Antibody responses of domestic animals to salivary antigens of Triatoma infestans as biomarkers for low-level infestation of triatomines

International Journal for Parasitology

Volumn 39, Issue 9, 2009, Pages 1021-1029

  Schwarz, Alexandra ^a,b   Sternberg, Jeremy M ^a   Johnston, Valerie ^a   Medrano Mercado, Nora ^c   Anderson, Jennifer M ^d   Hume, Jen C C ^e   Valenzuela, Jesus G ^d   Schaub, Günter A ^b   Billingsley, Peter F ^f  

^a UNIVERSITY OF ABERDEEN   (United Kingdom)

^b RUHR UNIVERSITY BOCHUM   (Germany)

^c UNIVERSIDAD MAYOR DE SAN SIMÓN   (Bolivia)

^d NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES   (United States)

^e Entomology Section   (United States)

^f SANARIA INC   (United States)

Author keywords

Antibody responses; Chagas disease; Chickens; Cross reactivity; Guinea pigs; Salivary proteins; Surveillance; Triatoma infestans

Indexed keywords

BIOLOGICAL MARKER; IMMUNOGLOBULIN G; PARASITE ANTIGEN;

ANTIBODY; ANTIGEN; ARTHROPOD; BIOMARKER; BIRD; DISEASE CONTROL; DISEASE RESISTANCE; DOMESTIC SPECIES; IMMUNE RESPONSE; PARASITE INFESTATION; PROTEIN;

ANTIBODY RESPONSE; ANTIBODY TITER; ANTIGEN RECOGNITION; ARTHROPOD; ARTICLE; BOLIVIA; CHAGAS DISEASE; CHICKEN; CHILE; CIMEX; CONTROLLED STUDY; CROSS REACTION; DISEASE CARRIER; ENZYME LINKED IMMUNOSORBENT ASSAY; GUINEA PIG; HOST PARASITE INTERACTION; IMMUNE RESPONSE; IMMUNOGENICITY; INFESTATION; MOSQUITO; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PSYCHODIDAE; SPECIES DIFFERENCE; TICK; TRIATOMA INFESTANS; TRYPANOSOMA CRUZI; VECTOR CONTROL; WESTERN BLOTTING;

ANIMALS; ANIMALS, DOMESTIC; ANTIBODY FORMATION; BIOLOGICAL MARKERS; BOLIVIA; CHAGAS DISEASE; CHICKENS; CHILE; GUINEA PIGS; HUMANS; MOLECULAR SEQUENCE DATA; PSYCHODIDAE; SALIVARY PROTEINS AND PEPTIDES; TRIATOMA;

CHILE; SOUTH AMERICA;

ANIMALIA; ARTHROPODA; CAVIA; CIMICIDAE; GALLUS GALLUS; IXODIDA; PHLEBOTOMINAE; TRIATOMA INFESTANS; TRYPANOSOMA CRUZI;

EID: 67349176393     PISSN: 00207519     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpara.2009.01.010     Document Type: Article

References (52)

1. Amino R., Tanaka A.S., and Schenkman S. Triapsin, an unusual activatable serine protease from the saliva of the hematophagous vector of Chagas disease Triatoma infestans (Hemiptera: Reduviidae). Insect. Biochem. Mol. Biol. 31 (2001) 465-472
2. Barbosa S.E., Diotaiuti L., Soares R.P., and Pereira M.H. Differences in saliva composition among three Brazilian populations of Panstrongylus megistus (Hemiptera, Reduviidae). Acta Trop. 72 (1999) 91-98
3. Barbosa S.E., Diotaiuti L., Braga E.M., and Pereira M.H. Variability of the salivary proteins of 20 Brazilian populations of Panstrongylus megistus (Hemiptera: Reduviidae: Triatominae). Acta Trop. 92 (2004) 25-33
4. Barral A., Honda E., Caldas A., Costa J., Vinhas V., Rowton E.D., Valenzuela J.G., Charlab R., Barral-Netto M., and Ribeiro J.M. Human immune response to sand fly salivary gland antigens: a useful epidemiological marker?. Am. J. Trop. Med. Hyg. 62 (2000) 740-745
5. Billingsley P.F., Baird J., Mitchell J.A., and Drakeley C. Immune interactions between mosquitoes and their hosts. Parasite Immunol. 28 (2006) 143-153
6. Cecere M.C., Gürtler R.E., Canale D.M., Chuit R., and Cohen J.E. Effects of partial housing improvement and insecticide spraying on the reinfestation dynamics of Triatoma infestans in rural northwestern Argentina. Acta Trop. 84 (2002) 101-116
7. Champagne D.E. Antihemostatic molecules from saliva of blood-feeding arthropods. Pathophysiol. Haemost. Thromb. 34 (2005) 221-227
8. Chapman M.D., Marshall N.A., and Saxon A. Identification and partial purification of species-specific allergens from Triatoma protracta (Heteroptera, Reduviidae). J. Allergy Clin. Immun. 78 (1986) 436-442
9. Chippaux J.P., Postigo J.R., Santalla J.A., Schneider D., and Brutus L. Epidemiological evaluation of Chagas disease in a rural area of southern Bolivia. Trans. R. Soc. Trop. Med. Hyg. 102 (2008) 578-584
10. Cornelie S., Remoue F., Doucoure S., Ndiaye T., Sauvage F.X., Boulanger D., and Simondon F. An insight into immunogenic salivary proteins of Anopheles gambiae in African children. Malar. J. 6 (2007) 75
11. Dias, J.C.P., Schofield, C.J., 1999. The evolution of Chagas disease (American trypanosomiasis) control after 90 years since Carlos Chagas discovery. Mem Inst Oswaldo Cruz 94 (Suppl. 1), 103-121.
12. Dias J.C.P., Silveira A.C., and Schofield C.J. The impact of Chagas disease control in Latin America: a review. Mem. Inst. Oswaldo Cruz 97 (2002) 603-612
13. Dimopoulos G., Richman A., Müller H.M., and Kafatos F.C. Molecular immune responses of the mosquito Anopheles gambiae to bacteria and malaria parasites. Proc. Natl. Acad. Sci. USA 94 (1997) 11508-11513
14. 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
15. Drakeley C.J., Corran P.H., Coleman P.G., Tongren J.E., McDonald S.L.R., Carneiro I., Malima R., Lusingu J., Manjurano A., Nkya W.M.M., Lemnge M.M., Cox J., Reyburn H., and Riley E.M. Estimating medium- and long-term trends in malaria transmission by using serological markers of malaria exposure. Proc. Natl. Acad. Sci. USA 102 (2005) 5108-5113
16. Fox I., and Bayona I.G. Circulating precipitating antibodies in the rabbit from the bites of Rhodnius prolixus as shown by agar-gel tests. J. Parasitol. 54 (1968) 1239-1240
17. Gomes R.B., Brodskyn C., de Oliveira C.I., Costa J., Miranda J.C., Caldas A., Valenzuela J.G., Barral-Netto M., and Barral A. Seroconversion against Lutzomyia longipalpis saliva concurrent with the development of anti-Leishmania chagasi delayed-type hypersensitivity. J. Infect. Dis. 186 (2002) 1530-1534
18. Gürtler R.E., Kitron U., Cecere M.C., Segura E.L., and Cohen J.E. Sustainable vector control and management of Chagas disease in the Gran Chaco, Argentina. Proc. Natl. Acad. Sci. USA 104 (2007) 16194-16199
19. Hecht M.M., Bussacos A.C., Lozzi S.P., Santana J.M., and Teixeira A.R. Triatoma infestans chooses to feed upon immune prey. Am. J. Trop. Med. Hyg. 75 (2006) 893-900
20. Heukeshoven J., and Dernick R. Characterization of a solvent system for separation of water-insoluble poliovirus proteins by reversed-phase high-performance liquid chromatography. J. Chromatogr. 326 (1985) 91-101
21. Hostomska J., Rohousova I., Volfova V., Stanneck D., Mencke N., and Volf P. Kinetics of canine antibody response to saliva of the sand fly Lutzomyia longipalpis. Vector Borne Zoonotic Dis. 8 (2008) 443-450
22. Inokuma H., Ohno K., and Onishi T. Is the detection of anti-Rhipicephalus sanguineus (Rs24p) antibodies a valuable epidemiological tool of tick infestation in dogs?. Vet. Res. 31 (2000) 365-369
23. Kalvachova P., Hribalova V., Kodym P., and Volf P. Modulation of murine lymphocyte responsiveness by the saliva of Rhodnius prolixus (Hemiptera: Reduviidae). J. Med. Entomol. 36 (1999) 341-344
24. Kollien A.H., and Schaub G.A. The development of Trypanosoma cruzi (Trypanosomatidae) in the reduviid bug Triatoma infestans (Insecta): influence of starvation. J. Eukaryot. Microbiol. 45 (1998) 59-63
25. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
26. Lane R.S., Moss R.B., Hsu Y.P., Wei T., Mesirow M.L., and Kuo M.M. Anti-arthropod saliva antibodies among residents of a community at high risk for Lyme disease in California. Am. J. Trop. Med. Hyg. 61 (1999) 850-859
27. Lanzaro G.C., Lopes A.H., Ribeiro J.M., Shoemaker C.B., Warburg A., Soares M., and Titus R.G. Variation in the salivary peptide, maxadilan, from species in the Lutzomyia longipalpis complex. Insect. Mol. Biol. 8 (1999) 267-275
28. Marshall N. Allergy to Triatoma protracta (Heteroptera: Reduviidae). II. Antigen production in vitro. J. Med. Entomol. 19 (1982) 253-254
29. Milleron R.S., Mutebi J.P., Valle S., Montoya A., Yin H., Soong L., and Lanzaro G.C. Antigenic diversity in maxadilan, a salivary protein from the sand fly vector of American visceral leishmaniasis. Am. J. Trop. Med. Hyg. 70 (2004) 286-293
30. Modi G.B., and Tesh R.B. A simple technique for mass rearing Lutzomyia longipalpis and Phlebotomus papatasi (Diptera: Psychodidae) in the laboratory. J. Med. Entomol. 20 (1983) 568-569
31. Nascimento R.J., Santana J.M., Lozzi S.P., Araujo C.N., and Teixeira A.R. Human IgG1 and IgG4: the main antibodies against Triatoma infestans (Hemiptera: Reduviidae) salivary gland proteins. Am. J. Trop. Med. Hyg. 65 (2001) 219-226
32. Orlandi-Pradines E., Almeras L., Denis de Senneville L., Barbe S., Remoue F., Villard C., Cornelie S., Penhoat K., Pascual A., Bourgouin C., Fontenille D., Bonnet J., Corre-Catelin N., Reiter P., Pages F., Laffite D., Boulanger D., Simondon F., Pradines B., Fusai T., and Rogier C. Antibody response against saliva antigens of Anopheles gambiae and Aedes aegypti in travellers in tropical Africa. Microbes Infect. 9 (2007) 1454-1462
33. Pineda V., Montalvo E., Alvarez D., Santamaria A.M., Calzada J.E., and Saldana A. Feeding sources and trypanosome infection index of Rhodnius pallescens in a Chagas disease endemic area of Amador County, Panama. Rev. Inst. Med. Trop. Sao Paulo 50 (2008) 113-116
34. Pinnas J.L., Lindberg R.E., Chen T.M.W., and Meinke G.C. Studies of kissing bug sensitive patients - Evidence for the lack of cross-reactivity between Triatoma protracta and Triatoma rubida salivary-gland extracts. J. Allergy Clin. Immun. 77 (1986) 364-370
35. Poinsignon A., Cornelie S., Remoue F., Grebaut P., Courtin D., Garcia A., and Simondon F. Human/vector relationships during human African trypanosomiasis: initial screening of immunogenic salivary proteins of Glossina species. Am. J. Trop. Med. Hyg. 76 (2007) 327-333
36. Ramsey J.M., and Schofield C.J. Control of Chagas disease vectors. Salud Publica Mex. 45 (2003) 123-128
37. Remoue F., Cisse B., Ba F., Sokhna C., Herve J.P., Boulanger D., and Simondon F. Evaluation of the antibody response to Anopheles salivary antigens as a potential marker of risk of malaria. Trans. R. Soc. Trop. Med. Hyg. 100 (2006) 363-370
38. Ribeiro J.M. Blood-feeding arthropods: live syringes or invertebrate pharmacologists?. Infect. Agents Dis. 4 (1995) 143-152
39. Rohousova I., Ozensoy S., Ozbel Y., and Volf P. Detection of species-specific antibody response of humans and mice bitten by sand flies. Parasitology 130 (2005) 493-499
40. Rohousova I., Volf P., and Lipoldova M. Modulation of murine cellular immune response and cytokine production by salivary gland lysate of three sand fly species. Parasite Immunol. 27 (2005) 469-473
41. Rohousova I., and Volf P. Sand fly saliva: effects on host immune response and Leishmania transmission. Folia Parasit. 53 (2006) 161-171
42. Sanders M.L., Jaworski D.C., Sanchez J.L., DeFraites R.F., Glass G.E., Scott A.L., Raha S., Ritchie B.C., Needham G.R., and Schwartz B.S. Antibody to a cDNA-derived calreticulin protein from Amblyomma americanum as a biomarker of tick exposure in humans. Am. J. Trop. Med. Hyg. 59 (1998) 279-285
43. Schaub G.A. Trypanosoma cruzi: quantitative studies of the development of two strains in small intestine and rectum of the vector Triatoma infestans. Exp. Parasitol. 68 (1989) 260-273
44. Schaub G.A. Kissing bugs. In: Mehlhorn H. (Ed). Encyclopedia of Parasitology Vol. 1 (2008), Springer-Verlag, Heidelberg 684-686
45. Schaub G.A., and Schottelius J. Identification of trypanosomes isolated from Reduviidae from North Chile. Z. Parasitenkd. 70 (1984) 3-9
46. Schofield C.J., Jannin J., and Salvatella R. The future of Chagas disease control. Trends Parasitol. 22 (2006) 583-588
47. Schwartz B.S., Ford D.P., Childs J.E., Rothman N., and Thomas R.J. Anti-tick saliva antibody: a biologic marker of tick exposure that is a risk factor for Lyme disease seropositivity. Am. J. Epidemiol. 134 (1991) 86-95
48. Schwartz B.S., Nadelman R.B., Fish D., Childs J.E., Forseter G., and Wormser G.P. Entomologic and demographic correlates of anti-tick saliva antibody in a prospective study of tick bite subjects in Westchester County, New York. Am. J. Trop. Med. Hyg. 48 (1993) 50-57
49. Toloza A.C., Germano M., Cueto G.M., Vassena C., Zerba E., and Picollo M.I. Differential patterns of insecticide resistance in eggs and first instars of Triatoma infestans (Hemiptera: Reduviidae) from Argentina and Bolivia. J. Med. Entomol. 45 (2008) 421-426
50. Volf P., Grubhoffer L., and Hosek P. Characterisation of salivary gland antigens of Triatoma infestans and antigen-specific serum antibody response in mice exposed to bites of T. Infestans. Vet. Parasitol. 47 (1993) 327-337
51. Volf P., Hostomska J., and Rohousova I. Molecular crosstalks in Leishmania-sandfly-host relationships. Parasite 15 (2008) 237-243
52. WHO. New global effort to eliminate Chagas disease. Wkly Epidemiol. Rec. 82 (2007) 259-260