Publications by authors named "Oliver Chiu Kit Ma"

An in-house-developed target amplicon sequencing by next-generation sequencing technology (TB-NGS) enables simultaneous detection of resistance-related mutations in (MTB) against 8 anti-tuberculosis drug classes. In this multi-center study, we investigated the clinical utility of incorporating TB-NGS for rapid drug-resistant MTB detection in high endemic regions in southeast China. From January 2018 to November 2019, 4,047 respiratory specimens were available from patients suffering lower respiratory tract infections in Hong Kong and Guangzhou, among which 501 were TB-positive as detected by in-house IS6110-qPCR assay with diagnostic sensitivity and specificity of 97.

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Background: The emergence of Mycobacterium tuberculosis with complex drug resistance profiles necessitates a rapid and comprehensive drug susceptibility test for guidance of patient treatment. We developed two targeted-sequencing workflows based on Illumina MiSeq and Nanopore MinION for the prediction of drug resistance in M. tuberculosis toward 12 antibiotics.

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Article Synopsis
  • An evaluation was conducted on the effectiveness of a new in-house duplex nested IS6110 real-time PCR assay for diagnosing pulmonary tuberculosis (TB) quickly and accurately.
  • The study analyzed 503 sputum samples, determining the diagnostic accuracy using ROC curve analysis, resulting in a high sensitivity of 97.2% and specificity of 99.7% at an optimal Ct value of 24.140.
  • The IS6110-qPCR assay showed no cross-reactivity with other non-tuberculous mycobacteria and is deemed a cost-effective option for TB screening, especially in resource-limited areas facing high TB rates.
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Multidrug-resistant tuberculosis (MDR-TB) is posing a major threat to global TB control. In this study, we focused on two consecutive MDR-TB isolated from the same patient before and after the initiation of anti-TB treatment. To better understand the genomic characteristics of MDR-TB, Single Molecule Real-Time (SMRT) Sequencing and comparative genomic analyses was performed to identify mutations that contributed to the stepwise development of drug resistance and growth fitness in MDR-TB under challenge of anti-TB drugs.

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