Author(s): E. Nieves , Y. Sánchez , H. Sánchez , M. Rondón, N. González & J. Carrero
Journal: Journal of Vector Borne Diseases
ISSN 0972-9062
Volume: 49;
Issue: 1;
Start page: 8;
Date: 2012;
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Keywords: Immunogenicity | leishmaniasis | Phlebotominae | salivary proteins
ABSTRACT
Background & objectives: The saliva of the Phlebotominae is highly immunogenic to the vertebrate host and isa determining factor in the Leishmania infection. The aim of this work was to study the saliva of Lutzomyiaovallesi as a possible risk marker for the transmission of Leishmania.Methods: Two populations of L. ovallesi from different geographical areas and subjected to different environmentalconditions were compared by geometric morphometry of the wings, by protein profile analysis of salivary glandsand by assessing the presence of anti-saliva protein in human sera confronted with laboratory L. ovallesi saliva.Results: The results showed differences in the isometric size and structure of the wings but no allometric effects.Protein profiles of salivary glands of both the L. ovallesi populations studied were found to be similar, based on11 protein bands with molecular weights ranging from 16 to 99 kDa. Anti-saliva antibodies were present inhuman sera, but human sera infected and uninfected with leishmaniasis could not be differentiated.Interpretation & conclusion: We conclude that the saliva of laboratory-reared L. ovallesi is representative ofthat of the wild population. It is suggested to study the presence of anti-saliva antibodies in other species ofsandflies and mosquitoes
Journal: Journal of Vector Borne Diseases
ISSN 0972-9062
Volume: 49;
Issue: 1;
Start page: 8;
Date: 2012;
VIEW PDF
DOWNLOAD PDF Original pageKeywords: Immunogenicity | leishmaniasis | Phlebotominae | salivary proteins
ABSTRACT
Background & objectives: The saliva of the Phlebotominae is highly immunogenic to the vertebrate host and isa determining factor in the Leishmania infection. The aim of this work was to study the saliva of Lutzomyiaovallesi as a possible risk marker for the transmission of Leishmania.Methods: Two populations of L. ovallesi from different geographical areas and subjected to different environmentalconditions were compared by geometric morphometry of the wings, by protein profile analysis of salivary glandsand by assessing the presence of anti-saliva protein in human sera confronted with laboratory L. ovallesi saliva.Results: The results showed differences in the isometric size and structure of the wings but no allometric effects.Protein profiles of salivary glands of both the L. ovallesi populations studied were found to be similar, based on11 protein bands with molecular weights ranging from 16 to 99 kDa. Anti-saliva antibodies were present inhuman sera, but human sera infected and uninfected with leishmaniasis could not be differentiated.Interpretation & conclusion: We conclude that the saliva of laboratory-reared L. ovallesi is representative ofthat of the wild population. It is suggested to study the presence of anti-saliva antibodies in other species ofsandflies and mosquitoes
