Publications by authors named "Yothin Hinwan"

Article Synopsis
  • Adult-onset immunodeficiency (AOID) is linked to anti-IFN-γ autoantibodies (auAbs), which may increase susceptibility to disseminated nontuberculous mycobacterial (dNTM) infections, alongside other molecular factors.
  • A study involving dNTM patients assessed plasma anti-IFN-γ auAb levels through ELISA and whole-blood RNA sequencing, showing significantly higher auAb levels in active cases compared to inactive patients and healthy controls.
  • The research found that active infection was marked by over-expressed inflammatory pathways, under-expressed type-2 immunity pathways, and elevated plasma IL-8 levels, suggesting IL-8 could potentially serve as a key mediator in
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Background: Next-generation sequencing of , the infectious agent causing tuberculosis, is improving the understanding of genomic diversity of circulating lineages and strain-types, and informing knowledge of drug resistance mutations. An increasingly popular approach to characterizing genomes (size: 4.4 Mbp) and variants (.

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Melioidosis caused by Burkholderia pseudomallei (Bp) is a public health threat. Genomic-epidemiology research on this deadly disease is scarce. We investigated whole-genome sequences of Bp isolates in relation to environmental source and drug susceptibility.

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Melioidosis is caused by Burkholderia pseudomallei (Bp) acquired from the environment. Conventional identification methods for environmental Bp are challenging due to the presence of closely related species. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is accurate for bacterial identification, but has been little used to identify Bp from environmental samples.

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Mycobacterium avium complex (MAC) infections are a significant clinical challenge. Determining drug-susceptibility profiles and the genetic basis of drug resistance is crucial for guiding effective treatment strategies. This study aimed to determine the drug-susceptibility profiles of MAC clinical isolates and to investigate the genetic basis conferring drug resistance using whole-genome sequencing (WGS) analysis.

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