Atypical morphological characteristics and surface antigen expression of Burkholderia pseudomallei in naturally

R Nanagara1, K Vipulakorn, S Suwannaroj

  • 1Department of Medicine, Faculty of Medicine, KhonKaen University , KhonKaen 40002 , Thailand.

Modern Rheumatology
|January 4, 2014
PubMed

Insights

Burkholderia pseudomallei causes difficult-to-treat melioidosis. In human tissues, this bacterium appears atypical and suppresses surface antigens, aiding survival against host defenses and antibiotics.

Area of Science:

  • Microbiology
  • Immunology
  • Pathogenesis

Background:

  • Melioidosis, caused by Burkholderia pseudomallei, is a severe infection with protracted and difficult-to-eradicate courses.
  • Mechanisms of host defense and antibiotic evasion by B. pseudomallei remain poorly understood.

Purpose of the Study:

  • To compare morphological characteristics and surface antigen expression of B. pseudomallei in naturally infected human synovial tissues versus cultured bacteria.
  • To investigate bacterial adaptation strategies in vivo.

Main Methods:

  • Immunoelectron microscopy was used on synovial biopsies from four B. pseudomallei septic arthritis patients.
  • Pathogenic B. pseudomallei from culture media served as positive controls.
  • A polyclonal antibody to whole cell B. pseudomallei was employed for immunogold staining.

Main Results:

  • B. pseudomallei particles were observed both extracellularly and intracellularly within synovial tissues.
  • Intracytoplasmic bacteria and mononuclear phagosomes with microcolony-like structures were identified.
  • Bacteria in synovial samples showed atypical morphology with reduced electron lucent granules and weaker surface antigen expression compared to controls.

Conclusions:

  • Atypical forms of B. pseudomallei with suppressed surface antigens were found in naturally infected human synovial tissues.
  • These adaptations likely contribute to bacterial survival against host immune surveillance and antibiotic treatment.
  • Understanding these mechanisms is crucial for developing effective melioidosis therapies.

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