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Detection of Four Human Coronaviruses in Respiratory Infections in Children: A One-Year Study in Colorado

Identifieur interne : 000798 ( PascalFrancis/Curation ); précédent : 000797; suivant : 000799

Detection of Four Human Coronaviruses in Respiratory Infections in Children: A One-Year Study in Colorado

Auteurs : Samuel R. Dominguez [États-Unis] ; Christine C. Robinson [États-Unis] ; Kathryn V. Holmes [États-Unis]

Source :

RBID : Pascal:09-0379754

Descripteurs français

English descriptors

Abstract

Lower respiratory tract infections are the leading cause of death in children worldwide. Studies on the epidemiology and clinical associations of the four human non-SARS human coronaviruses (HCoVs) using sensitive polymerase chain reaction (PCR) assays are needed to evaluate the clinical significance of HCoV infections worldwide. Pediatric respiratory specimens (1,683) submitted to a diagnostic virology laboratory over a 1-year period (December 2004-November 2005) that were negative for seven respiratory viruses by conventional methods were tested for RNA of four HCoVs using sensitive RT-PCR assays. Coronavirus RNAs were detected in 84 (5.0%) specimens: HCoV-NL63 in 37 specimens, HCoV-OC43 in 34, HCoV-229E in 11, and HCoVHKU1 in 2. The majority of HCoV infections occurred during winter months, and over 62% were in previously healthy children. Twenty-six (41%) coronavirus positive patients had evidence of a lower respiratory tract infection (LRTI), 17 (26%) presented with vomiting and/or diarrhea, and 5 (8%) presented with meningoencephalitis or seizures. Respiratory specimens from one immunocompromised patient were persistently positive for HCoV-229E RNA for 3 months. HCoV-NL63-positive patients were nearly twice as likely to be hospitalized (P=0.02) and to have a LRTI (P=0.04) than HCoV-OC43-positive patients. HCoVs are associated with a small, but significant number (at least 2.4% of total samples submitted), of both upper and lower respiratory tract illnesses in children in Colorado. Our data raise the possibility that HCoV may play a role in gastrointestinal and CNS disease. Additional studies are needed to investigate the potential roles of HCoVs in these diseases. J. Med. Virol.
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A11 03  1    @1 HOLMES (Kathryn V.)
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A14 02      @1 Department of Pathology and Laboratory Medicine, The Children's Hospital, University of Colorado Denver School of Medicine @2 Aurora, Colorado @3 USA @Z 2 aut.
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C01 01    ENG  @0 Lower respiratory tract infections are the leading cause of death in children worldwide. Studies on the epidemiology and clinical associations of the four human non-SARS human coronaviruses (HCoVs) using sensitive polymerase chain reaction (PCR) assays are needed to evaluate the clinical significance of HCoV infections worldwide. Pediatric respiratory specimens (1,683) submitted to a diagnostic virology laboratory over a 1-year period (December 2004-November 2005) that were negative for seven respiratory viruses by conventional methods were tested for RNA of four HCoVs using sensitive RT-PCR assays. Coronavirus RNAs were detected in 84 (5.0%) specimens: HCoV-NL63 in 37 specimens, HCoV-OC43 in 34, HCoV-229E in 11, and HCoVHKU1 in 2. The majority of HCoV infections occurred during winter months, and over 62% were in previously healthy children. Twenty-six (41%) coronavirus positive patients had evidence of a lower respiratory tract infection (LRTI), 17 (26%) presented with vomiting and/or diarrhea, and 5 (8%) presented with meningoencephalitis or seizures. Respiratory specimens from one immunocompromised patient were persistently positive for HCoV-229E RNA for 3 months. HCoV-NL63-positive patients were nearly twice as likely to be hospitalized (P=0.02) and to have a LRTI (P=0.04) than HCoV-OC43-positive patients. HCoVs are associated with a small, but significant number (at least 2.4% of total samples submitted), of both upper and lower respiratory tract illnesses in children in Colorado. Our data raise the possibility that HCoV may play a role in gastrointestinal and CNS disease. Additional studies are needed to investigate the potential roles of HCoVs in these diseases. J. Med. Virol.
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C03 02  X  FRE  @0 Rhinovirus @2 NW @5 03
C03 02  X  ENG  @0 Rhinovirus @2 NW @5 03
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C03 03  X  FRE  @0 Détection @5 05
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C07 04  X  SPA  @0 Picornaviridae @2 NW
C07 05  X  FRE  @0 Homme
C07 05  X  ENG  @0 Human
C07 05  X  SPA  @0 Hombre
C07 06  X  FRE  @0 Etats-Unis @2 NG
C07 06  X  ENG  @0 United States @2 NG
C07 06  X  SPA  @0 Estados Unidos @2 NG
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N21       @1 271

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<fC07 i1="05" i2="X" l="SPA">
<s0>Hombre</s0>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Etats-Unis</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>United States</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Estados Unidos</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Amérique du Nord</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>North America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>America del norte</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Amérique</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>America</s0>
<s2>NG</s2>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Infection</s0>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Infection</s0>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Infección</s0>
</fC07>
<fN21>
<s1>271</s1>
</fN21>
</pA>
</standard>
</inist>
</record>

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