Table 2.
Illustrative works described in the literature employing nanostructures for the detection of animal pathogens
| Target pathogen(s) | Nanostructuresa | Transduction mechanism | LOD or sensitivity | References |
|---|---|---|---|---|
| Canine parvovirus | PNA | Fluorescence | 40–2,000 copies/μl (89.8 %) | [105] |
| Influenza virus (H5) | MB | Fluorescence | 0.6 nM | [37] |
| Influenza virus (H5N1) | GNPs and Ag enhancer | Light scattering | 103 TCID50 units | [69] |
| Influenza virus (H5N1) | DNA aptamer | SPR | 1.28 HAU | [87] |
| Influenza virus (H1N1) | GNPs | Fluorescence and surface-enhanced Raman scattering | – | [93] |
| Influenza virus (H5N1) | Complementary oxide semiconductor (CMOS) | Impedance spectroscopy | 5 nM (10−11 F) | [98] |
| Influenza virus (H5N1) | DNA aptamer/hydrogel | QCM | 0.0128 HAU | [102] |
| 16 avian influenza viruses | Magnetic beads | Colorimetry (HA test and LAT test) and RT-PCR | 16–1,024 HAU | [106] |
| Feline calicivirus | Liposomes | Fluorescence | 1.6 × 105 PFU/ml | [5] |
| Pestiviruses (Classical swine fever virus; Border disease virus; Bovine viral diarrhea virus 1 and 2) | Magnetic beads | Optic (visual; microscopy; chip reader) | – | [55] |
| Alexandrium sp. complex | PNA and cyanine-derived fluorophore (DiSC2(5)) | Colorimetry | – | [89] |
| B. anthracis | SWCNT | Raman spectroscopy | – | [97] |
| B. anthracis | Electrically active magnetic NPs | Cyclic voltammetry | 0.01 ng/μl | [94] |
| B. anthracis | GNPs | QCM | 3.5 × 102 CFU/ml | [95] |
| B. anthracis; S. enteritidis | GNPs, magnetic NPs and NP tracers (PbS and CdS) | Square wave anodic stripping voltammetry | 50 pg/ml | [90] |
| E. coli | DNA aptamer | Impedance spectroscopy | 10−7 M | [79] |
| E. coli | Alginic acid-coated Co magnetic beads | Transmission electron microscopy | 10 cells/ml | [86] |
| E. coli | Fe2O3/Au magnetic NP and magnetic NPs | Amperometry | 5 CFU/ml | [99] |
| E. coli O157:H7 | Aluminum anodized oxide (AAO) nanopore membrane | Cyclic voltammetry and impedance spectroscopy | 0.5 nM | [91] |
| E. coli O157:H7 | Magnetic beads and QDs | Fluorescence | 250 zM | [104] |
| F. tularensis | MB | Fluorescence | – | [84] |
| M. avium | GNPs | Colorimetry | 1.875 ng/μl (87.5–100 %) | [100] |
| M. tuberculosis; M. bovis | GNPs | Colorimetry | 5 × 10−8 M | [85] |
| S. aureus | GNPs/poly-3,4-ethylenedioxythiophene (PEDOT) film | Chronoamperometry | ≤150 pM | [96] |
| S. aureus | GNPs/PANI nanofibers | Cyclic voltammetry | pM range | [101] |
| S. aureus (MRSA) | PNA | Impedance spectroscopy | 10 pM | [103] |
| Y. enterocolitica | Carbon ionic liquid electrode and V2O5 nanobelt/MWCNT/chitosan | Differential pulse voltammetry | 1.76 × 10−12 M | [92] |
| C. perfringens; C. tetani; S. pneumoniae; P. aeruginosa; E. coli | GNPs | QCM | 1.5 × 102 CFU/ml (94.12 %) | [83] |
| Salmonellae | GNPs and Ag enhancer | Colorimetry | 104 cells | [88] |
aMicro-scaled magnetic particle labels are also considered in this table