Expression of cellular components in granulomatous inflammatory response in Piaractus mesopotamicus model

PLoS One. 2015 Mar 26;10(3):e0121625. doi: 10.1371/journal.pone.0121625. eCollection 2015.

Abstract

The present study aimed to describe and characterize the cellular components during the evolution of chronic granulomatous inflammation in the teleost fish pacus (P. mesopotamicus) induced by Bacillus Calmette-Guerin (BCG), using S-100, iNOS and cytokeratin antibodies. 50 fish (120±5.0 g) were anesthetized and 45 inoculated with 20 μL (40 mg/mL) (2.0 x 10(6) CFU/mg) and five inoculated with saline (0,65%) into muscle tissue in the laterodorsal region. To evaluate the inflammatory process, nine fish inoculated with BCG and one control were sampled in five periods: 3rd, 7th, 14th, 21st and 33rd days post-inoculation (DPI). Immunohistochemical examination showed that the marking with anti-S-100 protein and anti-iNOS antibodies was weak, with a diffuse pattern, between the third and seventh DPI. From the 14th to the 33rd day, the marking became stronger and marked the cytoplasm of the macrophages. Positivity for cytokeratin was initially observed in the 14th DPI, and the stronger immunostaining in the 33rd day, period in which the epithelioid cells were more evident and the granuloma was fully formed. Also after the 14th day, a certain degree of cellular organization was observed, due to the arrangement of the macrophages around the inoculated material, with little evidence of edema. The arrangement of the macrophages around the inoculum, the fibroblasts, the lymphocytes and, in most cases, the presence of melanomacrophages formed the granuloma and kept the inoculum isolated in the 33rd DPI. The present study suggested that the granulomatous experimental model using teleost fish P. mesopotamicus presented a similar response to those observed in mammals, confirming its importance for studies of chronic inflammatory reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Fishes
  • Granuloma / etiology*
  • Granuloma / pathology*
  • Keratins / metabolism
  • Muscles / metabolism
  • Muscles / microbiology
  • Muscles / pathology
  • Mycobacterium bovis
  • Nitric Oxide Synthase Type II / metabolism
  • S100 Proteins / metabolism

Substances

  • S100 Proteins
  • Keratins
  • Nitric Oxide Synthase Type II

Associated data

  • figshare/10.6084/M9.FIGSHARE.1311737
  • figshare/10.6084/M9.FIGSHARE.1311738

Grants and funding

This study was supported by São Paulo Research Foundation—FAPESP (grant 2010/08624-5). WGM was supported by a PhD scholarship from FAPESP (grant 2009/17640-7). The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.