1. Validation and utilization of an internally controlled multiplex Real-time RT-PCR assay for simultaneous detection of enteroviruses and enterovirus A71 associated with hand foot and mouth disease.
- Author
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Thanh TT, Anh NT, Tham NT, Van HM, Sabanathan S, Qui PT, Ngan TT, Van TT, Nguyet LA, Ny NT, Thanh le TM, Chai OK, Perera D, Viet do C, Khanh TH, Ha do Q, Tuan HM, Wong KT, Hung NT, Chau NV, Thwaites G, van Doorn HR, and Van Tan L
- Subjects
- Animals, Asia, Child, Child, Preschool, Enterovirus classification, Enterovirus genetics, Female, Humans, Infant, Male, Multiplex Polymerase Chain Reaction standards, Pharynx virology, Real-Time Polymerase Chain Reaction standards, Rectum virology, Reference Standards, Reverse Transcriptase Polymerase Chain Reaction standards, Sensitivity and Specificity, Enterovirus isolation & purification, Enterovirus Infections diagnosis, Multiplex Polymerase Chain Reaction methods, Real-Time Polymerase Chain Reaction methods, Reverse Transcriptase Polymerase Chain Reaction methods
- Abstract
Background: Hand foot and mouth disease (HFMD) is a disease of public health importance across the Asia-Pacific region. The disease is caused by enteroviruses (EVs), in particular enterovirus A71 (EV-A71). In EV-A71-associated HFMD, the infection is sometimes associated with severe manifestations including neurological involvement and fatal outcome. The availability of a robust diagnostic assay to distinguish EV-A71 from other EVs is important for patient management and outbreak response., Methods: We developed and validated an internally controlled one-step single-tube real-time RT-PCR in terms of sensitivity, linearity, precision, and specificity for simultaneous detection of EVs and EV-A71. Subsequently, the assay was then applied on throat and rectal swabs sampled from 434 HFMD patients., Results: The assay was evaluated using both plasmid DNA and viral RNA and has shown to be reproducible with a maximum assay variation of 4.41 % and sensitive with a limit of detection less than 10 copies of target template per reaction, while cross-reactivity with other EV serotypes was not observed. When compared against a published VP1 nested RT-PCR using 112 diagnostic throat and rectal swabs from 112 children with a clinical diagnosis of HFMD during 2014, the multiplex assay had a higher sensitivity and 100 % concordance with sequencing results which showed EVs in 77/112 (68.8 %) and EV-A71 in 7/112 (6.3 %). When applied to clinical diagnostics for 322 children, the assay detected EVs in throat swabs of 257/322 (79.8 %) of which EV-A71 was detected in 36/322 (11.2 %) children. The detection rate increased to 93.5 % (301/322) and 13.4 % (43/322) for EVs and EV-A71, respectively, when rectal swabs from 65 throat-negative children were further analyzed., Conclusion: We have successfully developed and validated a sensitive internally controlled multiplex assay for rapid detection of EVs and EV-A71, which is useful for clinical management and outbreak control of HFMD.
- Published
- 2015
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