4.8 Article

A versatile loop-mediated isothermal amplification microchip platform for Streptococcus pneumoniae and Mycoplasma pneumoniae testing at the point of care

Journal

BIOSENSORS & BIOELECTRONICS
Volume 126, Issue -, Pages 373-380

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2018.11.011

Keywords

Microfluidic chip; Loop-mediated isothermal amplification; Pathogens; Remote visualization; Point-of-care testing

Funding

  1. National Natural Science Foundation of China [81671975]
  2. Shanghai Health System Talent Training Program [2017BR001]
  3. Shanghai Health and Family Planning Commission [20164005]
  4. Cross Research Fund of Biomedical Engineering of Shanghai Jiaotong University [YG2017MS46]
  5. General Program of Shanghai Municipal Commission of Health and Family Planning [201440435]

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Community-acquired pneumonia (CAP) is the leading cause of mortality in children under five years of age, globally. Given that Streptococcus pneumoniae (S. pneumoniae) and Mycoplasma pneumoniae (M. pneumoniae) are the most common pathogens associated with CAP requiring hospital admission, a simple, low cost, highly sensitive method is in great need for immediate and early diagnosis of CAP. Herein, we report a versatile microfluidic chip platform integrated with loop-mediated isothermal amplification (LAMP) for simultaneous S. pneumoniae and M. pneumoniae testing at the point of care. The platform includes a polymer/paper microfluidic chip and a portable device. On-chip magnetic particle-based nucleic acid extraction is used for concentration of pathogens' genomic DNA and is followed by LAMP. The portable device has the function of heating the microfluidic chip, and photographing and transmitting the result to a smartphone. Complete extraction of the DNA using the microfluidic chip took similar to 15 min versus > 1.5 h with a phenol-chloroform method. The analytical sensitivity of the assay was determined to be 20 fg by testing serial dilutions of target DNA ranging from 2 ng to 2 fg per reaction. We evaluated the clinical sensitivity and specificity of the IP mu chip assay using 63 randomly selected oropharyngeal swabs and bronchoalveolar lavage fluid specimens from children. For comparison, these specimens were also tested against real-time PCR assay (M. pneumoniae), conventional PCR assay (S. pneumoniae), and culture tests (S. pneumoniae). These results yielded positive and negative predictive values for M. pneumoniae testing with the IP mu chip platform of 96.9% and 100%, respectively. Compared with S. pneumoniae IP chip, the clinical sensitivity of S. pneumoniae PCR and culture tests was 60% and 40%, respectively, while clinical specificity of the two tests was 100%. This versatile IP mu chip platform has great potential for point of care testing of different kinds of pathogens, especially for developing nations.

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