Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.

Cystic Fibrosis (CF) is the most prevalent autosomal recessive disease in the Caucasian population. A cystic fibrosis transmembrane conductance regulator knockout (CFTR-/-) pig that displays most of the features of the human CF disease has been recently developed. However, CFTR-/- pigs presents a 10...

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Main Authors: Antoine Guillon, Claire Chevaleyre, Celine Barc, Mustapha Berri, Hans Adriaensen, François Lecompte, Thierry Villemagne, Jérémy Pezant, Rémi Delaunay, Joseph Moënne-Loccoz, Patricia Berthon, Andrea Bähr, Eckhard Wolf, Nikolai Klymiuk, Sylvie Attucci, Reuben Ramphal, Pierre Sarradin, Dominique Buzoni-Gatel, Mustapha Si-Tahar, Ignacio Caballero
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4658176?pdf=render
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spelling doaj-d7872b42283e49d48ce296eacc12fdee2020-11-25T01:35:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011011e014345910.1371/journal.pone.0143459Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.Antoine GuillonClaire ChevaleyreCeline BarcMustapha BerriHans AdriaensenFrançois LecompteThierry VillemagneJérémy PezantRémi DelaunayJoseph Moënne-LoccozPatricia BerthonAndrea BährEckhard WolfNikolai KlymiukSylvie AttucciReuben RamphalPierre SarradinDominique Buzoni-GatelMustapha Si-TaharIgnacio CaballeroCystic Fibrosis (CF) is the most prevalent autosomal recessive disease in the Caucasian population. A cystic fibrosis transmembrane conductance regulator knockout (CFTR-/-) pig that displays most of the features of the human CF disease has been recently developed. However, CFTR-/- pigs presents a 100% prevalence of meconium ileus that leads to death in the first hours after birth, requiring a rapid diagnosis and surgical intervention to relieve intestinal obstruction. Identification of CFTR-/- piglets is usually performed by PCR genotyping, a procedure that lasts between 4 to 6 h. Here, we aimed to develop a procedure for rapid identification of CFTR-/- piglets that will allow placing them under intensive care soon after birth and immediately proceeding with the surgical correction.Male and female CFTR+/- pigs were crossed and the progeny was examined by computed tomography (CT) scan to detect the presence of meconium ileus and facilitate a rapid post-natal surgical intervention. Genotype was confirmed by PCR. CT scan presented a 94.4% sensitivity to diagnose CFTR-/- piglets. Diagnosis by CT scan reduced the birth-to-surgery time from a minimum of 10 h down to a minimum of 2.5 h and increased the survival of CFTR-/- piglets to a maximum of 13 days post-surgery as opposed to just 66 h after later surgery.CT scan imaging of meconium ileus is an accurate method for rapid identification of CFTR-/- piglets. Early CT detection of meconium ileus may help to extend the lifespan of CFTR-/- piglets and, thus, improve experimental research on CF, still an incurable disease.http://europepmc.org/articles/PMC4658176?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Antoine Guillon
Claire Chevaleyre
Celine Barc
Mustapha Berri
Hans Adriaensen
François Lecompte
Thierry Villemagne
Jérémy Pezant
Rémi Delaunay
Joseph Moënne-Loccoz
Patricia Berthon
Andrea Bähr
Eckhard Wolf
Nikolai Klymiuk
Sylvie Attucci
Reuben Ramphal
Pierre Sarradin
Dominique Buzoni-Gatel
Mustapha Si-Tahar
Ignacio Caballero
spellingShingle Antoine Guillon
Claire Chevaleyre
Celine Barc
Mustapha Berri
Hans Adriaensen
François Lecompte
Thierry Villemagne
Jérémy Pezant
Rémi Delaunay
Joseph Moënne-Loccoz
Patricia Berthon
Andrea Bähr
Eckhard Wolf
Nikolai Klymiuk
Sylvie Attucci
Reuben Ramphal
Pierre Sarradin
Dominique Buzoni-Gatel
Mustapha Si-Tahar
Ignacio Caballero
Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
PLoS ONE
author_facet Antoine Guillon
Claire Chevaleyre
Celine Barc
Mustapha Berri
Hans Adriaensen
François Lecompte
Thierry Villemagne
Jérémy Pezant
Rémi Delaunay
Joseph Moënne-Loccoz
Patricia Berthon
Andrea Bähr
Eckhard Wolf
Nikolai Klymiuk
Sylvie Attucci
Reuben Ramphal
Pierre Sarradin
Dominique Buzoni-Gatel
Mustapha Si-Tahar
Ignacio Caballero
author_sort Antoine Guillon
title Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
title_short Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
title_full Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
title_fullStr Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
title_full_unstemmed Computed Tomography (CT) Scanning Facilitates Early Identification of Neonatal Cystic Fibrosis Piglets.
title_sort computed tomography (ct) scanning facilitates early identification of neonatal cystic fibrosis piglets.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Cystic Fibrosis (CF) is the most prevalent autosomal recessive disease in the Caucasian population. A cystic fibrosis transmembrane conductance regulator knockout (CFTR-/-) pig that displays most of the features of the human CF disease has been recently developed. However, CFTR-/- pigs presents a 100% prevalence of meconium ileus that leads to death in the first hours after birth, requiring a rapid diagnosis and surgical intervention to relieve intestinal obstruction. Identification of CFTR-/- piglets is usually performed by PCR genotyping, a procedure that lasts between 4 to 6 h. Here, we aimed to develop a procedure for rapid identification of CFTR-/- piglets that will allow placing them under intensive care soon after birth and immediately proceeding with the surgical correction.Male and female CFTR+/- pigs were crossed and the progeny was examined by computed tomography (CT) scan to detect the presence of meconium ileus and facilitate a rapid post-natal surgical intervention. Genotype was confirmed by PCR. CT scan presented a 94.4% sensitivity to diagnose CFTR-/- piglets. Diagnosis by CT scan reduced the birth-to-surgery time from a minimum of 10 h down to a minimum of 2.5 h and increased the survival of CFTR-/- piglets to a maximum of 13 days post-surgery as opposed to just 66 h after later surgery.CT scan imaging of meconium ileus is an accurate method for rapid identification of CFTR-/- piglets. Early CT detection of meconium ileus may help to extend the lifespan of CFTR-/- piglets and, thus, improve experimental research on CF, still an incurable disease.
url http://europepmc.org/articles/PMC4658176?pdf=render
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