• Yanfei Zhou, Stefan Fernandez, In-Kyu Yoon, Sriluck Simasathien, Veerachai Watanaveeradej, Yu Yang, Omely A Marte-Salcedo, Deidra J Shuck-Lee, Stephen J Thomas, Jun Hang, and Richard G Jarman.
• Viral Diseases Branch, Walter Reed Army Institute of Research, Silver Spring, Maryland.
• Am. J. Trop. Med. Hyg. 2016 Sep 7; 95 (3): 663-669.

AbstractNumerous pathogens cause respiratory infections with similar symptoms. Routine diagnostics detect only a limited number of pathogens, leaving a gap in respiratory illness etiology surveillance. This study evaluated next-generation sequencing for unbiased pathogen identification. Respiratory samples collected in Thailand, Philippines, Bhutan, and Nepal, that were negative by several molecular and immunofluorescence assays, underwent viral cultivation. Samples which demonstrated cytopathic effect in culture (N = 121) were extracted and tested by Luminex xTAG respiratory viral panel (RVP) assay and deep sequencing by Roche 454 FLX Titanium system. Using RVP assay, 52 (43%) samples were positive for enterovirus or rhinovirus and another three were positive for respiratory syncytial virus B, parainfluenza 4, and adenovirus. Deep sequencing confirmed the Luminex assay results and identified additional viral pathogens. Human enteroviruses, including Enterovirus A type 71 and 12 types of Enterovirus B (EV-B) were identified from a hospital in Bangkok. Phylogenetic and recombination analysis showed high correlation of VP1 gene-based phylogeny with genome-wide phylogeny and the frequent genetic exchange among EV-B viruses. The high number and diversity of enteroviruses in the hospital in Bangkok suggests prevalent existence. The metagenomic approach used in our study enabled comprehensive diagnoses of respiratory viruses.© The American Society of Tropical Medicine and Hygiene.

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