Pathogen-associated molecular patterns activate expression of genes involved in cell proliferation, immunity and detoxification in the amebocyte-producing organ of the snail Biomphalaria glabrata. (March 2016)

• Record Type: Journal Article
• Authors: Zhang, Si-Ming; Loker, Eric S.; Sullivan, John T.
• Is Part Of: Developmental and comparative immunology. Volume 56(2016)
• Page Start: 25
• Page End: 36
• Publication Date: 2016-03
• Subjects: Biomphalaria glabrata -- Mollusk -- Amebocyte-producing organ (APO) -- Pathogen associated molecular pattern (PAMP) -- Aminoacyl-tRNA synthetase -- GiMAP; Immunology -- Periodicals; Developmental immunology -- Periodicals; 616.079
• DOI: 10.1016/j.dci.2015.11.008
• Languages: English
• ISSNs: 0145-305X

Abstract

Abstract: The anterior pericardial wall of the snail Biomphalaria glabrata has been identified as a site of hemocyte production, hence has been named the amebocyte-producing organ (APO). A number of studies have shown that exogenous abiotic and biotic substances, including pathogen associated molecular patterns (PAMPs), are able to stimulate APO mitotic activity and/or enlarge its size, implying a role for the APO in innate immunity. The molecular mechanisms underlying such responses have not yet been explored, in part due to the difficulty in obtaining sufficient APO tissue for gene expression studies. By using a modified RNA extraction technique and microarray technology, we investigated transcriptomic responses of APOs dissected from snails at 24 h post-injection with two bacterial PAMPs, lipopolysaccharide (LPS) and peptidoglycan (PGN), or with fucoidan (FCN), which may mimic fucosyl-rich glycan PAMPs on sporocysts of Schistosoma mansoni . Based upon the number of genes differentially expressed, LPS exhibited the strongest activity, relative to saline-injected controls. A concurrent activation of genes involved in cell proliferation, immune response and detoxification metabolism was observed. A gene encoding checkpoint 1 kinase, a key regulator of mitosis, was highly expressed after stimulation by LPS. Also, seven different aminoacyl-tRNA synthetases that play an essential role in protein synthesis were found to be highly expressed. In addition to stimulating genes involved in cell proliferation, the injected substances, especially LPS, also induced expression of a number of immune-related genes including arginase, peptidoglycan recognition protein short form, tumor necrosis factor receptor, ficolin, calmodulin, bacterial permeability increasing proteins and E3 ubiquitin-protein ligase. Importantly, significant up-regulation was observed in four GiMAP (GTPase of immunity-associated protein) genes, a result which provides the first evidence suggesting an immune role of GiMAP in protostome animals. Moreover, altered expression of genes encoding cytochrome P450, glutathione-S-transferase, multiple drug resistance protein as well as a large number of genes encoding enzymes associated with degradation and detoxification metabolism was elicited in response to the injected substances. Highlights: This is the first transcriptome study in the APO of the snail Biomphalaria glabrata. The data support histological observations of high mitotic activity in the APO following challenge with PAMPs. PAMPs elicit immune responses by up-regulating expression of immune genes and increasing proliferation of hemocytes. Compared to FCN and PGN, LPS is a more potent PAMP in activating gene expression. Role of arginase and GiMAP in snail immunity is suggested. Biotransformation activity is enhanced in the APO following exposure to PAMPs.