity of 100% and a sensitivity up to 8 x 10(−1) fg/2μl O. lupi adult-DNA and up to 3.6 x 10(−1) pg/2μl of mfs-DNA (corresponding to 1 x 10(−2) mfs/2μl). Only 9.5% O. lupi-infected skin samples were positive for cPCR with a sensitivity of 8 x 10(−1) pg/2μl of DNA. Out of 152 blackflies and mosquitoes/midges, eight specimens experimentally infected (n = 1 S. erythrocephalum; n = 1 S. ornatum; n = 6 Simulium sp.) were positive by qPCR. The qPCR assay herein standardized represents an important step forward in the diagnosis of zoonotic onchocercosis caused by O. lupi, especially for the detection and quantification of low number of mfs. This assay provides a fundamental contribution for the establishment of surveillance strategies aiming at assessing the presence of O. lupi in carnivores and in insect species acting as potential intermediate hosts. The O. lupi qPCR assay will enable disease progress monitoring as well as the diagnosis of apparently clinical healthy dogs and cats. Public Library of Science 2018-04-04 /pmc/articles/PMC5902036/ /pubmed/29617361 http://dx.doi.org/10.1371/journal.pntd.0006402 Text en © 2018 Latrofa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Latrofa, Maria Stefania
Annoscia, Giada
Colella, Vito
Cavalera, Maria Alfonsa
Maia, Carla
Martin, Coralie
Šlapeta, Jan
Otranto, Domenico
A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title_full A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title_fullStr A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title_full_unstemmed A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title_short A real-time PCR tool for the surveillance of zoonotic Onchocerca lupi in dogs, cats and potential vectors
title_sort real-time pcr tool for the surveillance of zoonotic onchocerca lupi in dogs, cats and potential vectors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902036/
https://www.ncbi.nlm.nih.gov/pubmed/29617361
http://dx.doi.org/10.1371/journal.pntd.0006402
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