Table 2.
Method | Treatment | Detection | Type of sample | Target virus | References |
---|---|---|---|---|---|
Molecular | Proteinase and RNase | RT‐PCR | Cell culture | FCV HAV, MNoV, poliovirus 1, | Nuanualsuwan & Cliver (2002, 2003); Baert et al. (2008) |
Proteinase and RNase | qNASBA | Stool samples and cell culture | NoV, FCV | Lamhoujeb et al. (2008, 2009) | |
RNase protection assay | qRT‐PCR | Stool samples and cell culture | NoV, FCV | Topping et al. (2009) | |
5’ NTR RT‐PCR | Cell culture | HAV | Bhattacharya et al. (2004); Li et al. (2002, 2004) | ||
Long target region (LTR) qRT‐PCR | Cell culture | HAV, poliovirus 1, F‐specific RNA phages | Li et al. (2002); Simonet & Gantzer (2006a, b) | ||
Cell culture + molecular | Attachment to cell monolayer | RT‐PCR | Cell culture | HAV, poliovirus 1, FCV | Nuanualsuwan & Cliver (2003) |
Virus replication in cell culture (ICC: integrated cell culture) | RT‐PCR | Different types of water, sewage effluent, faecal specimens and cell culture | AdV, AstV, EV, poliovirus, RV, HAV, MS2 | Blackmer et al. (2000); Chapron et al. (2000); Jiang et al. (2004); Ko et al. (2003, 2005); Lee & Kim (2002); Lee & Jeong (2004); Li et al. (2009); Nuanualsuwan & Cliver (2003); Reynolds et al. (1996); Shieh et al. (2008) | |
Immunological +molecular | Antibody capture | RT‐PCR | Different types of water, faecal samples and cell culture | HAV, NoV, poliovirus 1, FCV | Gilpatrick et al. (2000); Myrmel et al. (2000); Schwab et al. (1996) |
Immunomagnetic separation | qRT‐PCR | Artificially contaminated groundwater | HAV | Abd El Galil et al. (2004) |
RT‐PCR, reverse transcriptase PCR; qRT‐PCR, reverse transcriptase real‐time PCR; qNASBA, real‐time nucleic acid sequence–based amplification; FCV, feline calicivirus; mNoV, murine NoV.
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