Abstract

Synthetic peptide vaccines were designed to target the neuropeptides innervating Ixodes ricinus salivary glands and hindgut and they were tested for their capacity to afford protective immunity against nymphs or larvae and Anaplasma phagocytophilum-infected nymph infestation, in mice and sheep, respectively. In both models, the assembly of SIFamide (SIFa) or myoinhibitory peptide (MIP) neuropeptides into multiple antigenic peptide constructs (MAPs) elicited a robust IgG antibody response following immunization. Nevertheless, no observable detrimental impact on nymphs was evidenced in mice, and, unfortunately, the number of engorged nymphs on sheep was insufficient for firm conclusions to be drawn, including for bacterial transmission. Regarding larvae, while vaccination of the sheep did not globally diminish tick feeding success or development, analyses of animals at the individual level revealed a negative correlation between anti-SIFa and MIP antibody levels and larva-to-nymph molting success for both antigens. Our results provide a proof of principle and precedent for the use of MAPs for the induction of immunity against tick peptide molecules. Although the present study did not provide the expected level of protection, it inaugurates a new strategy for protection against ticks based on the immunological targeting of key components of their nervous system.

Highlights

  • Among the 27 most important vector-borne diseases of humans listed by the World HealthOrganization (WHO), six are tick-borne diseases

  • The vaccine candidates were synthetized as multiple antigenic peptides multiple antigenic peptide constructs (MAPs) in which four copies of the same peptide were formulated on a lysine-based backbone (LifeTein, New Jersey, NJ, USA)

  • Based on the results obtained here, we conclude that vaccine-mediated protection against nymphs in mice and larvae on sheep could not be demonstrated in the present study, despite a promising negative correlation between antibody levels of anti-myoinhibitory peptide (MIP) and larva to nymph molting success

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Summary

Introduction

Among the 27 most important vector-borne diseases of humans listed by the World HealthOrganization (WHO), six are tick-borne diseases. Ixodes ricinus is the most abundant and widespread tick species in Europe and owing to both socio-economic and environmental changes exhibits ongoing changes in its distribution with respect to previously recognized endemic zones [2]. An attractive strategy for controlling ticks is based on the identification of tick molecules of critical importance in the tick life cycle that could represent protective antigens on which anti-tick vaccines could be based [4]. This concept holds the promise of establishing an effective and environmentally benign control measure for these medically important arthropods along with the pathogens they transmit [5,6,7]. For the anti-tick vaccines developed to date, protection appears to be provided by vaccine-elicited antibodies that are ingurgitated with blood and that interact with the targeted antigen within the tick body, thereby interfering with its biological function

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