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International external quality assessment study for molecular detection of Lassa virus.
Nikisins, Sergejs; Rieger, Toni; Patel, Pranav; Müller, Rolf; Günther, Stephan; Niedrig, Matthias.
Afiliação
  • Nikisins S; Highly Pathogenic Viruses (ZBS 1), Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany; European Public Health Microbiology Training Programme (EUPHEM), European Centre for Disease Prevention and Control (ECDC), Stockholm, Sweden.
  • Rieger T; Bernhard-Nocht-Institute for Tropical Medicine, WHO Collaborating Centre for Arboviruses and Hemorrhagic Fever Reference and Research, Hamburg, Germany.
  • Patel P; Highly Pathogenic Viruses (ZBS 1), Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany.
  • Müller R; Biomatrica, San Diego, California, United States of America.
  • Günther S; Bernhard-Nocht-Institute for Tropical Medicine, WHO Collaborating Centre for Arboviruses and Hemorrhagic Fever Reference and Research, Hamburg, Germany.
  • Niedrig M; Highly Pathogenic Viruses (ZBS 1), Centre for Biological Threats and Special Pathogens, Robert Koch Institute, Berlin, Germany.
PLoS Negl Trop Dis ; 9(5): e0003793, 2015 May.
Article em En | MEDLINE | ID: mdl-25996783
Lassa virus (LASV) is a causative agent of hemorrhagic fever in West Africa. In recent years, it has been imported several times to Europe and North America. The method of choice for early detection of LASV in blood is RT-PCR. Therefore, the European Network for Diagnostics of 'Imported' Viral Diseases (ENIVD) performed an external quality assessment (EQA) study for molecular detection of LASV. A proficiency panel of 13 samples containing various concentrations of inactivated LASV strains Josiah, Lib-1580/121, CSF, or AV was prepared. Samples containing the LASV-related lymphocytic choriomeningitis virus (LCMV) and negative sera were included as specificity controls. Twenty-four laboratories from 17 countries (13 European, one African, one Asian, two American countries) participated in the study. Thirteen laboratories (54%) reported correct results, 4 (17%) laboratories reported 1 to 2 false-negative results, and 7 (29%) laboratories reported 3 to 5 false-negative results. This EQA study indicates that most participating laboratories have a good or acceptable performance in molecular detection of LASV. However, several laboratories need to review and improve their diagnostic procedures.
Assuntos

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Reação em Cadeia da Polimerase Via Transcriptase Reversa / Laboratórios / Vírus Lassa Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans País/Região como assunto: Africa / America do norte / Europa Idioma: En Revista: PLoS Negl Trop Dis Assunto da revista: MEDICINA TROPICAL Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Temas: ECOS / Aspectos_gerais Bases de dados: MEDLINE Assunto principal: Reação em Cadeia da Polimerase Via Transcriptase Reversa / Laboratórios / Vírus Lassa Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Humans País/Região como assunto: Africa / America do norte / Europa Idioma: En Revista: PLoS Negl Trop Dis Assunto da revista: MEDICINA TROPICAL Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Suécia