2020
DOI: 10.1016/j.diagmicrobio.2020.115015
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Detection of herpes simplex and varicella-zoster virus from skin lesions: comparison of RT-PCR and isothermal amplification for rapid identification

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Cited by 12 publications
(4 citation statements)
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“…However, all subjects with available medical records were examined by a rapid examination kit. Moreover, concordance between the rapid identification kit and RT-PCR was 99.3% [ 28 ]. It is, therefore, considered that the inconsistency of diagnosis between medical institutions would be negligible.…”
Section: Discussionmentioning
confidence: 99%
“…However, all subjects with available medical records were examined by a rapid examination kit. Moreover, concordance between the rapid identification kit and RT-PCR was 99.3% [ 28 ]. It is, therefore, considered that the inconsistency of diagnosis between medical institutions would be negligible.…”
Section: Discussionmentioning
confidence: 99%
“…As with other isothermal reactions, only simple heating apparatus is required, however, the higher temperature reaction of HDA negates the ability to use ambient temperatures for amplification. HDA functions in the presence of other biological agents, and can be used alongside crude samples, without the need for DNA or RNA extraction (Kim et al, 2011;Li et al, 2013;Jevšnik et al, 2020).…”
Section: Helicase-dependent Amplificationmentioning
confidence: 99%
“…Recent studies by Jevšnik et al have compared the effective detection of herpes simplex and varicella-zoster virus from skin lesions using a commercially available test, the RT-PCR (Argene, BioMerieux, Verniolle, France) test, performed on LC480 platform (Roche Applied Science, Mannheim, Germany) and the HDA assay (Solana HSV1 + 2/VZV assay, Quidel Corporation, San Diego, CA, USA). Both tests showed good agreement of 98.3% for HSV-1 and 99.3% for VZV [ 127 ]. The limit of detection of RT-PCR reagents was about 107 copies/mL.…”
Section: Detection Of Hsv In Lesionsmentioning
confidence: 99%