2019
Click-conjugated photon-upconversion nanoparticles in an immunoassay for honeybee pathogen Melissococcus plutonius
POLÁCHOVÁ, Veronika, Matěj PASTUCHA, Zuzana MIKUŠOVÁ, Matthias Jürgen MICKERT, Antonín HLAVÁČEK et. al.Základní údaje
Originální název
Click-conjugated photon-upconversion nanoparticles in an immunoassay for honeybee pathogen Melissococcus plutonius
Autoři
POLÁCHOVÁ, Veronika (203 Česká republika, domácí), Matěj PASTUCHA (203 Česká republika, domácí), Zuzana MIKUŠOVÁ (703 Slovensko, domácí), Matthias Jürgen MICKERT (276 Německo), Antonín HLAVÁČEK (203 Česká republika), Hans-Heiner GORRIS (276 Německo), Petr SKLÁDAL (203 Česká republika, domácí) a Zdeněk FARKA (203 Česká republika, garant, domácí)
Vydání
Nanoscale, Cambridge, Royal Society of Chemistry, 2019, 2040-3364
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10406 Analytical chemistry
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 6.895
Kód RIV
RIV/00216224:14740/19:00108343
Organizační jednotka
Středoevropský technologický institut
UT WoS
000466774500026
Klíčová slova anglicky
Bacteria detection; European foulbrood diagnosis; Upconversion-linked immunosorbent assay; ULISA; Antibody development; Apis mellifera
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 24. 10. 2024 12:54, Mgr. Adéla Pešková
Anotace
V originále
European foulbrood (EFB) is an infectious disease affecting honeybee larvae caused by the bacterium Melissococcus plutonius. The enzyme-linked immunosorbent assay (ELISA) is the gold standard for antibody-based bacteria detection, however, its sensitivity is not high enough to reveal early-stage EFB infection. Photon-upconversion nanoparticles (UCNPs) are lanthanide-doped nanomaterials that emit light of shorter wavelength under near-infrared (NIR) excitation and thus avoid optical background interference. After conjugation with specific biorecognition molecules, UCNPs can be used as ultrasensitive labels in immunoassays. Here, we introduce a method for conjugation of UCNPs with streptavidin based on copper-free click chemistry, which involves surface modification of UCNPs with alkyne-modified bovine serum albumin (BSA) that prevents the non-specific binding and provides reactive groups for conjugation with streptavidin-azide. To develop a sandwich upconversion-linked immunosorbent assay (ULISA) for M. plutonius detection, we have prepared a rabbit polyclonal anti-Melissococcus antibody. The specific capture of the bacteria was followed by binding of biotinylated antibody and UCNP–BSA–streptavidin conjugate for a highly sensitive upconversion readout. The assay yielded an LOD of 340 CFU mL-1 with a wide working range up to 10^9 CFU mL-1, which is 400 times better than the LOD of the conventional ELISA. The practical applicability of the ULISA was successfully demonstrated by detecting M. plutonius in spiked real samples of bees, larvae and bottom hive debris. These results show a great potential of the assay for early diagnosis of EFB, which can prevent uncontrolled spreading of the infection and losses of honeybee colonies.
Návaznosti
LQ1601, projekt VaV |
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MUNI/A/1575/2018, interní kód MU |
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TJ01000386, projekt VaV |
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90043, velká výzkumná infrastruktura |
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