Ramalho-Ortigão Marcelo, Jochim Ryan C, Anderson Jennifer M, Lawyer Phillip G, Pham Van-My, Kamhawi Shaden, Valenzuela Jesus G
Vector Molecular Biology Unit, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
BMC Genomics. 2007 Aug 30;8:300. doi: 10.1186/1471-2164-8-300.
In sandflies, the blood meal is responsible for the induction of several physiologic processes that culminate in egg development and maturation. During blood feeding, infected sandflies are also able to transmit the parasite Leishmania to a suitable host. Many blood-induced molecules play significant roles during Leishmania development in the sandfly midgut, including parasite killing within the endoperitrophic space. In this work, we randomly sequenced transcripts from three distinct high quality full-length female Phlebotomus papatasi midgut-specific cDNA libraries from sugar-fed, blood-fed and Leishmania major-infected sandflies. Furthermore, we compared the transcript expression profiles from the three different cDNA libraries by customized bioinformatics analysis and validated these findings by semi-quantitative PCR and real-time PCR.
Transcriptome analysis of 4010 cDNA clones resulted in the identification of the most abundant P. papatasi midgut-specific transcripts. The identified molecules included those with putative roles in digestion and peritrophic matrix formation, among others. Moreover, we identified sandfly midgut transcripts that are expressed only after a blood meal, such as microvilli associated-like protein (PpMVP1, PpMVP2 and PpMVP3), a peritrophin (PpPer1), trypsin 4 (PpTryp4), chymotrypsin PpChym2, and two unknown proteins. Of interest, many of these overabundant transcripts such as PpChym2, PpMVP1, PpMVP2, PpPer1 and PpPer2 were of lower abundance when the sandfly was given a blood meal in the presence of L. major.
This tissue-specific transcriptome analysis provides a comprehensive look at the repertoire of transcripts present in the midgut of the sandfly P. papatasi. Furthermore, the customized bioinformatic analysis allowed us to compare and identify the overall transcript abundance from sugar-fed, blood-fed and Leishmania-infected sandflies. The suggested upregulation of specific transcripts in a blood-fed cDNA library were validated by real-time PCR, suggesting that this customized bioinformatic analysis is a powerful and accurate tool useful in analysing expression profiles from different cDNA libraries. Additionally, the findings presented in this work suggest that the Leishmania parasite is modulating key enzymes or proteins in the gut of the sandfly that may be beneficial for its establishment and survival.
在白蛉中,血餐可诱导多种生理过程,最终导致卵子发育和成熟。在吸血过程中,受感染的白蛉还能够将利什曼原虫传播给合适的宿主。许多由血液诱导的分子在利什曼原虫在白蛉中肠发育过程中发挥重要作用,包括在内营养空间内杀死寄生虫。在这项研究中,我们从取食糖水、取食血液和感染硕大利什曼原虫的雌性巴氏白蛉中肠特异性高质量全长cDNA文库中随机测序转录本。此外,我们通过定制的生物信息学分析比较了来自三个不同cDNA文库的转录本表达谱,并通过半定量PCR和实时PCR验证了这些发现。
对4010个cDNA克隆进行转录组分析,鉴定出巴氏白蛉中肠特异性最丰富的转录本。鉴定出的分子包括那些在消化和围食膜形成等过程中可能发挥作用的分子。此外,我们鉴定出仅在取食血液后才表达的白蛉中肠转录本,如微绒毛相关样蛋白(PpMVP1、PpMVP2和PpMVP3)、一种围食膜蛋白(PpPer1)、胰蛋白酶4(PpTryp4)、胰凝乳蛋白酶PpChym2和两种未知蛋白。有趣的是,当白蛉在硕大利什曼原虫存在的情况下取食血液时,许多这些过量表达的转录本,如PpChym2、PpMVP1、PpMVP2、PpPer1和PpPer2的丰度较低。
这种组织特异性转录组分析全面展示了巴氏白蛉中肠中存在的转录本库。此外,定制的生物信息学分析使我们能够比较和鉴定取食糖水、取食血液和感染利什曼原虫的白蛉的总体转录本丰度。通过实时PCR验证了取食血液的cDNA文库中特定转录本的上调,这表明这种定制的生物信息学分析是一种强大而准确的工具,可以用于分析不同cDNA文库的表达谱。此外,这项研究中的发现表明,利什曼原虫寄生虫正在调节白蛉肠道中的关键酶或蛋白质,这可能有利于其建立和生存。