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Assessment of a multiplex RT-PCR for Simultaneous, Rapid Screening of Common Viral Infections of Central Nervous System: A Prospective Study for Enteroviruses and Herpesviruses


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Fig. 1

The multiplex PCR assay’s specificity was examined using PCR mixes containing all two-primer pairs and a single template (cDNA/DNA) from the positive controls. Lane 1: standard 100-bp DNA ladder marker. Lane 2: the mixture of enterovirus (440 bp) and HSV (292 bp) positive controls. Lane 3: enterovirus (440 bp), Lane 4: HSV (292 bp), Lane 5: negative control (E. coli)
The multiplex PCR assay’s specificity was examined using PCR mixes containing all two-primer pairs and a single template (cDNA/DNA) from the positive controls. Lane 1: standard 100-bp DNA ladder marker. Lane 2: the mixture of enterovirus (440 bp) and HSV (292 bp) positive controls. Lane 3: enterovirus (440 bp), Lane 4: HSV (292 bp), Lane 5: negative control (E. coli)

Fig. 2

Comparison of the sensitivity between multiplex PCR and monoplex PCR for the 10-fold serial dilutions of positive controls. (A): HSV (292 bp) (B): Enteroviruses (440 bp)
Comparison of the sensitivity between multiplex PCR and monoplex PCR for the 10-fold serial dilutions of positive controls. (A): HSV (292 bp) (B): Enteroviruses (440 bp)
eISSN:
1732-2693
Idioma:
Inglés
Calendario de la edición:
Volume Open
Temas de la revista:
Life Sciences, Molecular Biology, Microbiology and Virology, Medicine, Basic Medical Science, Immunology