Sample Preparation and qPCR Detection of Tuberculosis on a Centrifugal Microfluidic Cartridge Enabling Molecular Downstream Resistance Profiling ^†

Abstract

Tuberculosis (TB) is still one of the world’s deadliest infections. Fast detection of the pathogen M. tuberculosis (MTB) and its genetic resistance markers substantially improves treatment success and outcome. A key element for rapid genetic diagnostics is the efficient extraction of DNA from sputum for qPCR detection at the point of care. We present the fully automated sample preparation of MTB DNA from 3 mL of liquefied sputum and qPCR detection of MTB on a centrifugal microfluidic cartridge. Our method achieves a limit of detection (LoD) between 17 and 57 CFU/mL and provides a purified DNA solution for molecular downstream testing, such as targeted NGS.

1. Introduction

Only a few fully automated point-of-care solutions are available for TB diagnostics [1,2], and none of them provide extracted DNA for subsequent comprehensive antibiotic resistance testing from the same sample. Here, we present a new sample preparation of MTB DNA using centrifugal microfluidics, a technology dedicated to implementing complex workflows on compact cartridges [3]. However, to date, fully automated centrifugal microfluidic sample-to-answer approaches have only been demonstrated for small sample volumes [4] or nasal swabs [5]. The combination of a liquefaction and inactivation (LI) reagent with a filter and lysis (FL) module allows us to increase sample volumes 15-fold from 200 µL to 3000 µL. It enables the detection of MTB on the cartridge and the provision of the DNA solution in a detachable DNA tube for subsequent resistance profiling.

2. Materials and Methods

The cavity for the FL module is integrated into an injection-molded cartridge (Figure 1A,B). A polyethylene frit (PE3510, SPC Technologies, diameter of 9 mm) and a glass microfiber filter (GMF150, Whatman, diameter of 10 mm) are fixed with a press-fit O-ring (8 × 1.25 mm, FKM, IR-Dichtungstechnik). The custom-developed LI reagent consists of 45% isopropanol, 3% NaOH, 0.5% N-lauroyl-sarcosine, and 0.2% Tween. 1 mL of sputum is mixed with 2 mL of LI reagent and incubated for 20 min.

3. Results and Discussion

For the automation of sample preparation and qPCR detection of MTB from sputum on a centrifugal microfluidic cartridge, the FL module is the key element. It enables the efficient provision of MTB DNA from sputum and consists of a filter frit and a bacteria enrichment filter (Figure 1A). The externally inactivated, liquefied sputum sample is added to the cartridge and filtered, retaining MTB in the bacteria enrichment filter (Figure 2A). A washing step is performed to reduce interfering sputum and LI reagent residues. This is followed by thermal lysis to release the MTB DNA. With this method, large sample volumes of up to 3 mL can be automatically processed and analyzed. Spiking dilutions of H37Rv in sputum identified a LoD between 17 and 57 CFU/mL (Figure 2B). One important achievement is the inactivation and structural weakening of the hard-to-lyse MTB during the LI step while not losing the DNA. MTB DNA can be efficiently released by thermal lysis and subsequently used for qPCR-based MTB detection on the cartridge. Resistance profiles can be generated externally downstream using the DNA solution obtained via the DNA tube interface, as depicted in Figure 1C.