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. Author manuscript; available in PMC: 2024 Feb 19.
Published in final edited form as: J Med Microbiol. 2020 Feb 3;69(2):218–227. doi: 10.1099/jmm.0.001123

Table 1.

PCR primer sequences for amplification of cag PAI and vacA genes

Gene Primer name Sequence Reference
cagA*, CAGTF 5’ACCCTAGTCGGTAATGGG [69]
CAGTR 5’GCTTTAGCTTCTGAYACYGC [69]
A2530S 5’GTTAARAATRGTGTRAAYGG [70]
3000AS 5’TTTAGCTTCTGATACCGC [70]
cagE cagEAF 5’TTGAAAACTTCAAGGATAGGATAGAGC [13]
cagEAR 5’GCCTAGCGTAATATCACCATTACCC [13]
cagEBF 5’AGTGATGCTTTGAGTCGCAAGTC [71]
cagEBR 5’TGGGGCAATAGTGTGATGACG [71]
cagT cagTAF 5’CCATGTTTATACGCCTGTGT [54]
cagTAR 5’CATCACCACACCCTTTTGAT [54]
cagTBF 5’TCTAAAAAGATTACGCTCATAGGCG [72]
cagTBR 5’CTTTGGCTTGCATGTTCAAGTTGCC [72]
virD4 virD4BF 5’TTTCATAGGTTCTATGGCAAGCGGG [73]
virD4BR 5’TTAGCGCCATTCCTACCATAACC [73]
virD4AF 5’TTTATGATGATAATCGATCGCC [73]
virD4AR 5’GAACGCCTGCCCTGCGTAAGCG [73]
Right end cagPAI 3’F 5’GGCTCAAGCTCGGAATGAT
emptyR 5’CTCTTTTTGTGCCTTTGATTGAA
Left end cagPAI emptyF 5’CCAAATACATTTTGGCTAAATAAAC
5’R 5’GCTTATCAGTCAAATTGTTTTTG
vacA s1a SS1F 5’GTCAGCATCACACCGCAAC [29]
VAIR 5’CTGCTTGAATGCGCCAAAC [29]
vacA s1b SS3F 5’AGCGCCATACCGCAAGAG [29]
VAIR 5’CTGCTTGAATGCGCCAAAC [29]
vacA s1c S1cF 5’CTYGCTTTAGTRGGGYTA [74]
VAIR 5’CTGCTTGAATGCGCCAAAC [29]
vacA s2 SS2F 5’GCTAACACGCCAAATGATCC [29]
VAIR 5’CTGCTTGAATGCGCCAAAC [29]
vacA m1a VA3F 5’GGTCAAAATGCGGTCATGG [29]
VA3R 5’CTAATGCCATTGGTACCTGTAGAAAC [29]
vacA m1b VAMF 5’CCCCAATGCAGTCATGGAT [75]
VAMR 5’GCTGTTAGTGCCTAAAGAAGCAT [75]
vacA m2 VA4F 5’GGAGCCCCAGGAAACATTG [29]
VA4R 5’TGTCATAACTAGCGCCTTGCAC [29]
vacA i1 F1 5’GTTGGGATTGGGGGAATGCCG [63]
c1R 5’TTAATTTAACGCTGTTTGAAG [63]
vacA i2 F1 5’GTTGGGATTGGGGGAATGCCG [63]
c2R 5’GATCAACGCTCTGATTTGA [63]
*

Also used to determine the EPIYA sequence for cagA-positive samples.

Sample is considered to have an intact cagPAI if all of these genes are present.