Gut membrane proteins as candidate antigens for immunization of mice against the tick Amblyomma sculptum

•Amblyomma sculptum is one the most important tick species in south America.•Few works have focused on the search for anti-A. sculptum vaccines.•Concealed gut proteins may be promissing vaccine antigens against A. sculptum.•A chimeric protein was constructed with promising efficacy against A. sculpt...

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Published inVaccine Vol. 42; no. 21; p. 126141
Main Authors Costa, Gabriel C.A., Ribeiro, Izabela C.T., Giunchetti, Rodolfo C., Gontijo, Nelder F., Sant'Anna, Mauricio R.V., Pereira, Marcos H., Pessoa, Grasielle C.D., Koerich, Leonardo B., Oliveira, Fabiano, Valenzuela, Jesus G., Fujiwara, Ricardo T., Bartholomeu, Daniella C., Araujo, Ricardo N.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 30.08.2024
Elsevier Limited
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Abstract •Amblyomma sculptum is one the most important tick species in south America.•Few works have focused on the search for anti-A. sculptum vaccines.•Concealed gut proteins may be promissing vaccine antigens against A. sculptum.•A chimeric protein was constructed with promising efficacy against A. sculptum.•Vaccine induced a reduction in female fertility and nymph mortality. Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins − AsMucin, AsAPP, and AsLAMP − and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.
AbstractList Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins - AsMucin, AsAPP, and AsLAMP - and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins - AsMucin, AsAPP, and AsLAMP - and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.
Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins − AsMucin, AsAPP, and AsLAMP − and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.
•Amblyomma sculptum is one the most important tick species in south America.•Few works have focused on the search for anti-A. sculptum vaccines.•Concealed gut proteins may be promissing vaccine antigens against A. sculptum.•A chimeric protein was constructed with promising efficacy against A. sculptum.•Vaccine induced a reduction in female fertility and nymph mortality. Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins − AsMucin, AsAPP, and AsLAMP − and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.
Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF). Tick gut proteins play an essential role in blood feeding, digestion, and protection of gut epithelium. Therefore, many of these were investigated as potential vaccine targets for tick-control strategies. The present study aimed to select transcripts corresponding to putative immunogenic proteins in the A. sculptum gut epithelial membrane, produce recombinant proteins and evaluate them as antigens against A. sculptum infestations. Three gut proteins - AsMucin, AsAPP, and AsLAMP - and a chimeric protein (rAsChimera) based on 22 peptides containing putative B cell epitopes from seven different gut proteins were evaluated as anti-A. sculptum antigens. Mice immunizations revealed that all recombinant targets elicited humoral response with significantly increased IgG levels compared to controls. For rAsChimera, IgG levels remained significantly higher than controls up to 75 days after the end of the immunization. Challenge trials revealed that vaccination with the chimeric protein was the most effective against A. sculptum, inducing 100 % nymph mortality and reaching 80.8 % efficacy against females. The other three proteins did not induce relevant protection, as AsAPP had only 26.6 % efficacy, whereas AsMucin and AsLAMP induced no protection. These data indicate that targeting gut protein immunogenic regions may be an effective strategy for a vaccine formulation againstA. sculptum.
ArticleNumber 126141
Author Koerich, Leonardo B.
Pessoa, Grasielle C.D.
Valenzuela, Jesus G.
Bartholomeu, Daniella C.
Ribeiro, Izabela C.T.
Sant'Anna, Mauricio R.V.
Giunchetti, Rodolfo C.
Oliveira, Fabiano
Araujo, Ricardo N.
Gontijo, Nelder F.
Pereira, Marcos H.
Fujiwara, Ricardo T.
Costa, Gabriel C.A.
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  givenname: Mauricio R.V.
  surname: Sant'Anna
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  givenname: Marcos H.
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  givenname: Grasielle C.D.
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  fullname: Pessoa, Grasielle C.D.
  organization: Department of Parasitology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
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  givenname: Leonardo B.
  surname: Koerich
  fullname: Koerich, Leonardo B.
  organization: Department of Parasitology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
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  givenname: Fabiano
  surname: Oliveira
  fullname: Oliveira, Fabiano
  organization: Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, United States
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  givenname: Jesus G.
  surname: Valenzuela
  fullname: Valenzuela, Jesus G.
  organization: Vector Molecular Biology Section, Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, United States
– sequence: 11
  givenname: Ricardo T.
  surname: Fujiwara
  fullname: Fujiwara, Ricardo T.
  organization: Department of Parasitology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
– sequence: 12
  givenname: Daniella C.
  surname: Bartholomeu
  fullname: Bartholomeu, Daniella C.
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  givenname: Ricardo N.
  orcidid: 0000-0002-1272-4386
  surname: Araujo
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  email: rnaraujo@icb.ufmg.br
  organization: Department of Parasitology, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil
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Keywords Concealed antigens
Anti-tick vaccine
Intestine
Gut epithelium
Hematophagy
Tick control
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Snippet •Amblyomma sculptum is one the most important tick species in south America.•Few works have focused on the search for anti-A. sculptum vaccines.•Concealed gut...
Amblyomma sculptum is widely distributed in Brazil and is the main vector of Rickettsia rickettsii, the causative agent of the Brazilian spotted fever (BSF)....
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SubjectTerms Amblyomma - immunology
Amblyomma sculptum
Amino acids
Animals
Anti-tick vaccine
Antigens
Antigens - immunology
Brazil
Cloning
Concealed antigens
Digestive system
Digestive tract
E coli
Effectiveness
Epithelium
Epitopes
Female
Females
Gut epithelium
Hematophagy
Immune response (humoral)
Immunization
Immunization - methods
Immunogenicity
Immunoglobulin G
Immunoglobulin G - blood
Immunoglobulin G - immunology
Intestine
Male
Membrane proteins
Membrane Proteins - genetics
Membrane Proteins - immunology
Membranes
Mice
Mice, Inbred BALB C
Peptides
Plasmids
Proteins
Recombinant Proteins - genetics
Recombinant Proteins - immunology
Rickettsia rickettsii - immunology
Tick control
Tick Infestations - immunology
Tick Infestations - prevention & control
Vaccines
Title Gut membrane proteins as candidate antigens for immunization of mice against the tick Amblyomma sculptum
URI https://dx.doi.org/10.1016/j.vaccine.2024.07.042
https://www.ncbi.nlm.nih.gov/pubmed/39033080
https://www.proquest.com/docview/3094374459
https://www.proquest.com/docview/3083216146/abstract/
Volume 42
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