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Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX
The structure genes spike (S), nucleocapsid (N), membrane (M), small membrane (sM) of a porcine epidemic diarrhea virus (PEDV) strain DX isolated in Gansu province, North-west of China, were cloned, sequenced and compared with published sequences of PEDV strains. The nucleotide sequences encoding th...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SP Wuhan Institute of Virology, CAS
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091100/ http://dx.doi.org/10.1007/s12250-009-2982-y |
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author | Li, Jian-qiang Liu, Ji-xing Lan, Xi Cheng, Jie Wu, Run Lou, Zhong-Zi Yin, Xiang-ping Li, Xue-rui Li, Bao-yu Yang, Bin Li, Zhi-yong |
author_facet | Li, Jian-qiang Liu, Ji-xing Lan, Xi Cheng, Jie Wu, Run Lou, Zhong-Zi Yin, Xiang-ping Li, Xue-rui Li, Bao-yu Yang, Bin Li, Zhi-yong |
author_sort | Li, Jian-qiang |
collection | PubMed |
description | The structure genes spike (S), nucleocapsid (N), membrane (M), small membrane (sM) of a porcine epidemic diarrhea virus (PEDV) strain DX isolated in Gansu province, North-west of China, were cloned, sequenced and compared with published sequences of PEDV strains. The nucleotide sequences encoding the entire S, sM, M and N genes open reading frame (ORF) of DX were 4 152, 231, 681 and 1 326 bases long respectively. There were transcription regulatory sequences (TRSs) upstream of the initiator ATG of the S, N and M genes. The amino acids sequences of S, M and N contained 30, 3 and 7 potential asparagine (N)-linked glycosylation sites. Homologous analysis and phylogenetic trees showed that DX had the closest relationship with strains LJB/06, JS-2004-2Z and CH/HLJH/06 that were also isolated from China and indicated the prevalence of some PEDV isolates in China were widespread since the JS-2004-2Z strain originated from the south of the China, and LJB/06 and CH/HLJH/06 were isolated from northeast China. The N gene was cloned using two primers which contained Nco I and BamH I restriction enzyme sites and subcloned into expression vector pET30a. The recombinant plasmid was then transformed into E.coli Rossta. SDS-PAGE showed there was a protein of about 55kDa as expected and Western blot indicated the N protein had biological activity. |
format | Online Article Text |
id | pubmed-7091100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | SP Wuhan Institute of Virology, CAS |
record_format | MEDLINE/PubMed |
spelling | pubmed-70911002020-03-24 Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX Li, Jian-qiang Liu, Ji-xing Lan, Xi Cheng, Jie Wu, Run Lou, Zhong-Zi Yin, Xiang-ping Li, Xue-rui Li, Bao-yu Yang, Bin Li, Zhi-yong Virol Sin Article The structure genes spike (S), nucleocapsid (N), membrane (M), small membrane (sM) of a porcine epidemic diarrhea virus (PEDV) strain DX isolated in Gansu province, North-west of China, were cloned, sequenced and compared with published sequences of PEDV strains. The nucleotide sequences encoding the entire S, sM, M and N genes open reading frame (ORF) of DX were 4 152, 231, 681 and 1 326 bases long respectively. There were transcription regulatory sequences (TRSs) upstream of the initiator ATG of the S, N and M genes. The amino acids sequences of S, M and N contained 30, 3 and 7 potential asparagine (N)-linked glycosylation sites. Homologous analysis and phylogenetic trees showed that DX had the closest relationship with strains LJB/06, JS-2004-2Z and CH/HLJH/06 that were also isolated from China and indicated the prevalence of some PEDV isolates in China were widespread since the JS-2004-2Z strain originated from the south of the China, and LJB/06 and CH/HLJH/06 were isolated from northeast China. The N gene was cloned using two primers which contained Nco I and BamH I restriction enzyme sites and subcloned into expression vector pET30a. The recombinant plasmid was then transformed into E.coli Rossta. SDS-PAGE showed there was a protein of about 55kDa as expected and Western blot indicated the N protein had biological activity. SP Wuhan Institute of Virology, CAS 2009-05-28 /pmc/articles/PMC7091100/ http://dx.doi.org/10.1007/s12250-009-2982-y Text en © Wuhan Institute of Virology, CAS and Springer-Verlag GmbH 2009 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Li, Jian-qiang Liu, Ji-xing Lan, Xi Cheng, Jie Wu, Run Lou, Zhong-Zi Yin, Xiang-ping Li, Xue-rui Li, Bao-yu Yang, Bin Li, Zhi-yong Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title | Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title_full | Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title_fullStr | Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title_full_unstemmed | Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title_short | Cloning the structure genes and expression the N gene of porcine epidemic diarrhea virus DX |
title_sort | cloning the structure genes and expression the n gene of porcine epidemic diarrhea virus dx |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7091100/ http://dx.doi.org/10.1007/s12250-009-2982-y |
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