AI Article Synopsis

  • Recent advancements in tuberculosis (TB) diagnostics have improved patient survival rates, but challenges with early detection persist due to inefficiency and high costs of existing methods.
  • A new portable, user-friendly, and affordable biosensor device has been developed for the early detection of TB, using a label-free surface plasmon resonance (SPR) method to quantify heat shock protein X (HspX) directly in sputum samples.
  • This biosensor achieves impressive sensitivity with a limit of detection at 0.63 ng/mL and a limit of quantification at 2.12 ng/mL, demonstrating significant differences in HspX levels between TB-infected patients and non-infected individuals.

Article Abstract

Advancements that occurred during the last years in the diagnosis of (), the causative agent of tuberculosis infection, have prompted increased survival rates of patients. However, limitations related to the inefficiency of an early detection still remain; some techniques and laboratory methods do not have enough specificity and most instruments are expensive and require handling by trained staff. In order to contribute to a prompt and effective diagnosis of tuberculosis, we report the development of a portable, user-friendly, and low-cost biosensor device for its early detection. By using a label-free surface plasmon resonance (SPR) biosensor, we have established a direct immunoassay for the direct detection and quantification of the heat shock protein X (HspX) of , a well-established biomarker of this pathogen, directly in pretreated sputum samples. The method relies on highly specific monoclonal antibodies that are previously immobilized on the plasmonic sensor surface. This technology allows for the direct detection of the biomarker without amplification steps, showing a limit of detection (LOD) of 0.63 ng mL and a limit of quantification (LOQ) of 2.12 ng mL. The direct analysis in pretreated sputum shows significant differences in the HspX concentration in patients with tuberculosis (with concentration levels in the order of 116-175 ng mL) compared with non-tuberculosis infected patients (values below the LOQ of the assay).

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http://dx.doi.org/10.1021/acsinfecdis.9b00502DOI Listing

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