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- Publisher Website: 10.1016/j.jcv.2006.10.001
- Scopus: eid_2-s2.0-33845346442
- PMID: 17112780
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Article: Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong
Title | Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong |
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Authors | |
Keywords | Maximum-likelihood Neighbour-joining Phylogenetics S-gene SARS-CoV Single nucleotide variation |
Issue Date | 2007 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv |
Citation | Journal Of Clinical Virology, 2007, v. 38 n. 1, p. 19-26 How to Cite? |
Abstract | Background: The spike glycoprotein (S) gene of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) has been useful in analyzing the molecular epidemiology of the 2003 SARS outbreaks. Objectives: To characterize complete SARS-CoV S-gene sequences from Hong Kong. Study design: Fifty-six SARS-CoV S-gene sequences, obtained from patients who presented with SARS to the Prince of Wales Hospital during March-May 2003, were analysed using a maximum likelihood (ML) approach, together with 138 other (both human and animal) S-gene sequences downloaded from GenBank. Results: The maximum-likelihood (ML) trees showed little evolution occurring within these 56 sequences. Analysis with the other sequences, showed three distinct SARS clusters, closely correlated to previously defined early, middle and late phases of the 2003 international SARS outbreaks. In addition, two new single nucleotide variations (SNVs), T21615A and T21901A, were discovered, not previously reported elsewhere. Conclusions: The ML approach to the reconstruction of tree phylogenies is known to be superior to the more popular, less computationally and time-demanding neighbour-joining (NJ) approach. The ML analysis in this study confirms the previously reported SARS epidemiology analysed mostly using the NJ approach. The two new SNVs reported here are most likely due to the tissue-culture passaging of the clinical samples. © 2006 Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/79274 |
ISSN | 2023 Impact Factor: 4.0 2023 SCImago Journal Rankings: 1.344 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Tang, JW | en_HK |
dc.contributor.author | Cheung, JLK | en_HK |
dc.contributor.author | Chu, IMT | en_HK |
dc.contributor.author | Ip, M | en_HK |
dc.contributor.author | Hui, M | en_HK |
dc.contributor.author | Peiris, M | en_HK |
dc.contributor.author | Chan, PKS | en_HK |
dc.date.accessioned | 2010-09-06T07:52:42Z | - |
dc.date.available | 2010-09-06T07:52:42Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | Journal Of Clinical Virology, 2007, v. 38 n. 1, p. 19-26 | en_HK |
dc.identifier.issn | 1386-6532 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/79274 | - |
dc.description.abstract | Background: The spike glycoprotein (S) gene of the severe acute respiratory syndrome-associated coronavirus (SARS-CoV) has been useful in analyzing the molecular epidemiology of the 2003 SARS outbreaks. Objectives: To characterize complete SARS-CoV S-gene sequences from Hong Kong. Study design: Fifty-six SARS-CoV S-gene sequences, obtained from patients who presented with SARS to the Prince of Wales Hospital during March-May 2003, were analysed using a maximum likelihood (ML) approach, together with 138 other (both human and animal) S-gene sequences downloaded from GenBank. Results: The maximum-likelihood (ML) trees showed little evolution occurring within these 56 sequences. Analysis with the other sequences, showed three distinct SARS clusters, closely correlated to previously defined early, middle and late phases of the 2003 international SARS outbreaks. In addition, two new single nucleotide variations (SNVs), T21615A and T21901A, were discovered, not previously reported elsewhere. Conclusions: The ML approach to the reconstruction of tree phylogenies is known to be superior to the more popular, less computationally and time-demanding neighbour-joining (NJ) approach. The ML analysis in this study confirms the previously reported SARS epidemiology analysed mostly using the NJ approach. The two new SNVs reported here are most likely due to the tissue-culture passaging of the clinical samples. © 2006 Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jcv | en_HK |
dc.relation.ispartof | Journal of Clinical Virology | en_HK |
dc.rights | Journal of Clinical Virology. Copyright © Elsevier BV. | en_HK |
dc.subject | Maximum-likelihood | en_HK |
dc.subject | Neighbour-joining | en_HK |
dc.subject | Phylogenetics | en_HK |
dc.subject | S-gene | en_HK |
dc.subject | SARS-CoV | en_HK |
dc.subject | Single nucleotide variation | en_HK |
dc.title | Characterizing 56 complete SARS-CoV S-gene sequences from Hong Kong | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1386-6532&volume=38&issue=1&spage=19&epage=26&date=2007&atitle=Characterizing+56+complete+SARS-CoV+S-gene+sequences+from+Hong+Kong | en_HK |
dc.identifier.email | Peiris, M: malik@hkucc.hku.hk | en_HK |
dc.identifier.authority | Peiris, M=rp00410 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jcv.2006.10.001 | en_HK |
dc.identifier.pmid | 17112780 | - |
dc.identifier.scopus | eid_2-s2.0-33845346442 | en_HK |
dc.identifier.hkuros | 134628 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33845346442&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 38 | en_HK |
dc.identifier.issue | 1 | en_HK |
dc.identifier.spage | 19 | en_HK |
dc.identifier.epage | 26 | en_HK |
dc.identifier.isi | WOS:000243736900004 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Tang, JW=10341387300 | en_HK |
dc.identifier.scopusauthorid | Cheung, JLK=7202072287 | en_HK |
dc.identifier.scopusauthorid | Chu, IMT=7103327448 | en_HK |
dc.identifier.scopusauthorid | Ip, M=7102423261 | en_HK |
dc.identifier.scopusauthorid | Hui, M=24075844900 | en_HK |
dc.identifier.scopusauthorid | Peiris, M=7005486823 | en_HK |
dc.identifier.scopusauthorid | Chan, PKS=32067487100 | en_HK |
dc.identifier.issnl | 1386-6532 | - |