E-NTPDase and E-ADA activities in rats experimental infected by Cryptococcus neoformans

Vet Microbiol. 2014 Nov 7;174(1-2):206-13. doi: 10.1016/j.vetmic.2014.09.007. Epub 2014 Sep 23.

Abstract

Cryptococcus neoformans, the etiological agent of cryptococcosis, is an opportunistic fungal pathogen of immunocompromised individuals. The aim of this study was to evaluate the activities of E-NTPDase and E-ADA in rats experimentally infected by C. neoformans var. grubii. Adult rats (35) were divided in two groups: 18 for the control group (uninfected) (A), and 17 for the infected group (B). Each group was separated into three sub-groups (A1, A2, A3-B1, B2, B3), and samples were collected on 10, 20, and 30 days post-infection (PI). Leukocyte counts, IFN-γ, TNF-α, IgM, IgG levels, and E-NTPDase and E-ADA activities were analyzed. It was possible to observe that IgG and IgM seric levels of infected rats were significantly elevated (P<0.01) on days 10, 20 and 30 PI, as well as the levels of TNF-α and INF-γ when compared to uninfected rodents. Regarding E-NTPDase activity in lymphocytes, it was possible to observe that the ATP hydrolysis was significantly decreased on days 20 (P<0.01) and 30 PI (P<0.05), while ADP hydrolysis was significantly reduced only on day 20 PI (P<0.01) when compared with uninfected group. Seric E-ADA activity had a significant reduction (P<0.01) during all three evaluated periods when compared to the control group, while E-ADA activity in lymphocytes increased significantly (P<0.01) when compared to the group A on day 10 PI; however on days 20 and 30 PI, its activity was considerable reduced in lymphocytes of infected animals (P<0.01). Therefore, it is possible to conclude that the infection caused by C. neoformans in immunocompetent rats leads to changes in the purinergic signaling (NTPDase and E-ADA), concomitantly with an inflammatory response (increased levels of cytokines and immunoglobulins) associated with inflammatory infiltrates and histological lesions in the lung.

Keywords: Cryptococcosis; Enzyme activity; Lymphocytes; Purinergic signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Deaminase / metabolism*
  • Animals
  • Antigens, CD / metabolism*
  • Apyrase / metabolism*
  • Cryptococcosis / enzymology*
  • Cryptococcosis / immunology
  • Cryptococcus neoformans / immunology*
  • Cytokines / blood
  • Histological Techniques
  • Leukocyte Count
  • Lymphocytes / metabolism
  • Rats
  • Time Factors

Substances

  • Antigens, CD
  • Cytokines
  • Adenosine Deaminase
  • Apyrase
  • CD39 antigen