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Identification of Highly Specific and Cross‐Reactive Antigens of Leishmania Species by Antibodies from Leishmania (Leishmania) chagasi Naturally Infected Dogs
Author(s) -
Vale A. M.,
Fujiwara R. T.,
Da Silva Neto A. F.,
Miret J. A.,
Alvarez D. C. C.,
Da Silva J. C. F.,
CamposNeto A.,
Reed S.,
Mayrink W.,
Nascimento E.
Publication year - 2009
Publication title -
zoonoses and public health
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.87
H-Index - 65
eISSN - 1863-2378
pISSN - 1863-1959
DOI - 10.1111/j.1863-2378.2008.01183.x
Subject(s) - antigen , leishmania chagasi , biology , heterologous , visceral leishmaniasis , virology , leishmaniasis , immunogen , leishmania , antibody , cross reactivity , leishmania braziliensis , immunology , microbiology and biotechnology , cutaneous leishmaniasis , cross reactions , genetics , parasite hosting , gene , monoclonal antibody , world wide web , computer science
Summary The Leishmania species present a genetic homology that ranges from 69 to 90%. Because of this homology, heterologous antigens have been used in the immunodiagnosis and vaccine development against Leishmania infections. In the current work, we describe the identification of species‐specific and cross‐reactive antigens among several New World Leishmania species, using symptomatic and asymptomatic naturally Leishmania chagasi ‐infected dog sera. Soluble antigens from five strains of New World Leishmania were separated by electrophoresis in SDS‐PAGE and immunoblotted. Different proteins were uniquely recognized in the L. chagasi panel by either symptomatic or asymptomatic dog sera suggesting their use as markers for the progression of disease and diagnosis of the initial (sub‐clinical) phase of the infection. Cross‐reactive antigens were identified using heterologous antigenic panels ( L. amazonensis strains PH8 and BH6, L. guyanensis and L. braziliensis ). L. guyanensis panel showed the highest cross‐reactivity against L. chagasi specific antibodies, suggesting that proteins from this extract might be suitable for the diagnosis of visceral canine leishmaniasis. Interestingly, the 51 and 97 kDa proteins of Leishmania were widely recognized (77.8% to 100%) among all antigenic panels tested, supporting their potential use for immunodiagnosis. Finally, we identified several leishmanial antigens that might be useful for routine diagnosis and seroepidemiological studies of the visceral canine leishmaniasis.