Evaluation of the function of a type I peritrophic matrix as a physical barrier for midgut epithelium invasion by mosquito-borne pathogens in Aedes aegypti

Vector-Borne and Zoonotic Diseases

Volumn 8, Issue 5, 2008, Pages 701-712

  Kato, Nobutaka ^a   Mueller, Christopher R ^a   Fuchs, Jeremy F ^a   McElroy, Kate ^b   Wessely, Vilena ^a   Higgs, Stephen ^b   Christensen, Bruce M ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b University of Texas Medical Branch School of Medicine   (United States)

Author keywords

Mosquito(es)

Indexed keywords

CHITIN SYNTHASE;

AEDES AEGYPTI; ANIMAL TISSUE; ARTICLE; BRUGIA PAHANGI; CONTROLLED STUDY; DENGUE VIRUS; EVALUATION; FEMALE; INTESTINE EPITHELIUM; MIDGUT; MOSQUITO; NONHUMAN; NUCLEOTIDE SEQUENCE; OOCYTE; PLASMODIUM; PLASMODIUM GALLINACEUM; PRIORITY JOURNAL; PROTEIN EXPRESSION; RNA INTERFERENCE;

AEDES; ANIMALS; BRUGIA PAHANGI; CHICKENS; DENGUE VIRUS; FEMALE; GASTROINTESTINAL TRACT; GERBILLINAE; HOST-PATHOGEN INTERACTIONS; INSECT VECTORS; OVIPOSITION; PLASMODIUM GALLINACEUM;

AEDES AEGYPTI; BRUGIA PAHANGI; DENGUE VIRUS; PLASMODIUM GALLINACEUM;

EID: 53549085423     PISSN: 15303667     EISSN: None     Source Type: Journal    
DOI: 10.1089/vbz.2007.0270     Document Type: Article

References (31)

1. Abraham, EG, Jacobs-Lorena, M. Mosquito midgut barriers to malaria parasite development. Insect Biochem Mol Biol 2004; 34:667-671.
2. Bartholomay, LC, Cho, WL, Rocheleau, TA, Boyle, JP, et al. Description of the transcriptomes of immune response-activated hemocytes from the mosquito vectors Aedes aegypti and Armigeres subalbatus. Infect Immun 2004; 72:4114-4126.
3. Beerntsen, BT, James, AA, Christensen, BM. Genetics of mosquito vector competence. Microbiol Mol Biol Rev 2000; 64:115-137.
4. Billingsley, PF, Rudin, W. The role of the mosquito peritrophic membrane in bloodmeal digestion and infectivity of Plasmodium species. J Parasitol 1992; 78:430-440.
5. Billker, O, Lindo, V, Panico, M, Etienne, AE, et al. Identification of xanthurenic acid as the putative inducer of malaria development in the mosquito. Nature 1998; 392:289-292.
6. Borovdsy, D. Proteolytic enzymes and blood digestion in the mosquito, Culex nigripalpus. Arch Insect Biochem Physiol 1986; 3:147-160.
7. Chamberlain, RW, Sudia, WD. Mechanism of transmission of viruses by mosquitoes. Annu Rev Entomol 1961; 6:371-390.
8. Christensen, BM, Sutherland, RD. Brugia pahangi: Exsheathment and midgut penetration in Aedes aegypti. Trans Am Microscop Soc 1984; 103:423-433.
9. Christophides, GK, Vlachou, D, Kafatos, FC. Comparative and functional genomics of the innate immune system in the malaria vector Anopheles gambiae. Immunol Rev 2004; 198:127-148.
10. de la Vega, H, Specht, CA, Liu, Y, Robbins, PW. Chitinases are a multi-gene family in Aedes, Anopheles and Drosophila. Insect Mol Biol 1998; 7:233-239.
11. Garcia, GE, Wirtz, RA, Barr, JR, Woolfitt, A, et al. Xanthurenic acid induces gametogenesis in Plasmodium, the malaria parasite. J Biol Chem 1998; 273:12003-12005.
12. Gass, RF, Yeates, RA. In vitro damage of cultured ookinetes of Plasmodium gallinaceum by digestive proteinases from susceptible Aedes aegypti. Acta Trop 1979; 36:243-252.
13. Graf, R, Raikhel, AS, Brown, MR, Lea, AO, et al. Mosquito trypsin: immunocytochemical localization in the midgut of blood-fed Aedes aegypti (L.). Cell Tissue Res 1986; 245:19-27.
14. Han, YS, Thompson, J, Kafatos, FC, Barillas-Mury, C. Molecular interactions between Anopheles stephensi midgut cells and Plasmodium berghei: the time bomb theory of ookinete invasion of mosquitoes. EMBO J 2000; 19:6030-6040.
15. Hardy, JL, Houk, EJ, Kramer, LD, Reeves, WC. Intrinsic factors affecting vector competence of mosquitoes for arboviruses. Annu Rev Entomol 1983; 28:229-262.
16. Higgs, S. How do mosquito vectors live with their viruses? In: Microbe-Vector Interactions. In: Gillespie, SH, Smith, GL, Osbourn, A, eds. Vector-Borne Diseases. Cambridge, UK, Cambridge University Press, 2004:103-137.
17. Houk, EJ, Obie, F, Hardy, JL. Peritrophic membrane formation and the midgut barrier to arboviral infection in the mosquito, Culex tarsalis Coquillett (Insecta, Diptera). Acta Trop 1979; 36:39-45.
18. Huber, M, Cabib, E, Miller, LH. Malaria parasite chitinase and penetration of the mosquito peritrophic membrane. Proc Natl Acad Sci U S A 1991; 88:2807-2810.
19. Kato, N, Mueller, CR, Fuchs, JF, Wessely, V, et al. Regulatory mechanisms of chitin biosynthesis and roles of chitin in peritrophic matrix formation in the midgut of adult Aedes aegypti. Insect Biochem Mol Biol 2006; 36:1-9.
20. Kogan, PH. Substitute blood meal for investigating and maintaining Aedes aegypti (Diptera: Culicidae). J Med Entomol 1990; 27:709-712.
21. Lehane, MJ. Peritrophic matrix structure and function. Annu Rev Entomol 1997; 42:525-550.
22. Moskalyk, LA, Oo, MM, Jacobs-Lorena, M. Peritrophic matrix proteins of Anopheles gambiae and Aedes aegypti. Insect Mol Biol 1996; 5:261-268.
23. Orihel, TC. The peritrophic membrane: its role as a barrier to infection of the arthropod host. In: Maramorosch, K, Shope, RE, eds. Invertebrate Immunity Mechanisms of Invertebrate Vector-Parasite Relations. New York, Academic Press, 1975:65-73.
24. Perrone, JB, Spielman, A. Microfilarial perforation of the midgut of a mosquito. J Parasitol 1986; 72:723-727.
25. Perrone, JB, Spielman, A. Time and site of assembly of the peritrophic membrane of the mosquito Aedes aegypti. Cell Tissue Res 1988; 252:473-478.
26. Shahabuddin, M, Toyoshima, T, Aikawa, M, Kaslow, DC. Transmission- blocking activity of a chitinase inhibitor and activation of malarial parasite chitinase by mosquito protease. Proc Natl Acad Sci U S A 1993; 90:4266-4270.
27. Shao, L, Devenport, M, Jacobs-Lorena, M. The peritrophic matrix of hematophagous insects. Arch Insect Biochem Physiol 2001; 47:119-125.
28. Stohler, HR. The peritrophic membrane in blood sucking Diptera in relation to their role as vectors of blood parasites. Acta Trop 1961; 18:263-266.
29. Van Handel, E, Romoser, WS. Proteolytic activity in the ectoperitrophic fluid of blood-fed Culex nigripalpus. Med Vet Entomol 1987; 1:251-255.
30. Villalon, JM, Ghosh, A, Jacobs-Lorena, M. The peritrophic matrix limits the rate of digestion in adult Anopheles stephensi and Aedes aegypti mosquitoes. J Insect Physiol 2003; 49:891-895.
31. Wang, P, Granados, RR. Molecular structure of the peritrophic membrane (PM): identification of potential PM target sites for insect control. Arch Insect Biochem Physiol 2001; 47:110-118.