Detailed Information on Publication Record
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.Basic information
Original name
Click-conjugated photon-upconversion nanoparticles in an immunoassay for honeybee pathogen Melissococcus plutonius
Authors
POLÁCHOVÁ, Veronika (203 Czech Republic, belonging to the institution), Matěj PASTUCHA (203 Czech Republic, belonging to the institution), Zuzana MIKUŠOVÁ (703 Slovakia, belonging to the institution), Matthias Jürgen MICKERT (276 Germany), Antonín HLAVÁČEK (203 Czech Republic), Hans-Heiner GORRIS (276 Germany), Petr SKLÁDAL (203 Czech Republic, belonging to the institution) and Zdeněk FARKA (203 Czech Republic, guarantor, belonging to the institution)
Edition
Nanoscale, Cambridge, Royal Society of Chemistry, 2019, 2040-3364
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10406 Analytical chemistry
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 6.895
RIV identification code
RIV/00216224:14740/19:00108343
Organization unit
Central European Institute of Technology
UT WoS
000466774500026
Keywords in English
Bacteria detection; European foulbrood diagnosis; Upconversion-linked immunosorbent assay; ULISA; Antibody development; Apis mellifera
Tags
International impact, Reviewed
Změněno: 24/10/2024 12:54, Mgr. Adéla Pešková
Abstract
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.
Links
LQ1601, research and development project |
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MUNI/A/1575/2018, interní kód MU |
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TJ01000386, research and development project |
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90043, large research infrastructures |
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