A nanoparticle-based method for culture-free bacterial DNA enrichment from whole blood.

Point-of-care (POC) diagnostics are one of the quick and sensitive detection approaches used in current clinical applications, but always face a performance tradeoff between time-to-result and assay sensitivity. One critical setting where these limitations are evident is the detection of sepsis, where 6-10mL of whole blood may contain as little as one bacterial colony forming unit (cfu). The large sample volume, complex nature of the sample and low analyte concentration necessitates signal enhancement using culture-based or molecular amplification techniques. In the time-critical diagnosis of sepsis, waiting for up to 24h to produce sufficient DNA for analysis is not possible. As a consequence, there is a need for integrated sample preparation methods that could enable shorter detection times, whilst maintaining high analytical performance. We report the development of a culture-free bacterial enrichment method to concentrate bacteria from whole blood in less than 3h. The method relies on triple-enrichment steps to magnetically concentrate bacterial cells and their DNA with a 500-fold reduction in sample volume (from 10 to 0.02mL). Using this sample preparation method, sensitive qPCR detection of the extracted S. aureus bacterial DNA was achieved with a detection limit of 5±0.58cfu/mL within a total elapsed time of 4h; much faster than conventional culture-based approaches. The method could be fully automated for integration into clinical practice for point-of-care or molecular detection of bacterial DNA from whole blood.

[1]  R. Zengerle,et al.  Microfluidic lab-on-a-chip platforms: requirements, characteristics and applications. , 2010, Chemical Society reviews.

[2]  P. Yager,et al.  Point-of-care diagnostics for global health. , 2008, Annual review of biomedical engineering.

[3]  A. Elaissari,et al.  Magnetic particles: From preparation to lab-on-a-chip, biosensors, microsystems and microfluidics applications , 2016 .

[4]  J. Justin Gooding,et al.  Electrochemical DNA Hybridization Biosensors , 2002 .

[5]  Vincent M. Rotello,et al.  Applications of Nanoparticles in Biology , 2008 .

[6]  Rapid detection of bacterial cell from whole blood: Integration of DNA sample preparation into single micro-PCR chip , 2011 .

[7]  Samuel K Sia,et al.  Commercialization of microfluidic point-of-care diagnostic devices. , 2012, Lab on a chip.

[8]  Angelika Niemz,et al.  Point-of-care nucleic acid testing for infectious diseases. , 2011, Trends in biotechnology.

[9]  Joseph Wang,et al.  Nanoparticle-based electrochemical DNA detection , 2003 .

[10]  D. Di Carlo,et al.  Continuous scalable blood filtration device using inertial microfluidics , 2010, Biotechnology and bioengineering.

[11]  Utkan Demirci,et al.  Portable microfluidic chip for detection of Escherichia coli in produce and blood , 2012, International journal of nanomedicine.

[12]  Tassaneewan Laksanasopin,et al.  Point-of-Care Diagnostics: Recent Developments in a Connected Age. , 2017, Analytical chemistry.

[13]  David E. Williams,et al.  Point of care diagnostics: status and future. , 2012, Analytical chemistry.

[14]  Hakho Lee,et al.  A magneto-DNA nanoparticle system for rapid detection and phenotyping of bacteria. , 2013, Nature nanotechnology.

[15]  W. Russ Algar,et al.  Toward point-of-care diagnostics with consumer electronic devices: the expanding role of nanoparticles , 2015 .

[16]  D. Alland,et al.  Highly Sensitive Detection of Staphylococcus aureus Directly from Patient Blood , 2012, PloS one.

[17]  K. Lewis,et al.  Persister cells and tolerance to antimicrobials. , 2004, FEMS microbiology letters.

[18]  Philippe Colson,et al.  Modern clinical microbiology: new challenges and solutions , 2013, Nature Reviews Microbiology.

[19]  R. Bhattacharyya,et al.  Direct detection and drug-resistance profiling of bacteremias using inertial microfluidics. , 2015, Lab on a chip.

[20]  Pedro Estrela,et al.  Point-of-Care Diagnostics in Low Resource Settings: Present Status and Future Role of Microfluidics , 2015, Biosensors.

[21]  Helen H. Lee,et al.  Sample preparation: a challenge in the development of point-of-care nucleic acid-based assays for resource-limited settings. , 2007, The Analyst.

[22]  Andrea Pavesi,et al.  Advances in microfluidics in combating infectious diseases , 2016, Biotechnology Advances.

[23]  M. Tabrizian,et al.  Microfluidic designs and techniques using lab-on-a-chip devices for pathogen detection for point-of-care diagnostics. , 2012, Lab on a chip.

[24]  Anthony P F Turner,et al.  Biosensors: sense and sensibility. , 2013, Chemical Society reviews.

[25]  Christopher B. Raub,et al.  Sequestration of bacteria from whole blood by optimized microfluidic cross-flow filtration for Rapid Antimicrobial Susceptibility Testing , 2015 .

[26]  J. Puckridge,et al.  The dissociation of proteins by chaotropic salts. , 1973, The Journal of biological chemistry.

[27]  Richard A Robison,et al.  Rapid separation of bacteria from blood—review and outlook , 2016, Biotechnology progress.

[28]  Robert Wilson The use of gold nanoparticles in diagnostics and detection. , 2008, Chemical Society reviews.

[29]  M. Mäki Bacterial and fungal DNA extraction from positive blood culture bottles: a manual and an automated protocol. , 2015, Methods in molecular biology.

[30]  C. Schrader,et al.  PCR inhibitors – occurrence, properties and removal , 2012, Journal of applied microbiology.

[31]  Miqin Zhang,et al.  Design and fabrication of magnetic nanoparticles for targeted drug delivery and imaging. , 2010, Advanced drug delivery reviews.

[32]  D. Ecker,et al.  Improved Sensitivity for Molecular Detection of Bacterial and Candida Infections in Blood , 2014, Journal of Clinical Microbiology.

[33]  Roland Zengerle,et al.  Automated nucleic acid extraction from whole blood, B. subtilis, E. coli, and Rift Valley fever virus on a centrifugal microfluidic LabDisk , 2015 .

[34]  K. J. Jeong,et al.  Synthetic ligand-coated magnetic nanoparticles for microfluidic bacterial separation from blood. , 2014, Nano letters.

[35]  Anubhav Tripathi,et al.  Microfluidic Sample Preparation for Medical Diagnostics. , 2015, Annual review of biomedical engineering.

[36]  Kwang S. Kim,et al.  Fast DNA sequencing with a graphene-based nanochannel device. , 2011, Nature nanotechnology.

[37]  Jongyoon Han,et al.  Large-Volume Microfluidic Cell Sorting for Biomedical Applications. , 2015, Annual review of biomedical engineering.

[38]  Ye Ai,et al.  Separation of Escherichia coli Bacteria from Peripheral Blood Mononuclear Cells Using Standing Surface Acoustic Waves , 2013, Analytical chemistry.

[39]  M. Cooper,et al.  Surface Ligand Density of Antibiotic-Nanoparticle Conjugates Enhances Target Avidity and Membrane Permeabilization of Vancomycin-Resistant Bacteria. , 2017, Bioconjugate chemistry.

[40]  H. Postma,et al.  Rapid sequencing of individual DNA molecules in graphene nanogaps. , 2008, Nano letters.

[41]  J. Yother Capsules of Streptococcus pneumoniae and other bacteria: paradigms for polysaccharide biosynthesis and regulation. , 2011, Annual review of microbiology.

[42]  James R. Knight,et al.  Genome sequencing in microfabricated high-density picolitre reactors , 2005, Nature.

[43]  Jeffrey N. Weiser,et al.  The role of Streptococcus pneumoniae virulence factors in host respiratory colonization and disease , 2008, Nature Reviews Microbiology.

[44]  L. Barth Reller,et al.  Detection of Bloodstream Infections in Adults: How Many Blood Cultures Are Needed? , 2006, Journal of Clinical Microbiology.

[45]  Nathaniel C. Cady,et al.  Nucleic Acid-based Detection of Bacterial Pathogens Using Integrated Microfluidic Platform Systems , 2009, Sensors.

[46]  H. Brismar,et al.  Microfluidic-based isolation of bacteria from whole blood for sepsis diagnostics , 2014, Biotechnology Letters.

[47]  Joseph Wang Electrochemical nucleic acid biosensors , 2002 .

[48]  Alan Ashworth,et al.  Noninvasive Detection of HER2 Amplification with Plasma DNA Digital PCR , 2013, Clinical Cancer Research.

[49]  Gwo-Bin Lee,et al.  Nucleic acid amplification using microfluidic systems. , 2013, Lab on a chip.

[50]  Mehmet Toner,et al.  Blood-on-a-chip. , 2005, Annual review of biomedical engineering.

[51]  P. François,et al.  Molecular diagnosis of bloodstream infections: planning to (physically) reach the bedside , 2010, Current opinion in infectious diseases.