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Epidemiological and genetic correlates of severe acute respiratory syndrome coronavirus infection in the hospital with the highest nosocomial infection rate in Taiwan in 2003

Identifieur interne : 004457 ( Main/Exploration ); précédent : 004456; suivant : 004458

Epidemiological and genetic correlates of severe acute respiratory syndrome coronavirus infection in the hospital with the highest nosocomial infection rate in Taiwan in 2003

Auteurs : Yi-Ming Arthur Chen [Taïwan] ; Shu-Yuan Liang [Taïwan] ; Yi-Ping Shih [Taïwan] ; Chia-Yen Chen [Taïwan] ; Yuan-Ming Lee [Taïwan] ; LING CHANG [Taïwan] ; Shiao-Ying Jung [Taïwan] ; Mei-Shang Ho [Taïwan] ; Kung-Yee Liang [Taïwan] ; Hour-Young Chen [Taïwan] ; Yu-Jiun Chan [Taïwan] ; Da-Chen Chu [Taïwan]

Source :

RBID : Pascal:06-0127171

Descripteurs français

English descriptors

Abstract

Taiwan experienced a series of outbreaks of nosocomial severe acute respiratory syndrome (SARS) infections in 2003. Two months after the final outbreak, we recruited 658 employees from the hospital that suffered the first and most severe SARS infections to help us investigate epidemiological and genetic factors associated with the SARS coronavirus (SARS-CoV). SARS-CoV infections were detected by using enzyme immunoassays and confirmed by a combination of Western blot assays, neutralizing antibody tests, and commercial SARS tests. Risk factors were analyzed via questionnaire responses and sequence-specific oligonucleotide probes of human leukocyte antigen (HLA) alleles. Our results indicate that 3% (20/658) of the study participants were seropositive, with one female nurse identified as a subclinical case. Identified SARS-CoV infection risk factors include working in the same building as the hospital's emergency room and infection ward, providing direct care to SARS patients, and carrying a Cw*0801 HLA allele. The odds ratio for contracting a SARS-CoV infection among persons with either a homozygous or a heterozygous Cw*0801 genotype was 4.4 (95% confidence interval, 1.5 to 12.9; P = 0.007).

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Le document en format XML

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<term>Adult</term>
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<term>Blotting, Western</term>
<term>Coronavirus</term>
<term>Cross Infection (epidemiology)</term>
<term>Cross Infection (virology)</term>
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</keywords>
<keywords scheme="MESH" type="chemical" qualifier="blood" xml:lang="en">
<term>Antibodies, Viral</term>
</keywords>
<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en">
<term>Taiwan</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en">
<term>Cross Infection</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>HLA-C Antigens</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Antigènes HLA-C</term>
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="sang" xml:lang="fr">
<term>Anticorps antiviraux</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infection croisée</term>
<term>Syndrome respiratoire aigu sévère</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Cross Infection</term>
<term>Severe Acute Respiratory Syndrome</term>
</keywords>
<keywords scheme="MESH" qualifier="épidémiologie" xml:lang="fr">
<term>Infection croisée</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Taïwan</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Animals</term>
<term>Blotting, Western</term>
<term>Disease Outbreaks</term>
<term>Enzyme-Linked Immunosorbent Assay</term>
<term>Female</term>
<term>Histocompatibility Testing</term>
<term>Hospitals, Urban</term>
<term>Humans</term>
<term>Male</term>
<term>Mice</term>
<term>Middle Aged</term>
<term>Neutralization Tests</term>
<term>Risk Factors</term>
<term>Surveys and Questionnaires</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Animaux</term>
<term>Coronavirus</term>
<term>Enquêtes et questionnaires</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Flambées de maladies</term>
<term>Génétique</term>
<term>Humains</term>
<term>Hôpitaux urbains</term>
<term>Incidence</term>
<term>Mâle</term>
<term>Souris</term>
<term>Taiwan</term>
<term>Microbiologie</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Infection nosocomiale</term>
<term>Technique de Western</term>
<term>Test ELISA</term>
<term>Test d'histocompatibilité</term>
<term>Tests de neutralisation</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Taïwan</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr">
<term>Génétique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Taiwan experienced a series of outbreaks of nosocomial severe acute respiratory syndrome (SARS) infections in 2003. Two months after the final outbreak, we recruited 658 employees from the hospital that suffered the first and most severe SARS infections to help us investigate epidemiological and genetic factors associated with the SARS coronavirus (SARS-CoV). SARS-CoV infections were detected by using enzyme immunoassays and confirmed by a combination of Western blot assays, neutralizing antibody tests, and commercial SARS tests. Risk factors were analyzed via questionnaire responses and sequence-specific oligonucleotide probes of human leukocyte antigen (HLA) alleles. Our results indicate that 3% (20/658) of the study participants were seropositive, with one female nurse identified as a subclinical case. Identified SARS-CoV infection risk factors include working in the same building as the hospital's emergency room and infection ward, providing direct care to SARS patients, and carrying a Cw*0801 HLA allele. The odds ratio for contracting a SARS-CoV infection among persons with either a homozygous or a heterozygous Cw*0801 genotype was 4.4 (95% confidence interval, 1.5 to 12.9; P = 0.007).</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Taïwan</li>
</country>
</list>
<tree>
<country name="Taïwan">
<noRegion>
<name sortKey="Chen, Yi Ming Arthur" sort="Chen, Yi Ming Arthur" uniqKey="Chen Y" first="Yi-Ming Arthur" last="Chen">Yi-Ming Arthur Chen</name>
</noRegion>
<name sortKey="Chan, Yu Jiun" sort="Chan, Yu Jiun" uniqKey="Chan Y" first="Yu-Jiun" last="Chan">Yu-Jiun Chan</name>
<name sortKey="Chen, Chia Yen" sort="Chen, Chia Yen" uniqKey="Chen C" first="Chia-Yen" last="Chen">Chia-Yen Chen</name>
<name sortKey="Chen, Hour Young" sort="Chen, Hour Young" uniqKey="Chen H" first="Hour-Young" last="Chen">Hour-Young Chen</name>
<name sortKey="Chu, Da Chen" sort="Chu, Da Chen" uniqKey="Chu D" first="Da-Chen" last="Chu">Da-Chen Chu</name>
<name sortKey="Ho, Mei Shang" sort="Ho, Mei Shang" uniqKey="Ho M" first="Mei-Shang" last="Ho">Mei-Shang Ho</name>
<name sortKey="Jung, Shiao Ying" sort="Jung, Shiao Ying" uniqKey="Jung S" first="Shiao-Ying" last="Jung">Shiao-Ying Jung</name>
<name sortKey="Lee, Yuan Ming" sort="Lee, Yuan Ming" uniqKey="Lee Y" first="Yuan-Ming" last="Lee">Yuan-Ming Lee</name>
<name sortKey="Liang, Kung Yee" sort="Liang, Kung Yee" uniqKey="Liang K" first="Kung-Yee" last="Liang">Kung-Yee Liang</name>
<name sortKey="Liang, Shu Yuan" sort="Liang, Shu Yuan" uniqKey="Liang S" first="Shu-Yuan" last="Liang">Shu-Yuan Liang</name>
<name sortKey="Ling Chang" sort="Ling Chang" uniqKey="Ling Chang" last="Ling Chang">LING CHANG</name>
<name sortKey="Shih, Yi Ping" sort="Shih, Yi Ping" uniqKey="Shih Y" first="Yi-Ping" last="Shih">Yi-Ping Shih</name>
</country>
</tree>
</affiliations>
</record>

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