色氨酸及其衍生物在疟媒蚊体内疟原虫发育中的作用

Hiroyuki Matsuoka, Meiji Arai, Hajime Yoshida, Ryuta Hattori, Yuichi Kasahara, Makoto Hirai
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引用次数: 1

摘要

黄嘌呤酸(XA)是昆虫眼色素合成单色通路色氨酸代谢的侧反应产物,可诱导疟原虫配子体发生。利用高效液相色谱电化学检测系统,成功地测定了蚊子组织中XA的含量。在取血的中肠中,XA含量不足以激活配子细胞。我们发现蚊子的唾液腺含有足够的XA来激活配子体,蚊子在吸血过程中将唾液摄取到中肠。综上所述,XA很可能在吸血过程中从唾液腺排出,并被吞咽到中肠,在那里它影响疟疾配子细胞。在本研究中,我们比较了幼蚊(羽化后2-3日龄)和老蚊(羽化后12-14日龄)的传播功效。幼龄组全身及唾液腺XA含量较高。从患有疟疾的同一只老鼠身上采血后,年轻组中肠上出现的卵囊数量也更高。当两组蚊子用培养的疟原虫卵母细胞喂血时,两组蚊子的卵囊数量相似,这表明幼蚊和老年蚊子从卵母细胞到卵囊的发育条件相似。综合这些结果,我们得出结论,传播效能受唾液腺中XA含量的控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of tryptophan and its derivatives for development of malaria parasite in vector mosquito

Xanthurenic acid (XA), a lateral reaction product of tryptophan metabolism in the omochrome pathway of eye pigment synthesis in insects, induces gametogenesis of malaria parasites. We have succeeded in measuring XA contents in the mosquito tissues using a high performance liquid chromatography with electrochemical detection system. XA content is not enough for activating gametocytes in the midgut where blood meal is taken. We have found that the salivary gland of mosquito contains a sufficient amount of XA for activating gametocytes and mosquito ingests saliva into the midgut during blood feeding. Taken together, it is likely that XA is discharged from salivary gland during blood feeding and is swallowed to the midgut where it affects malaria gametocytes. In the present study, we compared young mosquitoes (2–3 day-old after emergence) with old mosquitoes (12–14 day-old after emergence) in terms of transmission efficacy. XA contents in whole body and the salivary gland were larger in the young group. Numbers of oocyst developed on the midgut after taking blood from the same mouse with malaria were also higher in the young group. When both groups fed a blood meal with cultured ookinetes of malaria parasites, the numbers of oocyst were similar in both groups, suggesting that conditions for development from ookinetes to oocysts were similar in young and old mosquitoes. Taking these results together, we conclude that transmission efficacy is controlled by the amount of XA in the salivary gland.

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