Immunity to Lutzomyia whitmani Saliva Protects against Experimental Leishmania braziliensis Infection

PLoS Negl Trop Dis. 2016 Nov 3;10(11):e0005078. doi: 10.1371/journal.pntd.0005078. eCollection 2016 Nov.

Abstract

Background: Previous works showed that immunization with saliva from Lutzomyia intermedia, a vector of Leishmania braziliensis, does not protect against experimental infection. However, L. braziliensis is also transmitted by Lutzomyia whitmani, a sand fly species closely related to Lu. intermedia. Herein we describe the immune response following immunization with Lu. whitmani saliva and the outcome of this response after L. braziliensis infection.

Methods and findings: BALB/c mice immunized with Lu. whitmani saliva developed robust humoral and cellular immune responses, the latter characterized by an intense cellular infiltrate and production of IFN-γ and IL-10, by both CD4+ and CD8+ cells. Mice immunized as above and challenged with L. braziliensis plus Lu. whitmani saliva displayed significantly smaller lesions and parasite load at the challenge site. This protection was associated with a higher (p<0.05) IFN-γ production in response to SLA stimulation. Long-term persisting immunity was also detected in mice immunized with Lu. whitmani saliva. Furthermore, individuals residing in an endemic area for cutaneous leishmaniasis (CL) presented antibody responses to Lu. whitmani saliva. However CL patients, with active lesions, displayed a lower humoral response to Lu. whitmani saliva compared to individuals with subclinical Leishmania infection.

Conclusion: Pre-exposure to Lu. whitmani saliva induces protection against L. braziliensis in a murine model. We also show that Lu. whitmani salivary proteins are immunogenic in naturally exposed individuals. Our results reinforce the importance of investigating the immunomodulatory effect of saliva from different species of closely related sand flies.

MeSH terms

  • Animals
  • Antibodies, Protozoan / blood
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Disease Models, Animal
  • Female
  • Humans
  • Immunity, Cellular
  • Immunity, Humoral
  • Immunization
  • Immunoglobulin G / blood
  • Immunomodulation
  • Insect Vectors / immunology*
  • Insect Vectors / parasitology
  • Interferon-gamma / immunology
  • Interleukin-10 / immunology
  • Leishmania braziliensis / immunology*
  • Leishmaniasis, Cutaneous / immunology*
  • Leishmaniasis, Cutaneous / parasitology
  • Leishmaniasis, Cutaneous / prevention & control
  • Mice
  • Mice, Inbred BALB C
  • Parasite Load
  • Prospective Studies
  • Psychodidae / immunology*
  • Psychodidae / parasitology
  • Saliva / chemistry
  • Saliva / immunology*
  • Salivary Proteins and Peptides / immunology*

Substances

  • Antibodies, Protozoan
  • Immunoglobulin G
  • Salivary Proteins and Peptides
  • Interleukin-10
  • Interferon-gamma

Grants and funding

This work was funded in part by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq - 400695/2012-0) and Fundação de Amparo à Pesquisa da Bahia (FAPESB INT 0003/2013), Brazil. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.