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Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression

The porcine epidemic diarrhoea virus (PEDV) devastates the health of piglets but may not infect piglets whose CMP-N-glycolylneuraminic acid hydroxylase (CMAH) gene is mutated (knockouts, KO) by using CRISPR/Cas9 gene editing techniques. This hypothesis was tested by using KO piglets that were challe...

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Autores principales: Tu, Ching-Fu, Chuang, Chin-kai, Hsiao, Kai-Hsuan, Chen, Chien-Hong, Chen, Chi-Min, Peng, Su-Hei, Su, Yu-Hsiu, Chiou, Ming-Tang, Yen, Chon-Ho, Hung, Shao-Wen, Yang, Tien-Shuh, Chen, Chuan-Mu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541307/
https://www.ncbi.nlm.nih.gov/pubmed/31141512
http://dx.doi.org/10.1371/journal.pone.0217236
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author Tu, Ching-Fu
Chuang, Chin-kai
Hsiao, Kai-Hsuan
Chen, Chien-Hong
Chen, Chi-Min
Peng, Su-Hei
Su, Yu-Hsiu
Chiou, Ming-Tang
Yen, Chon-Ho
Hung, Shao-Wen
Yang, Tien-Shuh
Chen, Chuan-Mu
author_facet Tu, Ching-Fu
Chuang, Chin-kai
Hsiao, Kai-Hsuan
Chen, Chien-Hong
Chen, Chi-Min
Peng, Su-Hei
Su, Yu-Hsiu
Chiou, Ming-Tang
Yen, Chon-Ho
Hung, Shao-Wen
Yang, Tien-Shuh
Chen, Chuan-Mu
author_sort Tu, Ching-Fu
collection PubMed
description The porcine epidemic diarrhoea virus (PEDV) devastates the health of piglets but may not infect piglets whose CMP-N-glycolylneuraminic acid hydroxylase (CMAH) gene is mutated (knockouts, KO) by using CRISPR/Cas9 gene editing techniques. This hypothesis was tested by using KO piglets that were challenged with PEDV. Two single-guide RNAs targeting the CMAH gene and Cas9 mRNA were microinjected into the cytoplasm of newly fertilized eggs. Four live founders generated and proven to be biallelic KO, lacking detectable N-glycolylneuraminic acid (NGNA). The founders were bred, and homozygous offspring were obtained. Two-day-old (in exps. I, n = 6, and III, n = 15) and 3-day-old (in exp. II, n = 9) KO and wild-type (WT, same ages in respective exps.) piglets were inoculated with TCID(50) 1x10(3) PEDV and then fed 20 mL of infant formula (in exps. I and II) or sow’s colostrum (in exp. III) every 4 hours. In exp. III, the colostrum was offered 6 times and was then replaced with Ringer/5% glucose solution. At 72 hours post-PEDV inoculation (hpi), the animals either deceased or euthanized were necropsied and intestines were sampled. In all 3 experiments, the piglets showed apparent outward clinical manifestations suggesting that infection occurred despite the CMAH KO. In exp. I, all 6 WT piglets and only 1 of 6 KO piglets died at 72 hpi. Histopathology and immunofluorescence staining showed that the villus epithelial cells of WT piglets were severely exfoliated, but only moderate exfoliation and enterocyte vacuolization was observed in KO piglets. In exp. II, delayed clinical symptoms appeared, yet the immunofluorescence staining/histopathologic inspection (I/H) scores of the two groups differed little. In exp. III, the animals exhibited clinical and pathological signs after inoculation similar to those in exp. II. These results suggest that porcine CMAH KO with nullified NGNA expression are not immune to PEDV but that this KO may lessen the severity of the infection and delay its occurrence.
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spelling pubmed-65413072019-06-05 Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression Tu, Ching-Fu Chuang, Chin-kai Hsiao, Kai-Hsuan Chen, Chien-Hong Chen, Chi-Min Peng, Su-Hei Su, Yu-Hsiu Chiou, Ming-Tang Yen, Chon-Ho Hung, Shao-Wen Yang, Tien-Shuh Chen, Chuan-Mu PLoS One Research Article The porcine epidemic diarrhoea virus (PEDV) devastates the health of piglets but may not infect piglets whose CMP-N-glycolylneuraminic acid hydroxylase (CMAH) gene is mutated (knockouts, KO) by using CRISPR/Cas9 gene editing techniques. This hypothesis was tested by using KO piglets that were challenged with PEDV. Two single-guide RNAs targeting the CMAH gene and Cas9 mRNA were microinjected into the cytoplasm of newly fertilized eggs. Four live founders generated and proven to be biallelic KO, lacking detectable N-glycolylneuraminic acid (NGNA). The founders were bred, and homozygous offspring were obtained. Two-day-old (in exps. I, n = 6, and III, n = 15) and 3-day-old (in exp. II, n = 9) KO and wild-type (WT, same ages in respective exps.) piglets were inoculated with TCID(50) 1x10(3) PEDV and then fed 20 mL of infant formula (in exps. I and II) or sow’s colostrum (in exp. III) every 4 hours. In exp. III, the colostrum was offered 6 times and was then replaced with Ringer/5% glucose solution. At 72 hours post-PEDV inoculation (hpi), the animals either deceased or euthanized were necropsied and intestines were sampled. In all 3 experiments, the piglets showed apparent outward clinical manifestations suggesting that infection occurred despite the CMAH KO. In exp. I, all 6 WT piglets and only 1 of 6 KO piglets died at 72 hpi. Histopathology and immunofluorescence staining showed that the villus epithelial cells of WT piglets were severely exfoliated, but only moderate exfoliation and enterocyte vacuolization was observed in KO piglets. In exp. II, delayed clinical symptoms appeared, yet the immunofluorescence staining/histopathologic inspection (I/H) scores of the two groups differed little. In exp. III, the animals exhibited clinical and pathological signs after inoculation similar to those in exp. II. These results suggest that porcine CMAH KO with nullified NGNA expression are not immune to PEDV but that this KO may lessen the severity of the infection and delay its occurrence. Public Library of Science 2019-05-29 /pmc/articles/PMC6541307/ /pubmed/31141512 http://dx.doi.org/10.1371/journal.pone.0217236 Text en © 2019 Tu 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
Tu, Ching-Fu
Chuang, Chin-kai
Hsiao, Kai-Hsuan
Chen, Chien-Hong
Chen, Chi-Min
Peng, Su-Hei
Su, Yu-Hsiu
Chiou, Ming-Tang
Yen, Chon-Ho
Hung, Shao-Wen
Yang, Tien-Shuh
Chen, Chuan-Mu
Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title_full Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title_fullStr Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title_full_unstemmed Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title_short Lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the CMP-N-glycolylneuraminic acid hydroxylase gene with CRISPR/Cas9 to nullify N-glycolylneuraminic acid expression
title_sort lessening of porcine epidemic diarrhoea virus susceptibility in piglets after editing of the cmp-n-glycolylneuraminic acid hydroxylase gene with crispr/cas9 to nullify n-glycolylneuraminic acid expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541307/
https://www.ncbi.nlm.nih.gov/pubmed/31141512
http://dx.doi.org/10.1371/journal.pone.0217236
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