An. gambiae gSG6-P1 evaluation as a proxy for human-vector contact in the Americas: A pilot study

Parasites and Vectors

Volumn 8, Issue 1, 2015, Pages

  Londono Renteria, Berlin ^a   Drame, Papa M ^b   Weitzel, Thomas ^c   Rosas, Reinaldo ^d   Gripping, Crystal ^e   Cardenas, Jenny C ^f   Alvares, Marcela ^g   Wesson, Dawn M ^e   Poinsignon, Anne ^h   Remoue, Franck ^h   Colpitts, Tonya M ^a  

^a UNIVERSITY OF SOUTH CAROLINA SCHOOL OF MEDICINE   (United States)

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

^c UNIVERSIDAD DEL DESARROLLO   (Chile)

^d HOSPITAL MILITAR DE SANTIAGO   (Chile)

^e TULANE UNIVERSITY   (United States)

^f Hospital Los Patios   (Colombia)

^g Hospital Emiro Quintero Canizales   (Colombia)

^h Institut de Recherche pour le Développement IRD   (Côte d’Ivoire)

Author keywords

[No Author keywords available]

Indexed keywords

GSG6 P1; IMMUNOGLOBULIN G ANTIBODY; PEPTIDE; UNCLASSIFIED DRUG; ANTIBODY; IMMUNOGLOBULIN G; INSECT PROTEIN; SALIVA PROTEIN;

ADULT; ANOPHELES GAMBIAE; ANTIBODY BLOOD LEVEL; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; ENDEMIC DISEASE; ENZYME LINKED IMMUNOSORBENT ASSAY; HOST PARASITE INTERACTION; HUMAN; IMMUNE RESPONSE; MALARIA; MOSQUITO BITE; NONHUMAN; OPTICAL DENSITY; PARASITE VECTOR; PILOT STUDY; WESTERN HEMISPHERE; ADOLESCENT; ANIMAL; BLOOD; CHILE; COLOMBIA; FEMALE; IMMUNOLOGY; INSECT BITE; INSECT VECTOR; MALE; NORTH CAROLINA; PARASITOLOGY; PHYSIOLOGY; PLASMODIUM; SEASON; TRAVEL; YOUNG ADULT;

ADOLESCENT; ANIMALS; ANOPHELES GAMBIAE; ANTIBODIES; CHILE; COLOMBIA; ENZYME-LINKED IMMUNOSORBENT ASSAY; FEMALE; HUMANS; IMMUNOGLOBULIN G; INSECT BITES AND STINGS; INSECT PROTEINS; INSECT VECTORS; MALARIA; MALE; NORTH CAROLINA; PILOT PROJECTS; PLASMODIUM; SALIVARY PROTEINS AND PEPTIDES; SEASONS; TRAVEL; YOUNG ADULT;

EID: 84944710594     PISSN: None     EISSN: 17563305     Source Type: Journal    
DOI: 10.1186/s13071-015-1160-3     Document Type: Article

References (45)

1. Nilsson SK, Childs LM, Buckee C, Marti M. Targeting human transmission biology for malaria elimination. PLoS Pathog. 2015;11(6):e1004871.
2. WHO Malaria Report 2014. WWMR. 2014.
3. Guerra CA, Gikandi PW, Tatem AJ, Noor AM, Smith DL, Hay SI, et al. The limits and intensity of Plasmodium falciparum transmission: implications for malaria control and elimination worldwide. PLoS Med. 2008;5(2):e38.
4. Quintero JP, Siqueira AM, Tobon A, Blair S, Moreno A, Arevalo-Herrera M, et al. Malaria-related anaemia: a Latin American perspective. Mem Inst Oswaldo Cruz. 2011;106 Suppl 1:91-104.
5. Barabutis N, Siejka A, Schally AV, Block NL, Cai R, Varga JL. Activation of mitogen-activated protein kinases by a splice variant of GHRH receptor. J Mol Endocrinol. 2010;44(2):127-34.
6. Schneider BS, Higgs S. The enhancement of arbovirus transmission and disease by mosquito saliva is associated with modulation of the host immune response. Trans R Soc Trop Med Hyg. 2008;102(5):400-8.
7. Schneider BS, Mathieu C, Peronet R, Mecheri S. Anopheles stephensi saliva enhances progression of cerebral malaria in a murine model. Vector Borne Zoonotic Dis. 2011;11(4):423-32.
8. Rajamanonmani R, Nkenfou C, Clancy P, Yau YH, Shochat SG, Sukupolvi-Petty S, et al. On a mouse monoclonal antibody that neutralizes all four dengue virus serotypes. J Gen Virol. 2009;90(Pt 4):799-809.
9. Birley MH, Charlewood JD. Sporozoite rate and malaria prevalence. Parasitol Today. 1987;3(8):231-2.
10. Duffy PE, Fried M. Malaria in the pregnant woman. Curr Top Microbiol Immunol. 2005;295:169-200.
11. Kline DL. Traps and trapping techniques for adult mosquito control. J Am Mosq Control Assoc. 2006;22(3):490-6.
12. Mboera LE. Sampling techniques for adult Afrotropical malaria vectors and their reliability in the estimation of entomological inoculation rate. Tanzan Health Res Bull. 2005;7(3):117-24.
13. Hiwat H, Andriessen R, Rijk M, Koenraadt CJ, Takken W. Carbon dioxide baited trap catches do not correlate with human landing collections of Anopheles aquasalis in Suriname. Mem Inst Oswaldo Cruz. 2011;106(3):360-4.
14. Margos G, Navarette S, Butcher G, Davies A, Willers C, Sinden RE, et al. Interaction between host complement and mosquito-midgut-stage Plasmodium berghei. Infect Immun. 2001;69(8):5064-71.
15. Londono-Renteria BL, Eisele TP, Keating J, James MA, Wesson DM. Antibody response against Anopheles albimanus (Diptera: Culicidae) salivary protein as a measure of mosquito bite exposure in Haiti. J Med Entomol. 2010;47(6):1156-63.
16. Londono-Renteria B, Cardenas JC, Cardenas LD, Christofferson RC, Chisenhall DM, Wesson DM, et al. Use of anti-Aedes aegypti salivary extract antibody concentration to correlate risk of vector exposure and dengue transmission risk in Colombia. PLoS One. 2013;8(12):e81211.
17. Lombardo F, Ronca R, Rizzo C, Mestres-Simon M, Lanfrancotti A, Curra C, et al. The Anopheles gambiae salivary protein gSG6: an anopheline-specific protein with a blood-feeding role. Insect Biochem Mol Biol. 2009;39(7):457-66.
18. Ndille EE, Dubot-Peres A, Doucoure S, Mouchet F, Cornelie S, Sidavong B, et al. Human IgG antibody response to Aedes aegypti Nterm-34 kDa salivary peptide as an indicator to identify areas at high risk for dengue transmission: a retrospective study in urban settings of Vientiane city, Lao PDR. Trop Med Int Health. 2014;19(5):576-80.
19. Ribeiro JM, Mans BJ, Arca B. An insight into the sialome of blood-feeding Nematocera. Insect Biochem Mol Biol. 2010;40(11):767-84.
20. Poinsignon A, Cornelie S, Mestres-Simon M, Lanfrancotti A, Rossignol M, Boulanger D, et al. Novel peptide marker corresponding to salivary protein gSG6 potentially identifies exposure to Anopheles bites. PLoS One. 2008;3(6):e2472.
21. Poinsignon A, Cornelie S, Ba F, Boulanger D, Sow C, Rossignol M, et al. Human IgG response to a salivary peptide, gSG6-P1, as a new immunoepidemiological tool for evaluating low-level exposure to Anopheles bites. Malar J. 2009;8:198.
22. Sagna AB, Sarr JB, Gaayeb L, Drame PM, Ndiath MO, Senghor S, et al. gSG6-P1 salivary biomarker discriminates micro-geographical heterogeneity of human exposure to Anopheles bites in low and seasonal malaria areas. Parasit Vectors. 2013;6:68.
23. Drame PM, Machault V, Diallo A, Cornelie S, Poinsignon A, Lalou R, et al. IgG responses to the gSG6-P1 salivary peptide for evaluating human exposure to Anopheles bites in urban areas of Dakar region, Senegal. Malar J. 2012;11:72.
24. Rizzo C, Ronca R, Fiorentino G, Verra F, Mangano V, Poinsignon A, et al. Humoral response to the Anopheles gambiae salivary protein gSG6: a serological indicator of exposure to Afrotropical malaria vectors. PLoS One. 2011;6(3):e17980.
25. Orlandi-Pradines E, Almeras L, Denis de Senneville L, Barbe S, Remoue F, Villard C, et al. Antibody response against saliva antigens of Anopheles gambiae and Aedes aegypti in travellers in tropical Africa. Microbes Infect. 2007;9(12-13):1454-62.
26. Drame PM, Poinsignon A, Besnard P, Cornelie S, Le Mire J, Toto JC, et al. Human antibody responses to the Anopheles salivary gSG6-P1 peptide: a novel tool for evaluating the efficacy of ITNs in malaria vector control. PLoS One. 2010;5(12):e15596.
27. Drame PM, Diallo A, Poinsignon A, Boussari O, Dos Santos S, Machault V, et al. Evaluation of the effectiveness of malaria vector control measures in urban settings of Dakar by a specific anopheles salivary biomarker. PLoS One. 2013;8(6):e66354.
28. Hobbs JH, Sexton JD, St Jean Y, Jacques JR. The biting and resting behavior of Anopheles albimanus in northern Haiti. J Am Mosq Control Assoc. 1986;2(2):150-3.
29. Mekuria Y, Williams DC, Tidwell MA, Santana TA. Studies of the susceptibility of Anopheles albimanus and Anopheles vestitipennis from Dajabon, Dominican Republic, to insecticides. J Am Mosq Control Assoc. 1990;6(4):645-50.
30. Molina AM. Sistemas de Informacion Geografica para el Analisis de la Distribucion Espacial de la Malaria en Colombia. Revista EIA. 2008;9:20.
31. Víctor Alberto Olano HLB, Sáenz R, Quiñones ML, Molina JA. Mapas preliminares de la distribución de especies de Anopheles vectores de malaria en Colombia. Biomedica. 2001;21(4):7.
32. Padley D, Moody AH, Chiodini PL, Saldanha J. Use of a rapid, single-round, multiplex PCR to detect malarial parasites and identify the species present. Ann Trop Med Parasitol. 2003;97(2):131-7.
33. Calvo E, Andersen J, Francischetti IM, deL Capurro M, deBianchi AG, James AA, et al. The transcriptome of adult female Anopheles darlingi salivary glands. Insect Mol Biol. 2004;13(1):73-88.
34. Calvo E, Pham VM, Marinotti O, Andersen JF, Ribeiro JM. The salivary gland transcriptome of the neotropical malaria vector Anopheles darlingi reveals accelerated evolution of genes relevant to hematophagy. BMC Genomics. 2009;10:57.
35. Rizzo C, Ronca R, Fiorentino G, Mangano VD, Sirima SB, Nebie I, et al. Wide cross-reactivity between Anopheles gambiae and Anopheles funestus SG6 salivary proteins supports exploitation of gSG6 as a marker of human exposure to major malaria vectors in tropical Africa. Malar J. 2011;10:206.
36. Nagarajan S, Chesla S, Cobern L, Anderson P, Zhu C, Selvaraj P. Ligand binding and phagocytosis by CD16 (Fc gamma receptor III) isoforms. Phagocytic signaling by associated zeta and gamma subunits in Chinese hamster ovary cells. J Biol Chem. 1995;270(43):25762-70.
37. Rodriguez JC, Uribe GA, Araujo RM, Narvaez PC, Valencia SH. Epidemiology and control of malaria in Colombia. Mem Inst Oswaldo Cruz. 2011;106 Suppl 1:114-22.
38. Badu K, Siangla J, Larbi J, Lawson BW, Afrane Y, Ong'echa J, et al. Variation in exposure to Anopheles gambiae salivary gland peptide (gSG6-P1) across different malaria transmission settings in the western Kenya highlands. Malar J. 2012;11:318.
39. Stone W, Bousema T, Jones S, Gesase S, Hashim R, Gosling R, et al. IgG responses to Anopheles gambiae salivary antigen gSG6 detect variation in exposure to malaria vectors and disease risk. PLoS One. 2012;7(6):e40170.
40. Olano VA, Brochero H, Sáenz R, Quiñones M, Molina J. Mapas preliminares de la distribución de especies de Anopheles vectores de malaria en Colombia. Biomedica. 2001;21(4):4.
41. Olano V, Carrasquilla G, Mendez F. [Transmission of urban malaria in Buenaventrua, Colombia: entomological features]. Pan Am J Public Health. 1997;1(4):287-94.
42. Caillouet KA, Keating J, Eisele TP. Characterization of aquatic mosquito habitat, natural enemies, and immature mosquitoes in the Artibonite Valley, Haiti. J Vector Ecol. 2008;33(1):191-7.
43. Kiszewski A, Mellinger A, Spielman A, Malaney P, Sachs SE, Sachs J. A global index representing the stability of malaria transmission. AmJTrop Med Hyg. 2004;70(5):486-98.
44. Kuadkitkan A, Wikan N, Fongsaran C, Smith DR. Identification and characterization of prohibitin as a receptor protein mediating DENV-2 entry into insect cells. Virology. 2010;406(1):149-61.
45. Ribeiro JM, Arca B, Lombardo F, Calvo E, Phan VM, Chandra PK, et al. An annotated catalogue of salivary gland transcripts in the adult female mosquito, Aedes aegypti. BMC Genomics. 2007;8:6.