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. 2024 Aug 21;44(1):58–69. doi: 10.12938/bmfh.2024-059

Table 1. Primer sequences and conditions used in quantitative polymerase chain reaction (PCR).

Target organism Standard strain Primer sequence (5′-3′) PCR product siza (bp) 3-step amplification Reference

Denaturation Annealing Elongation
Prevotella spp. Faecalibacterium prausnitzii F: CACRGTAAACGATGGATGCC 527–529 94℃ for 20 s 55℃ for 20 s 72℃ for 30 s [28]
JCM31915 R: GGTCGGGTTGCAGACC
Lactobacillus spp. Lactobacillus plantarum F: AGCAGTAGGGAATCTTCCA 341 95℃ for 15 s 58℃ for 20 s 72℃ for 30 s [29]
22A-3 R: CACCGCTACACATGGAG
Bifidobacterium spp. Bifidobacterium F: TCGCGTC(C/T)GGTGTGAAAG 549–563 95℃ for 15 s 58℃ for 20 s 72℃ for 30 s [29]
longumJCM1217 R: CCACATCCAGC(A/G)TCCAC
Fusobacterium spp Fusobacterium nucleatum F: CCCTTCAGTGCCGCAGT 248 95℃ for 15 s 61℃ for 15 s 72℃ for 30 s [29]
JCM8532 R: GTCGCAGGATGTCAAGAC
Bacteroides spp. Bacteroides thetaiotaomicron F: GGTGTCGGCTTAAGTGCCAT 495 95℃ for 15 s 68℃ for 20 s 72℃ for 30 s [29]
DSMZ 2079 R: CGGATGTAAGGGCCGTGC
Faecalibacterium Faecalibacterium prausnitzii F: GGAGGAAGAAGGTCTTCGG 248 95℃ for 15 s 60℃ for 15 s 72℃ for 30 s [30]
prausnitzii DSMZ 17677 R: AATTCCGCCTACCTCTGCACT