Immune Defenses of the Invasive Apple Snail Pomacea canaliculata (Caenogastropoda, Ampullariidae): Phagocytic Hemocytes in the Circulation and the Kidney

• Published in: PloS one 2015-04, Vol.10 (4), p.e0123964-e0123964
• Main Authors: Cueto, Juan A, Rodriguez, Cristian, Vega, Israel A, Castro-Vazquez, Alfredo
• Format: Article
• Language: English
• Subjects: Animals; Bacteria; Beads; Circulation; Collagen; Collagenase; Confocal; Confocal microscopy; Cytometry; Cytoplasm; Electron density; Electron microscopy; Electrons; Enzymes; Escherichia coli - physiology; Exposure; Flow Cytometry; Fluorescence; Fluorescent Dyes - metabolism; Glycogen; Gram-negative bacteria; Granular materials; Granules; Granulocytes; Hemocytes; Hemocytes - immunology; Hemocytes - ultrastructure; Kidney - cytology; Kidney - metabolism; Kidney - ultrastructure; Kidneys; Leukocytes (eosinophilic); Leukocytes (granulocytic); Light microscopy; Meningitis; Microorganisms; Microscopy; Mollusks; Nonnative species; Nuclei; Phagocytes; Phagocytosis; Phagosomes; Phase contrast; Pomacea canaliculata; Public health; Scanning microscopy; Snails - immunology; Transmission electron microscopy; Yeasts
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0123964

Hemocytes in the circulation and kidney islets, as well as their phagocytic responses to microorganisms and fluorescent beads, have been studied in Pomacea canaliculata, using flow cytometry, light microscopy (including confocal laser scanning microscopy) and transmission electron microscopy (TEM). Three circulating hemocyte types (hyalinocytes, agranulocytes and granulocytes) were distinguished by phase contrast microscopy of living cells and after light and electron microscopy of fixed material. Also, three different populations of circulating hemocytes were separated by flow cytometry, which corresponded to the three hemocyte types. Hyalinocytes showed a low nucleus/cytoplasm ratio, and no apparent granules in stained material, but showed granules of moderate electron density under TEM (L granules) and at least some L granules appear acidic when labeled with LysoTracker Red. Both phagocytic and non-phagocytic hyalinocytes lose most (if not all) L granules when exposed to microorganisms in vitro. The phagosomes formed differed whether hyalinocytes were exposed to yeasts or to Gram positive or Gram negative bacteria. Agranulocytes showed a large nucleus/cytoplasm ratio and few or no granules. Granulocytes showed a low nucleus/cytoplasm ratio and numerous eosinophilic granules after staining. These granules are electron dense and rod-shaped under TEM (R granules). Granulocytes may show merging of R granules into gigantic ones, particularly when exposed to microorganisms. Fluorescent bead exposure of sorted hemocytes showed phagocytic activity in hyalinocytes, agranulocytes and granulocytes, but the phagocytic index was significantly higher in hyalinocytes. Extensive hemocyte aggregates ('islets') occupy most renal hemocoelic spaces and hyalinocyte-like cells are the most frequent component in them. Presumptive glycogen deposits were observed in most hyalinocytes in renal islets (they also occur in the circulation but less frequently) and may mean that hyalinocytes participate in the storage and circulation of this compound. Injection of microorganisms in the foot results in phagocytosis by hemocytes in the islets, and the different phagosomes formed are similar to those in circulating hyalinocytes. Dispersed hemocytes were obtained after kidney collagenase digestion and cell sorting, and they were able to phagocytize fluorescent beads. A role for the kidney as an immune barrier is proposed for this snail.