Efficacy of the Vaccine Candidate Based on the P0 Peptide against Dermacentor nitens and Ixodes ricinus Ticks
Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
20-05736S
Czech Science Foundation
110RT0541
Programa Iberoamericano de Ciencia y Tecnología para el Desarrollo
Internal Grant
Centro de Ingeniería Genética y Biotecnología
Internal Grant
nstituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Portugal
PubMed
38003829
PubMed Central
PMC10675505
DOI
10.3390/pathogens12111365
PII: pathogens12111365
Knihovny.cz E-zdroje
- Klíčová slova
- P0 protein, anti-tick vaccine, tick control, ticks, vaccination,
- Publikační typ
- časopisecké články MeSH
The control of ticks through vaccination offers a sustainable alternative to the use of chemicals that cause contamination and the selection of resistant tick strains. However, only a limited number of anti-tick vaccines have reached commercial realization. In this sense, an antigen effective against different tick species is a desirable target for developing such vaccines. A peptide derived from the tick P0 protein (pP0) conjugated to a carrier protein has been demonstrated to be effective against the Rhipicephalus microplus, Rhipicephalus sanguineus, and Amblyomma mixtum tick species. The aim of this work was to assess the efficacy of this peptide when conjugated to the Bm86 protein against Dermacentor nitens and Ixodes ricinus ticks. An RNAi experiment using P0 dsRNA from I. ricinus showed a dramatic reduction in the feeding of injected female ticks on guinea pigs. In the follow-up vaccination experiments, rabbits were immunized with the pP0-Bm86 conjugate and challenged simultaneously with larvae, nymphs, and the adults of I. ricinus ticks. In the same way, horses were immunized with the pP0-Bm86 conjugate and challenged with D. nitens larva. The pP0-Bm86 conjugate showed efficacies of 63% and 55% against I. ricinus and D. nitens ticks, respectively. These results, combined with previous reports of efficacy for this conjugate, show the promising potential for its development as a broad-spectrum anti-tick vaccine.
Center for Genetic Engineering and Biotechnology 31st Avenue and 190 Havana 10600 Cuba
Instituto de Saúde Ambiental Faculdade de Medicina Universidade de Lisboa 1649 004 Lisboa Portugal
National Laboratory of Parasitology Avenue San Antonio Rincón Km 1 1 2 Artemisa 32500 Cuba
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Bickerton M., Rochlin I., González J., McSorley K., Toledo A. Field applications of granular and liquid pyrethroids, carbaryl, and IGRs to control the asian longhorned tick (Haemaphysalis longicornis) and impacts on nontarget invertebrates. Ticks Tick-Borne Dis. 2022;13:102054. doi: 10.1016/j.ttbdis.2022.102054. PubMed DOI
Mutavi F., Heitkönig I., Wieland B., Aarts N., Van Paassen A. Tick treatment practices in the field: Access to, knowledge about, and on-farm use of acaricides in Laikipia, Kenya. Ticks Tick-Borne Dis. 2021;12:101757. doi: 10.1016/j.ttbdis.2021.101757. PubMed DOI
Dhang P., Koehler P., Pereira R., Dye II D.D. Key Questions in Urban Pest Management: A Study and Revision Guide. CAB International; Oxfordshire, UK: 2022.
Kunz S.E., Kemp D.H. Insecticides and acaricides: Resistance and environmental impact. Rev. Sci. Tech. 1994;13:1249–1286. doi: 10.20506/rst.13.4.816. PubMed DOI
Agwunobi D.O., Yu Z., Liu J. A retrospective review on ixodid tick resistance against synthetic acaricides: Implications and perspectives for future resistance prevention and mitigation. Pestic. Biochem. Physiol. 2021;173:104776. doi: 10.1016/j.pestbp.2021.104776. PubMed DOI
De Rouck S., İnak E., Dermauw W., Van Leeuwen T. A review of the molecular mechanisms of acaricide resistance in mites and ticks. Insect Biochem. Mol. Biol. 2023;159:103981. doi: 10.1016/j.ibmb.2023.103981. PubMed DOI
Klafke G.M., Miller R.J., Tidwell J.P., Thomas D.B., Sanchez D., Feria Arroyo T.P., Perez de Leon A.A. High-resolution melt (HRM) analysis for detection of SNPs associated with pyrethroid resistance in the southern cattle fever tick, Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) Int. J. Parasitol. Drugs Drug Resist. 2019;9:100–111. doi: 10.1016/j.ijpddr.2019.03.001. PubMed DOI PMC
Sagar S.V., Saini K., Sharma A.K., Kumar S., Kumar R., Fular A., Shakya M., Upadhaya D., Nagar G., Samanta S., et al. Acaricide resistance in Rhipicephalus microplus collected from selected districts of Madhy Pradesh, Uttar Pradesh and Punjab states of India. Trop. Anim. Health Prod. 2019;52:611–618. doi: 10.1007/s11250-019-02048-0. PubMed DOI
Rodríguez-Valle M., Mendez L., Valdez M., Redondo M., Montero Espinosa C., Vargas M., Lleonart Cruz R.L., Pérez Barrios H., Seoane G., Serrano Ramirez E., et al. Integrated control of Boophilus microplus ticks in Cuba based on vaccination with the anti-tick vaccine GavacTM. Exp. Appl. Acarol. 2004;34:375–382. doi: 10.1007/s10493-004-1389-6. PubMed DOI
Suarez M., Rubi J., Pérez D., Cordova V., Salazar Y., Vielma A., Barrios F., Gil C.A., Segura N., Carrillo Y., et al. High impact and effectiveness of Gavac™ vaccine in the national program for control of bovine ticks Rhipicephalus microplus in Venezuela. Livest. Sci. 2016;187:48–52. doi: 10.1016/j.livsci.2016.02.005. DOI
De la Fuente J., Estrada-Peña A. Why New Vaccines for the Control of Ectoparasite Vectors Have Not Been Registered and Commercialized? Vaccines. 2019;7:75. doi: 10.3390/vaccines7030075. PubMed DOI PMC
Smith D.R., Hungerford J., Willadsen P., Cobon G.S. The development of TickGARD: A commercial vaccine against the cattle tick Boophilus microplus; Proceedings of the 8th International Congress of Parasitology; Kuşadası, Turkey. 10–14 October 1994.
Alvarez D.O., Corona-González B., Rodríguez-Mallón A., Rodríguez Gonzalez I., Alfonso P., Noda Ramos A.A., Díaz-Sánchez A.A., González Navarrete M., Rodríguez Fernández R., Méndez Mellor L. Ticks and tick-borne diseases in Cuba, half a century of scientific research. Pathogens. 2020;9:616. doi: 10.3390/pathogens9080616. PubMed DOI PMC
Encinosa Guzmán P.E., Fernández C., Cano Argüelles A.L., Fuentes Castillo A., García Y., Rodríguez R., Fernández Y., Bello Y., González Y., Mendez L., et al. Characterization of two Cuban colonies of Rhipicephalus microplus ticks. Vet. Parasitol. Reg. Stud. Rep. 2021;25:100591. doi: 10.1016/j.vprsr.2021.100591. PubMed DOI
Šlapeta J., Chandra S., Halliday B. The “tropical lineage” of the brown dog tick Rhipicephalus sanguineus sensu lato identified as Rhipicephalus linnaei (Audouin, 1826) Int. J. Parasitol. 2021;51:431–436. doi: 10.1016/j.ijpara.2021.02.001. PubMed DOI
Encinosa P.E., Bello Y., Rodríguez-Mallon A. Genetic and biological characterization of a Cuban tick strain from Rhipicephalus sanguineus complex and its sensitivity to different chemical acaricides. Int. J. Acarol. 2016;42:18–25. doi: 10.1080/01647954.2015.1113309. DOI
Sanches G.S., Evora P.M., Mangold A.J., Jittapalapong S., Rodriguez-Mallon A., Guzman P.E., Bechara G.H., Camargo-Mathias M.I. Molecular, biological, and morphometric comparisons between different geographical populations of Rhipicephalus sanguineus sensu lato (Acari: Ixodidae) Vet. Parasitol. 2016;215:78–87. doi: 10.1016/j.vetpar.2015.11.007. PubMed DOI
Estrada-Peña A., Jongejan F. Ticks feeding on humans: A review of records on human-biting Ixodoidea with special reference to pathogen transmission. Exp. Appl. Acarol. 1999;23:685–715. doi: 10.1023/A:1006241108739. PubMed DOI
Dantas-Torres F., Figueredo L.A., Brandao-Filho S.P. Rhipicephalus sanguineus (Acari: Ixodidae), the brown dog tick, parasitizing humans in Brazil. Rev. Soc. Bras. Med. Trop. 2006;39:64–67. doi: 10.1590/S0037-86822006000100012. PubMed DOI
Dantas-Torres F. Biology and ecology of the brown dog tick, Rhipicephalus sanguineus. Parasit. Vectors. 2010;3:26. doi: 10.1186/1756-3305-3-26. PubMed DOI PMC
Encinosa P.E., García Y., Lleonart R., Aliaga D., Fernández Y., Bello Y., la Guardia C.d., González Y., Díaz A., Estrada M.P., et al. Morphological and molecular characterization supporting Amblyomma mixtum presence in Cuba. Ticks Tick-Borne Dis. 2021;12:101602. doi: 10.1016/j.ttbdis.2020.101602. PubMed DOI
Charles R.A., Bermúdez S., Banović P., Alvarez D.O., Díaz-Sánchez A.A., Corona-González B., Etter E.M.C., Rodríguez González I., Ghafar A., Jabbar A., et al. Ticks and Tick-Borne Diseases in Central America and the Caribbean: A One Health Perspective. Pathogens. 2021;10:1273. doi: 10.3390/pathogens10101273. PubMed DOI PMC
Kahl O., Gray J.S. The biology of Ixodes ricinus with emphasis on its ecology. Ticks Tick-Borne Dis. 2023;14:102114. doi: 10.1016/j.ttbdis.2022.102114. PubMed DOI
Gray J., Kahl O., Zintl A. What do we still need to know about Ixodes ricinus? Ticks Tick-Borne Dis. 2021;12:101682. doi: 10.1016/j.ttbdis.2021.101682. PubMed DOI
Rodríguez-Mallon A., Fernández E., Encinosa P.E., Bello Y., Méndez-Pérez L., Cepero L., Pérez D., González M., Garay H., Reyes O., et al. A novel tick antigen shows high vaccine efficacy against the dog tick, Rhipicephalus sanguineus. Vaccine. 2012;30:1782–1789. doi: 10.1016/j.vaccine.2012.01.011. PubMed DOI
Sanchez-Madrid F., Vidales F.J., Ballesta J.P. Functional role of acidic ribosomal proteins. Interchangeability of proteins from bacterial and eukaryotic cells. Biochemistry. 1981;20:3263–3266. doi: 10.1021/bi00514a043. PubMed DOI
Kurtzman C.P. Description of Komagataella phaffii sp. nov. and the transfer of Pichia pseudopastoris to the methylotrophic yeast genus Komagataella. Int. J. Syst. Evol. Microbiol. 2005;55:973–976. doi: 10.1099/ijs.0.63491-0. PubMed DOI
Canales M., Enriquez A., Ramos E., Cabrera D., Dandie H., Soto A., Falcon V., Rodriguez M., de la Fuente J. Large-scale production in Pichia pastoris of the recombinant vaccine Gavac against cattle tick. Vaccine. 1997;15:414–422. doi: 10.1016/S0264-410X(96)00192-2. PubMed DOI
Garcia-Garcia J.C., Soto A., Nigro F., Mazza M., Joglar M., Hechevarria M., Lamberti J., de la Fuente J. Adjuvant and immunostimulating properties of the recombinant Bm86 protein expressed in Pichia pastoris. Vaccine. 1998;16:1053–1055. doi: 10.1016/S0264-410X(97)00266-1. PubMed DOI
Rodríguez-Mallon A., Encinosa P.E., Méndez-Pérez L., Bello Y., Rodríguez Fernández R., Garay H., Cabrales A., Méndez L., Borroto C., Estrada M. High efficacy of a 20 amino acid peptide of the acidic ribosomal protein P0 against the cattle tick, Rhipicephalus microplus. Ticks Tick-Borne Dis. 2015;6:530–537. doi: 10.1016/j.ttbdis.2015.04.007. PubMed DOI
Rodríguez-Mallon A., Encinosa Guzmán P.E., Bello Soto Y., Rosales Perdomo K., Montero Espinosa C., Vargas M., Estrada García M.P. A chemical conjugate of the tick P0 peptide is efficacious against Amblyomma mixtum. Transbound. Emerg. Dis. 2019;67:175–177. doi: 10.1111/tbed.13455. PubMed DOI
Rodriguez Mallon A., Javier Gonzalez L., Encinosa Guzman P.E., Bechara G.H., Sanches G.S., Pousa S., Cabrera G., Cabrales A., Garay H., Mejias R., et al. Functional and mass spectrometric evaluation of an anti-tick antigen based on the P0 peptide conjugated to Bm86 protein. Pathogens. 2020;9:513. doi: 10.3390/pathogens9060513. PubMed DOI PMC
González L.J., Encinosa Guzmán P.E., Machado W., Pousa S., Leyva A., Arguelles A.L.C., Cabrera G., Espinosa L.A., Parra R., Hernández R. Synthesis, LC-MS/MS analysis, and biological evaluation of two vaccine candidates against ticks based on the antigenic P0 peptide from R. sanguineus linked to the p64K carrier protein from Neisseria meningitidis. Anal. Bioanal. Chem. 2021;413:5885–5900. doi: 10.1007/s00216-021-03569-0. PubMed DOI PMC
Gong H., Liao M., Zhou J., Hatta T., Huang P., Zhang G., Kanuka H., Nishikawa Y., Xuan X., Fujisaki K. Gene silencing of ribosomal protein P0 is lethal to the tick Haemaphysalis longicornis. Vet. Parasitol. 2008;151:268–278. doi: 10.1016/j.vetpar.2007.11.015. PubMed DOI
Zhang Y., Cui J., Zhou Y., Cao J., Gong H., Zhang H., Zhou J. Liposome mediated double-stranded RNA delivery to silence ribosomal protein P0 in the tick Rhipicephalus haemaphysaloides. BMC Ecol. 2018;9:638–644. doi: 10.1016/j.ttbdis.2018.01.015. PubMed DOI PMC
de la Fuente J., Manzano-Roman R., Naranjo V., Kocan K.M., Zivkovic Z., Blouin E.F., Canales M., Almazan C., Galindo R.C., Step D.L., et al. Identification of protective antigens by RNA interference for control of the lone star tick, Amblyomma americanum. Vaccine. 2010;28:1786–1795. doi: 10.1016/j.vaccine.2009.12.007. PubMed DOI
Wojda I., Cytrynska M., Frajnt M., Jakubowicz T. Protein kinases CKI and CKII are implicated in modification of ribosomal proteins of the yeast Trichosporon cutaneum. Acta Biochim. Pol. 2002;49:947–957. doi: 10.18388/abp.2002_3754. PubMed DOI
Yacoub A., Kelley M.R., Deutsch W.A. Drosophila ribosomal protein PO contains apurinic/apyrimidinic endonuclease activity. Nucleic Acids Res. 1996;24:4298–4303. doi: 10.1093/nar/24.21.4298. PubMed DOI PMC
Sehgal A., Kumar N., Carruthers V.B., Sharma S. Translocation of ribosomal protein P0 onto the Toxoplasma gondii tachyzoite surface. Int. J. Parasitol. 2003;33:1589–1594. doi: 10.1016/S0020-7519(03)00267-4. PubMed DOI
Singh S., Sehgal A., Waghmare S., Chakraborty T., Goswami A., Sharma S. Surface expression of the conserved ribosomal protein P0 on parasite and other cells. Mol. Biochem. Parasitol. 2002;119:121–124. doi: 10.1016/S0166-6851(01)00394-2. PubMed DOI
Radulović Ž.M., Kim T.K., Porter L.M., Sze S.H., Lewis L., Mulenga A. A 24-48 h fed Amblyomma americanum tick saliva immuno-proteome. BMC Genom. 2014;15:518. doi: 10.1186/1471-2164-15-518. PubMed DOI PMC
Tirloni L., Reck J., Soares Terra R.M., Martins J.R., Mulenga A., Sherman N.E., Fox J.W., Yates J.R., Termignoni C., Pinto A.F.M., et al. Proteomic analysis of cattle tick Rhipicephalus (Boophilus) microplus saliva: A comparison between partially and fully engorged females. PLoS ONE. 2014;9:e94831. doi: 10.1371/journal.pone.0094831. PubMed DOI PMC
Coumou J., Wagemakers A., Trentelman J.J., Nijhof A.M., Hovius J.W. Vaccination against Bm86 homologues in rabbits does not impair Ixodes ricinus feeding or oviposition. PLoS ONE. 2014;10:e0123495. doi: 10.1371/journal.pone.0123495. PubMed DOI PMC
Garcia-Garcia J.C., Gonzalez I.L., Gonzalez D.M., Valdes M., Mendez L., Lamberti J., D’Agostino B., Citroni D., Fragoso H., Ortiz M., et al. Sequence variations in the Boophilus microplus Bm86 locus and implications for immunoprotection in cattle vaccinated with this antigen. Exp. Appl. Acarol. 1999;23:883–895. doi: 10.1023/A:1006270615158. PubMed DOI
Ben Said M., Galai Y., Mhadhbi M., Jedidi M., de la Fuente J., Darghouth M.A. Molecular characterization of Bm86 gene orthologs from Hyalomma excavatum, Hyalomma dromedarii and Hyalomma marginatum marginatum and comparison with a vaccine candidate from Hyalomma scupense. Vet. Parasitol. 2012;190:230–240. doi: 10.1016/j.vetpar.2012.05.017. PubMed DOI
Garcia-Garcia J.C., Montero C., Rodriguez M., Soto A., Redondo M., Valdes M., Mendez L., de la Fuente J. Effect of particulation on the immunogenic and protective properties of the recombinant Bm86 antigen expressed in Pichia pastoris. Vaccine. 1998;16:374–380. doi: 10.1016/S0264-410X(97)80915-2. PubMed DOI
de la Fuente J., Rodriguez M., Montero C., Redondo M., Garcia-Garcia J.C., Mendez L., Serrano E., Valdes M., Enriquez A., Canales M., et al. Vaccination against ticks (Boophilus spp.): The experience with the Bm86-based vaccine GavacTM. Genet. Anal. 1999;15:143–148. doi: 10.1016/S1050-3862(99)00018-2. PubMed DOI
NRC . Guide for the Care and Use of Laboratory Animals: Eighth Edition. The National Academies Press; Washington, DC, USA: 2011.
Fuentes Castillo A., Armenteros Zaldívar Y., Ledesma Bravo F.L., Bello Soto Y., Rodríguez Fernández R., Méndez L. Obtaining Dermacentor nitens Ticks (Neumann, 1897) (Acari: Ixodidae) in Cattle in BioTicks. Elfos Scientiae; Varadero, Cuba: 2022.
Untergasser A., Cutcutache I., Koressaar T., Ye J., Faircloth B.C., Remm M., Rozen S.G. Primer3—New capabilities and interfaces. Nucleic Acids Res. 2012;40:e115. doi: 10.1093/nar/gks596. PubMed DOI PMC
Hajdusek O., Sojka D., Kopacek P., Buresova V., Franta Z., Sauman I., Winzerling J., Grubhoffer L. Knockdown of proteins involved in iron metabolism limits tick reproduction and development. Proc. Natl. Acad. Sci. USA. 2009;106:1033–1038. doi: 10.1073/pnas.0807961106. PubMed DOI PMC
Perez-Perez D., Bechara G.H., Machado R.Z., Andrade G.M., Del Vecchio R.E., Pedroso M.S., Hernandez M.V., Farnos O. Efficacy of the Bm86 antigen against immature instars and adults of the dog tick Rhipicephalus sanguineus (Latreille, 1806) (Acari: Ixodidae) Vet. Parasitol. 2010;167:321–326. doi: 10.1016/j.vetpar.2009.09.034. PubMed DOI