Proof of Concept for a Portable Platform for Molecular Diagnosis of Tropical Diseases: On-Chip Ready-to-Use Real-Time Quantitative PCR for Detection of Trypanosoma cruzi or Plasmodium spp

Although molecular diagnostics is well established in clinical laboratories, its full potential has not been extended to field settings. Typically, diagnostic real-time quantitative PCR (qPCR) reagents require temperature-controlled transportation and storage. Furthermore, thermocyclers are bulky an...

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Veröffentlicht in:The Journal of molecular diagnostics : JMD 2019-09, Vol.21 (5), p.839-851
Hauptverfasser: Rampazzo, Rita C P, Graziani, Ana Cláudia, Leite, Keren K, Surdi, Jhully Anni, Biondo, Cheysa A, Costa, Maykon L N, Jacomasso, Thiago, Cereda, Marco, De Fazio, Marco, Bianchessi, Marco A, Moreira, Otacílio C, Britto, Constança, Costa, Joana D N, Góes, Viviane M, da Silva, Alexandre J, Krieger, Marco A, Costa, Alexandre D T
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container_issue 5
container_start_page 839
container_title The Journal of molecular diagnostics : JMD
container_volume 21
creator Rampazzo, Rita C P
Graziani, Ana Cláudia
Leite, Keren K
Surdi, Jhully Anni
Biondo, Cheysa A
Costa, Maykon L N
Jacomasso, Thiago
Cereda, Marco
De Fazio, Marco
Bianchessi, Marco A
Moreira, Otacílio C
Britto, Constança
Costa, Joana D N
Góes, Viviane M
da Silva, Alexandre J
Krieger, Marco A
Costa, Alexandre D T
description Although molecular diagnostics is well established in clinical laboratories, its full potential has not been extended to field settings. Typically, diagnostic real-time quantitative PCR (qPCR) reagents require temperature-controlled transportation and storage. Furthermore, thermocyclers are bulky and fragile, requiring good infrastructure for optimal operation. These major hurdles strongly limit use of molecular-based tests in low-resource scenarios. Herein, Trypanosoma cruzi or Plasmodium spp. DNA were detected with qPCR using commercial equipment (ABI7500 instrument) and a prototype platform comprising a portable device and a silicon chip, named Q3-Plus. In addition, a ready-to-use reaction format, where all qPCR reagents are stored on plate or on chip, was compared with the traditional freezer-stored format. No significant differences were observed in detecting T. cruzi or Plasmodium spp. DNA between thermocyclers, as well as between reagents' formats, for storage periods of up to 28 days (at 2°C to 8°C or 21°C to 23°C, respectively). When challenged with patients' samples, the Q3-Plus system performed as efficiently as the standard equipment for Plasmodium spp. DNA detection, showing it to be a valuable solution to malaria point-of-care diagnostics. Detection of T. cruzi DNA in chronic patients' samples using the Q3-Plus system yielded approximately 50% efficiency relative to the ABI7500. These results are essential to support future endeavors to bring molecular diagnostics to the point of care, where most needed.
doi_str_mv 10.1016/j.jmoldx.2019.04.008
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title Proof of Concept for a Portable Platform for Molecular Diagnosis of Tropical Diseases: On-Chip Ready-to-Use Real-Time Quantitative PCR for Detection of Trypanosoma cruzi or Plasmodium spp
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