Detection of Japanese Encephalitis Virus RNA in human throat samples in Laos : a pilot study

Autor: Malee Seephonelee, Paul N. Newton, Audrey Dubot-Pérès, Tehmina Bharucha, Marc Lecuit, Onanong Sengvilaipaseuth, Xavier de Lamballerie, Malavanh Vongsouvath, Jean-David Pommier, Géraldine Piorkowski, Manivanh Vongsouvath, Sayaphet Rattanavong, Christopher Gorman
Přispěvatelé: Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), Mahidol University [Bangkok]-Mahosot Hospital, University College of London [London] (UCL), Unité des Virus Emergents (UVE), Institut de Recherche pour le Développement (IRD)-Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Biologie des Infections - Biology of Infection, Institut Pasteur [Paris] (IP)-Institut National de la Santé et de la Recherche Médicale (INSERM), Université Paris Descartes - Paris 5 (UPD5), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Unité de Virologie / Virology Unit [Phnom Penh], Institut Pasteur du Cambodge, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), University of Oxford, The SEAe project was supported by Total Foundation, Horizon 2020 research and innovation programme EVAg under grant agreement N° 653316, the Institute of Research for Development (IRD), Aix-Marseille University and the Wellcome Trust of Great Britain. The research was implemented in collaboration with ComAcross project (www.onehealthsea.org/comacross) thanks to the financial support of the European Union (EuropeAid, INNOVATE contract 315-047), European Project: 653316,H2020,H2020-INFRAIA-2014-2015,EVAg(2015), Bousquet, nathalie, European Virus Archive goes global - EVAg - - H20202015-04-01 - 2019-03-31 - 653316 - VALID, Aix Marseille Université (AMU)-Institut de Recherche pour le Développement (IRD)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pasteur [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Oxford [Oxford]
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Male
viruses
Pilot Projects
Antibodies
Viral

Serology
0302 clinical medicine
030212 general & internal medicine
Child
Encephalitis Virus
Japanese

[SDV.MP.VIR] Life Sciences [q-bio]/Microbiology and Parasitology/Virology
education.field_of_study
Multidisciplinary
Middle Aged
3. Good health
Vaccination
medicine.anatomical_structure
Molecular Diagnostic Techniques
Laos
Child
Preschool

[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
RNA
Viral

Medicine
Female
Encephalitis
Adult
Adolescent
Science
030231 tropical medicine
Population
Enzyme-Linked Immunosorbent Assay
Real-Time Polymerase Chain Reaction
Virus
Article
03 medical and health sciences
Young Adult
Throat
medicine
Humans
Serologic Tests
education
Encephalitis
Japanese

Retrospective Studies
Molecular epidemiology
business.industry
Japanese encephalitis
medicine.disease
Virology
Immunoglobulin M
Pharynx
business
Zdroj: Scientific Reports, Vol 8, Iss 1, Pp 1-5 (2018)
Scientific Reports
Scientific Reports, 2018, 8 (1), pp.8018. ⟨10.1038/s41598-018-26333-4⟩
Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.8018. ⟨10.1038/s41598-018-26333-4⟩
ISSN: 2045-2322
Popis: International audience; Japanese encephalitis virus (JEV) is the most commonly identified cause of acute encephalitis syndrome (AES) in Asia. The WHO recommended test is anti-JEV IgM-antibody-capture-enzyme-linked-immunosorbent-assay (JEV MAC-ELISA). However, data suggest this has low positive predictive value, with false positives related to other Flavivirus infections and vaccination. JEV RT-PCR in cerebrospinal fluid (CSF) and/or serum is highly specific, but is rarely positive; 0–25% of patients that fulfil the WHO definition of JE (clinical Acute Encephalitis Syndrome (AES) and JEV MAC-ELISA positive). Testing other body fluids by JEV RT-qPCR may improve the diagnosis. As a pilot study thirty patients admitted to Mahosot Hospital 2014–2017, recruited to the SouthEast -Asia-Encephalitis study, were tested by JEV MAC-ELISA and two JEV real-time RT-PCR (RT-qPCR) assays (NS2A and NS3). Eleven (36.7%) were JEV MAC-ELISA positive. Available CSF and serum samples of these patients were JEV RT-qPCR negative but 2 (7%) had JEV RNA detected in their throat swabs. JEV RNA was confirmed by re-testing, and sequencing of RT-qPCR products. As the first apparent report of JEV RNA detection in human throat samples, the provides new perspectives on human JEV infection, potentially informing improving JEV detection. We suggest that testing patients' throat swabs for JEV RNA is performed, in combination with molecular and serological CSF and serum investigations, on a larger scale to investigate the epidemiology of the presence of JEV in human throats. Throat swabs are an easy and non-invasive tool that could be rolled out to a wider population to improve knowledge of JEV molecular epidemiology. Evidence continues to implicate Japanese encephalitis virus (JEV) as a major cause of encephalitis in Asia, with recent evidence of possible autochthonous transmission in Africa 1–3. Among the key factors in its persistent role as a public health problem are the limitations of existing diagnostic tests, our understanding of its epidemiology and inadequate implementation of vaccination programmes. The conventional mainstay of JEV encephalitis diagnosis is serology, with serum and cerebrospinal fluid (CSF) anti-JEV IgM antibody capture enzyme-linked immunosorbent assays (JEV MAC-ELISA) recommended by the World Health Organization (WHO) 4. However, there are concerns about the accuracy of JEV MAC-ELISA for diagnosing JEV. Low positive predictive value of JEV MAC-ELISA has been reported 5 , and there are recognised difficulties with false positives related to vaccination and in areas where other Flavivirus infections are endemic 6,7. Diagnosis of JEV by Reverse-Transcription (RT)-PCR is highly specific, and enables improved understanding of the molecular epidemiology of JEV 8. However, JEV RT-PCR testing of CSF and serum samples has low sensitivity , rarely positive in patients at presentation (0–25% that fulfil the WHO definition of Acute Encephalitis
Databáze: OpenAIRE