» Articles » PMID: 38351361

High-affinity Truncated Aptamers for Detection of Cronobacter Spp with Magnetic Separation-assisted DNAzyme-driven 3D DNA Walker

Overview
Journal Mikrochim Acta
Specialties Biotechnology
Chemistry
Date 2024 Feb 13
PMID 38351361
Authors
Affiliations
Soon will be listed here.
Abstract

After optimizing the original aptamer sequence by truncation strategy, a magnetic separation-assisted DNAzyme-driven 3D DNA walker fluorescent aptasensor was developed for detecting the food-borne pathogen Cronobacter species. Iron oxide magnetic nanoparticles (MNPs) modified with a hybrid of truncated aptamer probe and DNAzyme strand (AP-E1) denoted as MNPs@AP-E1, were employed as capture probes. Simultaneously, a DNAzyme-driven 3D-DNA walker was utilized as the signal amplification element. The substrate strand (Sub) was conjugated with the gold nanoparticles (AuNPs), resulting in the formation of AuNPs@Sub, which served as a 3D walking track. In the presence of the target bacteria and Mg, E1-DNAzyme was activated and moved along AuNPs@Sub, continuously releasing the signal probe. Under optimized conditions, a strong linear correlation was observed for Cronobacter sakazakii (C. sakazakii) in the concentration range 10 to 10 CFU mL, with a low detection limit of 2 CFU mL. The fluorescence signal responses for different Cronobacter species exhibited insignificant differences, with a relative standard deviation of 3.6%. Moreover, the aptasensor was successfully applied to determine  C. sakazakii in real samples with recoveries of 92.86%-108.33%. Therefore, the novel method could be a good candidate for ultra-sensitive and selective detection of Cronobacter species without complex manipulation.

Citing Articles

Aptamer's Structure Optimization for Better Diagnosis and Treatment of Glial Tumors.

Koshmanova A, Artyushenko P, Shchugoreva I, Fedotovskaya V, Luzan N, Kolovskaya O Cancers (Basel). 2024; 16(23).

PMID: 39682297 PMC: 11640682. DOI: 10.3390/cancers16234111.

References
1.
Jackson E, Sonbol H, Masood N, Forsythe S . Genotypic and phenotypic characteristics of Cronobacter species, with particular attention to the newly reclassified species Cronobacter helveticus, Cronobacter pulveris, and Cronobacter zurichensis. Food Microbiol. 2014; 44:226-35. DOI: 10.1016/j.fm.2014.06.013. View

2.
Craven H, McAuley C, Hannah M, Duffy L, Fegan N, Forsythe S . Applicability of Enterobacteriaceae and coliforms tests as indicators for Cronobacter in milk powder factory environments. Food Microbiol. 2020; 94:103642. DOI: 10.1016/j.fm.2020.103642. View

3.
Hawkins R, Lissner C, SANFORD J . Enterobacter sakazakii bacteremia in an adult. South Med J. 1991; 84(6):793-5. DOI: 10.1097/00007611-199106000-00033. View

4.
Shukla S, Haldorai Y, Bajpai V, Rengaraj A, Hwang S, Song X . Electrochemical coupled immunosensing platform based on graphene oxide/gold nanocomposite for sensitive detection of Cronobacter sakazakii in powdered infant formula. Biosens Bioelectron. 2018; 109:139-149. DOI: 10.1016/j.bios.2018.03.010. View

5.
Zhu Y, Wang D . Rapid Detection of Enterobacter Sakazakii in milk Powder using amino modified chitosan immunomagnetic beads. Int J Biol Macromol. 2016; 93(Pt A):615-622. DOI: 10.1016/j.ijbiomac.2016.09.024. View