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利用RNA干扰抑制长须罗蛉中胰蛋白酶的表达可提高利什曼原虫的存活率。

Inhibition of trypsin expression in Lutzomyia longipalpis using RNAi enhances the survival of Leishmania.

作者信息

Sant'anna Mauricio Rv, Diaz-Albiter Hector, Mubaraki Murad, Dillon Rod J, Bates Paul A

机构信息

Biomedical and Life Sciences, Lancaster University, Lancaster, UK.

出版信息

Parasit Vectors. 2009 Dec 9;2(1):62. doi: 10.1186/1756-3305-2-62.

Abstract

BACKGROUND

Leishmania parasites must overcome several barriers to achieve transmission by their sand fly vectors. One of the earliest threats is exposure to enzymes during blood meal digestion. Trypsin-like enzymes appear to be detrimental to parasite survival during the very early phase of development as amastigotes transform into promastigote stages. Here, we investigate whether parasites can affect trypsin secretion by the sand fly midgut epithelium and if inhibition of this process is of survival value to the parasites.

RESULTS

Infections of Lutzomyia longipalpis with Leishmania mexicana were studied and these showed that infected sand flies produced less trypsin-like enzyme activity during blood meal digestion when compared to uninfected controls. RNA interference was used to inhibit trypsin 1 gene expression by micro-injection into the thorax, as trypsin 1 is the major blood meal induced trypsin activity in the sand fly midgut. Injection of specific double stranded RNA reduced trypsin 1 expression as assessed by RT-PCR and enzyme assays, and also led to increased numbers of parasites in comparison with mock-injected controls. Injection by itself was observed to have an inhibitory effect on the level of infection, possibly through stimulation of a wound repair or immune response by the sand fly.

CONCLUSION

Leishmania mexicana was shown to be able to modulate trypsin secretion by Lutzomyia longipalpis to its own advantage, and direct inhibition of trypsin gene expression led to increased parasite numbers in the midguts of infected flies. Successful application of RNA interference methodology to Leishmania-infected sand flies now opens up the use of this technique to study a wide range of sand fly genes and their role in the parasite-vector interaction.

摘要

背景

利什曼原虫寄生虫必须克服多个障碍才能通过其沙蝇媒介实现传播。最早的威胁之一是在血餐消化过程中暴露于酶。在无鞭毛体转变为前鞭毛体阶段的发育早期,类胰蛋白酶似乎对寄生虫的存活有害。在此,我们研究寄生虫是否能影响沙蝇中肠上皮细胞的胰蛋白酶分泌,以及抑制这一过程对寄生虫的生存是否具有价值。

结果

对感染墨西哥利什曼原虫的长须罗蛉进行了研究,结果表明,与未感染的对照相比,感染的沙蝇在血餐消化过程中产生的类胰蛋白酶活性较低。通过向胸腔显微注射RNA干扰来抑制胰蛋白酶1基因的表达,因为胰蛋白酶1是沙蝇中肠中血餐诱导的主要胰蛋白酶活性。通过RT-PCR和酶分析评估,注射特定的双链RNA可降低胰蛋白酶1的表达,与模拟注射的对照相比,还导致寄生虫数量增加。观察到注射本身对感染水平有抑制作用,可能是通过刺激沙蝇的伤口修复或免疫反应。

结论

已证明墨西哥利什曼原虫能够调节长须罗蛉的胰蛋白酶分泌以使其自身受益,直接抑制胰蛋白酶基因表达会导致感染沙蝇中肠内的寄生虫数量增加。RNA干扰方法在感染利什曼原虫的沙蝇中的成功应用,现在开辟了利用该技术研究多种沙蝇基因及其在寄生虫与媒介相互作用中的作用的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca16/2796656/ecd62f5fb040/1756-3305-2-62-1.jpg

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本文引用的文献

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The role of NF-kappaB factor REL2 in the Aedes aegypti immune response.
Insect Biochem Mol Biol. 2009 Apr;39(4):303-14. doi: 10.1016/j.ibmb.2009.01.007. Epub 2009 Feb 7.
2
Dengue virus type 2 infections of Aedes aegypti are modulated by the mosquito's RNA interference pathway.
PLoS Pathog. 2009 Feb;5(2):e1000299. doi: 10.1371/journal.ppat.1000299. Epub 2009 Feb 13.
3
Visceral leishmaniasis in Brazil: trends and challenges.
Cad Saude Publica. 2008 Dec;24(12):2941-7. doi: 10.1590/s0102-311x2008001200024.
5
Gene silencing in phlebotomine sand flies: Xanthine dehydrogenase knock down by dsRNA microinjections.
Insect Biochem Mol Biol. 2008 Jun;38(6):652-60. doi: 10.1016/j.ibmb.2008.03.012. Epub 2008 Apr 4.
6
Conserved mosquito/parasite interactions affect development of Plasmodium falciparum in Africa.
PLoS Pathog. 2008 May 16;4(5):e1000069. doi: 10.1371/journal.ppat.1000069.
7
Leishmania chitinase facilitates colonization of sand fly vectors and enhances transmission to mice.
Cell Microbiol. 2008 Jun;10(6):1363-72. doi: 10.1111/j.1462-5822.2008.01132.x. Epub 2008 Feb 19.
9
Constitutive and blood meal-induced trypsin genes in Lutzomyia longipalpis.
Arch Insect Biochem Physiol. 2007 Oct;66(2):53-63. doi: 10.1002/arch.20198.
10
Leishmania manipulation of sand fly feeding behavior results in enhanced transmission.
PLoS Pathog. 2007 Jun;3(6):e91. doi: 10.1371/journal.ppat.0030091.

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