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Table 2 List of PCR primers used in this study with optimal amplification conditions

From: Monitoring of Poyang lake water for sewage contamination using human enteric viruses as an indicator

Virus

Primer name

Primer Sequence (5′ → 3′)

Length (bp)

Amplification condition

Reference

TA

Mg (mM)

Primer (μM)

BSA

 

NoV GI

QNIF4

CGCTGGATGCGNTTCCAT

8

6

58

2.0

0.4

Yes

Loisy et al., 2005

NV1LCR

CCTTAGACGCCATCATCATTTAC

NoV GII

COG2F

CARGARBCNATGTTYAGRTGGATGAG

9

7

58

2.0

0.8

Yes

Kageyama et al., 2003

COG2R

TCGACGCCATCTTCATTCACA

EoV

EQ-1

ACATGGTGTGAAGAGTCTATTGAGCT

1

4

2

60

1.5

0.6

Yes

Dierssen et al., 2008

EQ-2

CCAAAGTAGTCGGTTCCGC

AdV

ADV-F

GCCACGGTGGGGTTTCTAAACTT

1

3

2

54

1.5

0.6

Yes

Gunson et al., 2009

ADV-R

GCCCCAGTGGTCTTACATGCACATC

  1. aNoV GI, human norovirus genotype I; NoV GII, human norovirus genotype II; EoV, human enterovirus; AdV, human adenovirus