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. 2014 Mar 10;2014:648520. doi: 10.1155/2014/648520

Table 3.

Primer sequences and product sizes used in this study.

Pathogen Target Sequence 5′-3′ Size References
Shigella and EIEC ipaH AGGTGACACTATAGAATA aACCATGCTCGCAGAGAAACT 213 [10]
GTACGACTCACTATAGGGA bTCAGTACAGCATGCCATGGT

Vibrio parahaemolyticus tlh AGGTGACACTATAGAATAACTCAACACAAGAAGAGATCGACAA 246 [30]
GTACGACTCACTATAGGGAGATGAGCGGTTGATGTCCAA

EHEC and EPEC eaeA AGGTGACACTATAGAATAAGGTCGTCGTGTCTGCTA 293 [31]
GTACGACTCACTATAGGGACCGTGGTTGCTTGCGTTTG

Salmonella invA AGGTGACACTATAGAATAGTGAAATTATCGCCACGTTCGGGCAA 323 [32]
GTACGACTCACTATAGGGATCATCGCACCGTCAAAGGAACC

Yersinia ail AGGTGACACTATAGAATATAATGTGTACGCTGCGAG 389 [5]
GTACGACTCACTATAGGGAGACGTCTTACTTGCACTG

Vibrio cholerae ctx AGGTGACACTATAGAATAACAGTAACTTAGATATTGCTCCAG 507 This study
GTACGACTCACTATAGGGAACCATTCTTAAAAGTAATGATAGCCA

Campylobacter jejuni mapA AGGTGACACTATAGAATACTATTTTATTTTTGAGTGCTTGTG 627 [33]
GTACGACTCACTATAGGGAGCTTTATTTGCCATTTGTTTTATTA

Noroviruses GI RDRP AGGTGACACTATAGAATACGCTGGATGCGCTTCCATGA 162 [21]
GTACGACTCACTATAGGGAGCAAGAGGGTCAGAAGCATT

Rotavirus VP6 AGGTGACACTATAGAATAAAGTCTTCCACATGGAGGT 210 Modified [21]
GTACGACTCACTATAGGGAARRTTICCAATTCCTCCAGT

Norovirus GII RDRP AGGTGACACTATAGAATACAGACAAGAGCCAATGTTCA 279 Modified [21]
GTACGACTCACTATAGGGATTTCTAATCCAGGGGTCAATT

Human astrovirus ORF1a AGGTGACACTATAGAATACGTCATTATTTGTTGTCATA 326 [21]
GTACGACTCACTATAGGGACATGTGCTGCTGTTACTATG

Enteric adenovirus Hexon AGGTGACACTATAGAATATGTACAAGCCAGNTGTAGCTC 388 This study
GTACGACTCACTATAGGGAAAGCAGTAATTTGGCANTTCGT

Human bocavirus 1c VP1 AGGTGACACTATAGAATAAAACCCATCACTCTCAATGCTT 412 This study
GTACGACTCACTATAGGGACAGTATGTCTTCTTTCTGGACG

Human bocavirus 2 VP1 AGGTGACACTATAGAATAAAATCCACCACTATCCATGCTC 412 This study
GTACGACTCACTATAGGGACGGTGTGTCTTCTTTCTGGTCT

aUniversal primers-F: AGGTGACACTATAGAATA; buniversal primers-R: GTACGACTCACTATAGGGA; cthe primers for HBoV1 and HBoV2 are equally mixed, the amplicon sizes of both PCR products are exactly the same, and the primers are located at the same position in the corresponding viral genome; this method is able to identify the presence of HBoV1 and HBoV2 but cannot classify the subtypes.