Literature DB >> 20446698

Nanoliter multiplex PCR arrays on a SlipChip.

Feng Shen1, Wenbin Du, Elena K Davydova, Mikhail A Karymov, Janmajay Pandey, Rustem F Ismagilov.   

Abstract

The SlipChip platform was tested to perform high-throughput nanoliter multiplex PCR. The advantages of using the SlipChip platform for multiplex PCR include the ability to preload arrays of dry primers, instrument-free sample manipulation, small sample volume, and high-throughput capacity. The SlipChip was designed to preload one primer pair per reaction compartment and to screen up to 384 different primer pairs with less than 30 nanoliters of sample per reaction compartment. Both a 40-well and a 384-well design of the SlipChip were tested for multiplex PCR. In the geometries used here, the sample fluid was spontaneously compartmentalized into discrete volumes even before slipping of the two plates of the SlipChip, but slipping introduced additional capabilities that made devices more robust and versatile. The wells of this SlipChip were designed to overcome potential problems associated with thermal expansion. By using circular wells filled with oil and overlapping them with square wells filled with the aqueous PCR mixture, a droplet of aqueous PCR mixture was always surrounded by the lubricating fluid. In this design, during heating and thermal expansion, only oil was expelled from the compartment and leaking of the aqueous solution was prevented. Both 40-well and 384-well devices were found to be free from cross-contamination, and end point fluorescence detection provided reliable readout. Multiple samples could also be screened on the same SlipChip simultaneously. Multiplex PCR was validated on the 384-well SlipChip with 20 different primer pairs to identify 16 bacterial and fungal species commonly presented in blood infections. The SlipChip correctly identified five different bacterial or fungal species in separate experiments. In addition, the presence of the resistance gene mecA in methicillin resistant Staphylococcus aureus (MRSA) was identified. The SlipChip will be useful for applications involving PCR arrays and lays the foundation for new strategies for diagnostics, point-of-care devices, and immobilization-based arrays.

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Year:  2010        PMID: 20446698      PMCID: PMC2916686          DOI: 10.1021/ac1007249

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  77 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-05       Impact factor: 11.205

4.  Evaluation of the Xpert methicillin-resistant Staphylococcus aureus (MRSA) assay using the GeneXpert real-time PCR platform for rapid detection of MRSA from screening specimens.

Authors:  Angela S Rossney; Celine M Herra; Gráinne I Brennan; Pamela M Morgan; Brian O'Connell
Journal:  J Clin Microbiol       Date:  2008-08-06       Impact factor: 5.948

5.  Limited T-cell receptor beta-chain heterogeneity among interleukin 2 receptor-positive synovial T cells suggests a role for superantigen in rheumatoid arthritis.

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Journal:  Proc Natl Acad Sci U S A       Date:  1991-12-01       Impact factor: 11.205

6.  Detection of Staphylococcus aureus by polymerase chain reaction amplification of the nuc gene.

Authors:  O G Brakstad; K Aasbakk; J A Maeland
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Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

9.  Integrated portable genetic analysis microsystem for pathogen/infectious disease detection.

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10.  Large scale multiplex PCR improves pathogen detection by DNA microarrays.

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  31 in total

1.  Theoretical design and analysis of multivolume digital assays with wide dynamic range validated experimentally with microfluidic digital PCR.

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Review 2.  The role of physiological heterogeneity in microbial population behavior.

Authors:  Mary E Lidstrom; Michael C Konopka
Journal:  Nat Chem Biol       Date:  2010-09-17       Impact factor: 15.040

3.  Individually addressable arrays of replica microbial cultures enabled by splitting SlipChips.

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Journal:  Integr Biol (Camb)       Date:  2014-08       Impact factor: 2.192

4.  Robust dipstick urinalysis using a low-cost, micro-volume slipping manifold and mobile phone platform.

Authors:  Gennifer T Smith; Nicholas Dwork; Saara A Khan; Matthew Millet; Kiran Magar; Mehdi Javanmard; Audrey K Ellerbee Bowden
Journal:  Lab Chip       Date:  2016-05-24       Impact factor: 6.799

5.  Behavior of a train of droplets in a fluidic network with hydrodynamic traps.

Authors:  Swastika S Bithi; Siva A Vanapalli
Journal:  Biomicrofluidics       Date:  2010-12-06       Impact factor: 2.800

Review 6.  Slip-driven microfluidic devices for nucleic acid analysis.

Authors:  Weiyuan Lyu; Mengchao Yu; Haijun Qu; Ziqing Yu; Wenbin Du; Feng Shen
Journal:  Biomicrofluidics       Date:  2019-07-12       Impact factor: 2.800

7.  The potential impact of droplet microfluidics in biology.

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Journal:  Anal Chem       Date:  2013-03-15       Impact factor: 6.986

8.  Digital PCR on a SlipChip.

Authors:  Feng Shen; Wenbin Du; Jason E Kreutz; Alice Fok; Rustem F Ismagilov
Journal:  Lab Chip       Date:  2010-07-01       Impact factor: 6.799

9.  Gene-targeted microfluidic cultivation validated by isolation of a gut bacterium listed in Human Microbiome Project's Most Wanted taxa.

Authors:  Liang Ma; Jungwoo Kim; Roland Hatzenpichler; Mikhail A Karymov; Nathaniel Hubert; Ira M Hanan; Eugene B Chang; Rustem F Ismagilov
Journal:  Proc Natl Acad Sci U S A       Date:  2014-06-25       Impact factor: 11.205

10.  Mechanistic evaluation of the pros and cons of digital RT-LAMP for HIV-1 viral load quantification on a microfluidic device and improved efficiency via a two-step digital protocol.

Authors:  Bing Sun; Feng Shen; Stephanie E McCalla; Jason E Kreutz; Mikhail A Karymov; Rustem F Ismagilov
Journal:  Anal Chem       Date:  2013-01-16       Impact factor: 6.986

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