Impaired cellular immune response to injected bacteria after knockdown of ferritin genes in the hard tick Haemaphysalis longicornis. Issue 3 (June 2016)

• Record Type: Journal Article
• Authors: Galay, Remil Linggatong; Takechi, Rie; Umemiya-Shirafuji, Rika; Talactac, Melbourne Rio; Maeda, Hiroki; Kusakisako, Kodai; Mochizuki, Masami; Fujisaki, Kozo; Tanaka, Tetsuya
• Is Part Of: Parasitology international. Volume 65:Issue 3(2016:Jun.)
• Page Start: 251
• Page End: 257
• Publication Date: 2016-06
• Subjects: Ticks -- Ferritin -- Innate immunity -- Iron; Parasitology -- Periodicals; Parasites -- Periodicals; Parasitic Diseases -- Periodicals; Parasitology -- Periodicals; Parasitologie -- Périodiques; 571.99905
• DOI: 10.1016/j.parint.2016.01.007
• Languages: English
• ISSNs: 1383-5769

Abstract

Abstract: Iron is an indispensable element for most microorganisms, including many pathogenic bacteria. Iron-withholding is a known component of the innate immunity, particularly of vertebrate hosts. Ticks are vectors of multiple pathogens and reports have shown that they naturally harbor several bacterial species. Thus, tick innate immunity must be crucial in limiting bacterial population to tolerable level that will not cause adverse effects. We have previously characterized two types of the iron-binding protein ferritin (HlFER) in the hard tick Haemaphysalis longicornis, known to be a vector of some protozoan parasites and rickettsiae, and showed their antioxidant function and importance in blood feeding and reproduction. Here we examined the possible role of HlFERs in tick immunity against bacterial infection. After silencing Hlfer genes, adult ticks were injected with live enhanced green fluorescence protein-expressing Escherichia coli, and then monitored for survival rate. Hemolymph that included hemocytes was collected for microscopic examination to observe cellular immune response, and for E. coli culture to determine bacterial viability after injection in the ticks. The expression of some antimicrobial peptides in whole ticks was also analyzed by RT-PCR. Hlfer -silenced ticks had a significantly lower survival rate than control ticks after E. coli injection. Greater number of bacteria inside and outside the hemocytes and higher bacterial colony counts after culture with hemolymph were also observed in Hlfer -silenced ticks. However, no difference on the expression of antimicrobial peptides was observed. These results suggest that ferritin molecules might be important in the cellular immune response of ticks to some bacteria. Graphical abstract: Highlights: Hlfer -silenced ticks had lower survival rate than control after bacterial injection. The expression of HlFERs in the hemocytes is stimulated by bacterial injection. Hemocytes of Hlfer -silenced ticks were filled with E. coli 72 h after injection. Hemolymph of Hlfer -silenced ticks yielded more E. coli colonies after culture. Hlfer -silencing did not affect the transcription of antimicrobial peptides.