Genomic Sequencing of a SARS Coronavirus Isolate That Predated the Metropole Hotel Case Cluster in Hong Kong
Identifieur interne : 000E88 ( Pmc/Corpus ); précédent : 000E87; suivant : 000E89Genomic Sequencing of a SARS Coronavirus Isolate That Predated the Metropole Hotel Case Cluster in Hong Kong
Auteurs : Stephen S C. Chim ; Yu-Kwan Tong ; Emily C W. Hung ; Rossa W K. Chiu ; Y M Dennis LoSource :
- Clinical Chemistry [ 0009-9147 ] ; 2004.
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DOI: 10.1373/clinchem.2003.025536
PubMed: 14709660
PubMed Central: 7108164
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Genomic Sequencing of a SARS Coronavirus Isolate That Predated the Metropole Hotel Case Cluster in Hong Kong</title><author><name sortKey="Chim, Stephen S C" sort="Chim, Stephen S C" uniqKey="Chim S" first="Stephen S C" last="Chim">Stephen S C. Chim</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Tong, Yu Kwan" sort="Tong, Yu Kwan" uniqKey="Tong Y" first="Yu-Kwan" last="Tong">Yu-Kwan Tong</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Hung, Emily C W" sort="Hung, Emily C W" uniqKey="Hung E" first="Emily C W" last="Hung">Emily C W. Hung</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Chiu, Rossa W K" sort="Chiu, Rossa W K" uniqKey="Chiu R" first="Rossa W K" last="Chiu">Rossa W K. Chiu</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Lo, Y M Dennis" sort="Lo, Y M Dennis" uniqKey="Lo Y" first="Y M Dennis" last="Lo">Y M Dennis Lo</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">14709660</idno><idno type="pmc">7108164</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7108164</idno><idno type="RBID">PMC:7108164</idno><idno type="doi">10.1373/clinchem.2003.025536</idno><date when="2004">2004</date><idno type="wicri:Area/Pmc/Corpus">000E88</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000E88</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Genomic Sequencing of a SARS Coronavirus Isolate That Predated the Metropole Hotel Case Cluster in Hong Kong</title><author><name sortKey="Chim, Stephen S C" sort="Chim, Stephen S C" uniqKey="Chim S" first="Stephen S C" last="Chim">Stephen S C. Chim</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Tong, Yu Kwan" sort="Tong, Yu Kwan" uniqKey="Tong Y" first="Yu-Kwan" last="Tong">Yu-Kwan Tong</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Hung, Emily C W" sort="Hung, Emily C W" uniqKey="Hung E" first="Emily C W" last="Hung">Emily C W. Hung</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Chiu, Rossa W K" sort="Chiu, Rossa W K" uniqKey="Chiu R" first="Rossa W K" last="Chiu">Rossa W K. Chiu</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Lo, Y M Dennis" sort="Lo, Y M Dennis" uniqKey="Lo Y" first="Y M Dennis" last="Lo">Y M Dennis Lo</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author></analytic><series><title level="j">Clinical Chemistry</title><idno type="ISSN">0009-9147</idno><idno type="eISSN">1530-8561</idno><imprint><date when="2004">2004</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Clin Chem</journal-id><journal-id journal-id-type="iso-abbrev">Clin. Chem</journal-id><journal-id journal-id-type="publisher-id">clinchem</journal-id><journal-id journal-id-type="publisher-id">Clin. Chem.</journal-id><journal-title-group><journal-title>Clinical Chemistry</journal-title></journal-title-group><issn pub-type="ppub">0009-9147</issn><issn pub-type="epub">1530-8561</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">14709660</article-id><article-id pub-id-type="pmc">7108164</article-id><article-id pub-id-type="doi">10.1373/clinchem.2003.025536</article-id><article-id pub-id-type="publisher-id">clinchem0231</article-id><article-categories><subj-group subj-group-type="heading"><subject>Technical Briefs</subject></subj-group></article-categories><title-group><article-title>Genomic Sequencing of a SARS Coronavirus Isolate That Predated the Metropole Hotel Case Cluster in Hong Kong</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Chim</surname><given-names>Stephen S C</given-names></name><xref ref-type="aff" rid="AFF1"></xref></contrib><contrib contrib-type="author"><name><surname>Tong</surname><given-names>Yu-Kwan</given-names></name><xref ref-type="aff" rid="AFF1"></xref></contrib><contrib contrib-type="author"><name><surname>Hung</surname><given-names>Emily C W</given-names></name><xref ref-type="aff" rid="AFF2"></xref></contrib><contrib contrib-type="author"><name><surname>Chiu</surname><given-names>Rossa W K</given-names></name><xref ref-type="aff" rid="AFF1"></xref></contrib><contrib contrib-type="author"><name><surname>Lo</surname><given-names>Y M Dennis</given-names></name><xref ref-type="corresp" rid="C1"></xref><email>loym@cuhk.edu.hk</email><xref ref-type="aff" rid="AFF1"></xref></contrib></contrib-group><aff id="AFF1"><label>1</label><institution>Departments of Chemical Pathology and</institution></aff><aff id="AFF2"><label>2</label><institution>Paediatrics</institution>, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, New Territories, Hong Kong</aff><author-notes><corresp id="C1">Address correspondence to this author at: Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Room 38023, 1/F Clinical Sciences Bldg., 30-32 Ngan Shing St., Shatin, New Territories, Hong Kong SAR; fax 852-2194-6171, e-mail <email>loym@cuhk.edu.hk</email></corresp></author-notes><pub-date pub-type="ppub"><month>1</month><year>2004</year></pub-date><pub-date pub-type="epub" iso-8601-date="2004-01-01"><day>01</day><month>1</month><year>2004</year></pub-date><volume>50</volume><issue>1</issue><fpage>231</fpage><lpage>233</lpage><permissions><copyright-statement>© 2004 The American Association for Clinical Chemistry</copyright-statement><copyright-year>2004</copyright-year><license license-type="publisher-standard" xlink:href="https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model"><license-p>This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (<ext-link ext-link-type="uri" xlink:href="https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model">https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model</ext-link>)</license-p></license><license><license-p>This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.</license-p></license></permissions><self-uri xlink:href="clinchem0231.pdf"></self-uri></article-meta></front><body><p>The epidemic of severe acute respiratory syndrome (SARS) swept across the globe, with reported cases in more than 30 countries. As of July 11, 2003, the number of reported probable cases was 8437, with 813 deaths (<xref rid="R1" ref-type="bibr">1</xref>). A novel coronavirus, SARS-CoV, was promptly implicated as the causative agent (<xref rid="R2" ref-type="bibr">2</xref>)(<xref rid="R3" ref-type="bibr">3</xref>)(<xref rid="R4" ref-type="bibr">4</xref>). Macaques infected with SARS-CoV subsequently developed respiratory symptoms and pathology similar to SARS patients, thus fulfilling the Koch postulates (<xref rid="R5" ref-type="bibr">5</xref>). Efforts in sequencing the viral genome promptly followed, and the genomic sequence revealed little homology to previously characterized strains of coronaviruses (<xref rid="R6" ref-type="bibr">6</xref>)(<xref rid="R7" ref-type="bibr">7</xref>). The complete genomic sequences of several SARS-CoV isolates have since been made publicly available (<ext-link ext-link-type="uri" xlink:href="http://www.ncbi.nlm.nih.gov">www.ncbi.nlm.nih.gov</ext-link>).</p><p>Several sequence variations exist among isolates. In general, based on these sequence variations, the majority of the isolates can be segregated into two groups: isolates that were obtained from individuals who were epidemiologically linked to and those who were not linked to the Metropole Hotel in Hong Kong (<xref rid="R8" ref-type="bibr">8</xref>)(<xref rid="R9" ref-type="bibr">9</xref>)(<xref rid="R10" ref-type="bibr">10</xref>). Ruan et al. (<xref rid="R10" ref-type="bibr">10</xref>) compared the genomic sequences of 14 SARS-CoV isolates and suggested that a haplotype comprising four nucleotide positions, namely, 9404, 17564, 22222, and 27827 [GenBank accession no. AY274119 (<xref rid="R7" ref-type="bibr">7</xref>)], clearly defined two distinct genotypes. Isolates that were epidemiologically linked to the Metropole Hotel cluster have the configuration T:T:T:T, as opposed to the sequence C:G:C:C seen in the unassociated strains. (Note: The usage of the DNA-based code for the designation of SARS-CoV haplotypes does not imply that this virus possesses a DNA genome.)</p><p>SARS was first reported in Guangdong Province, China, in November 2002 (<xref rid="R11" ref-type="bibr">11</xref>). Isolates that demonstrated the C:G:C:C haplotype were epidemiologically traceable to the early part of the epidemic (<xref rid="R9" ref-type="bibr">9</xref>). On the other hand, SARS was first reported in Hong Kong when a cluster of cases was noted among visitors to the Metropole Hotel. This case cluster comprised international travelers who subsequently brought SARS to other countries, including Vietnam, Canada, and Singapore (<xref rid="R11" ref-type="bibr">11</xref>). Epidemiologic investigations revealed that the cases were traceable to a nephrologist from Guangdong Province, China, who checked into the hotel on February 21, 2003 (<xref rid="R8" ref-type="bibr">8</xref>)(<xref rid="R11" ref-type="bibr">11</xref>). These data suggest that since the emergence of SARS-CoV in southern China, at least two strains of the virus had emerged (<xref rid="R9" ref-type="bibr">9</xref>).</p><p>We recently confirmed a case of SARS that presented in Hong Kong before the report of the case cluster at the Metropole Hotel. It would be of interest to determine whether this strain is related to either of the reported groups. This patient, designated A, presented to a hospital in Hong Kong on February 17, 2003, with a 2-day history of fever, chills, rigors, dry cough, and intense malaise. She resided in the US, but before symptom onset, she had been visiting her ailing mother in Guangzhou, China. Her mother died on February 12, 2003, of a cause unknown to the family. After admission, patient A deteriorated rapidly and required intensive care. Her chest radiograph revealed patchy infiltration, and serologic testing subsequently showed markedly increased antibody titers against SARS-CoV. Four household members and two healthcare workers later developed fever and respiratory symptoms.</p><p>In view of the distinct epidemiologic history, serum samples were retrieved from patient A. Viral RNA was extracted from 280 μL of the patient’s serum with a QIAamp Viral RNA Mini Kit (Qiagen), according to the manufacturer’s instructions, and eluted in 50 μL of RNase-free water; 11 μL of viral RNA was then reverse transcribed by Superscript III (Invitrogen) with reverse primers (PCR-R) targeting regions on the SARS-CoV genome that flank 20 selected polymorphic sites. Because polymorphisms seen in a single isolate could potentially be a result of culture or sequencing artifacts, we selected the target sites based on polymorphisms that were shared by at least two SARS-CoV isolates published in GenBank at the time of this study. The product was then amplified with use of 14 pairs of forward (PCR-F) and reverse (PCR-R) primers in a cDNA polymerase mixture (BD Clontech), with initial denaturation at 95 °C for 1 min and 35 cycles of denaturation at 95 °C for 0.5 min, annealing at 55 °C for 0.5 min, and extension at 68 °C for 1.5 min, and a final extension at 68 °C for 10 min. Seminested PCR was performed with the PCR-F and BSEQ-R series of primers with the same thermal profile. Primer sequences are available in the Data Supplement accompanying the online version of this Technical Brief at<ext-link ext-link-type="uri" xlink:href="http://www.clinchem.org/content/vol50/issue1/">http://www.clinchem.org/content/vol50/issue1/</ext-link> . Multiple negative PCR controls were included in each amplification.</p><p>The DNA of each amplicon was sequenced by the dideoxy dye terminator method on an automated DNA sequencer (3100 Genetic Analyzer; Applied Biosystems) based on capillary electrophoresis. The PCR-F, ASEQ-F, BSEQ-F, ASEQ-R, and BSEQ-R series of oligonucleotides were used as sequencing primers. Sequences were edited and aligned, and comparisons were made with the SeqScape software (Applied Biosystems). Regions that revealed nucleotide substitutions were confirmed by resequencing with a combination of different primer sets to ensure the quality of the sequencing data. On the whole, the sequencing covered one-third of the virus genome (<xref ref-type="fig" rid="F1">Fig. 1</xref> ) and was deposited at GenBank (accession nos. AY443086 to AY443095).</p><fig id="F1" orientation="portrait" position="float"><label>Figure 1.
</label><caption><p>Partial genomic sequence of SARS-CoV isolate CUHK-L2.</p><p>Regions of the CUHK-L2 isolate that were sequenced are indicated in <italic>black</italic>. <italic>Arrows</italic> indicate sites used for haplotype comparison. Open reading frames and nucleotide positions are shown in reference to the Tor2 sequence. <italic>Orf1ab</italic>, <italic>S</italic>, <italic>E</italic>, <italic>M</italic>, and <italic>N</italic> denote orf 1ab polyprotein, spike glycoprotein, envelope protein, membrane protein, and nucleocapsid protein, respectively.</p></caption><graphic xlink:href="zcy0010446250001"></graphic></fig><p>In contrast to the SARS-CoV isolates sequenced to date, the viral genomic sequence obtained from patient A, CUHK-L2, revealed a haplotype configuration of T:G:C:C (<xref rid="T1" ref-type="table">Table 1</xref> ), which represents a combination of the two genotypes that typify the isolates associated and those not associated with the Metropole Hotel (<xref rid="R10" ref-type="bibr">10</xref>). This is particularly interesting in view of the epidemiologic history of patient A. She had a history of travel to southern China, whereas her presentation clearly predated the Metropole Hotel cluster. The CUHK-L2 sequence represents the third SARS-CoV genotype directly traceable to southern China early in the course of the SARS epidemic, with a transitory sequence that bridges the two major genotypes reported earlier.</p><table-wrap id="T1" orientation="portrait" position="float"><label>Table 1.
</label><caption><p>Haplotype comparison of SARS CoV strains from Hong Kong and two transitory genotypes.</p></caption><table frame="hsides" rules="groups"><thead><tr><th colspan="1" rowspan="3" align="center" valign="bottom">Nucleotide position<sup>1</sup></th><th colspan="10" rowspan="1" align="center" valign="bottom">Isolate (GenBank accession no.)</th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="3" align="center" valign="bottom">Amino acid</th></tr><tr><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="4" rowspan="1" align="center" valign="bottom">Linked to Metropole Hotel</th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="2" rowspan="1" align="center" valign="bottom">Transitory</th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="4" rowspan="1" align="center" valign="bottom">Not linked to Metropole Hotel</th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th><th colspan="1" rowspan="1" align="center" valign="bottom"></th></tr><tr><th colspan="1" rowspan="1" align="left" valign="bottom"></th><th colspan="1" rowspan="1" align="left" valign="bottom">Tor2 (AY274119)</th><th colspan="1" rowspan="1" align="left" valign="bottom">Urbani (AY278741)</th><th colspan="1" rowspan="1" align="left" valign="bottom">SIN2500 (AY283794)</th><th colspan="1" rowspan="1" align="left" valign="bottom">CUHK-Su10 (AY282752)</th><th colspan="1" rowspan="1" align="left" valign="bottom">CUHK-L2 (AY443086–AY443095)</th><th colspan="1" rowspan="1" align="left" valign="bottom">CUHK-W1 (AY278554)</th><th colspan="1" rowspan="1" align="left" valign="bottom">BJ01 (AY278488)</th><th colspan="1" rowspan="1" align="left" valign="bottom">BJ02 (AY278487)</th><th colspan="1" rowspan="1" align="left" valign="bottom">BJ03 (AY278490)</th><th colspan="1" rowspan="1" align="left" valign="bottom">GZ01 (AY278489)</th><th colspan="1" rowspan="1" align="left" valign="bottom"></th></tr></thead><tbody><tr><td colspan="1" rowspan="1" align="left" valign="top">9404<sup>2</sup></td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">T, valine; C, alanine</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">17564<sup>2</sup></td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">T, aspartic acid; G, glutamic acid</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">19838</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">Silent</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">21721</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">G</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">A</td><td colspan="1" rowspan="1" align="left" valign="top">G, glycine; A, aspartate</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">22222<sup>2</sup></td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">T, isoleucine; C, threonine</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">27243</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">C, proline; T, leucine</td></tr><tr><td colspan="1" rowspan="1" align="left" valign="top">27827<sup>2</sup></td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">T</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">C</td><td colspan="1" rowspan="1" align="left" valign="top">Noncoding</td></tr></tbody></table><table-wrap-foot><fn id="fn_1"><label>1</label><p>Nucleotide positions are stated in reference to the Tor2 sequence.</p></fn><fn id="fn_2"><label>2</label><p>Part of the four-nucleotide haplotype reported by Ruan et al. (<xref rid="R10" ref-type="bibr">10</xref>).</p></fn></table-wrap-foot></table-wrap><p>We then compared the CUHK-L2 sequence with the complete genomic sequences of other SARS-CoV isolates. We note that in addition to the four-nucleotide haplotype, the nucleotide sequences at three additional positions, 19838, 21721, and 27243 (<xref rid="T1" ref-type="table">Table 1</xref> ), also distinctly segregated the isolates associated with the Metropole Hotel from the unassociated strains with the exception of CUHK-L2 and CUHK-W1 (GenBank accession no. AY278554). Although the isolates that are or are not linked to the Metropole Hotel showed a sequence of A:G:C or G:A:T, respectively, both CUHK-L2 and CUHK-W1 had a configuration that is a combination of the two haplotypes, A:A:C. CUHK-W1, as reported previously (<xref rid="R9" ref-type="bibr">9</xref>), was isolated from a patient who presented at approximately the same time as a major hospital outbreak in Hong Kong (<xref rid="R12" ref-type="bibr">12</xref>). The latter hospital outbreak was epidemiologically linked to the hotel cluster. However, similar to CUHK-L2, the CUHK-W1 isolate was obtained from a patient who had no connection with the Metropole Hotel but had been traveling in southern China before symptom onset (<xref rid="R9" ref-type="bibr">9</xref>).</p><p>When we used the combined haplotype consisting of all seven nucleotides (<xref rid="T1" ref-type="table">Table 1</xref> ), the segregation between the genotypes linked or not linked to the Metropole Hotel became less distinctive. CUHK-L2 shares three and CUHK-W1 shares two common nucleotide sequences with the hotel-linked isolates, whereas the remaining four nucleotides for CUHK-L2 and five nucleotides for CUHK-W1 are in common with the isolates not linked to the Metropole Hotel. Epidemiologically, CUHK-L2 and CUHK-W1 were obtained from patients who presented before or around the time of the report of the hotel cluster. Thus, there is both temporal and molecular evidence to suggest that CUHK-L2 and CUHK-W1 may represent two transitory strains of SARS-CoV that bridge the evolution between the earlier SARS-CoV strains and those that are linked to the Metropole Hotel.</p><p>These data confirm that during the early part of the epidemic, the SARS-CoV was undergoing gradual evolution. However, at present, it is uncertain whether these cumulative changes contributed to the infectivity and propagation efficiency of the SARS-CoV and, thus, the development of the SARS epidemic. 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