Seixas Adriana, Friesen Kevin J, Kaufman W Reuben
Centro de Biotecnologia, Universidade Federal do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, CEP 91501-970, Brazil.
J Insect Physiol. 2008 Jul;54(7):1175-83. doi: 10.1016/j.jinsphys.2008.05.004. Epub 2008 Jun 26.
Earlier work from our laboratory indicated that injection of 20-hydroxyecdysone (20E) into non-vitellogenic female Amblyomma hebraeum ticks stimulates the synthesis of vitellogenin (Vg), but not its uptake into oocytes [Friesen, K., Kaufman, W.R., 2004. Effects of 20-hydroxyecdysone and other hormones on egg development, and identification of a vitellin-binding protein in the ovary of the tick, Amblyomma hebraeum. Journal of Insect Physiology 50, 519-529]. In contrast, Thompson et al. [Thompson, D.M., Khalil, S.M.S., Jeffers, L.A., Ananthapadmanaban, U., Sonenshine, D.E., Mitchell, R.D., Osgood, C.J., Apperson, C.S., Roe, M.R., 2005. In vivo role of 20-hydroxyecdysone in the regulation of the vitellogenin mRNA and egg development in the American dog tick, Dermacentor variabilis (Say). Journal of Insect Physiology 51, 1105-1116] demonstrated that injection of 20E into virgin female Dermacentor variabilis ticks stimulated both vitellogenesis and Vg uptake into oocytes. In addition to the species difference in the two studies there were substantially different methods for injecting 20E. In our earlier work we injected small partially fed ticks after removing them from the host. Thompson et al. injected the females while they remained attached to the host. So in this study we repeated our earlier experiments on A. hebraeum using on-host injection. We also injected 20E into off-host ticks with or without haemolymph collected from engorged ticks (days 2-10 post-engorgement), or from large partially fed mated ticks in the rapid phase of engorgement, to see whether we might detect a 'vitellogenin uptake factor' (VUF) in haemolymph. Off-host injection of 20E (0.45microg/g body weight (bw)) did not induce ovary development beyond that of vehicle-injected controls. But ticks in this study, receiving 20E plus haemolymph from engorged ticks, showed a significant increase in ovary weight beyond that of 20E alone (1.31+/-0.05% bw; 34 for 20E plus haemolymph and 1.03+/-0.05% bw; 25 for 20E alone). However, in normal engorged A. hebraeum, the ovary exceeds 7% bw at the onset of oviposition. As in our earlier work, in this study 20E stimulated Vg-synthesis (3.9+/-0.5mgVt-equivalents/ml) beyond that occurring in vehicle-injected ticks (0.76+/-0.14mgVt-equivalents/ml), and there was a further increase in ticks injected with 20E plus haemolymph from engorged ticks (8.9+/-1.0mgVt-equivalents/ml). On-host injection of 20E alone (6microg20E/g bw) did not produce a statistically significant increase in oocyte length over that of vehicle-injected controls, whereas on-host injection of 20E plus engorged haemolymph resulted in significantly larger oocytes (261+/-57microm) compared to vehicle-injected controls (132+/-11microm), compared to 20E alone (131+/-12microm), or haemolymph alone (124+/-24microm). There was a marked stimulation of Vg-synthesis by 31microg20E/g bw (6.0+/-1.5mgVt-equivalents/ml) compared to vehicle-injected controls (1.02+/-33mgVt-equivalents/ml). Vt accumulation by ovaries was significantly greater in ticks treated with haemolymph (12+/-3microgVt/mg ovary) or 20E plus haemolymph (56+/-26microgVt/mg ovary) compared to vehicle-injected controls (5.1+/-1.5microgVt/mg ovary). There was also a significant effect of 6microg20E/g bw plus engorged haemolymph on ovary weight (1.74+/-0.29% bw) compared to vehicle-injected ticks (0.95+/-0.10% bw), but not compared to ticks injected with 20E alone (1.25+/-0.19% bw). We conclude that at least some of the differences observed between the two laboratories relate to the species difference, and that there is some evidence that the engorged haemolymph of A. hebraeum contains a VUF.
我们实验室早期的研究表明,向未形成卵黄的雌性希伯来花蜱注射20-羟基蜕皮酮(20E)可刺激卵黄原蛋白(Vg)的合成,但不会刺激其摄取进入卵母细胞[弗里森,K.,考夫曼,W.R.,2004年。20-羟基蜕皮酮和其他激素对蜱虫卵发育的影响,以及在希伯来花蜱卵巢中鉴定一种卵黄磷蛋白结合蛋白。昆虫生理学杂志50,519-529]。相比之下,汤普森等人[汤普森,D.M.,哈利勒,S.M.S.,杰弗斯,L.A.,阿南塔帕德马纳班,U.,索嫩申,D.E.,米切尔,R.D.,奥斯古德,C.J.,阿珀森,C.S.,罗,M.R.,2005年。20-羟基蜕皮酮在美洲犬蜱(Dermacentor variabilis(Say))中对卵黄原蛋白mRNA和卵发育调控的体内作用。昆虫生理学杂志51,1105-1116]证明,向未交配的雌性美洲犬蜱注射20E可刺激卵黄生成和Vg摄取进入卵母细胞。除了两项研究中的物种差异外,注射20E的方法也有很大不同。在我们早期的研究中,我们在将小的部分饱血的蜱从宿主身上移除后进行注射。汤普森等人在雌性蜱仍附着在宿主身上时进行注射。因此,在本研究中,我们使用在宿主上注射的方法重复了我们早期对希伯来花蜱的实验。我们还向离宿主的蜱注射20E,同时注射或不注射从饱血蜱(饱血后2-10天)或处于快速饱血阶段的大型部分饱血交配蜱收集的血淋巴,以观察我们是否能在血淋巴中检测到“卵黄原蛋白摄取因子”(VUF)。离宿主注射20E(0.45微克/克体重(bw))并未诱导卵巢发育超过注射溶剂的对照组。但在本研究中,接受20E加饱血蜱血淋巴的蜱,其卵巢重量比仅注射20E的蜱有显著增加(1.31±0.05%bw;20E加饱血蜱血淋巴组为34,仅注射20E组为1.03±0.05%bw;25)。然而,在正常饱血的希伯来花蜱中,产卵开始时卵巢超过7%bw。与我们早期的研究一样,在本研究中,20E刺激Vg合成(3.9±0.5毫克Vt当量/毫升)超过注射溶剂的蜱(0.76±0.14毫克Vt当量/毫升),并且在注射20E加饱血蜱血淋巴的蜱中进一步增加(8.9±1.0毫克Vt当量/毫升)。仅在宿主上注射20E(6微克20E/克bw)与注射溶剂的对照组相比,未使卵母细胞长度产生统计学上的显著增加,而在宿主上注射20E加饱血血淋巴导致卵母细胞显著更大(261±57微米),与注射溶剂的对照组(132±11微米)相比,与仅注射20E(131±12微米)或仅注射血淋巴(124±24微米)相比。与注射溶剂的对照组(1.02±33毫克Vt当量/毫升)相比,31微克20E/克bw显著刺激Vg合成(6.0±1.5毫克Vt当量/毫升)。与注射溶剂的对照组(5.1±1.5微克Vt/毫克卵巢)相比,用饱血血淋巴或20E加饱血血淋巴处理的蜱卵巢中Vt积累显著更高(12±3微克Vt/毫克卵巢或56±26微克Vt/毫克卵巢)。与注射溶剂的蜱(0.95±0.10%bw)相比,6微克20E/克bw加饱血血淋巴对卵巢重量也有显著影响(1.74±0.29%bw),但与仅注射20E的蜱(1.25±0.19%bw)相比无显著差异。我们得出结论,两个实验室观察到的至少一些差异与物种差异有关,并且有一些证据表明希伯来花蜱的饱血血淋巴中含有一种VUF。