Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites

Background: Malaria is the major parasitic disease worldwide caused by Plasmodium infection. The objective of integrated malaria control programs is to decrease malaria transmission, which needs specific tools to be accurately assessed. In areas where the transmission is low or has been substantially reduced, new complementary tools have to be developed to improve surveillance. A recent approach, based on the human antibody response to Anopheles salivary proteins, has been shown to be efficient in evaluating human exposure to Anopheles bites. The aim of the present study was to identify new An. gambiae salivary proteins as potential candidate biomarkers of human exposure to P. falciparum-infective bites. Methods: Experimental infections of An. gambiae by wild P. falciparum were carried out in semi-field conditions. Then a proteomic approach, combining 2D-DIGE and mass spectrometry, was used to identify the overexpressed salivary proteins in infected salivary glands compared to uninfected An. gambiae controls. Subsequently, a peptide design of each potential candidate was performed in silico and their antigenicity was tested by an epitope-mapping technique using blood from individuals exposed to Anopheles bites. Results: Five salivary proteins (gSG6, gSG1b, TRIO, SG5 and long form D7) were overexpressed in the infected salivary glands. Eighteen peptides were designed from these proteins and were found antigenic in children exposed to the Anopheles bites. Moreover, the results showed that the presence of wild P. falciparum in salivary glands modulates the expression of several salivary proteins and also appeared to induce post-translational modifications. Conclusions: This study is, to our knowledge, the first that compares the sialome of An. gambiae both infected and not infected by wild P. falciparum, making it possible to mimic the natural conditions of infection. This is a first step toward a better understanding of the close interactions between the parasite and the salivary gland of mosquitoes. In addition, these results open the way to define biomarkers of infective bites of Anopheles, which could, in the future, improve the estimation of malaria transmission and the evaluation of malaria vector control tools.

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Main Authors: Marie, Alexandra, Holzmuller, Philippe, Tchioffo, Majoline T., Rossignol, Marie, Demettre, Edith, Seveno, Martial, Corbel, Vincent, Awono-Ambéné, Parfait, Morlais, Isabelle, Remoue, Franck, Cornelie, Sylvie
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Language:eng
Subjects:L73 - Maladies des animaux, L72 - Organismes nuisibles des animaux,
Online Access:http://agritrop.cirad.fr/575732/
http://agritrop.cirad.fr/575732/1/document_575732.pdf
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spelling dig-cirad-fr-5757322022-04-15T09:45:42Z http://agritrop.cirad.fr/575732/ http://agritrop.cirad.fr/575732/ Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites. Marie Alexandra, Holzmuller Philippe, Tchioffo Majoline T., Rossignol Marie, Demettre Edith, Seveno Martial, Corbel Vincent, Awono-Ambéné Parfait, Morlais Isabelle, Remoue Franck, Cornelie Sylvie. 2014. Parasites and Vectors, 7 (599), 13 p.https://doi.org/10.1186/s13071-014-0599-y <https://doi.org/10.1186/s13071-014-0599-y> Researchers Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites Marie, Alexandra Holzmuller, Philippe Tchioffo, Majoline T. Rossignol, Marie Demettre, Edith Seveno, Martial Corbel, Vincent Awono-Ambéné, Parfait Morlais, Isabelle Remoue, Franck Cornelie, Sylvie eng 2014 Parasites and Vectors L73 - Maladies des animaux L72 - Organismes nuisibles des animaux Background: Malaria is the major parasitic disease worldwide caused by Plasmodium infection. The objective of integrated malaria control programs is to decrease malaria transmission, which needs specific tools to be accurately assessed. In areas where the transmission is low or has been substantially reduced, new complementary tools have to be developed to improve surveillance. A recent approach, based on the human antibody response to Anopheles salivary proteins, has been shown to be efficient in evaluating human exposure to Anopheles bites. The aim of the present study was to identify new An. gambiae salivary proteins as potential candidate biomarkers of human exposure to P. falciparum-infective bites. Methods: Experimental infections of An. gambiae by wild P. falciparum were carried out in semi-field conditions. Then a proteomic approach, combining 2D-DIGE and mass spectrometry, was used to identify the overexpressed salivary proteins in infected salivary glands compared to uninfected An. gambiae controls. Subsequently, a peptide design of each potential candidate was performed in silico and their antigenicity was tested by an epitope-mapping technique using blood from individuals exposed to Anopheles bites. Results: Five salivary proteins (gSG6, gSG1b, TRIO, SG5 and long form D7) were overexpressed in the infected salivary glands. Eighteen peptides were designed from these proteins and were found antigenic in children exposed to the Anopheles bites. Moreover, the results showed that the presence of wild P. falciparum in salivary glands modulates the expression of several salivary proteins and also appeared to induce post-translational modifications. Conclusions: This study is, to our knowledge, the first that compares the sialome of An. gambiae both infected and not infected by wild P. falciparum, making it possible to mimic the natural conditions of infection. This is a first step toward a better understanding of the close interactions between the parasite and the salivary gland of mosquitoes. In addition, these results open the way to define biomarkers of infective bites of Anopheles, which could, in the future, improve the estimation of malaria transmission and the evaluation of malaria vector control tools. article info:eu-repo/semantics/article Journal Article info:eu-repo/semantics/publishedVersion http://agritrop.cirad.fr/575732/1/document_575732.pdf application/pdf Cirad license info:eu-repo/semantics/openAccess https://agritrop.cirad.fr/mention_legale.html https://doi.org/10.1186/s13071-014-0599-y 10.1186/s13071-014-0599-y info:eu-repo/semantics/altIdentifier/doi/10.1186/s13071-014-0599-y info:eu-repo/semantics/altIdentifier/purl/https://doi.org/10.1186/s13071-014-0599-y
institution CIRAD FR
collection DSpace
country Francia
countrycode FR
component Bibliográfico
access En linea
databasecode dig-cirad-fr
tag biblioteca
region Europa del Oeste
libraryname Biblioteca del CIRAD Francia
language eng
topic L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
spellingShingle L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
Marie, Alexandra
Holzmuller, Philippe
Tchioffo, Majoline T.
Rossignol, Marie
Demettre, Edith
Seveno, Martial
Corbel, Vincent
Awono-Ambéné, Parfait
Morlais, Isabelle
Remoue, Franck
Cornelie, Sylvie
Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
description Background: Malaria is the major parasitic disease worldwide caused by Plasmodium infection. The objective of integrated malaria control programs is to decrease malaria transmission, which needs specific tools to be accurately assessed. In areas where the transmission is low or has been substantially reduced, new complementary tools have to be developed to improve surveillance. A recent approach, based on the human antibody response to Anopheles salivary proteins, has been shown to be efficient in evaluating human exposure to Anopheles bites. The aim of the present study was to identify new An. gambiae salivary proteins as potential candidate biomarkers of human exposure to P. falciparum-infective bites. Methods: Experimental infections of An. gambiae by wild P. falciparum were carried out in semi-field conditions. Then a proteomic approach, combining 2D-DIGE and mass spectrometry, was used to identify the overexpressed salivary proteins in infected salivary glands compared to uninfected An. gambiae controls. Subsequently, a peptide design of each potential candidate was performed in silico and their antigenicity was tested by an epitope-mapping technique using blood from individuals exposed to Anopheles bites. Results: Five salivary proteins (gSG6, gSG1b, TRIO, SG5 and long form D7) were overexpressed in the infected salivary glands. Eighteen peptides were designed from these proteins and were found antigenic in children exposed to the Anopheles bites. Moreover, the results showed that the presence of wild P. falciparum in salivary glands modulates the expression of several salivary proteins and also appeared to induce post-translational modifications. Conclusions: This study is, to our knowledge, the first that compares the sialome of An. gambiae both infected and not infected by wild P. falciparum, making it possible to mimic the natural conditions of infection. This is a first step toward a better understanding of the close interactions between the parasite and the salivary gland of mosquitoes. In addition, these results open the way to define biomarkers of infective bites of Anopheles, which could, in the future, improve the estimation of malaria transmission and the evaluation of malaria vector control tools.
format article
topic_facet L73 - Maladies des animaux
L72 - Organismes nuisibles des animaux
author Marie, Alexandra
Holzmuller, Philippe
Tchioffo, Majoline T.
Rossignol, Marie
Demettre, Edith
Seveno, Martial
Corbel, Vincent
Awono-Ambéné, Parfait
Morlais, Isabelle
Remoue, Franck
Cornelie, Sylvie
author_facet Marie, Alexandra
Holzmuller, Philippe
Tchioffo, Majoline T.
Rossignol, Marie
Demettre, Edith
Seveno, Martial
Corbel, Vincent
Awono-Ambéné, Parfait
Morlais, Isabelle
Remoue, Franck
Cornelie, Sylvie
author_sort Marie, Alexandra
title Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
title_short Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
title_full Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
title_fullStr Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
title_full_unstemmed Anopheles gambiae salivary protein expression modulated by wild Plasmodium falciparum infection: Highlighting of new antigenic peptides as candidates of An. gambiae bites
title_sort anopheles gambiae salivary protein expression modulated by wild plasmodium falciparum infection: highlighting of new antigenic peptides as candidates of an. gambiae bites
url http://agritrop.cirad.fr/575732/
http://agritrop.cirad.fr/575732/1/document_575732.pdf
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