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<records>
  <record>
    <language>eng</language>
    <publisher>Science and Education Publishing</publisher>
    <journalTitle>American Journal of Infectious Diseases and Microbiology</journalTitle>
    <eissn>2328-4064</eissn>
    <publicationDate>2015-02-01</publicationDate>
    <volume>3</volume>
    <issue>1</issue>
    <startPage>6</startPage>
    <endPage>13</endPage>
    <doi>10.12691/ajidm-3-1-2</doi>
    <publisherRecordId>AJIDM2015312</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Detection and Molecular Characterization of Respiratory Syncytial Virus (RSV) in Children with Respiratory Signs in Khartoum State, Sudan 2011-2012</title>
    <authors>
      <author>
        <name>Sahar O Khalil</name>
        <email>saharosmankhalil@yahoo.com</email>
        <affiliationId>1</affiliationId>
      </author>
      <author>
        <name>Khalid A Enan</name>
        <affiliationId>2</affiliationId>
      </author>
      <author>
        <name>Ali. Y. H</name>
        <affiliationId>3</affiliationId>
      </author>
      <author>
        <name>Bashir Salim</name>
        <affiliationId>4</affiliationId>
      </author>
      <author>
        <name>Isam M Elkhidir</name>
        <affiliationId>5</affiliationId>
      </author>
    </authors>
    <affiliationsList>
      <affiliationName affiliationId="1">Department of Microbiology, University of science and technology, P.O. Box: 30, Omdurman, Sudan</affiliationName>
      <affiliationName affiliationId="2">Department of Virology, Central Laboratory, Ministry of science and Technology, P.O. Box 7099, Khartoum</affiliationName>
      <affiliationName affiliationId="3">Department of Virology, Veterinary research Institute, P.O. Box 80 67, Khartoum, Sudan</affiliationName>
      <affiliationName affiliationId="4">Department of Parasitology, Faculty of Veterinary Medicine, University of Khartoum, 13314 Khartoum-North, Sudan</affiliationName>
      <affiliationName affiliationId="5">Department of Microbiology and Parasitology, Faculty of Medicine, University of Khartoum, Khartoum, Sudan</affiliationName>
    </affiliationsList>
    <abstract language="eng">Background: The present study was to investigate the incidence of the respiratory syncytial virus infection in children and to characterize the RSV circulating in Khartoum state during 2011-12 winter seasons. Methodology: Throat swab specimens collected from 224 children less than 5 years old, with respiratory tract infections admitted at Khartoum Hospitals in winter season (2011- 2012), were screened for RSV using direct immunofluorescence assay (DFA) and reverse transcription- polymerase chain reaction (RT-). Isolation in cell culture followed by nucleotide sequencing and bioinformatics analysis based on the G gene, were done for the RT- positive RSV samples. Results: Out of 224 patients, RSV infections were detected in 136 (60.7%) patients, by using DFA technique, and 44 (19.6%) patients using RT-PCR. 22 strains of RSV were isolated in Hep-2 cell line. The clinical symptoms including Bronchiolitis, Pneumonia, Asthma and Allergy showed significantly different rates (p&lt;0.05) in having RSV infection, (P-value = 0.017, 0.002, 0.0001, 0.0001) respectively. Bioinformatics analysis of nucleotide sequences of 7 cell culture isolated RSV strains revealed that all analyzed RSV belonged to the RSV-A genotype. Phylogenetic tree of RSV-A sequences showed that, all Sudanese strains were grouped with strains from Belgium and Saudi Arabia. Conclusions: This is the first report on molecular characterization that describes the circulation of RSV genotype in Sudan. DFA and RT-PCR offers rapid methods for detection of RSV in hospitalized children with Respiratory tract infection (RTI).</abstract>
    <fullTextUrl format="pdf">http://pubs.sciepub.com/ajidm/3/1/2/ajidm-3-1-2.pdf</fullTextUrl>
    <keywords language="eng">
      <keyword>respiratory tract infection</keyword>
      <keyword>respiratory syncytial viruses</keyword>
      <keyword>reverse transcription polymerase chain reaction</keyword>
      <keyword>direct immunofluorescence assay</keyword>
      <keyword>khartoum</keyword>
    </keywords>
  </record>
</records>