“…TaqMan quantitative real-time RT-PCR assays have also been developed and used for the specific detection and quantitation of North American eastern equine encephalitis (EEE) and western equine encephalitis (WEE) RNAs based on amplification of 69 bp and 67 bp of the corresponding genome sequences, respectively (Lambert et al, 2003;Vina-Rodriguez et al, 2016). In addition, the PCR-based detection methods have also been successfully employed for the detection of pathogenic DNA viruses such as adenoviruses (Allard et al, 1990), herpes viruses (Shimada et al, 2017), polyomaviruses (Vanchiere et al, 2005), poxviruses (Scaramozzino et al, 2007;Putkuri et al, 2009) and pathogenic RNA viruses such as Ebola (Cherpillod et al, 2016), Zika , SARS (Chan et al, 2004b), MERS-CoV (Lu et al, 2014), H5N1 (Ng et al, 2005;Karo-karo et al, 2019), Chikungunya , coxsackievirus (Wiyatno et al, 2016), rhinovirus C (Wiyatno et al, 2018), etc. Other molecular methods for detecting pathogenic viruses such as direct nucleic acid detection by a biosensor (Saylan et al, 2019) and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) diagnostics using CRISPR-CRISPR-associated system (CRISPR-Cas) (Chertow, 2018) have also been developed.…”