Accorsi Alice, Benatti Stefania, Ross Eric, Nasi Milena, Malagoli Davide
Stowers Institute for Medical Research, Kansas City, MO, USA; Howard Hughes Medical Institute, Stowers Institute for Medical Research, Kansas City, MO, USA.
Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Dev Comp Immunol. 2017 Jul;72:37-43. doi: 10.1016/j.dci.2017.02.001. Epub 2017 Feb 3.
The golden apple snail Pomacea canaliculata is an invasive pest originating from South America. It has already been found in Asia, the southern United States and more recently in the EU. Aiming to target the immune system of the snail as a way to control its spreading, we have developed organ-specific transcriptomes and looked for molecules controlling replication and differentiation of snail hemocytes. The prokineticin domain-containing protein Astakine 1 is the only cytokine known thus far capable of regulating invertebrate hematopoiesis, and we analyzed the transcriptomes looking for molecules containing a prokineticin domain. We have identified a prokineticin-like protein (PlP), that we called Pc-plp and we analyzed by real-time PCR (qPCR) its expression. In control snails, highest levels of Pc-plp were detected in the digestive gland, the ampulla (i.e., a hemocyte reservoir) and the pericardial fluid (i.e., the hematopoietic district). We tested Pc-plp expression after triggering hematopoiesis via multiple hemolymph withdrawals, or during bacterial challenge through LPS injection. In both cases a reduction of Pc-plp mRNA was observed. The multiple hemolymph withdrawals caused a significant decrease of Pc-plp mRNA in pericardial fluid and circulating hemocytes, while the LPS injection promoted the Pc-plp mRNA drop in anterior kidney, mantle and gills, organs that may act as immune barrier in molluscs. Our data indicate an important role for prokineticin domain-containing proteins as immunomodulators also in gastropods and their dynamic expression may serve as a biosensor to gauge the effectiveness of immunological interventions aimed at curtailing the spreading of the gastropod pest P. canaliculata.
福寿螺(Pomacea canaliculata)是一种原产于南美洲的入侵性害虫。它已在亚洲、美国南部被发现,最近在欧盟也有发现。为了以靶向福寿螺的免疫系统作为控制其传播的一种方式,我们开发了器官特异性转录组,并寻找控制福寿螺血细胞复制和分化的分子。含促动力蛋白结构域的蛋白Astakine 1是迄今为止已知的唯一能够调节无脊椎动物造血作用的细胞因子,我们分析转录组以寻找含有促动力蛋白结构域的分子。我们鉴定出一种促动力蛋白样蛋白(PlP),我们将其命名为Pc-plp,并通过实时定量PCR(qPCR)分析其表达。在对照福寿螺中,在消化腺、壶腹(即血细胞储存库)和心包液(即造血区域)中检测到最高水平的Pc-plp。我们通过多次采血触发造血作用后,或在通过注射脂多糖进行细菌攻击期间,测试了Pc-plp的表达。在这两种情况下,均观察到Pc-plp mRNA的减少。多次采血导致心包液和循环血细胞中Pc-plp mRNA显著下降,而注射脂多糖则促使前肾、外套膜和鳃中Pc-plp mRNA下降,这些器官可能是软体动物中的免疫屏障。我们的数据表明,含促动力蛋白结构域的蛋白作为免疫调节剂在腹足纲动物中也具有重要作用,其动态表达可能作为一种生物传感器来评估旨在遏制腹足纲害虫福寿螺传播的免疫干预措施的有效性。