Molecularly Imprinted Nanoparticle Ensembles for Rapidly Identifying S. epidermidis

Author:

Hlaoperm Chularat12,Sudjarwo Wisnu Arfian A.13,Ehrenbrandtner Jakob1,Kiss Endre4,Del Favero Giorgia45ORCID,Choowongkomon Kiattawee6ORCID,Rattanasrisomporn Jatuporn27ORCID,Lieberzeit Peter A.13ORCID

Affiliation:

1. University of Vienna, Faculty for Chemistry, Department of Physical Chemistry, Waehringer Strasse 42, A-1090 Wien, Austria

2. Center for Advanced Studies for Agriculture and Food, Kasetsart University Institute for Advanced Studies, Kasetsart University, Bangkok 10900, Thailand

3. University of Vienna, Faculty for Chemistry, Doctoral School of Chemistry, Waehringer Strasse 42, A-1090 Vienna, Austria

4. University of Vienna, Faculty for Chemistry, Core Facility Multimodal Imaging, Waehringer Strasse 38, A-1090 Vienna, Austria

5. University of Vienna, Faculty for Chemistry, Department of Food Chemistry and Toxicology, Waehringer Strasse 38, A-1090 Vienna, Austria

6. Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand

7. Department of Companion Animal Clinical Sciences, Faculty of Veterinary Medicine, Kasetsart University, Kamphaeng Saen Campus, Nakhon Pathom 73140, Thailand

Abstract

Staphylococcus epidermidis (S. epidermidis) belongs to methicillin-resistant bacteria strains that cause severe disease in humans. Herein, molecularly imprinted polymer (MIP) nanoparticles resulting from solid-phase synthesis on entire cells were employed as a sensing material to identify the species. MIP nanoparticles revealed spherical shapes with diameters of approximately 70 nm to 200 nm in scanning electron microscopy (SEM), which atomic force microscopy (AFM) confirmed. The interaction between nanoparticles and bacteria was assessed using height image analysis in AFM. Selective binding between MIP nanoparticles and S. epidermidis leads to uneven surfaces on bacteria. The surface roughness of S. epidermidis cells was increased to approximately 6.3 ± 1.2 nm after binding to MIP nanoparticles from around 1 nm in the case of native cells. This binding behavior is selective: when exposing Escherichia coli and Bacillus subtilis to the same MIP nanoparticle solutions, one cannot observe binding. Fluorescence microscopy confirms both sensitivity and selectivity. Hence, the developed MIP nanoparticles are a promising approach to identify (pathogenic) bacteria species.

Funder

University of Vienna

Office of the Ministry of Higher Education, Science, Research and Innovation; and the Thailand Science Research and Innovation through the Kasetsart University Reinventing University Program 2021

the Faculty of Veterinary Medicine, Kasetsart university; and the Kasetsart University Research and Development Institute (KURDI) Bangkok, Thailand

ASEAN-European Academic University Network

the Austrian Federal Ministry of Education, Science and Research

the OeAD—Austria’s Agency for Education and Internationalization

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Biochemistry,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

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