Interaction of the bacteria Xenorhabdus nematophila (Enterobactericeae) and Bacillus subtilis (Bacillaceae) with the hemocytes of larval Malacosoma disstria (Insecta: Lepidoptera: Lasiocampidae)

• Published in: Journal of invertebrate pathology 2007, Vol.94 (1), p.20-30
• Main Authors: Giannoulis, Paschalis, Brooks, Cory L., Dunphy, Gary B., Mandato, Craig A., Niven, Donald F., Zakarian, Robert J.
• Format: Article
• Language: English
• Subjects: Animals; antibacterial properties; apolipophorin; apolipophorin-III; Bacillaceae; Bacillus subtilis; Bacillus subtilis - physiology; Bacterial Adhesion; Biological and medical sciences; Biological control; cell-mediated immunity; Control; Fundamental and applied biological sciences. Psychology; Hemocytes; Hemocytes - microbiology; Hemolymph - microbiology; immune response; insect immunity; Insecta; Larva - metabolism; Larva - microbiology; larvae; Lasiocampidae; Lepidoptera; Lepidoptera - metabolism; Lepidoptera - microbiology; Lipopolysaccharides - metabolism; Lysozyme; Malacosoma; Malacosoma disstria; monophenol monooxygenase; Monophenol Monooxygenase - metabolism; Muramidase - metabolism; Phenoloxidase; Phytopathology. Animal pests. Plant and forest protection; Plasma protein; Protozoa. Invertebrates; Xenorhabdus; Xenorhabdus - physiology; Xenorhabdus nematophila
• ISSN: 0022-2011; 1096-0805
• DOI: 10.1016/j.jip.2006.08.010

Malacosoma disstria larvae are a pest of deciduous trees. Little is known on the interaction of bacteria with the immediate hemocytic antimicrobial responses of these insects. Incubating dead Xenorhabdus nematophila and Bacillus subtilis with a mixture of serum-free granular cells and plasmatocytes in vitro revealed differential bacterial-hemocyte adhesion and differential discharge of lysozyme and phenoloxidase but not total protein. Although active phenoloxidase adhered equally to both bacterial species, X. nematophila limited enzyme activation whereas B. subtilis enhanced activation. Serum with active phenoloxidase (as opposed to tropolone-inhibited phenoloxidase) and purified insect lysozyme increased bacterial-hemocyte adhesion of both bacterial species. An apolipophorin-III-like protein when incubated with hemocytes, limited their responses to glass slides and bacterial adhesion. However, initial binding of the protein to both bacteria increased granular cell levels with bacteria while lowering the plasmatocyte levels with adhering procaryotes. The protein also increased lysozyme and phenoloxidase activities. Although B. subtilis in vivo elicited a nodulation-based decline in total hemocyte counts and did not affect hemocyte viability, dead X. nematophila elevated hemocyte counts and damaged the hemocytes as lipopolysaccharide levels increased and X. nematophila emerged into the hemolymph. Apolipophorin-III-like protein once bound to the bacteria slowed their removal from the hemolymph.