Skip to main content
. 2023 Nov 9;12(22):4067. doi: 10.3390/foods12224067

Table 1.

HCR-based biosensors for foodborne pathogen detection.

Signal Transduction Detected Pathogens and Target Type Strategy Linear Range LOD Detection Time Food Samples Ref.
Colorimetry E. coli O157:H7; cell ELISA; HRP enzyme 5 × 102–1 × 107 CFU/mL 1.08 × 102 CFU/mL in pure culture and 2.6 × 102 CFU/mL in milk ~7.5 h Milk [32]
Salmonella spp. and S. aureus; DNA G-quadruplex DNAzyme 1–1 × 105 CFU/mL 10 CFU/mL 130 min Skim milk [33]
Escherichia coli; cell Two types of mechanisms based on AuNP 1 × 102–1 × 104 CFU/mL 10 CFU/mL ~80 min Tap water and milk [34]
S. aureus; mecA gene Multi-color; AuNBPs 10–100 pM 2.71 pM 1 h Milk [38]
L. monocytogenes; genomic DNA GOx/HRP enzyme cascade; Boolean logic function 0.1–10 nM (colorimetry); 0−50 nM (electrochemistry) 1.12 nM (colorimetry); 0.04 nM (electrochemistry) 2 h Vegetable, meat, and milk extracts [39]
Fluorescence S. enteritidis; invA gene MBs; hairpin labeled FAM 7.4 × 101–7.4 × 108 CFU/mL 74 CFU/mL ~2.5 h Lettuce [41]
Mycobacterium tuberculosis; IS6110 gene MBs; hairpin labeled TAMRA; turn-off 0.01–100 nM 10 pM ~2 h N/A [42]
emetic Bacillus cereus; genomic DNA MBs; hairpin labeled FAM; flow cytometry 7.6–7.6 × 106 CFU/mL 7.6 CFU/mL in buffer and 9.2 × 102 CFU/mL in milk ~4.5 h Milk [43]
S. enteritidis; invA gene “GO fluorescence” platform; hairpin labeled FAM; turn-on 4.2 × 101–4.2 × 107 CFU/mL 4.2 × 101 CFU/mL in buffer and 4.2 × 102 CFU/mL in milk 3.5 h Milk [44]
E. coli O157:H7; fliCh7 gene “PCR-HCR” dual-signal amplification; SYBR Green I embed dsDNA 7.2 × 101–7.2 × 106 CFU/mL 7.2 × 101 CFU/mL in buffer and 7.2 × 102 CFU/mL in milk ~3.5 h Milk [46]
S. aureus; DNA “HCR-3WJ-NEASA” circuit dual-signal amplification; CQ 10 pM–10 nM 6.7 pM 0.5 h Milk [47]
S. aureus; 16S rRNA “FAM-SYBR Green I” cooperative effect; “GO fluorescence” platform 50 pM–100 nM 50 pM ~1.5 h Milk [48]
MRSA; agrA gene transcription (its mRNA) “FAM-SYBR Green I” cooperative effect; “GO fluorescence” platform; strand-displacement polymerization reaction (SDPR) 10 fM–100 pM 10 fM ~1 h N/A [49]
MRSA; agrC gene transcription (its mRNA) “FAM-SYBR Green I” cooperative effect; “GO fluorescence” platform; Nb.BbvcI-assisted target recycling amplification (NATR) 10 fM–100 pM 7.5 fM 50 min N/A [50]
Vibrio Parahaemolyticus; gyrB gene FRET; four-way branch migration HCR circuits 0.2–60 nM 0.067 nM 90 min N/A [51]
S. Typhimurium; cell FRET; ratio fluorescence; CRISPR-Cas12a system and TDN-hHCR 10–108 CFU/mL 8 CFU/mL ~2.5 h Milk and egg white [53]
E. coli O157:H7; cell FRET; ratio fluorescence; CQ 4.9 × 101–4.9 × 106 CFU/mL 3.5 × 101 CFU/mL ~3 h Milk [54]
S. aureus; cell IFE; UCNPs; g-C3N4 NSs 10–106 CFU/mL 1 CFU/mL 3 h Tap water and milk [57]
Electrochemistry S. aureus; cell pMB NPs; DHCR 10–108 CFU/mL 1 CFU/mL ~3 h Milk and pear juice [69]
E. coli O157:H7; cell Fc-Dox; multiple amplification through the 3D DNA walker, RCA, and HCR 10–104 CFU/mL 7 CFU/mL ~2 h N/A [70]
S. aureus; 16S rRNA Silver wire across electrodes; hairpin labeled AuNPs 50–107 CFU/mL 50 CFU/mL 100 min Milk [71]
S. Typhimurium;cell CRISPR-Cas12a; electrode surface modification of electrical response reporting probes 104–108 CFU/mL 20 CFU/mL ~2.5 h Milk [72]
Clostridium Perfringens; DNA DNA-Walker; methylene blue; dual-mode output 1–108 CFU/g 1 CFU/g N/A Chicken, beef, duck, mutton, and pork [78]
Surface-enhanced Raman scattering S. aureus; cell Au@Ag/4-ATP; PDMS-based SERS platform 28–2.8 × 106 CFU/mL 0.25 CFU/mL 2.5 h Milk [80]
S. Typhimurium; cell AgNP/DAPI; competitive indirect strategies 10–105 CFU/mL 6 CFU/mL 3.5 h Milk [81]
S. Typhimurium; cell 4-NTP/AuNPs; G-quadruplex DNAzyme 5–105 CFU/mL 4 CFU/mL 105 min Milk and tap water [82]
POC test S. enteritidis; DNA Lateral flow; Sandwich structure 2.5 pM–500 nM 1.76 pM ~25 min N/A [83]
S. enteritidis; 16S rRNA Lateral flow; “initiators-on-a-string”complex 102–104 CFU/mL 53.65 CFU/mL ~40 min Milk [84]
E. coli O157:H7; 16S rRNA Lateral flow; ISD 102–105 CFU/mL 102 CFU/mL ~1.5 h Milk [85]
Vibrio parahaemolyticus; cell Lateral flow; MBs; sandwich structure 103–108 CFU/mL 2.6 × 103 CFU/mL 67 min Shrimp [92]
E. coli O157:H7; cell Microfluidic chip; PtNPs 5 × 102–5 × 107 CFU/mL 250 CFU/mL in buffer and 400 CFU/mL in milk 75 min Milk [95]
S. aureus; S. enteritidis Microfluidic chip; multi-mode analysis 3.6 × 101–3.6 × 106 CFU/mL 4 and 8 CFU/mL, respectively 15 min Nonfat milk powder and raw ground pork [96]
E. coli O157:H7; cell Pregnancy test strips and MOF; sandwich structure 103–107 CFU/mL 530 CFU/mL 86 min Milk [93]
S. aureus; cell Personal glucose meter; the invertase catalyzes sucrose into glucose 3–3 × 103 CFU/mL 2 CFU/mL 4.5 h Peach juice, milk, and water samples [94]
Others
Surface plasmon resonance (SPR) S. aureus, Klebsiella pneumoniae and Escherichia coli; DNA MNAzyme 1 × 102–1 × 106 CFU/mL 67 CFU/mL of S. aureus, 57 CFU/mL of K. pneumonia and 61 CFU/mL of E. coli 4 h N/A [97]
Chemiluminescence (CL) L. monocytogenes; hlyA gene Cloth-based microfluidics; G-quadruplex DNAzyme 2 × 10−3–2 × 106 pM 1.1 fM 80 min Milk [98]
Electrochemiluminescence (ECL) E. coli O157:H7; genomic DNA Cloth-based microfluidics; Ru(bpy)32+ 102–107 CFU/mL 38 CFU/mL ~100 min Milk [99]

Note: N/A means not available.