Analysis of ESTs from Lutzomyia longipalpis sand flies and their contribution toward understanding the insect-parasite relationship

Genomics

Volumn 88, Issue 6, 2006, Pages 831-840

  Dillon, Rod J ^a   Ivens, Al C ^b   Churcher, Carol ^b   Holroyd, Nancy ^b   Quail, Michael A ^b   Rogers, Matthew E ^a   Soares, M Bento ^c   Bonaldo, Maria F ^c   Casavant, Thomas L ^d   Lehane, Mike J ^a   Bates, Paul A ^a  

^a LIVERPOOL SCHOOL OF TROPICAL MEDICINE   (United Kingdom)

^b WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^c NORTHWESTERN UNIVERSITY   (United States)

^d University of Iowa   (United States)

Author keywords

Expressed sequence tag; Genomics; Immunity; Leishmania; Lutzomyia; Midgut; Parasite

Indexed keywords

BACTERIAL PROTEIN; CASPASE; CONTIG; GALECTIN; GLUTAMATE AMMONIA LIGASE; PEROXIDASE; SCAVENGER RECEPTOR; SERINE PROTEINASE INHIBITOR; THIOESTER;

ARTICLE; CONTROLLED STUDY; DNA LIBRARY; EXPRESSED SEQUENCE TAG; GENE; GENE SEQUENCE; IMMUNE RESPONSE; INSECT GENETICS; LUTZOMYIA LONGIPALPIS; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PSYCHODIDAE; SEQUENCE ANALYSIS; VISCERAL LEISHMANIASIS;

ANIMALS; COMPUTATIONAL BIOLOGY; EXPRESSED SEQUENCE TAGS; HOST-PARASITE RELATIONS; INSECT PROTEINS; LEISHMANIA; MOLECULAR SEQUENCE DATA; PSYCHODIDAE; SEQUENCE ANALYSIS, DNA;

INSECTA; LUTZOMYIA LONGIPALPIS; PHLEBOTOMINAE;

EID: 33751083846     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/j.ygeno.2006.06.011     Document Type: Article

References (73)

1. Soares R.P.P., and Turco S.J. Lutzomyia longipalpis (Diptera: Psychodidae: Phlebotominae): a review. An. Acad. Bras. Cienc. 75 (2003) 441
2. Alexander B., de Carvalho R.L., McCallum H., and Pereira M.H. Role of the domestic chicken (Gallus gallus) in the epidemiology of urban visceral leishmaniasis in Brazil. Emerging Infect. Dis. 8 (2002) 1480-1485
3. Desjeux P., et al. Leishmaniasis. Nat. Rev. Microbiol. 2 (2004) 692-693
4. Roxstrom-Lindquist K., Terenius O., and Faye I. Parasite-specific immune response in adult Drosophila melanogaster: a genomic study. EMBO Rep. 5 (2004) 207-212
5. Dimopoulos G., et al. Genome expression analysis of Anopheles gambiae: responses to injury, bacterial challenge, and malaria infection. Proc. Natl. Acad. Sci. USA 99 (2002) 8814-8819
6. Valenzuela J.G., Garfield M., Rowton E.D., and Pham V.M. Identification of the most abundant secreted proteins from the salivary glands of the sand fly Lutzomyia longipalpis, vector of Leishmania chagasi. J. Exp. Biol. 207 (2004) 3717-3729
7. Ramalho-Ortigao J.M., Kamhawi S., Rowton E.D., Ribeiro J.M.C., and Valenzuela J.G. Cloning and characterization of trypsin- and chymotrypsin-like proteases from the midgut of the sand fly vector Phlebotomus papatasi. Insect Biochem. Mol. Biol. 33 (2003) 163-171
8. Ramalho-Ortigao J.M., and Traub-Cseko Y.M. Molecular characterization of Llchit1, a midgut chitinase cDNA from the leishmaniasis vector Lutzomyia longipalpis. Insect Biochem. Mol. Biol. 33 (2003) 279-287
9. Ramalho-Ortigao J.M., et al. Characterization of constitutive and putative differentially expressed mRNAs by means of expressed sequence tags, differential display reverse transcriptase-PCR and randomly amplified polymorphic DNA-PCR from the sand fly vector Lutzomyia longipalpis. Mem. Inst. Oswaldo Cruz 96 (2001) 105-111
10. Boulanger N., et al. Characterization of a defensin from the sand fly Phlebotomus duboscqi induced by challenge with bacteria or the protozoan parasite Leishmania major. Infect. Immun. 72 (2004) 7140-7146
11. Kamhawi S., et al. A role for insect galectins in parasite survival. Cell 119 (2004) 329-341
12. Aksoy S., Gibson W.C., and Lehane M.J. Interactions between tsetse and trypanosomes with implications for the control of trypanosomiasis. Adv. Parasitol. 53 (2003) 1-83
13. Sacks D., and Kamhawi S. Molecular aspects of parasite-vector and vector-host interactions in Leishmaniasis. Annu. Rev. Microbiol. 55 (2001) 453-483
14. Stierhof Y.D., et al. Filamentous proteophosphoglycan secreted by Leishmania promastigotes forms gel-like three-dimensional networks that obstruct the digestive tract of infected sandfly vectors. Eur. J. Cell Biol. 78 (1999) 675-689
15. Rogers M.E., Chance M.L., and Bates P.A. The role of promastigote secretory gel in the origin and transmission of the infective stage of Leishmania mexicana by the sandfly Lutzomyia longipalpis. Parasitology 124 (2002) 495-507
16. Rogers M.E., Ilg T., Nikolaev A.V., Ferguson M.A.J., and Bates P.A. Transmission of cutaneous leishmaniasis by sand flies is enhanced by regurgitation of fPPG. Nature 430 (2004) 463-467
17. Lehane M.J., et al. Adult midgut expressed sequence tags from the tsetse fly Glossina morsitans morsitans and expression analysis of putative immune response genes. Genome Biol. 4 (2003) R63
18. Severson D.W., Knudson D.L., Soares M.B., and Loftus B.J. Aedes aegypti genomics. Insect Biochem. Mol. Biol. 34 (2004) 715-721
19. Ewing B., and Green P. Base-calling of automated sequencer traces using Phred. II. Error probabilities. Genome Res. 8 (1998) 186-194
20. Walters L.L., Irons K.P., Modi G.B., and Tesh R.B. Refractory barriers in the sand fly Phlebotomus papatasi (Diptera, Psychodidae) to infection with Leishmania panamensis. Am. J. Trop. Med. Hyg. 46 (1992) 211-228
21. Niu L.L., Kiley L.M., Dasgupta R., Kohler P., and Christensen B.M. Three regulatory regions of the Aedes aegypti glutamine synthetase gene differentially regulate expression: identification of a crucial regulator in the first exon. Insect Mol. Biol. 12 (2003) 571-579
22. Terra W.R. The origin and functions of the insect peritrophic membrane and peritrophic gel. Arch. Insect Biochem. Physiol. 47 (2001) 47-61
23. Gaines P.J., Walmsley S.J., and Wisnewski N. Cloning and characterization of five cDNAs encoding peritrophin-A domains from the cat flea, Ctenocephalides felis. Insect Biochem. Mol. Biol. 33 (2003) 1061-1073
24. Theopold U., et al. Helix pomatia lectin, an inducer of Drosophila immune response, binds to hemomucin, a novel surface mucin. J. Biol. Chem. 271 (1996) 12708-12715
25. Shao L., Devenport M., Fujioka H., Ghosh A., and Jacobs-Lorena M. Identification and characterization of a novel peritrophic matrix protein, Ae-Aper50, and the microvillar membrane protein, AEG12, from the mosquito, Aedes aegypti. Insect Biochem. Mol. Biol. 35 (2005) 947-959
26. Morlais I., Mori A., Schneider J.R., and Severson D.W. A targeted approach to the identification of candidate genes determining susceptibility to Plasmodium gallinaceum in Aedes aegypti. Mol. Genet. Genom. 269 (2003) 753-764
27. Mahairaki V., Lycett G., Blass C., and Louis C. Beta-integrin of Anopheles gambiae: mRNA cloning and analysis of structure and expression. Insect Mol. Biol. 10 (2001) 217-223
28. Brittingham A., Chen G., McGwire B.S., Chang K.P., and Mosser D.M. Interaction of Leishmania gp63 with cellular receptors for fibronectin. Infect. Immun. 67 (1999) 4477-4484
29. Vasso Mahairaki G.L., Sidén-Kiamos I., Sinden R.E., and Louis C. Close association of invading Plasmodium berghei and β-integrin in the Anopheles gambiae midgut. Arch. Insect Biochem. Physiol. 60 (2005) 13-19
30. Ortega-Cava C.F., et al. Strategic compartmentalization of Toll-like receptor 4 in the mouse gut. J. Immunol. 170 (2003) 3977-3985
31. Dimopoulos G., Seeley D., Wolf A., and Kafatos F.C. Malaria infection of the mosquito Anopheles gambiae activates immune-responsive genes during critical transition stages of the parasite life cycle. EMBO J. 17 (1998) 6115-6123
32. Soares R.P.P., et al. Leishmania chagasi: lipophosphoglycan characterization and binding to the midgut of the sand fly vector Lutzomyia longipalpis. Mol. Biochem. Parasitol. 121 (2002) 213-224
33. Dillon R.J., and Lane R.P. Detection of Leishmania lipophosphoglycan binding proteins in the gut of the sand fly vector. Parasitology 118 (1999) 27-32
34. Osta M.A., Christophides G.K., and Kafatos F.C. Effects of mosquito genes on Plasmodium development. Science 303 (2004) 2030-2032
35. Christophides G.K., et al. Immunity-related genes and gene families in Anopheles gambiae. Science 298 (2002) 159-165
36. Blandin S., et al. Complement-like protein TEP1 is a determinant of vectorial capacity in the malaria vector Anopheles gambiae. Cell 116 (2004) 661-670
37. Choi J.Y., et al. Calreticulin enriched as an early-stage encapsulation protein in wax moth Galleria mellonella larvae. Dev. Comp. Immunol. 26 (2002) 335-343
38. Francischetti I.M.B., Valenzuela J.G., Pham V.M., Garfield M.K., and Ribeiro J.M.C. Toward a catalog for the transcripts and proteins (sialome) from the salivary gland of the malaria vector Anopheles gambiae. J. Exp. Biol. 205 (2002) 2429-2451
39. Danielli A., Kafatos F.C., and Loukeris T.G. Cloning and characterization of four Anopheles gambiae serpin isoforms, differentially induced in the midgut by Plasmodium berghei invasion. J. Biol. Chem. 278 (2003) 4184-4193
40. Danielli A., Barillas-Mury C., Kumar S., Kafatos F.C., and Loukeris T.G. Overexpression and altered nucleocytoplasmic distribution of Anopheles ovalbumin-like SRPN10 serpins in Plasmodium-infected midgut cells. Cell Microbiol. 7 (2005) 181-190
41. Abraham E.G., et al. Analysis of the Plasmodium and Anopheles transcriptional repertoire during ookinete development and midgut invasion. J. Biol. Chem. 279 (2004) 5573-5580
42. Tzou P., et al. Tissue-specific inducible expression of antimicrobial peptide genes in Drosophila surface epithelia. Immunity 13 (2000) 737-748
43. Vodovar N., et al. Drosophila host defense after oral infection by an entomopathogenic Pseudomonas species. Proc. Natl. Acad. Sci. USA 102 (2005) 11414-11419
44. Pal S., and Wu L. Guts and glory: balancing microbes and the immune response. Dev. Cell 8 (2005) 1-2
45. Kanda H., Igaki T., Kanuka H., Yagi T., and Miura M. Wengen, a member of the Drosophila tumor necrosis factor receptor superfamily, is required for Eiger signaling. J. Biol. Chem. 277 (2002) 28372-28375
46. Craig C.R., Fink J.L., Yagi Y., Ip Y.T., and Cagan R.L. A Drosophila p38 orthologue is required for environmental stress responses. EMBO Rep. 5 (2004) 1058-1063
47. Kim D.H., et al. A conserved p38 MAP kinase pathway in Caenorhabditis elegans innate immunity. Science 297 (2002) 623-626
48. Ha E.M., et al. An antioxidant system required for host protection against gut infection in Drosophila. Dev. Cell 8 (2005) 125-132
49. Hao Z., Kasumba I., and Aksoy S. Proventriculus (cardia) plays a crucial role in immunity in tsetse fly (Diptera: Glossinidiae). Insect Biochem. Mol. Biol. 33 (2003) 1155-1164
50. Munks R.J.L., et al. Antioxidant gene expression in the blood-feeding fly Glossina morsitans morsitans. Insect Mol. Biol. 14 (2005) 483-491
51. Bauer H., et al. Thioredoxin reductase from the malaria mosquito Anopheles gambiae-comparisons with the orthologous enzymes of Plasmodium falciparum and the human host. Eur. J. Biochem. 270 (2003) 4272-4281
52. Kumar S., Gupta L., Han Y.S., and Barillas-Mury C. Inducible peroxidases mediate nitration of Anopheles midgut cells undergoing apoptosis in response to Plasmodium invasion. J. Biol. Chem. 279 (2004) 53475-53482
53. Kumar S., and Barillas-Mury C. Ookinete-induced midgut peroxidases detonate the time bomb in anopheline mosquitoes. Insect Biochem. Mol. Biol. 35 (2005) 721-727
54. Souza A.V.G., Petretski J.H., Demasi M., Bechara E.J.H., and Oliveira P.L. Urate protects a blood-sucking insect against hemin-induced oxidative stress. Free Radic. Biol. Med. 22 (1997) 209
55. Bachali S., et al. Phylogenetic analysis of invertebrate lysozymes and the evolution of lysozyme function. J. Mol. Evol. 54 (2002) 652-664
56. Borovsky D., and Schlein Y. Trypsin and chymotrypsin-like enzymes of the sandfly Phlebotomus papatasi infected with Leishmania and their possible role in vector competence. Med. Vet. Entomol. 1 (1987) 235-242
57. Dillon R.J., and Lane R.P. Influence of Leishmania infection on blood-meal digestion in the sand flies Phlebotomus papatasi and Phlebotomus langeroni. Parasitol. Res. 79 (1993) 492-496
58. Pimenta P.F.P., Modi G.B., Pereira S.T., Shahabuddin M., and Sacks D.L. Novel role for the peritrophic matrix in protecting Leishmania from the hydrolytic activities of the sand fly midgut. Parasitology 115 (1997) 359-369
59. Jordao B.P., Capella A.N., Terra W.R., Ribeiro A.F., and Ferreira C. Nature of the anchors of membrane-bound aminopeptidase, amylase, and trypsin and secretory mechanisms in Spodoptera frugiperda (Lepidoptera) midgut cells. J. Insect Physiol. 45 (1999) 29-37
60. Rosenfeld A., and Vanderberg J.P. Plasmodium berghei: induction of aminopeptidase in malaria-resistant strain of Anopheles gambiae. Exp. Parasitol. 93 (1999) 101-104
61. Edwards M.J., et al. Characterization of a carboxypeptidase A gene from the mosquito, Aedes aegypti. Insect Mol. Biol. 9 (2000) 33-38
62. Leslie G., Barrett M., and Burchmore R. Leishmania mexicana: promastigotes migrate through osmotic gradients. Exp. Parasitol. 102 (2002) 117
63. Zheng L.B., Whang L.H.S., Kumar V., and Kafatos F.C. Two genes encoding midgut-specific maltase-like polypeptides from Anopheles gambiae. Exp. Parasitol. 81 (1995) 272-283
64. Schlein Y., Jacobson R.L., and Messer G. Leishmania infections damage the feeding mechanism of the sandfly vector and implement parasite transmission by bite. Proc. Natl. Acad. Sci. USA 89 (1992) 9944-9948
65. Joshi M.B., et al. Molecular characterization, expression, and in vivo analysis of LmexCht1; the chitinase of the human pathogen Leishmania mexicana. J. Biol. Chem. 280 (2005) 3847-3861
66. de la Vega H., Specht C.A., Liu Y., and Robbins P.W. Chitinases are a multi-gene family in Aedes, Anopheles and Drosophila. Insect Mol. Biol. 7 (1998) 233-239
67. Shi L., and Paskewitz S.M. Identification and molecular characterization of two immune-responsive chitinase-like proteins from Anopheles gambiae. Insect Mol. Biol. 13 (2004) 387-398
68. Rosetto M., et al. A mammalian-like lipase gene is expressed in the female reproductive accessory glands of the sand fly Phlebotomus papatasi (Diptera, Psychodidae). Insect Mol. Biol. 12 (2003) 501-508
69. Kallberg Y., Oppermann U., Jornvall H., and Persson B. Short-chain dehydrogenase/reductase (SDR) relationships: a large family with eight clusters common to human, animal, and plant genomes. Protein Sci. 11 (2002) 636-641
70. Ivens A.C., et al. The genome of the kinetoplastid parasite, Leishmania major. Science 309 (2005) 436-442
71. Lehane M.J., Wu D., and Lehane S.M. Midgut-specific immune molecules are produced by the blood-sucking insect Stomoxys calcitrans. Proc. Natl. Acad. Sci. USA 94 (1997) 11502-11507
72. Bonaldo M.D.F., Lennon G., and Soares M.B. Normalization and subtraction: two approaches to facilitate gene discovery. Genome Res. 6 (1996) 791-806
73. Bonfield J.K., Smith K., and Staden R. A new DNA sequence assembly program. Nucleic Acids Res. 23 (1995) 4992-4999