Dengue Virus Type 2 (DENV2)-Induced Oxidative Responses in Monocytes from Glucose-6-Phosphate Dehydrogenase (G6PD)-Deficient and G6PD Normal Subjects

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Abstract

Background:Dengue virus is endemic in peninsular Malaysia. The clinical manifestations vary depending on the incubation period of the virus as well as the immunity of the patients. Glucose-6-phosphate dehydrogenase (G6PD) deficiency is prevalent in Malaysia where the incidence is 3.2%. It has been noted that some G6PD-deficient individuals suffer from more severe clinical presentation of dengue infection. In this study, we aim to investigate the oxidative responses of DENV2-infected monocytes from G6PD-deficient individuals.Methodology:Monocytes from G6PD-deficient individuals were infected with DENV2 and infection rate, levels of oxidative species, nitric oxide (NO), superoxide anions (O2-), and oxidative stress were determined and compared with normal controls.Principal Findings:Monocytes from G6PD-deficient individuals exhibited significantly higher infection rates compared to normal controls. In an effort to explain the reason for this enhanced susceptibility, we investigated the production of NO and O2- in the monocytes of individuals with G6PD deficiency compared with normal controls. We found that levels of NO and O2- were significantly lower in the DENV-infected monocytes from G6PD-deficient individuals compared with normal controls. Furthermore, the overall oxidative stress in DENV-infected monocytes from G6PD-deficient individuals was significantly higher when compared to normal controls. Correlation studies between DENV-infected cells and oxidative state of monocytes further confirmed these findings.Conclusions/Significance:Altered redox state of DENV-infected monocytes from G6PD-deficient individuals appears to augment viral replication in these cells. DENV-infected G6PD-deficient individuals may contain higher viral titers, which may be significant in enhanced virus transmission. Furthermore, granulocyte dysfunction and higher viral loads in G6PD-deificient individuals may result in severe form of dengue infection. © 2014 Al-alimi et al.

Figures

  • Figure 1. G6PD levels in normal controls and G6PD-deficient subjects. G6PD levels were determined by a commercially available fluorimetric assay. The mean G6PD activity for G6PD-deficient individuals was 0.28560.26 IU/g Hb, compared to 13.5662.02 IU/g Hb for age matched normal controls. doi:10.1371/journal.pntd.0002711.g001
  • Figure 2. Growth curves of DENV2 in monocytes of G6PD-deficient and normal controls. The monocytes from G6PD-deficient and normal controls were infected with DENV2 at an MOI of 0.1. Cells and culture supernatants were harvested at 24, 48, 72, 96, 120 hours post-infection. Number of DENV infected cells were assayed by flow cytometry (A), whereas virus released by the infected cells was determined by Plaque assay (B). Number of infected cells as well as virus titer found to be significantly higher in infected monocytes from G6PD-deficient individuals compared to the normal controls. doi:10.1371/journal.pntd.0002711.g002
  • Figure 3. Production of nitric oxide (NO) in DENV-infected monocytes from G6PD-deficient, and normal controls. The production of nitric oxide (NO) in monocytes of both normal controls and G6PD-deficient donors increased significantly (p,0.001) after DENV2 infection. In a timedependent manner, monocytes from G6PD-deficient subjects produced significantly (p,0.001) lower NO than monocytes from normal controls. doi:10.1371/journal.pntd.0002711.g003
  • Figure 4. Production of superoxide anions (O2.2) in DENV-infected monocytes from G6PD-deficient, and normal controls. The production of superoxide anions (O2.2) in monocytes of both normal controls and G6PD-deficient donors increased significantly (p,0.001) after DENV2 infection. In a time-dependent manner, monocytes from G6PD-deficient subjects produced significantly (p,0.001) lower O2.2 than monocytes from normal controls. doi:10.1371/journal.pntd.0002711.g004
  • Figure 5. Oxidative stress accumulation in DENV-infected monocytes from G6PD-deficient and normal controls. The accumulation of oxidative stress in monocytes of both normal controls and G6PD-deficient donors increased significantly (p,0.001) after DENV2 infection. In a timedependent manner, monocytes from G6PD-deficient subjects accumulated significantly (p,0.001) higher oxidative stress compared to monocytes from normal controls. doi:10.1371/journal.pntd.0002711.g005
  • Figure 6. Correlation between DENV2 replication and NO, O2.2, and oxidative stress in monocytes from G6PD-deficient and normal controls. A significant moderate to strong correlation was found between the % infected monocytes and oxidative state (NO, O2.2, and oxidative stress) for monocytes from G6PD-deificient individuals (A) compared to normal controls (B). doi:10.1371/journal.pntd.0002711.g006

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Al-alimi, A. A., Ali, S. A., Al-Hassan, F. M., Idris, F. M., Teow, S. Y., & Mohd Yusoff, N. (2014). Dengue Virus Type 2 (DENV2)-Induced Oxidative Responses in Monocytes from Glucose-6-Phosphate Dehydrogenase (G6PD)-Deficient and G6PD Normal Subjects. PLoS Neglected Tropical Diseases, 8(3). https://doi.org/10.1371/journal.pntd.0002711

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