Publications by authors named "Zubeida Salaam-Dreyer"

Article Synopsis
  • The study examines how compensatory evolution affects the transmission of rifampicin-resistant tuberculosis in Khayelitsha, South Africa, highlighting its potential to mitigate fitness costs associated with drug resistance.
  • Over a period from 2008 to 2017, data from 2,161 individuals with multidrug or rifampicin-resistant tuberculosis were analyzed, finding that compensatory mutations were linked to more severe forms of the disease and a greater number of drug-resistance mutations.
  • The results indicate that compensatory evolution can lead to increased transmission rates of rifampicin-resistant tuberculosis, suggesting it plays a significant role in the spread of the disease, regardless of other influencing factors.
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Treatment of multidrug-resistant or rifampicin-resistant tuberculosis (MDR/RR-TB), although improved in recent years with shorter, more tolerable regimens, remains largely standardized and based on limited drug susceptibility testing (DST). More individualized treatment with expanded DST access is likely to improve patient outcomes. To assess the potential of TB drug resistance prediction based on whole-genome sequencing (WGS) to provide more effective treatment regimens, we applied current South African treatment recommendations to a retrospective cohort of MDR/RR-TB patients from Khayelitsha, Cape Town.

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Background: South Africa has a high burden of rifampicin-resistant tuberculosis (including multidrug-resistant [MDR] tuberculosis), with increasing rifampicin-monoresistant (RMR) tuberculosis over time. Resistance acquisition during first-line tuberculosis treatment could be a key contributor to this burden, and HIV might increase the risk of acquiring rifampicin resistance. We assessed whether HIV during previous treatment was associated with RMR tuberculosis and resistance acquisition among a retrospective cohort of patients with MDR or rifampicin-resistant tuberculosis.

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Rifampin monoresistance (RMR; rifampin resistance and isoniazid susceptibility) accounts for 38% of all rifampin-resistant tuberculosis (RR-TB) in South Africa and is increasing. We aimed to compare RMR-TB with multidrug-resistant TB (MDR-TB) in a setting with high TB, RR-TB, and HIV burdens. Patient-level clinical data and stored RR Mycobacterium tuberculosis isolates from 2008 to 2017 with available whole-genome sequencing (WGS) data were used to describe risk factors associated with RMR-TB and to compare RR-conferring mutations between RMR-TB and MDR-TB.

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