Simple and label-free pathogen enrichment via homobifunctional imidoesters using a microfluidic (SLIM) system for ultrasensitive pathogen detection in various clinical specimens

Abstract Diseases caused by pathogenic microorganisms including bacteria and viruses can cause serious medical issues including death and result in huge economic losses. Despite the myriad of recent advances in the rapid and accurate detection of pathogens, large volume clinical samples with a low concentration of pathogens continue to present challenges for diagnosis and surveillance. We here report a simple and label-free approach via homobifunctional imidoesters (HIs) with a microfluidic platform (SLIM) to efficiently enrich and extract pathogens at low concentrations from clinical samples. The SLIM system consists of an assembled double microfluidic chip for streamlining large volume processing and HIs for capturing pathogens and isolating nucleic acids by both electrostatic and covalent interaction without a chaotropic detergent or bulky instruments. The SLIM system significantly increases the enrichment and extraction rate of pathogens (up to 80% at 10 CFU (colony forming unit) in a 1 mL volume within 50 min). We demonstrated its clinical utility in large sample volumes from 46 clinical specimens including environmental swabs, saliva, and blood plasma. The SLIM system showed higher sensitivity with these samples and could detect pathogens that were below the threshold of detection with other methods. Finally, by combining our SLIM approach with an isothermal optical sensor, pathogens could be detected at a very high sensitivity in blood plasma samples within 80 min via enrichment, extraction and detection steps. Our SLIM system thus provides a simple, reliable, cost-effective and ultrasensitive pathogen diagnosis platform for use with large volume clinical samples and would thus have significant utility for various infectious diseases.

[1]  Ji Yeun Kim,et al.  Rapid Diagnosis of Tick-Borne Illnesses by Use of One-Step Isothermal Nucleic Acid Amplification and Bio-Optical Sensor Detection. , 2018, Clinical chemistry.

[2]  Nae Yoon Lee,et al.  An integrated microfluidic PCR system with immunomagnetic nanoparticles for the detection of bacterial pathogens , 2016, Biomedical microdevices.

[3]  Anthony S Fauci,et al.  The perpetual challenge of infectious diseases. , 2012, The New England journal of medicine.

[4]  E. Mardis Next-generation DNA sequencing methods. , 2008, Annual review of genomics and human genetics.

[5]  Michael C. McAlpine,et al.  Electrical detection of pathogenic bacteria via immobilized antimicrobial peptides , 2010, Proceedings of the National Academy of Sciences.

[6]  H. Pennington Politics, media and microbiologists , 2004, Nature Reviews Microbiology.

[7]  E. Lau,et al.  Kinetics of Serologic Responses to MERS Coronavirus Infection in Humans, South Korea , 2015, Emerging infectious diseases.

[8]  Obi L. Griffith,et al.  The Genome Sequence of the SARS-Associated Coronavirus , 2003, Science.

[9]  Y. Yeh,et al.  Point-of-Care Microdevices for Blood Plasma Analysis in Viral Infectious Diseases , 2014, Annals of Biomedical Engineering.

[10]  Douglas A. Granger,et al.  Integration of salivary biomarkers into developmental and behaviorally-oriented research: Problems and solutions for collecting specimens , 2007, Physiology & Behavior.

[11]  Tae Yoon Lee,et al.  A disposable lab-on-a-chip platform for highly efficient RNA isolation , 2018 .

[12]  A P Turner,et al.  Immunomagnetic separation with mediated flow injection analysis amperometric detection of viable Escherichia coli O157. , 1998, Analytical chemistry.

[13]  Tae Yoon Lee,et al.  Use of Dimethyl Pimelimidate with Microfluidic System for Nucleic Acids Extraction without Electricity. , 2017, Analytical chemistry.

[14]  O. Ozhelvaci,et al.  Evaluation of convenient pretreatment protocols for RNA virus metagenomics in serum and tissue samples. , 2015, Journal of virological methods.

[15]  S. Hanash,et al.  Emerging molecular biomarkers—blood-based strategies to detect and monitor cancer , 2011, Nature Reviews Clinical Oncology.

[16]  James E. Crowe,et al.  Structural Basis of Preexisting Immunity to the 2009 H1N1 Pandemic Influenza Virus , 2010, Science.

[17]  Jr-Lung Lin,et al.  Purification and enrichment of virus samples utilizing magnetic beads on a microfluidic system. , 2007, Lab on a chip.

[18]  Tae Yoon Lee,et al.  Dimethyl adipimidate/Thin film Sample processing (DTS); A simple, low-cost, and versatile nucleic acid extraction assay for downstream analysis , 2015, Scientific Reports.

[19]  E. Breitschwerdt,et al.  A combined approach for the enhanced detection and isolation of Bartonella species in dog blood samples: pre-enrichment liquid culture followed by PCR and subculture onto agar plates. , 2007, Journal of microbiological methods.

[20]  T. Kim,et al.  Molecular epidemiology and environmental contamination during an outbreak of parainfluenza virus 3 in a haematology ward , 2017, Journal of Hospital Infection.

[21]  David A. Rasko,et al.  Bacterial genome sequencing in the clinic: bioinformatic challenges and solutions , 2013, Nature Reviews Genetics.

[22]  Jennifer L. Gardy,et al.  Towards a genomics-informed, real-time, global pathogen surveillance system , 2017, Nature Reviews Genetics.

[23]  Ji Yeun Kim,et al.  Diagnostic Usefulness of Varicella-Zoster Virus Real-Time Polymerase Chain Reaction Analysis of DNA in Saliva and Plasma Specimens From Patients With Herpes Zoster , 2017, The Journal of infectious diseases.

[24]  Nigel Beard,et al.  Dealing with real samples: sample pre-treatment in microfluidic systems. , 2003, Lab on a chip.