The role of pilin protein of Xenorhabdus nematophila against immune defense reactions of insects

• Published in: Journal of insect physiology 2017-08, Vol.101, p.82-90
• Main Authors: Darsouei, Reyhaneh, Karimi, Javad, Dunphy, Gary B.
• Format: Article
• Language: English
• Subjects: Animals; Antimicrobial Cationic Peptides - genetics; Antimicrobial Cationic Peptides - metabolism; Antimicrobial peptides; Cellular defense; Fimbriae Proteins - genetics; Fimbriae Proteins - metabolism; Immunity, Innate; Insect pathology; Larva - growth & development; Larva - immunology; Larva - microbiology; Phenoloxidae; Phospholipase A2; Protease; Sequence Analysis, DNA; Spodoptera - growth & development; Spodoptera - immunology; Spodoptera - microbiology; Xenorhabdus - genetics; Xenorhabdus - physiology
• ISSN: 0022-1910; 1879-1611
• DOI: 10.1016/j.jinsphys.2017.07.003

[Display omitted] •Pilin protein was isolated from Xenorhabdus nematophila.•Main cellular and humoral defense reactions of S. exigua larvae addressed when treated with the pilin protein.•Expression of main AMPs transcript after treatment with pilin were suppressed.•This is first insight into the role of pilin against an insect humoral defense. Xenorhabdus nematophila is a symbiotic bacterium of the entomopathogenic nematode Steinernema carpocapsae (Weiser). It produces several toxic proteins which interfere with the immune system of insects. The current study shows that purified pilin protein could be a virulence trait of X. nematophila. The fifth instar larvae of Spodoptera exigua (Hübner) was injected with purified pilin. Changes in the cellular defenses in terms of total haemocyte counts and granulocyte percentage and humoral factors including total protease, phospholipase A2, and phenoloxidase activities (humoral defense) as well as the expression of the three main antimicrobial peptides attacin, cecropin, and spodoptericin were measured at specific times. The level of THC and granulocytes in larvae with different concentrations of pilin protein were less than the negative control. Also agglutination of haemocytes was observed 8–16h post-injection. The pilin protein activated phenoloxidase in the initial hour post-injection, by 2hpi, activity was stable. The activities of phospholipase A2 and protease activities reached maximum levels at 12 and 4hpi, respectively, and then decreased. The expressions of attacin, cecropin, and spodoptericin in larvae treated with pilin protein were up-regulated above that of the normal sample. The overexpression of cecropin was greater than the other antimicrobial protein mRNA transcripts. The spodoptericin expression had an irregular trend while expressions of attacin and cecropin reached maximum levels at 4hpi and then decreased. Generally, after the injection of pilin protein, the cellular and humoral immune system of S. exigua is activated but this toxin was able to inhibit them. This is the first report of the role of pilin protein when the bacterial symbiont of S. carpocapsae encounters the humoral defense of an insect.