Expanding the clinical and genetic spectrum of G6PD deficiency: The occurrence of BCGitis and novel missense mutation

Microb Pathog. 2017 Jan:102:160-165. doi: 10.1016/j.micpath.2016.11.025. Epub 2016 Nov 30.

Abstract

Glucose-6-phosphate dehydrogenase (G6PD) is a key enzyme in the pentose phosphate pathway that ensures sufficient production of coenzyme nicotinamide adenine dinucleotide phosphate (NADPH) by catalyzing the reduction of NADP+ to NADPH. Noteworthy, the latter mediates the production of reactive oxygen species (ROS) by phagocytic cells such as neutrophils and monocytes. Therefore, patients with severe forms of G6PD deficiency may present impaired NADPH oxidase activity and become susceptible to recurrent infections. This fact, highlights the importance to characterize the immunopathologic mechanisms underlying the susceptibility to infections in patients with G6PD deficiency. Here we report the first two cases of G6PD deficiency with Bacille Calmette-Guérin (BCG) adverse effect, besides jaundice, hemolytic anemia and recurrent infections caused by Staphylococcus aureus. The qualitative G6PD screening was performed and followed by oxidative burst analysis using flow cytometry. Genetic and in silico analyses were carried out by Sanger sequencing and mutation pathogenicity predicted using bioinformatics tools, respectively. Activated neutrophils and monocytes from patients displayed impaired oxidative burst. The genetic analysis revealed the novel missense mutation c.1157T>A/p.L386Q in G6PD. In addition, in silico analysis indicated that this mutation is pathogenic, thereby hampering the oxidative burst of neutrophils and monocytes from patients. Our data expand the clinical and genetic spectrum of G6PD deficiency, and suggest that impaired oxidative burst in this severe primary immune deficiency is an underlying immunopathologic mechanism that predisposes to mycobacterial infections.

Keywords: BCG; Coenzyme nicotinamide adenine dinucleotide phosphate; Glucose-6-phosphate dehydrogenase; Mutation; Reactive oxygen species; Vaccine.

MeSH terms

  • Amino Acid Substitution
  • BCG Vaccine / adverse effects
  • DNA Mutational Analysis
  • Genetic Association Studies
  • Glucosephosphate Dehydrogenase / chemistry
  • Glucosephosphate Dehydrogenase / genetics*
  • Glucosephosphate Dehydrogenase Deficiency / complications
  • Glucosephosphate Dehydrogenase Deficiency / diagnosis*
  • Glucosephosphate Dehydrogenase Deficiency / genetics*
  • Glucosephosphate Dehydrogenase Deficiency / immunology
  • Humans
  • Male
  • Models, Molecular
  • Monocytes / immunology
  • Monocytes / metabolism
  • Mutation, Missense
  • Mycobacterium bovis
  • Neutrophils / immunology
  • Neutrophils / metabolism
  • Oxidative Stress
  • Pedigree
  • Protein Conformation
  • Reactive Oxygen Species / metabolism
  • Respiratory Burst

Substances

  • BCG Vaccine
  • Reactive Oxygen Species
  • Glucosephosphate Dehydrogenase